Development of a colorectal cancer diagnostic model and dietary risk assessment through gut microbiome analysis

Colorectal cancer (CRC) is the third most common form of cancer and poses a critical public health threat due to the global spread of westernized diets high in meat, cholesterol, and fat. Although the link between diet and colorectal cancer has been well established, the mediating role of the gut mi...

Full description

Saved in:
Bibliographic Details
Published inExperimental & molecular medicine Vol. 51; no. 10; pp. 1 - 15
Main Authors Yang, Jinho, McDowell, Andrea, Kim, Eun Kyoung, Seo, Hochan, Lee, Won Hee, Moon, Chang-Mo, Kym, Sung-Min, Lee, Dong Ho, Park, Young Soo, Jee, Young-Koo, Kim, Yoon-Keun
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 03.10.2019
Springer Nature B.V
생화학분자생물학회
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Colorectal cancer (CRC) is the third most common form of cancer and poses a critical public health threat due to the global spread of westernized diets high in meat, cholesterol, and fat. Although the link between diet and colorectal cancer has been well established, the mediating role of the gut microbiota remains elusive. In this study, we sought to elucidate the connection between the gut microbiota, diet, and CRC through metagenomic analysis of bacteria isolated from the stool of CRC ( n  = 89) and healthy ( n  = 161) subjects. This analysis yielded a dozen genera that were significantly altered in CRC patients, including increased Bacteroides , Fusobacterium , Dorea , and Porphyromonas prevalence and diminished Pseudomonas , Prevotella , Acinetobacter , and Catenibacterium carriage. Based on these altered genera, we developed two novel CRC diagnostic models through stepwise selection and a simplified model using two increased and two decreased genera. As both models yielded strong AUC values above 0.8, the simplified model was applied to assess diet-based CRC risk in mice. Mice fed a westernized high-fat diet (HFD) showed greater CRC risk than mice fed a regular chow diet. Furthermore, we found that nonglutinous rice, glutinous rice, and sorghum consumption reduced CRC risk in HFD-fed mice. Collectively, these findings support the critical mediating role of the gut microbiota in diet-induced CRC risk as well as the potential of dietary grain intake to reduce microbiota-associated CRC risk. Further study is required to validate the diagnostic prediction models developed in this study as well as the preventive potential of grain consumption to reduce CRC risk. Colorectal cancer: Factors influencing cancer risk Tracing biomarkers of gut bacteria sheds light on how diet can affect gut composition and the risk of developing colorectal cancer (CRC). CRC is linked to diet, and scientists are examining how diet-associated changes in the gut microbiome may influence cancer risk. Yoon-Keun Kim, MD Healthcare Inc., Seoul, and Young-Koo Jee, Dankook University College of Medicine, Cheonan, South Korea, and co-workers analyzed bacterial populations in fecal samples from 89 CRC patients and 161 healthy controls. They found significant differences between patients and controls in 16 bacterial genera, these differences being potential biomarkers in diagnostic models for assessing CRC risk. The researchers used the models to determine CRC risk in mice fed diets, and found that the predicted risk was considerably reduced in mice on grain diets, especially rice or sorghum, compared to high fat diets.
AbstractList Colorectal cancer (CRC) is the third most common form of cancer and poses a critical public health threat due to the global spread of westernized diets high in meat, cholesterol, and fat. Although the link between diet and colorectal cancer has been well established, the mediating role of the gut microbiota remains elusive. In this study, we sought to elucidate the connection between the gut microbiota, diet, and CRC through metagenomic analysis of bacteria isolated from the stool of CRC (n = 89) and healthy (n = 161) subjects. This analysis yielded a dozen genera that were significantly altered in CRC patients, including increased Bacteroides, Fusobacterium, Dorea, and Porphyromonas prevalence and diminished Pseudomonas, Prevotella, Acinetobacter, and Catenibacterium carriage. Based on these altered genera, we developed two novel CRC diagnostic models through stepwise selection and a simplified model using two increased and two decreased genera. As both models yielded strong AUC values above 0.8, the simplified model was applied to assess diet-based CRC risk in mice. Mice fed a westernized high-fat diet (HFD) showed greater CRC risk than mice fed a regular chow diet. Furthermore, we found that nonglutinous rice, glutinous rice, and sorghum consumption reduced CRC risk in HFD-fed mice. Collectively, these findings support the critical mediating role of the gut microbiota in diet-induced CRC risk as well as the potential of dietary grain intake to reduce microbiota-associated CRC risk. Further study is required to validate the diagnostic prediction models developed in this study as well as the preventive potential of grain consumption to reduce CRC risk.
Colorectal cancer (CRC) is the third most common form of cancer and poses a critical public health threat due to the global spread of westernized diets high in meat, cholesterol, and fat. Although the link between diet and colorectal cancer has been well established, the mediating role of the gut microbiota remains elusive. In this study, we sought to elucidate the connection between the gut microbiota, diet, and CRC through metagenomic analysis of bacteria isolated from the stool of CRC ( n  = 89) and healthy ( n  = 161) subjects. This analysis yielded a dozen genera that were significantly altered in CRC patients, including increased Bacteroides , Fusobacterium , Dorea , and Porphyromonas prevalence and diminished Pseudomonas , Prevotella , Acinetobacter , and Catenibacterium carriage. Based on these altered genera, we developed two novel CRC diagnostic models through stepwise selection and a simplified model using two increased and two decreased genera. As both models yielded strong AUC values above 0.8, the simplified model was applied to assess diet-based CRC risk in mice. Mice fed a westernized high-fat diet (HFD) showed greater CRC risk than mice fed a regular chow diet. Furthermore, we found that nonglutinous rice, glutinous rice, and sorghum consumption reduced CRC risk in HFD-fed mice. Collectively, these findings support the critical mediating role of the gut microbiota in diet-induced CRC risk as well as the potential of dietary grain intake to reduce microbiota-associated CRC risk. Further study is required to validate the diagnostic prediction models developed in this study as well as the preventive potential of grain consumption to reduce CRC risk.
Colorectal cancer (CRC) is the third most common form of cancer and poses a critical public health threat due to the global spread of westernized diets high in meat, cholesterol, and fat. Although the link between diet and colorectal cancer has been well established, the mediating role of the gut microbiota remains elusive. In this study, we sought to elucidate the connection between the gut microbiota, diet, and CRC through metagenomic analysis of bacteria isolated from the stool of CRC ( n  = 89) and healthy ( n  = 161) subjects. This analysis yielded a dozen genera that were significantly altered in CRC patients, including increased Bacteroides , Fusobacterium , Dorea , and Porphyromonas prevalence and diminished Pseudomonas , Prevotella , Acinetobacter , and Catenibacterium carriage. Based on these altered genera, we developed two novel CRC diagnostic models through stepwise selection and a simplified model using two increased and two decreased genera. As both models yielded strong AUC values above 0.8, the simplified model was applied to assess diet-based CRC risk in mice. Mice fed a westernized high-fat diet (HFD) showed greater CRC risk than mice fed a regular chow diet. Furthermore, we found that nonglutinous rice, glutinous rice, and sorghum consumption reduced CRC risk in HFD-fed mice. Collectively, these findings support the critical mediating role of the gut microbiota in diet-induced CRC risk as well as the potential of dietary grain intake to reduce microbiota-associated CRC risk. Further study is required to validate the diagnostic prediction models developed in this study as well as the preventive potential of grain consumption to reduce CRC risk. Tracing biomarkers of gut bacteria sheds light on how diet can affect gut composition and the risk of developing colorectal cancer (CRC). CRC is linked to diet, and scientists are examining how diet-associated changes in the gut microbiome may influence cancer risk. Yoon-Keun Kim, MD Healthcare Inc., Seoul, and Young-Koo Jee, Dankook University College of Medicine, Cheonan, South Korea, and co-workers analyzed bacterial populations in fecal samples from 89 CRC patients and 161 healthy controls. They found significant differences between patients and controls in 16 bacterial genera, these differences being potential biomarkers in diagnostic models for assessing CRC risk. The researchers used the models to determine CRC risk in mice fed diets, and found that the predicted risk was considerably reduced in mice on grain diets, especially rice or sorghum, compared to high fat diets.
Colorectal cancer (CRC) is the third most common form of cancer and poses a critical public health threat due to theglobal spread of westernized diets high in meat, cholesterol, and fat. Although the link between diet and colorectalcancer has been well established, the mediating role of the gut microbiota remains elusive. In this study, we sought toelucidate the connection between the gut microbiota, diet, and CRC through metagenomic analysis of bacteriaisolated from the stool of CRC (n = 89) and healthy (n = 161) subjects. This analysis yielded a dozen genera that weresignificantly altered in CRC patients, including increased Bacteroides, Fusobacterium, Dorea, and Porphyromonasprevalence and diminished Pseudomonas, Prevotella, Acinetobacter, and Catenibacterium carriage. Based on thesealtered genera, we developed two novel CRC diagnostic models through stepwise selection and a simplified modelusing two increased and two decreased genera. As both models yielded strong AUC values above 0.8, the simplifiedmodel was applied to assess diet-based CRC risk in mice. Mice fed a westernized high-fat diet (HFD) showed greaterCRC risk than mice fed a regular chow diet. Furthermore, we found that nonglutinous rice, glutinous rice, and sorghumconsumption reduced CRC risk in HFD-fed mice. Collectively, these findings support the critical mediating role of thegut microbiota in diet-induced CRC risk as well as the potential of dietary grain intake to reduce microbiota-associatedCRC risk. Further study is required to validate the diagnostic prediction models developed in this study as well as thepreventive potential of grain consumption to reduce CRC risk. KCI Citation Count: 0
Colorectal cancer (CRC) is the third most common form of cancer and poses a critical public health threat due to the global spread of westernized diets high in meat, cholesterol, and fat. Although the link between diet and colorectal cancer has been well established, the mediating role of the gut microbiota remains elusive. In this study, we sought to elucidate the connection between the gut microbiota, diet, and CRC through metagenomic analysis of bacteria isolated from the stool of CRC (n = 89) and healthy (n = 161) subjects. This analysis yielded a dozen genera that were significantly altered in CRC patients, including increased Bacteroides, Fusobacterium, Dorea, and Porphyromonas prevalence and diminished Pseudomonas, Prevotella, Acinetobacter, and Catenibacterium carriage. Based on these altered genera, we developed two novel CRC diagnostic models through stepwise selection and a simplified model using two increased and two decreased genera. As both models yielded strong AUC values above 0.8, the simplified model was applied to assess diet-based CRC risk in mice. Mice fed a westernized high-fat diet (HFD) showed greater CRC risk than mice fed a regular chow diet. Furthermore, we found that nonglutinous rice, glutinous rice, and sorghum consumption reduced CRC risk in HFD-fed mice. Collectively, these findings support the critical mediating role of the gut microbiota in diet-induced CRC risk as well as the potential of dietary grain intake to reduce microbiota-associated CRC risk. Further study is required to validate the diagnostic prediction models developed in this study as well as the preventive potential of grain consumption to reduce CRC risk.Colorectal cancer (CRC) is the third most common form of cancer and poses a critical public health threat due to the global spread of westernized diets high in meat, cholesterol, and fat. Although the link between diet and colorectal cancer has been well established, the mediating role of the gut microbiota remains elusive. In this study, we sought to elucidate the connection between the gut microbiota, diet, and CRC through metagenomic analysis of bacteria isolated from the stool of CRC (n = 89) and healthy (n = 161) subjects. This analysis yielded a dozen genera that were significantly altered in CRC patients, including increased Bacteroides, Fusobacterium, Dorea, and Porphyromonas prevalence and diminished Pseudomonas, Prevotella, Acinetobacter, and Catenibacterium carriage. Based on these altered genera, we developed two novel CRC diagnostic models through stepwise selection and a simplified model using two increased and two decreased genera. As both models yielded strong AUC values above 0.8, the simplified model was applied to assess diet-based CRC risk in mice. Mice fed a westernized high-fat diet (HFD) showed greater CRC risk than mice fed a regular chow diet. Furthermore, we found that nonglutinous rice, glutinous rice, and sorghum consumption reduced CRC risk in HFD-fed mice. Collectively, these findings support the critical mediating role of the gut microbiota in diet-induced CRC risk as well as the potential of dietary grain intake to reduce microbiota-associated CRC risk. Further study is required to validate the diagnostic prediction models developed in this study as well as the preventive potential of grain consumption to reduce CRC risk.
Colorectal cancer (CRC) is the third most common form of cancer and poses a critical public health threat due to the global spread of westernized diets high in meat, cholesterol, and fat. Although the link between diet and colorectal cancer has been well established, the mediating role of the gut microbiota remains elusive. In this study, we sought to elucidate the connection between the gut microbiota, diet, and CRC through metagenomic analysis of bacteria isolated from the stool of CRC ( n  = 89) and healthy ( n  = 161) subjects. This analysis yielded a dozen genera that were significantly altered in CRC patients, including increased Bacteroides , Fusobacterium , Dorea , and Porphyromonas prevalence and diminished Pseudomonas , Prevotella , Acinetobacter , and Catenibacterium carriage. Based on these altered genera, we developed two novel CRC diagnostic models through stepwise selection and a simplified model using two increased and two decreased genera. As both models yielded strong AUC values above 0.8, the simplified model was applied to assess diet-based CRC risk in mice. Mice fed a westernized high-fat diet (HFD) showed greater CRC risk than mice fed a regular chow diet. Furthermore, we found that nonglutinous rice, glutinous rice, and sorghum consumption reduced CRC risk in HFD-fed mice. Collectively, these findings support the critical mediating role of the gut microbiota in diet-induced CRC risk as well as the potential of dietary grain intake to reduce microbiota-associated CRC risk. Further study is required to validate the diagnostic prediction models developed in this study as well as the preventive potential of grain consumption to reduce CRC risk. Colorectal cancer: Factors influencing cancer risk Tracing biomarkers of gut bacteria sheds light on how diet can affect gut composition and the risk of developing colorectal cancer (CRC). CRC is linked to diet, and scientists are examining how diet-associated changes in the gut microbiome may influence cancer risk. Yoon-Keun Kim, MD Healthcare Inc., Seoul, and Young-Koo Jee, Dankook University College of Medicine, Cheonan, South Korea, and co-workers analyzed bacterial populations in fecal samples from 89 CRC patients and 161 healthy controls. They found significant differences between patients and controls in 16 bacterial genera, these differences being potential biomarkers in diagnostic models for assessing CRC risk. The researchers used the models to determine CRC risk in mice fed diets, and found that the predicted risk was considerably reduced in mice on grain diets, especially rice or sorghum, compared to high fat diets.
Author Lee, Won Hee
Kim, Yoon-Keun
Seo, Hochan
McDowell, Andrea
Jee, Young-Koo
Moon, Chang-Mo
Yang, Jinho
Lee, Dong Ho
Kym, Sung-Min
Park, Young Soo
Kim, Eun Kyoung
Author_xml – sequence: 1
  givenname: Jinho
  surname: Yang
  fullname: Yang, Jinho
  organization: MD Healthcare Inc., Department of Health and Safety Convergence Science, Korea University
– sequence: 2
  givenname: Andrea
  surname: McDowell
  fullname: McDowell, Andrea
  organization: MD Healthcare Inc
– sequence: 3
  givenname: Eun Kyoung
  surname: Kim
  fullname: Kim, Eun Kyoung
  organization: MD Healthcare Inc
– sequence: 4
  givenname: Hochan
  surname: Seo
  fullname: Seo, Hochan
  organization: MD Healthcare Inc
– sequence: 5
  givenname: Won Hee
  surname: Lee
  fullname: Lee, Won Hee
  organization: MD Healthcare Inc
– sequence: 6
  givenname: Chang-Mo
  surname: Moon
  fullname: Moon, Chang-Mo
  organization: Department of Internal Medicine, School of Medicine, Ewha Womans University
– sequence: 7
  givenname: Sung-Min
  surname: Kym
  fullname: Kym, Sung-Min
  organization: Department of Internal Medicine, Inje University Haeundae Paik Hospital, Inje University College of Medicine
– sequence: 8
  givenname: Dong Ho
  orcidid: 0000-0002-6376-410X
  surname: Lee
  fullname: Lee, Dong Ho
  organization: Department of Internal Medicine, Seoul National University Bundang Hospital
– sequence: 9
  givenname: Young Soo
  surname: Park
  fullname: Park, Young Soo
  organization: Department of Internal Medicine, Seoul National University Bundang Hospital
– sequence: 10
  givenname: Young-Koo
  surname: Jee
  fullname: Jee, Young-Koo
  email: ykjee@dankook.ac.kr
  organization: Department of Internal Medicine, Dankook University College of Medicine
– sequence: 11
  givenname: Yoon-Keun
  surname: Kim
  fullname: Kim, Yoon-Keun
  email: ykkim@mdhc.kr
  organization: MD Healthcare Inc
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31582724$$D View this record in MEDLINE/PubMed
https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002518852$$DAccess content in National Research Foundation of Korea (NRF)
BookMark eNp9kk9rFTEUxYNU7Gv1A7iRgJu6GM2fSWZmI5SqbaFQkLoOmSQzL32Z5JlkCv325r2pVQt1Fcj9nZNzb-4ROPDBGwDeYvQRI9p-SpiQhlcIdxWimFb1C7AiqCMVrzE9AKtS5hXlmB6Co5RuESKsbupX4JBi1pKG1CsQvpg748J2Mj7DMEAJVXAhGpWlg0p6ZSLUVo4-pGwVnII2Dkqvy6XJMt7DaNMGypRMSnuPvI5hHtdwnDOcrIqht2EyRSLdfbLpNXg5SJfMm4fzGPz49vXm7KK6uj6_PDu9qhRrUK4azZimGA-4ZxJzSoZGkb7Fdc2JZL1UGjFJZU9a3aieEsow0x3vGDKaddrQY_Bh8fVxEBtlRZB2f45BbKI4_X5zKThuEWK8sJ8Xdjv3k9GqtBGlE9top9LhXvlvxdt18bkTvEWEN6wYnDwYxPBzNimLySZlnJPehDkJQlFJzgihBX3_BL0NcyzD2VOIo5ayulDv_k70GOX3vxUAL0AZcErRDI8IRmK3G2LZDVF2Q-x2Q-w0zRONsllmG3ZNWfdfJVmUqbziRxP_hH5e9At_Js5W
CitedBy_id crossref_primary_10_1093_mutage_geaa005
crossref_primary_10_3233_JBR_220076
crossref_primary_10_1002_cam4_70180
crossref_primary_10_3389_fimmu_2021_622064
crossref_primary_10_2147_CMAR_S252232
crossref_primary_10_1016_j_medmic_2024_100105
crossref_primary_10_1080_01635581_2024_2367266
crossref_primary_10_3389_fmicb_2023_1181328
crossref_primary_10_3390_medicina57030260
crossref_primary_10_2174_1389201023666221005103340
crossref_primary_10_2174_0115733947270529231116114913
crossref_primary_10_1111_jam_14943
crossref_primary_10_1007_s10552_020_01338_5
crossref_primary_10_3389_fonc_2022_982744
crossref_primary_10_4143_crt_2024_382
crossref_primary_10_3389_fimmu_2020_573158
crossref_primary_10_1016_j_jep_2024_118571
crossref_primary_10_3892_br_2021_1461
crossref_primary_10_3389_fmicb_2022_869523
crossref_primary_10_1016_j_csbj_2021_05_049
crossref_primary_10_1002_mco2_417
crossref_primary_10_1038_s41598_025_95010_0
crossref_primary_10_3389_fcimb_2024_1339750
crossref_primary_10_3389_fmicb_2022_990870
crossref_primary_10_3389_fonc_2023_1156246
crossref_primary_10_1186_s12967_024_04903_7
crossref_primary_10_1016_j_compbiomed_2024_109098
crossref_primary_10_1016_j_mcp_2024_101992
crossref_primary_10_22207_JPAM_16_2_39
crossref_primary_10_3389_fmicb_2023_1292490
crossref_primary_10_1038_s41598_023_31840_0
crossref_primary_10_1099_jmm_0_001706
crossref_primary_10_1016_j_compbiomed_2025_109813
crossref_primary_10_1016_j_lfs_2021_120202
crossref_primary_10_1038_s41598_024_53861_z
crossref_primary_10_3389_fonc_2021_664321
crossref_primary_10_1016_j_compbiomed_2021_104556
crossref_primary_10_1371_journal_pone_0255323
crossref_primary_10_3390_ijms21155389
crossref_primary_10_1016_j_semcancer_2021_05_018
crossref_primary_10_1016_j_neo_2022_100868
crossref_primary_10_1093_labmed_lmac072
crossref_primary_10_3390_pharmaceutics13050651
crossref_primary_10_15407_visn2021_11_024
crossref_primary_10_1016_j_genrep_2021_101375
crossref_primary_10_1038_s41598_022_19091_x
crossref_primary_10_1042_BSR20204113
crossref_primary_10_3389_fnut_2022_856408
crossref_primary_10_1016_j_molmet_2022_101529
crossref_primary_10_2217_crc_2020_0007
crossref_primary_10_1080_07420528_2020_1778717
crossref_primary_10_3389_fonc_2021_650026
crossref_primary_10_3748_wjg_v27_i45_7792
crossref_primary_10_3389_fonc_2022_1116780
crossref_primary_10_1021_acs_analchem_0c02627
crossref_primary_10_1016_j_lfs_2024_122462
crossref_primary_10_3748_wjg_v27_i19_2394
crossref_primary_10_3389_fcimb_2022_1013920
Cites_doi 10.1021/acs.jpcb.8b04610
10.1101/gr.126573.111
10.1038/nrmicro2819
10.1002/ijc.29704
10.1159/000084851
10.1016/j.jff.2015.03.020
10.1186/s40168-018-0451-2
10.12793/tcp.2018.26.3.103
10.1007/s00248-013-0245-9
10.18632/oncotarget.12449
10.1186/s40168-016-0160-7
10.3390/nu7010017
10.1038/ismej.2011.109
10.1054/bjoc.2001.1906
10.2307/2531595
10.1016/j.chom.2013.07.012
10.1007/s10096-014-2081-3
10.1093/femsec/fiv008
10.1186/s13568-018-0632-1
10.1172/JCI72334
10.1093/carcin/bgs112
10.1371/journal.pone.0040459
10.3748/wjg.v22.i2.501
10.1038/emm.2017.282
10.1136/gutjnl-2015-310912
10.1111/jth.12262
10.1136/bmjgast-2017-000145
10.1038/s41551-017-0181-y
10.1200/JCO.2008.17.4813
10.1093/carcin/20.8.1425
10.1152/ajpgi.00360.2012
10.1371/journal.pone.0088079
10.1002/sim.5328
10.1101/gr.126516.111
10.1093/jnci/djt300
10.3945/ajcn.112.056689
10.3389/fmicb.2018.01502
10.1007/s13304-016-0359-y
10.1371/journal.pone.0076520
10.1126/science.1223813
10.1186/s40824-017-0111-9
10.1371/journal.pone.0022109
10.1001/jama.293.2.172
10.1371/journal.pone.0039743
10.3390/nu8020078
ContentType Journal Article
Copyright The Author(s) 2019
2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Copyright_xml – notice: The Author(s) 2019
– notice: 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
DBID C6C
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7X7
7XB
88E
8FE
8FH
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
HCIFZ
K9.
LK8
M0S
M1P
M7P
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
7X8
5PM
ACYCR
DOI 10.1038/s12276-019-0313-4
DatabaseName Springer Nature OA Free Journals
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
ProQuest Health & Medical Collection (NC LIVE)
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
ProQuest SciTech Collection
ProQuest Natural Science Collection
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
Biological Science Collection
ProQuest Central
Natural Science Collection
ProQuest One Community College
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
SciTech Premium Collection (via ProQuest)
ProQuest Health & Medical Complete (Alumni)
ProQuest Biological Science Collection
ProQuest Health & Medical Collection
Medical Database
Biological Science Database
ProQuest Central Premium
ProQuest One Academic
Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
Korean Citation Index
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Publicly Available Content Database
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Natural Science Collection
ProQuest Central China
ProQuest Central
ProQuest One Applied & Life Sciences
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
Natural Science Collection
ProQuest Central Korea
Health & Medical Research Collection
Biological Science Collection
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest Biological Science Collection
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Biological Science Database
ProQuest SciTech Collection
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList Publicly Available Content Database
CrossRef


MEDLINE - Academic

MEDLINE
Database_xml – sequence: 1
  dbid: C6C
  name: Springer Nature Link OA Free Journals
  url: http://www.springeropen.com/
  sourceTypes: Publisher
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 4
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Anatomy & Physiology
Public Health
EISSN 2092-6413
EndPage 15
ExternalDocumentID oai_kci_go_kr_ARTI_6180056
PMC6802675
31582724
10_1038_s12276_019_0313_4
Genre Research Support, Non-U.S. Gov't
Journal Article
GrantInformation_xml – fundername: Ministry of Health and Welfare (Ministry of Health, Welfare and Family Affairs)
  grantid: H17C1996
  funderid: https://doi.org/10.13039/501100003625
– fundername: National Research Foundation of Korea (NRF)
  grantid: NRF-2016M3A9B6901516; NRF-2017M3A9F3047497
  funderid: https://doi.org/10.13039/501100003725
– fundername: National Research Foundation of Korea (NRF)
  grantid: NRF-2016M3A9B6901516
– fundername: Ministry of Health and Welfare (Ministry of Health, Welfare and Family Affairs)
  grantid: H17C1996
– fundername: National Research Foundation of Korea (NRF)
  grantid: NRF-2017M3A9F3047497
– fundername: ;
  grantid: NRF-2016M3A9B6901516; NRF-2017M3A9F3047497
– fundername: ;
  grantid: H17C1996
GroupedDBID ---
0R~
29G
2WC
3V.
5-W
53G
5GY
7X7
87B
88E
8FE
8FH
8FI
8FJ
8JR
9ZL
AAJSJ
ABUWG
ACGFO
ACGFS
ACPRK
ACSMW
ACYCR
ADBBV
AENEX
AFKRA
AHMBA
AJTQC
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
BBNVY
BENPR
BHPHI
BPHCQ
BVXVI
C1A
C6C
CCPQU
DIK
DU5
E3Z
EBLON
EBS
EF.
EJD
EMOBN
F5P
FYUFA
GROUPED_DOAJ
GX1
HCIFZ
HH5
HMCUK
HYE
LK8
M1P
M7P
M~E
NAO
OK1
PIMPY
PQQKQ
PROAC
PSQYO
RNS
RNT
RNTTT
RPM
SNYQT
TR2
UKHRP
W2D
XSB
AASML
AAYXX
CITATION
OVT
PHGZM
PHGZT
CGR
CUY
CVF
ECM
EIF
NPM
PJZUB
PPXIY
PQGLB
7XB
8FK
AZQEC
DWQXO
GNUQQ
K9.
PKEHL
PQEST
PQUKI
PRINS
PUEGO
7X8
5PM
AAADF
AAPBV
AFGXO
ID FETCH-LOGICAL-c570t-7d55d311f1b5a1632f7c2b814462a5bacd05a3ab28d7cb323515d96950ed59de3
IEDL.DBID 7X7
ISSN 1226-3613
2092-6413
IngestDate Tue Nov 21 21:39:17 EST 2023
Thu Aug 21 14:14:34 EDT 2025
Mon Jul 21 10:15:41 EDT 2025
Sat Aug 23 14:17:12 EDT 2025
Mon Jul 21 04:15:23 EDT 2025
Tue Jul 01 04:10:29 EDT 2025
Thu Apr 24 23:09:47 EDT 2025
Fri Feb 21 02:40:04 EST 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 10
Language English
License Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c570t-7d55d311f1b5a1632f7c2b814462a5bacd05a3ab28d7cb323515d96950ed59de3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0002-6376-410X
OpenAccessLink https://www.proquest.com/docview/2300608354?pq-origsite=%requestingapplication%
PMID 31582724
PQID 2300608354
PQPubID 2041975
PageCount 15
ParticipantIDs nrf_kci_oai_kci_go_kr_ARTI_6180056
pubmedcentral_primary_oai_pubmedcentral_nih_gov_6802675
proquest_miscellaneous_2301445223
proquest_journals_2300608354
pubmed_primary_31582724
crossref_primary_10_1038_s12276_019_0313_4
crossref_citationtrail_10_1038_s12276_019_0313_4
springer_journals_10_1038_s12276_019_0313_4
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2019-10-03
PublicationDateYYYYMMDD 2019-10-03
PublicationDate_xml – month: 10
  year: 2019
  text: 2019-10-03
  day: 03
PublicationDecade 2010
PublicationPlace London
PublicationPlace_xml – name: London
– name: United States
– name: Seoul
PublicationTitle Experimental & molecular medicine
PublicationTitleAbbrev Exp Mol Med
PublicationTitleAlternate Exp Mol Med
PublicationYear 2019
Publisher Nature Publishing Group UK
Springer Nature B.V
생화학분자생물학회
Publisher_xml – name: Nature Publishing Group UK
– name: Springer Nature B.V
– name: 생화학분자생물학회
References Yang, Kim, McDowell, Kim (CR16) 2018; 26
Kostic (CR25) 2012; 22
Keku (CR2) 2015; 308
Ou (CR7) 2013; 98
Kang (CR17) 2013; 8
Hendriksen (CR47) 2013; 11
DeLong, DeLong, Clarke-Pearson (CR20) 1988; 44
Rubinstein (CR28) 2013; 14
Chen (CR31) 2012; 7
Rodríguez, Mastronardi, Paz-Filho (CR12) 2013; 2
Chelakkot (CR18) 2018; 50
Arnold (CR1) 2017; 66
Darvin (CR45) 2015; 15
Castellarin (CR26) 2012; 22
Ho (CR30) 2018; 2
Nishiumi (CR51) 2012; 7
Gagnière (CR14) 2016; 22
Gorvitovskaia, Holmes, Huse (CR36) 2016; 4
Wang (CR22) 2012; 6
Ozdal (CR40) 2016; 8
Park (CR49) 2009; 27
Nam (CR38) 2011; 6
CR43
Conlon, Bird (CR39) 2015; 7
Nicholson (CR8) 2012; 336
Järvinen, Knekt, Hakulinen, Rissanen, Heliövaara (CR6) 2001; 85
Gao (CR33) 2015; 6
Sears, Geis, Housseau (CR15) 2014; 124
Tjalsma (CR35) 2012; 10
Liu (CR13) 2001; 19
Soler (CR9) 1999; 20
Gandomani (CR4) 2017; 4
Wu (CR23) 2013; 66
Ahn (CR24) 2013; 105
Zhang (CR41) 2016; 138
Mastronardi (CR11) 2005; 12
Ritchie (CR46) 2015; 91
Ahn, Segers, Hayes (CR32) 2012; 33
Hibberd (CR29) 2017; 4
Zhao (CR44) 2018; 122
Dai (CR34) 2018; 6
Liu, Defourny, Smid, Abee (CR21) 2018; 9
Seo, Lee, Cho (CR48) 2018; 22
Favoriti (CR3) 2016; 68
Zhu (CR10) 2016; 7
Flanagan (CR27) 2014; 33
Demler, Pencina, D’Agostino Sr (CR19) 2012; 31
Shin (CR50) 2014; 9
Jain, Li, Chen (CR37) 2018; 8
Chao (CR5) 2005; 293
Hudson (CR42) 2000; 9
AA Hibberd (313_CR29) 2017; 4
Z Dai (313_CR34) 2018; 6
A Chao (313_CR5) 2005; 293
T Ozdal (313_CR40) 2016; 8
W Chen (313_CR31) 2012; 7
H Tjalsma (313_CR35) 2012; 10
R Järvinen (313_CR6) 2001; 85
P Darvin (313_CR45) 2015; 15
M Arnold (313_CR1) 2017; 66
T Wang (313_CR22) 2012; 6
R Zhang (313_CR41) 2016; 138
L Flanagan (313_CR27) 2014; 33
JH Seo (313_CR48) 2018; 22
AJ Rodríguez (313_CR12) 2013; 2
N Wu (313_CR23) 2013; 66
J Ou (313_CR7) 2013; 98
J Yang (313_CR16) 2018; 26
AP Soler (313_CR9) 1999; 20
LE Ritchie (313_CR46) 2015; 91
HS Gandomani (313_CR4) 2017; 4
C Kang (313_CR17) 2013; 8
J Ahn (313_CR24) 2013; 105
JK Nicholson (313_CR8) 2012; 336
C Chelakkot (313_CR18) 2018; 50
J Ahn (313_CR32) 2012; 33
CL Sears (313_CR15) 2014; 124
Z Gao (313_CR33) 2015; 6
MR Rubinstein (313_CR28) 2013; 14
ER DeLong (313_CR20) 1988; 44
J Gagnière (313_CR14) 2016; 22
M Conlon (313_CR39) 2015; 7
TO Keku (313_CR2) 2015; 308
P Favoriti (313_CR3) 2016; 68
CA Mastronardi (313_CR11) 2005; 12
Y Liu (313_CR21) 2018; 9
313_CR43
AD Kostic (313_CR25) 2012; 22
Y Park (313_CR49) 2009; 27
JMT Hendriksen (313_CR47) 2013; 11
S Nishiumi (313_CR51) 2012; 7
OV Demler (313_CR19) 2012; 31
CL Ho (313_CR30) 2018; 2
EA Hudson (313_CR42) 2000; 9
G Zhu (313_CR10) 2016; 7
Z Liu (313_CR13) 2001; 19
Y Nam (313_CR38) 2011; 6
M Castellarin (313_CR26) 2012; 22
Y Zhao (313_CR44) 2018; 122
A Gorvitovskaia (313_CR36) 2016; 4
A Jain (313_CR37) 2018; 8
A Shin (313_CR50) 2014; 9
References_xml – volume: 2
  start-page: 211
  year: 2013
  end-page: 222
  ident: CR12
  article-title: Leptin as a risk factor for the development of colorectal cancer
  publication-title: Transl. Gastrointest. Cancer
– volume: 122
  start-page: 7855
  year: 2018
  end-page: 7861
  ident: CR44
  article-title: Ungerminated rice grains observed by femtosecond pulse laser second-harmonic generation microscopy
  publication-title: J. Phys. Chem. B
  doi: 10.1021/acs.jpcb.8b04610
– volume: 22
  start-page: 292
  year: 2012
  end-page: 298
  ident: CR25
  article-title: Genomic analysis identifies association of Fusobacterium with colorectal carcinoma
  publication-title: Genome Res.
  doi: 10.1101/gr.126573.111
– volume: 10
  start-page: 575
  year: 2012
  end-page: 582
  ident: CR35
  article-title: A bacterial driver–passenger model for colorectal cancer: beyond the usual suspects
  publication-title: Nat. Rev. Microbiol.
  doi: 10.1038/nrmicro2819
– volume: 138
  start-page: 555
  year: 2016
  end-page: 564
  ident: CR41
  article-title: Rice consumption and cancer incidence in US men and women
  publication-title: Int. J. Cancer
  doi: 10.1002/ijc.29704
– volume: 12
  start-page: 182
  year: 2005
  end-page: 188
  ident: CR11
  article-title: Lipopolysaccharide-induced leptin synthesis and release are differentially controlled by alpha-melanocyte-stimulating hormone
  publication-title: Neuroimmunomodulation
  doi: 10.1159/000084851
– volume: 15
  start-page: 193
  year: 2015
  end-page: 206
  ident: CR45
  article-title: Sorghum polyphenol suppresses the growth as well as metastasis of colon cancer xenografts through co-targeting jak2/STAT3 and PI3K/Akt/mTOR pathways
  publication-title: J. Funct. Foods
  doi: 10.1016/j.jff.2015.03.020
– volume: 6
  year: 2018
  ident: CR34
  article-title: Multi-cohort analysis of colorectal cancer metagenome identified altered bacteria across populations and universal bacterial markers
  publication-title: Microbiome
  doi: 10.1186/s40168-018-0451-2
– volume: 19
  start-page: 1009
  year: 2001
  end-page: 1014
  ident: CR13
  article-title: High fat diet enhances colonic cell proliferation and carcinogenesis in rats by elevating serum leptin
  publication-title: Int. J. Oncol.
– volume: 26
  start-page: 103
  year: 2018
  end-page: 110
  ident: CR16
  article-title: Microbe-derived extracellular vesicles as a smart drug delivery system
  publication-title: Transl. Clin. Pharmacol.
  doi: 10.12793/tcp.2018.26.3.103
– volume: 66
  start-page: 462
  year: 2013
  end-page: 470
  ident: CR23
  article-title: Dysbiosis signature of fecal microbiota in colorectal cancer patients
  publication-title: Microb. Ecol.
  doi: 10.1007/s00248-013-0245-9
– volume: 7
  start-page: 73711
  year: 2016
  end-page: 73724
  ident: CR10
  article-title: Lipopolysaccharide increases the release of VEGF-C that enhances cell motility and promotes lymphangiogenesis and lymphatic metastasis through the TLR4-NF-κB/JNK pathways in colorectal cancer
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.12449
– volume: 6
  start-page: 20
  year: 2015
  ident: CR33
  article-title: Microbiota disbiosis is associated with colorectal cancer
  publication-title: Front. Microbiol.
– volume: 4
  year: 2016
  ident: CR36
  article-title: Interpreting Prevotella and Bacteroides as biomarkers of diet and lifestyle
  publication-title: Microbiome
  doi: 10.1186/s40168-016-0160-7
– volume: 9
  start-page: 1163
  year: 2000
  end-page: 1170
  ident: CR42
  article-title: Characterization of potentially chemopreventive phenols in extracts of brown rice that inhibit the growth of human breast and colon cancer cells
  publication-title: Cancer Epidemiol. Biomark. Prev.
– volume: 7
  start-page: 17
  year: 2015
  end-page: 44
  ident: CR39
  article-title: The impact of diet and lifestyle on gut microbiota and human health
  publication-title: Nutrients
  doi: 10.3390/nu7010017
– volume: 6
  start-page: 320
  year: 2012
  end-page: 329
  ident: CR22
  article-title: Structural segregation of gut microbiota between colorectal cancer patients and healthy volunteers
  publication-title: ISME. J.
  doi: 10.1038/ismej.2011.109
– volume: 85
  start-page: 357
  year: 2001
  end-page: 361
  ident: CR6
  article-title: Dietary fat, cholesterol and colorectal cancer in a prospective study
  publication-title: Br. J. Cancer
  doi: 10.1054/bjoc.2001.1906
– volume: 44
  start-page: 837
  year: 1988
  end-page: 845
  ident: CR20
  article-title: Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach
  publication-title: Biometrics
  doi: 10.2307/2531595
– volume: 14
  start-page: 195
  year: 2013
  end-page: 206
  ident: CR28
  article-title: Fusobacterium nucleatum promotes colorectal carcinogenesis by modulating E-cadherin/ß-catenin signaling via its FadA adhesin
  publication-title: Cell. Host. Microbe
  doi: 10.1016/j.chom.2013.07.012
– volume: 33
  start-page: 1381
  year: 2014
  end-page: 1390
  ident: CR27
  article-title: Fusobacterium nucleatum associates with stages of colorectal neoplasia development, colorectal cancer and disease outcome
  publication-title: Eur. J. Clin. Microbiol. Infect. Dis.
  doi: 10.1007/s10096-014-2081-3
– volume: 91
  start-page: fiv008
  year: 2015
  ident: CR46
  article-title: Polyphenol-rich sorghum brans alter colon microbiota and impact species diversity and species richness after multiple bouts of dextran sodium sulfate-induced colitis
  publication-title: FEMS Microbiol. Ecol.
  doi: 10.1093/femsec/fiv008
– volume: 8
  year: 2018
  ident: CR37
  article-title: Similarities and differences in gut microbiome composition correlate with dietary patterns of Indian and Chinese adults
  publication-title: AMB Express
  doi: 10.1186/s13568-018-0632-1
– volume: 124
  start-page: 4166
  year: 2014
  end-page: 4172
  ident: CR15
  article-title: Bacteroides fragilis subverts mucosal biology: from symbiont to colon carcinogenesis
  publication-title: J. Clin. Invest.
  doi: 10.1172/JCI72334
– volume: 4
  start-page: 1656
  year: 2017
  end-page: 1675
  ident: CR4
  article-title: Colorectal cancer in the world: incidence, mortality and risk factors
  publication-title: BMRAT
– volume: 33
  start-page: 1055
  year: 2012
  end-page: 1058
  ident: CR32
  article-title: Periodontal disease, Porphyromonas gingivalis serum antibody levels and orodigestive cancer mortality
  publication-title: Carcinogenesis
  doi: 10.1093/carcin/bgs112
– volume: 7
  year: 2012
  ident: CR51
  article-title: A novel serum metabolomics-based diagnostic approach for colorectal cancer
  publication-title: PLoS. ONE
  doi: 10.1371/journal.pone.0040459
– volume: 22
  start-page: 501
  year: 2016
  end-page: 518
  ident: CR14
  article-title: Gut microbiota imbalance and colorectal cancer
  publication-title: World J. Gastroenterol.
  doi: 10.3748/wjg.v22.i2.501
– volume: 50
  year: 2018
  ident: CR18
  article-title: Akkermansia muciniphila-derived extracellular vesicles influence gut permeability through the regulation of tight junctions
  publication-title: Exp. Mol. Med.
  doi: 10.1038/emm.2017.282
– volume: 66
  start-page: 683
  year: 2017
  end-page: 691
  ident: CR1
  article-title: Global patterns and trends in colorectal cancer incidence and mortality
  publication-title: Gut
  doi: 10.1136/gutjnl-2015-310912
– volume: 11
  start-page: 129
  year: 2013
  end-page: 141
  ident: CR47
  article-title: Diagnostic and prognostic prediction models
  publication-title: J. Thromb. Haemost.
  doi: 10.1111/jth.12262
– volume: 4
  year: 2017
  ident: CR29
  article-title: Intestinal microbiota is altered in patients with colon cancer and modified by probiotic intervention
  publication-title: BMJ Open Gastroenterol.
  doi: 10.1136/bmjgast-2017-000145
– volume: 2
  start-page: 27
  year: 2018
  end-page: 37
  ident: CR30
  article-title: Engineered commensal microbes for diet-mediated colorectal-cancer chemoprevention
  publication-title: Nat. Biomed. Eng.
  doi: 10.1038/s41551-017-0181-y
– ident: CR43
– volume: 27
  start-page: 694
  year: 2009
  end-page: 698
  ident: CR49
  article-title: Validation of a colorectal cancer risk prediction model among white patients age 50 years and older
  publication-title: J. Clin. Oncol.
  doi: 10.1200/JCO.2008.17.4813
– volume: 20
  start-page: 1425
  year: 1999
  end-page: 1432
  ident: CR9
  article-title: Increased tight junctional permeability is associated with the development of colon cancer
  publication-title: Carcinogenesis
  doi: 10.1093/carcin/20.8.1425
– volume: 308
  start-page: G351
  year: 2015
  end-page: G363
  ident: CR2
  article-title: The gastrointestinal microbiota and colorectal cancer
  publication-title: Am. J. Physiol. Gastrointest. Liver Physiol.
  doi: 10.1152/ajpgi.00360.2012
– volume: 9
  year: 2014
  ident: CR50
  article-title: Risk prediction model for colorectal cancer: National Health Insurance Corporation study, Korea
  publication-title: PLoS. ONE
  doi: 10.1371/journal.pone.0088079
– volume: 31
  start-page: 2577
  year: 2012
  end-page: 2587
  ident: CR19
  article-title: Misuse of DeLong test to compare AUCs for nested models.
  publication-title: Stat. Med
  doi: 10.1002/sim.5328
– volume: 22
  start-page: 299
  year: 2012
  end-page: 306
  ident: CR26
  article-title: Fusobacterium nucleatum infection is prevalent in human colorectal carcinoma
  publication-title: Genome Res.
  doi: 10.1101/gr.126516.111
– volume: 105
  start-page: 1907
  year: 2013
  end-page: 1911
  ident: CR24
  article-title: Human gut microbiome and risk for colorectal cancer
  publication-title: J. Natl. Cancer Inst.
  doi: 10.1093/jnci/djt300
– volume: 98
  start-page: 111
  year: 2013
  end-page: 120
  ident: CR7
  article-title: Diet, microbiota, and microbial metabolites in colon cancer risk in rural Africans and African Americans
  publication-title: Am. J. Clin. Nutr.
  doi: 10.3945/ajcn.112.056689
– volume: 9
  start-page: 1502
  year: 2018
  ident: CR21
  article-title: Gram-positive bacterial extracellular vesicles and their impact on health and disease
  publication-title: Front. Microbio.
  doi: 10.3389/fmicb.2018.01502
– volume: 68
  start-page: 7
  year: 2016
  end-page: 11
  ident: CR3
  article-title: Worldwide burden of colorectal cancer: a review
  publication-title: Updates Surg.
  doi: 10.1007/s13304-016-0359-y
– volume: 8
  year: 2013
  ident: CR17
  article-title: Extracellular vesicles derived from gut microbiota, especially Akkermansia muciniphila, protect the progression of dextran sulfate sodium-induced colitis
  publication-title: PLoS. ONE
  doi: 10.1371/journal.pone.0076520
– volume: 336
  start-page: 1262
  year: 2012
  end-page: 1267
  ident: CR8
  article-title: Host-gut microbiota metabolic interactions
  publication-title: Science
  doi: 10.1126/science.1223813
– volume: 22
  year: 2018
  ident: CR48
  article-title: The market trend analysis and prospects of cancer molecular diagnostics kits
  publication-title: Biomater. Res.
  doi: 10.1186/s40824-017-0111-9
– volume: 6
  year: 2011
  ident: CR38
  article-title: Comparative analysis of Korean human gut microbiota by barcoded pyrosequencing
  publication-title: PLoS. ONE
  doi: 10.1371/journal.pone.0022109
– volume: 293
  start-page: 172
  year: 2005
  end-page: 182
  ident: CR5
  article-title: Meat consumption and risk of colorectal cancer
  publication-title: J. Am. Med. Assoc.
  doi: 10.1001/jama.293.2.172
– volume: 7
  year: 2012
  ident: CR31
  article-title: Human intestinal lumen and mucosa-associated microbiota in patients with colorectal cancer
  publication-title: PLoS. ONE
  doi: 10.1371/journal.pone.0039743
– volume: 8
  start-page: 78
  year: 2016
  ident: CR40
  article-title: The reciprocal interactions between polyphenols and gut microbiota and effects on bioaccessibility
  publication-title: Nutrients
  doi: 10.3390/nu8020078
– volume: 7
  start-page: 73711
  year: 2016
  ident: 313_CR10
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.12449
– volume: 12
  start-page: 182
  year: 2005
  ident: 313_CR11
  publication-title: Neuroimmunomodulation
  doi: 10.1159/000084851
– volume: 22
  year: 2018
  ident: 313_CR48
  publication-title: Biomater. Res.
  doi: 10.1186/s40824-017-0111-9
– volume: 8
  start-page: 78
  year: 2016
  ident: 313_CR40
  publication-title: Nutrients
  doi: 10.3390/nu8020078
– volume: 66
  start-page: 683
  year: 2017
  ident: 313_CR1
  publication-title: Gut
  doi: 10.1136/gutjnl-2015-310912
– volume: 138
  start-page: 555
  year: 2016
  ident: 313_CR41
  publication-title: Int. J. Cancer
  doi: 10.1002/ijc.29704
– volume: 7
  year: 2012
  ident: 313_CR51
  publication-title: PLoS. ONE
  doi: 10.1371/journal.pone.0040459
– volume: 22
  start-page: 299
  year: 2012
  ident: 313_CR26
  publication-title: Genome Res.
  doi: 10.1101/gr.126516.111
– volume: 19
  start-page: 1009
  year: 2001
  ident: 313_CR13
  publication-title: Int. J. Oncol.
– volume: 6
  start-page: 320
  year: 2012
  ident: 313_CR22
  publication-title: ISME. J.
  doi: 10.1038/ismej.2011.109
– volume: 6
  start-page: 20
  year: 2015
  ident: 313_CR33
  publication-title: Front. Microbiol.
– volume: 10
  start-page: 575
  year: 2012
  ident: 313_CR35
  publication-title: Nat. Rev. Microbiol.
  doi: 10.1038/nrmicro2819
– volume: 4
  year: 2016
  ident: 313_CR36
  publication-title: Microbiome
  doi: 10.1186/s40168-016-0160-7
– volume: 4
  start-page: 1656
  year: 2017
  ident: 313_CR4
  publication-title: BMRAT
– ident: 313_CR43
– volume: 98
  start-page: 111
  year: 2013
  ident: 313_CR7
  publication-title: Am. J. Clin. Nutr.
  doi: 10.3945/ajcn.112.056689
– volume: 14
  start-page: 195
  year: 2013
  ident: 313_CR28
  publication-title: Cell. Host. Microbe
  doi: 10.1016/j.chom.2013.07.012
– volume: 91
  start-page: fiv008
  year: 2015
  ident: 313_CR46
  publication-title: FEMS Microbiol. Ecol.
  doi: 10.1093/femsec/fiv008
– volume: 2
  start-page: 211
  year: 2013
  ident: 313_CR12
  publication-title: Transl. Gastrointest. Cancer
– volume: 9
  year: 2014
  ident: 313_CR50
  publication-title: PLoS. ONE
  doi: 10.1371/journal.pone.0088079
– volume: 6
  year: 2018
  ident: 313_CR34
  publication-title: Microbiome
  doi: 10.1186/s40168-018-0451-2
– volume: 50
  year: 2018
  ident: 313_CR18
  publication-title: Exp. Mol. Med.
  doi: 10.1038/emm.2017.282
– volume: 7
  start-page: 17
  year: 2015
  ident: 313_CR39
  publication-title: Nutrients
  doi: 10.3390/nu7010017
– volume: 336
  start-page: 1262
  year: 2012
  ident: 313_CR8
  publication-title: Science
  doi: 10.1126/science.1223813
– volume: 85
  start-page: 357
  year: 2001
  ident: 313_CR6
  publication-title: Br. J. Cancer
  doi: 10.1054/bjoc.2001.1906
– volume: 26
  start-page: 103
  year: 2018
  ident: 313_CR16
  publication-title: Transl. Clin. Pharmacol.
  doi: 10.12793/tcp.2018.26.3.103
– volume: 9
  start-page: 1502
  year: 2018
  ident: 313_CR21
  publication-title: Front. Microbio.
  doi: 10.3389/fmicb.2018.01502
– volume: 124
  start-page: 4166
  year: 2014
  ident: 313_CR15
  publication-title: J. Clin. Invest.
  doi: 10.1172/JCI72334
– volume: 8
  year: 2018
  ident: 313_CR37
  publication-title: AMB Express
  doi: 10.1186/s13568-018-0632-1
– volume: 6
  year: 2011
  ident: 313_CR38
  publication-title: PLoS. ONE
  doi: 10.1371/journal.pone.0022109
– volume: 9
  start-page: 1163
  year: 2000
  ident: 313_CR42
  publication-title: Cancer Epidemiol. Biomark. Prev.
– volume: 4
  year: 2017
  ident: 313_CR29
  publication-title: BMJ Open Gastroenterol.
  doi: 10.1136/bmjgast-2017-000145
– volume: 22
  start-page: 292
  year: 2012
  ident: 313_CR25
  publication-title: Genome Res.
  doi: 10.1101/gr.126573.111
– volume: 68
  start-page: 7
  year: 2016
  ident: 313_CR3
  publication-title: Updates Surg.
  doi: 10.1007/s13304-016-0359-y
– volume: 8
  year: 2013
  ident: 313_CR17
  publication-title: PLoS. ONE
  doi: 10.1371/journal.pone.0076520
– volume: 122
  start-page: 7855
  year: 2018
  ident: 313_CR44
  publication-title: J. Phys. Chem. B
  doi: 10.1021/acs.jpcb.8b04610
– volume: 308
  start-page: G351
  year: 2015
  ident: 313_CR2
  publication-title: Am. J. Physiol. Gastrointest. Liver Physiol.
  doi: 10.1152/ajpgi.00360.2012
– volume: 31
  start-page: 2577
  year: 2012
  ident: 313_CR19
  publication-title: Stat. Med
  doi: 10.1002/sim.5328
– volume: 27
  start-page: 694
  year: 2009
  ident: 313_CR49
  publication-title: J. Clin. Oncol.
  doi: 10.1200/JCO.2008.17.4813
– volume: 105
  start-page: 1907
  year: 2013
  ident: 313_CR24
  publication-title: J. Natl. Cancer Inst.
  doi: 10.1093/jnci/djt300
– volume: 33
  start-page: 1055
  year: 2012
  ident: 313_CR32
  publication-title: Carcinogenesis
  doi: 10.1093/carcin/bgs112
– volume: 66
  start-page: 462
  year: 2013
  ident: 313_CR23
  publication-title: Microb. Ecol.
  doi: 10.1007/s00248-013-0245-9
– volume: 2
  start-page: 27
  year: 2018
  ident: 313_CR30
  publication-title: Nat. Biomed. Eng.
  doi: 10.1038/s41551-017-0181-y
– volume: 22
  start-page: 501
  year: 2016
  ident: 313_CR14
  publication-title: World J. Gastroenterol.
  doi: 10.3748/wjg.v22.i2.501
– volume: 33
  start-page: 1381
  year: 2014
  ident: 313_CR27
  publication-title: Eur. J. Clin. Microbiol. Infect. Dis.
  doi: 10.1007/s10096-014-2081-3
– volume: 7
  year: 2012
  ident: 313_CR31
  publication-title: PLoS. ONE
  doi: 10.1371/journal.pone.0039743
– volume: 44
  start-page: 837
  year: 1988
  ident: 313_CR20
  publication-title: Biometrics
  doi: 10.2307/2531595
– volume: 293
  start-page: 172
  year: 2005
  ident: 313_CR5
  publication-title: J. Am. Med. Assoc.
  doi: 10.1001/jama.293.2.172
– volume: 20
  start-page: 1425
  year: 1999
  ident: 313_CR9
  publication-title: Carcinogenesis
  doi: 10.1093/carcin/20.8.1425
– volume: 11
  start-page: 129
  year: 2013
  ident: 313_CR47
  publication-title: J. Thromb. Haemost.
  doi: 10.1111/jth.12262
– volume: 15
  start-page: 193
  year: 2015
  ident: 313_CR45
  publication-title: J. Funct. Foods
  doi: 10.1016/j.jff.2015.03.020
SSID ssj0025474
Score 2.5159485
Snippet Colorectal cancer (CRC) is the third most common form of cancer and poses a critical public health threat due to the global spread of westernized diets high in...
Colorectal cancer (CRC) is the third most common form of cancer and poses a critical public health threat due to theglobal spread of westernized diets high in...
SourceID nrf
pubmedcentral
proquest
pubmed
crossref
springer
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 1
SubjectTerms 45/23
692/53/2421
692/699/67/2322
Aged
Animals
Bacteria - classification
Bacteria - genetics
Biomedical and Life Sciences
Biomedicine
Cancer
Cholesterol
Cholesterol - genetics
Colorectal cancer
Colorectal carcinoma
Colorectal Neoplasms - diagnosis
Colorectal Neoplasms - genetics
Colorectal Neoplasms - microbiology
Colorectal Neoplasms - pathology
Diet
Diet, High-Fat - adverse effects
Dietary intake
Digestive system
Feces - microbiology
Female
Gastrointestinal Microbiome - genetics
Gut microbiota
High cholesterol diet
High fat diet
Humans
Intestinal microflora
Male
Meat
Medical Biochemistry
Metagenome - genetics
Mice
Microbiomes
Microbiota
Microbiota - genetics
Middle Aged
Molecular Medicine
Prediction models
Public health
Risk Assessment
Stem Cells
Westernization
생화학
SummonAdditionalLinks – databaseName: Springer Nature HAS Fully OA
  dbid: AAJSJ
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Lb9QwELb6kBAXRFseCwUZhDiALBI7dpzjCrUqK5ULVOrNsmOnrNpNUJo99N8z4zxgKa2EcogUjy3bM7ZnMuNvCHkHR3Bi86Jk2ivJQEIssy5PWBFAeApZuZLjbeTTr-rkLFucy_Mtko53YWLQfoS0jNv0GB326TrlPEfbt2CINsiybbKLSO0g2rvz-eLbYrKyZBahl4FeMQGH1ejKFPp2IxuH0XbdVv_SM2-HS_7lM41H0fFj8mjQIem87_Ue2Qr1PjmYw4Ca1Q19T2NUZ_xdvk8enA7O8wPS_BEgRJuKWoqI1bjjQWMlcr-lvo-8g4ZpzJFDbe3hY-hse0MxDJ3aCcqTDjl-6MW6o6tlj-i0ClClxzl5Qs6Oj75_PmFDvgVWyjzpWO6l9CJNq9RJC3oar3LglEaLkVvpbOkTaYV1XPu8dIIL0IV8oQqZBC8LH8RTslM3dXhOKM-ClRV38FiEJNPOeqmyIgmhCCqIGUnGiTflAEaOOTGuTHSKC216XhnglUFemWxGPkxVfvZIHPcRvwVumstyaRA_G98XjblsDVgJX4xKNUKgzsjhyGwzrNxrAyZZolAvhTbeTMWw5tCRYuvQrCMNTAporjCOZ71sTF0SqdQ851A735CaiQD7s1lSL39EXG-lMR2YnJGPo3z97tadI33xX9QvyUOO4o8REOKQ7HTtOrwCrapzr4d19AvhIxu1
  priority: 102
  providerName: Springer Nature
Title Development of a colorectal cancer diagnostic model and dietary risk assessment through gut microbiome analysis
URI https://link.springer.com/article/10.1038/s12276-019-0313-4
https://www.ncbi.nlm.nih.gov/pubmed/31582724
https://www.proquest.com/docview/2300608354
https://www.proquest.com/docview/2301445223
https://pubmed.ncbi.nlm.nih.gov/PMC6802675
https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002518852
Volume 51
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
ispartofPNX Experimental and Molecular Medicine, 2019, 51(0), , pp.1-15
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1bb9MwFLbYJiGkCUHHJTAqgxAPIGtJHMfJEyrVplFpEwIm9c1yYmdUo8mWpg_795zjXEq5THmI5Eti5xzb55bvEPIWjmBfyzRniYkFAw7RTGfSZ6kF5klFkeUh_o18dh6fXkSzuZh3BrdVF1bZ74luozZVjjbyIxCV_Rjlhejj9Q3DrFHoXe1SaOyQPYQuQ66W843CJSKHwhyAiME4nFu9V5MnRysolKhLpwzRC1m0dS7tlHXxL5Hz78jJP9yn7lQ6eUQeduIknbT0f0zu2XJEDiYlqNLLW_qOugBPZzkfkftnnR99RPZbax1tf0I6INVvsUO0KqimCGaNmyE8PEfGqKlpg_LgRdSlz6G6NFBoG13fUoxQp3pA-aRd-h96uW7octGCPS0tdGkhUJ6Qi5Pj79NT1qViYLmQfsOkEcLwICiCTGgQ4cJCAhETVCZDLTKdG19orrMwMTLPeMhBTDJpnArfGpEay5-S3bIq7XNCw8hqUYQZXBrRypJMGxFHqW9tamPLPeL3hFB5h1OO6TJ-Kucv54lqaaeAdgpppyKPvB-6XLcgHXc1fgPUVVf5QiG0Nt4vK3VVK1AgPqs4SBAd1SOHPfFVt6hXasOCHnk9VMNyRB-LLm21dm3go4BQC_N41vLKMCQeiCSUIfSWW1w0NMDxbNeUix8O8jtOMFOY8MiHnt82w_rvTF_cPYmX5EGI_I_REPyQ7Db12r4CCavJxm4ZjcneZDL7NoP7p-PzL1-hdBpPx85q8Quygybl
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwEB61RQIkhGDLY6GAQcABZDWx4zwOCFVAtUu7PbXS3owTO-2q3aTsQ2j_FL-RmTx2WR69VTlEiu3Ezow9M57xNwCvUQR7JkoyHttQceQQw00aeTxxyDyJytNM0GnkwVHYOwm-DtVwA362Z2EorLJdE6uF2pYZ7ZHvoqrshaQvBB8vv3PKGkXe1TaFRs0WB27xA0226Yf-Z6TvGyH2vxx_6vEmqwDPVOTNeGSVstL3cz9VBrURkUfYn5jsImFUajLrKSNNKmIbZakUEiW-TcJEec6qxDqJ792EGyh4PTL2ouHKwFNBhfrso0rDJcrJ1osq490pPozIdk84oSXyYE0ObhaT_F8q7t-Rmn-4ayspuH8P7jbqK9ur-e0-bLiiA9t7BZru4wV7y6qA0mqnvgM3B43fvgN36t1BVh962obyt1glVubMMALPpsUXX54RI06YrYMA8UOsStfDTGHxoZuZyYJRRDwzS1RR1qQbYqfzGRuPanCpscMmNeTKAzi5FiI9hK2iLNxjYCJwRuUixcsQOlqcGqvCIPGcS1zoZBe8lhA6a3DRKT3Hha788zLWNe000k4T7XTQhXfLJpc1KMhVlV8hdfV5NtIE5U3301KfTzQaLH0d-jGhsXZhpyW-bhaRqV6xfBdeLotx-pNPxxSunFd18KegEo3jeFTzyrJL0lexiAS2jta4aFmB-rNeUozOKojxMKbMZKoL71t-W3XrvyN9cvUgXsCt3vHgUB_2jw6ewm1Bc4EiMeQObM0mc_cMtbtZ-ryaUgy-Xfcc_gUs-l5i
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3rb9MwED9tnTQhIQQdj8IAg4APTFYTJ87jA0KDrVoZqybEpH0zTuyMajQZfQj1X-Ov4y6vUR77NuVDpMRO7d6d7853_h3AC1TBjg7jlEcmkBw5RHOdhA6PLTJPLLMkFXQa-WgUHJz4H07l6Rr8bM7CUFplsyaWC7UpUtoj76Op7ARkL_j9rE6LON4bvL34zqmCFEVam3IaFYsc2uUPdN9mb4Z7SOuXQgz2P78_4HWFAZ7K0Jnz0EhpPNfN3ERqtExEFuLYIvKRhJaJTo0jtacTEZkwTTzhofY3cRBLxxoZG-vhd9dhIySvqAMb7_ZHx59ad0_6JQa0iwYO91BrNjFVL-rP8GFInnzMCTuR-ytacT2fZv8yeP_O2_wjeFvqxMFtuFUbs2y34r47sGbzLmzt5ujIT5bsFSvTS8t9-y5sHtVR_C7crPYKWXUEaguK3zKXWJExzQhKm5Zi_HhKbDllpkoJxB9iZfEepnODD-1cT5eM8uOZbjFGWV18iJ0t5mwyrqCmJha7VAAsd-HkWsh0Dzp5kdsHwIRvtcxEgpcmrLQo0UYGfuxYG9vAej1wGkKotEZJp2Id31QZrfciVdFOIe0U0U75PXjddrmoIEKuavwcqavO07EiYG-6nxXqfKrQfRmqwI0Im7UH2w3xVb2kzNSlAPTgWfsaFwOK8OjcFouyDf4paFLjPO5XvNIOyXNlJEKBvcMVLmob0HhW3-TjryXgeBBRnTLZg52G3y6H9d-ZPrx6Ek9hE-VXfRyODh_BDUGiQGkZ3jZ05tOFfYym3jx5UssUgy_XLca_ALHPY_0
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Development+of+a+colorectal+cancer+diagnostic+model+and+dietary+risk+assessment+through+gut+microbiome+analysis&rft.jtitle=Experimental+%26+molecular+medicine&rft.au=Yang%2C+Jinho&rft.au=McDowell%2C+Andrea&rft.au=Kim%2C+Eun+Kyoung&rft.au=Seo%2C+Hochan&rft.date=2019-10-03&rft.issn=1226-3613&rft.eissn=2092-6413&rft.volume=51&rft.issue=10&rft.spage=1&rft.epage=15&rft_id=info:doi/10.1038%2Fs12276-019-0313-4&rft.externalDBID=n%2Fa&rft.externalDocID=10_1038_s12276_019_0313_4
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1226-3613&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1226-3613&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1226-3613&client=summon