Association between serum 25-hydroxyvitamin D and global DNA methylation in visceral adipose tissue from colorectal cancer patients
Visceral adipose tissue (VAT) has been identified as the essential fat depot for pathogenetic theories that associateobesity and colon cancer. LINE-1 hypomethylation has been mostly detected in tumor colon tissue, but less is known about the epigenetic pattern in surrounding tissues. The aim was to...
Saved in:
Published in | BMC cancer Vol. 19; no. 1; pp. 93 - 7 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
BioMed Central Ltd
21.01.2019
BioMed Central BMC |
Subjects | |
Online Access | Get full text |
ISSN | 1471-2407 1471-2407 |
DOI | 10.1186/s12885-018-5226-4 |
Cover
Loading…
Abstract | Visceral adipose tissue (VAT) has been identified as the essential fat depot for pathogenetic theories that associateobesity and colon cancer. LINE-1 hypomethylation has been mostly detected in tumor colon tissue, but less is known about the epigenetic pattern in surrounding tissues. The aim was to analyze for the first time the potential relationship between serum vitamin D, obesity and global methylation (LINE-1) in the visceral adipose tissue (VAT) from patients with and without colorectal cancer.
A total of 55 patients with colorectal cancer and 35 control subjects participated in the study. LINE-1 DNA methylation in VAT was measured by pyrosequencing. Serum 25(OH)D levels were determined by ELISA.
Cancer patients had lower levels of LINE-1 methylation in VAT compared with the control group. In the subjects with colorectal cancer, LINE-1 DNA methylation levels were associated positively with vitamin D levels (r = 0,463; p < 0.001) and negatively with BMI (r = - 0.334, p = 0.01) and HOMA insulin resistance index (r = - 0.348, p = 0.01). Serum vitamin D was the main variable explaining the LINE-1% variance in the cancer group (β = 0.460, p < 0.001). In a multivariate analysis, subjects with higher LINE-1 methylation values had lower risk of developing colorectal cancer (OR = 0.53; IC95% =0.28-0.99) compared with the control group.
We showed for the first time an association between LINE-1 DNA methylation in VAT and vitamin D levels in subjects with colorectal cancer, highlighting the importance of VAT from cancer patients, which could be modified epigenetically compared to healthy subjects. |
---|---|
AbstractList | Visceral adipose tissue (VAT) has been identified as the essential fat depot for pathogenetic theories that associateobesity and colon cancer. LINE-1 hypomethylation has been mostly detected in tumor colon tissue, but less is known about the epigenetic pattern in surrounding tissues. The aim was to analyze for the first time the potential relationship between serum vitamin D, obesity and global methylation (LINE-1) in the visceral adipose tissue (VAT) from patients with and without colorectal cancer.
A total of 55 patients with colorectal cancer and 35 control subjects participated in the study. LINE-1 DNA methylation in VAT was measured by pyrosequencing. Serum 25(OH)D levels were determined by ELISA.
Cancer patients had lower levels of LINE-1 methylation in VAT compared with the control group. In the subjects with colorectal cancer, LINE-1 DNA methylation levels were associated positively with vitamin D levels (r = 0,463; p < 0.001) and negatively with BMI (r = - 0.334, p = 0.01) and HOMA insulin resistance index (r = - 0.348, p = 0.01). Serum vitamin D was the main variable explaining the LINE-1% variance in the cancer group (β = 0.460, p < 0.001). In a multivariate analysis, subjects with higher LINE-1 methylation values had lower risk of developing colorectal cancer (OR = 0.53; IC95% =0.28-0.99) compared with the control group.
We showed for the first time an association between LINE-1 DNA methylation in VAT and vitamin D levels in subjects with colorectal cancer, highlighting the importance of VAT from cancer patients, which could be modified epigenetically compared to healthy subjects. Visceral adipose tissue (VAT) has been identified as the essential fat depot for pathogenetic theories that associateobesity and colon cancer. LINE-1 hypomethylation has been mostly detected in tumor colon tissue, but less is known about the epigenetic pattern in surrounding tissues. The aim was to analyze for the first time the potential relationship between serum vitamin D, obesity and global methylation (LINE-1) in the visceral adipose tissue (VAT) from patients with and without colorectal cancer.BACKGROUNDVisceral adipose tissue (VAT) has been identified as the essential fat depot for pathogenetic theories that associateobesity and colon cancer. LINE-1 hypomethylation has been mostly detected in tumor colon tissue, but less is known about the epigenetic pattern in surrounding tissues. The aim was to analyze for the first time the potential relationship between serum vitamin D, obesity and global methylation (LINE-1) in the visceral adipose tissue (VAT) from patients with and without colorectal cancer.A total of 55 patients with colorectal cancer and 35 control subjects participated in the study. LINE-1 DNA methylation in VAT was measured by pyrosequencing. Serum 25(OH)D levels were determined by ELISA.METHODSA total of 55 patients with colorectal cancer and 35 control subjects participated in the study. LINE-1 DNA methylation in VAT was measured by pyrosequencing. Serum 25(OH)D levels were determined by ELISA.Cancer patients had lower levels of LINE-1 methylation in VAT compared with the control group. In the subjects with colorectal cancer, LINE-1 DNA methylation levels were associated positively with vitamin D levels (r = 0,463; p < 0.001) and negatively with BMI (r = - 0.334, p = 0.01) and HOMA insulin resistance index (r = - 0.348, p = 0.01). Serum vitamin D was the main variable explaining the LINE-1% variance in the cancer group (β = 0.460, p < 0.001). In a multivariate analysis, subjects with higher LINE-1 methylation values had lower risk of developing colorectal cancer (OR = 0.53; IC95% =0.28-0.99) compared with the control group.RESULTSCancer patients had lower levels of LINE-1 methylation in VAT compared with the control group. In the subjects with colorectal cancer, LINE-1 DNA methylation levels were associated positively with vitamin D levels (r = 0,463; p < 0.001) and negatively with BMI (r = - 0.334, p = 0.01) and HOMA insulin resistance index (r = - 0.348, p = 0.01). Serum vitamin D was the main variable explaining the LINE-1% variance in the cancer group (β = 0.460, p < 0.001). In a multivariate analysis, subjects with higher LINE-1 methylation values had lower risk of developing colorectal cancer (OR = 0.53; IC95% =0.28-0.99) compared with the control group.We showed for the first time an association between LINE-1 DNA methylation in VAT and vitamin D levels in subjects with colorectal cancer, highlighting the importance of VAT from cancer patients, which could be modified epigenetically compared to healthy subjects.CONCLUSIONSWe showed for the first time an association between LINE-1 DNA methylation in VAT and vitamin D levels in subjects with colorectal cancer, highlighting the importance of VAT from cancer patients, which could be modified epigenetically compared to healthy subjects. Abstract Background Visceral adipose tissue (VAT) has been identified as the essential fat depot for pathogenetic theories that associateobesity and colon cancer. LINE-1 hypomethylation has been mostly detected in tumor colon tissue, but less is known about the epigenetic pattern in surrounding tissues. The aim was to analyze for the first time the potential relationship between serum vitamin D, obesity and global methylation (LINE-1) in the visceral adipose tissue (VAT) from patients with and without colorectal cancer. Methods A total of 55 patients with colorectal cancer and 35 control subjects participated in the study. LINE-1 DNA methylation in VAT was measured by pyrosequencing. Serum 25(OH)D levels were determined by ELISA. Results Cancer patients had lower levels of LINE-1 methylation in VAT compared with the control group. In the subjects with colorectal cancer, LINE-1 DNA methylation levels were associated positively with vitamin D levels (r = 0,463; p < 0.001) and negatively with BMI (r = − 0.334, p = 0.01) and HOMA insulin resistance index (r = − 0.348, p = 0.01). Serum vitamin D was the main variable explaining the LINE-1% variance in the cancer group (β = 0.460, p < 0.001). In a multivariate analysis, subjects with higher LINE-1 methylation values had lower risk of developing colorectal cancer (OR = 0.53; IC95% =0.28–0.99) compared with the control group. Conclusions We showed for the first time an association between LINE-1 DNA methylation in VAT and vitamin D levels in subjects with colorectal cancer, highlighting the importance of VAT from cancer patients, which could be modified epigenetically compared to healthy subjects. |
ArticleNumber | 93 |
Audience | Academic |
Author | Clemente-Postigo, Mercedes Sánchez-Alcoholado, Lidia Crujeiras, Ana B. Torres, Esperanza Morcillo, Sonsoles Castellano-Castillo, Daniel Tinahones, Francisco José Macias-Gonzalez, Manuel |
Author_xml | – sequence: 1 givenname: Daniel surname: Castellano-Castillo fullname: Castellano-Castillo, Daniel – sequence: 2 givenname: Sonsoles surname: Morcillo fullname: Morcillo, Sonsoles – sequence: 3 givenname: Ana B. surname: Crujeiras fullname: Crujeiras, Ana B. – sequence: 4 givenname: Lidia surname: Sánchez-Alcoholado fullname: Sánchez-Alcoholado, Lidia – sequence: 5 givenname: Mercedes surname: Clemente-Postigo fullname: Clemente-Postigo, Mercedes – sequence: 6 givenname: Esperanza surname: Torres fullname: Torres, Esperanza – sequence: 7 givenname: Francisco José surname: Tinahones fullname: Tinahones, Francisco José – sequence: 8 givenname: Manuel orcidid: 0000-0002-6475-4704 surname: Macias-Gonzalez fullname: Macias-Gonzalez, Manuel |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30665376$$D View this record in MEDLINE/PubMed |
BookMark | eNp1ktuL1DAUxousuBf9A3yRgCD60DW3Ns2LMOx6GVgUvDyHNDmdydI2Y5OuO8_-46Z2V6ai5CEh5_d95Jx8p9lR73vIsqcEnxNSla8DoVVV5JhUeUFpmfMH2QnhguSUY3F0cD7OTkO4xpiIClePsmOGy7JgojzJfq5C8Mbp6HyPaog_AHoUYBg7RIt8u7eDv93fuKg716NLpHuLNq2vdYsuP65QB3G7b2dxqt-4YGBINW3dzgdA0YUwAmoG3yHjWz-AialsdJ84tEtC6GN4nD1sdBvgyd1-ln179_brxYf86tP79cXqKjeFFDHXjAqOy5pbK2lNaqCSMkENE6lNqk3BbQ2YaMDa1pTXmJZU8lpXpbCkbBg7y9azr_X6Wu0G1-lhr7x26veFHzZKD9GZFpSUtWaEWMmw5SVwyUTTaG4JsEJqKZPXm9lrN9YdWJP6SI0vTJeV3m3Vxt-oknFSiMng5Z3B4L-PEKLqpum1re7Bj0FRIiTHsmQ4oc9ndKPT01zf-ORoJlytiopwWkgydXf-DyotC50zKTiNS_cLwauFIDERbuNGjyGo9ZfPS_bFAbsF3cZt8O04_XxYgs8O5_JnIPeJS4CYATP4EAZolEnpmnzSc12rCFZTttWcbZWyraZsK56U5C_lvfn_Nb8AWs36eA |
CitedBy_id | crossref_primary_10_1080_15592294_2021_1950991 crossref_primary_10_23736_S2724_6507_20_03299_X crossref_primary_10_1155_2019_7406078 crossref_primary_10_1016_j_freeradbiomed_2022_10_003 crossref_primary_10_1007_s11888_021_00465_8 crossref_primary_10_3390_ijms21124484 crossref_primary_10_1002_mnfr_202100125 crossref_primary_10_7717_peerj_17105 crossref_primary_10_2147_TACG_S365613 crossref_primary_10_3390_jcm8071041 crossref_primary_10_1007_s11154_019_09522_y crossref_primary_10_2217_epi_2022_0288 crossref_primary_10_1039_D0FO01984D crossref_primary_10_3390_biom9070289 crossref_primary_10_1002_mco2_496 crossref_primary_10_1002_mnfr_202000437 crossref_primary_10_1016_j_jgg_2024_12_020 crossref_primary_10_1016_j_phanu_2020_100231 |
Cites_doi | 10.1158/1078-0432.CCR-08-3330 10.1016/j.jnutbio.2004.08.004 10.3748/wjg.v20.i18.5177 10.1111/j.1749-6632.2011.06096.x 10.1017/S0007114516000696 10.1515/cclm-2012-0624 10.1007/s12263-015-0480-4 10.2174/0929867324666161117155325 10.1186/1471-2407-14-712 10.1371/journal.pone.0034615 10.1038/nrendo.2014.94 10.1038/ng0894-536 10.1136/gutjnl-2015-310912 10.1038/ng1834 10.1038/nrg2640 10.1093/nar/gki987 10.1158/1055-9965.EPI-14-1161 10.1002/mnfr.201400079 10.1093/jnci/dju195 10.4161/15592294.2014.969617 10.1158/1055-9965.EPI-08-0926 10.1136/gut.2004.054718 10.1136/gut.2005.073163 10.3389/fendo.2014.00065 10.1136/gut.2009.183707 10.1371/journal.pone.0109478 10.1136/gutjnl-2013-304701 10.1177/003335490912400320 10.1016/S2213-8587(14)70134-2 10.1007/s00384-003-0539-3 10.2217/epi.11.22 10.18632/oncotarget.10998 10.1016/S0140-6736(89)91789-3 10.1186/s13148-018-0493-0 10.1111/acel.12030 10.1016/j.jsbmb.2016.11.020 10.1186/1476-4598-9-125 10.1038/ijo.2014.34. 10.1016/j.mrfmmm.2012.02.005 10.1016/j.gastrohep.2012.01.002. 10.1038/s41366-018-0065-6 10.1186/1475-2891-10-51 10.18632/oncotarget.4450 10.1186/1868-7083-4-10 |
ContentType | Journal Article |
Copyright | COPYRIGHT 2019 BioMed Central Ltd. The Author(s). 2019 |
Copyright_xml | – notice: COPYRIGHT 2019 BioMed Central Ltd. – notice: The Author(s). 2019 |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM ISR 7X8 5PM DOA |
DOI | 10.1186/s12885-018-5226-4 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Gale In Context: Science MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – 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 |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1471-2407 |
EndPage | 7 |
ExternalDocumentID | oai_doaj_org_article_99ba311d930d46e4937ffa4d1e359a99 PMC6341579 A581425913 30665376 10_1186_s12885_018_5226_4 |
Genre | Journal Article |
GrantInformation_xml | – fundername: NICOLAS MONARDES SAS SPAIN grantid: C-0029-2014 – fundername: CIBERobn MINISTERIO DE SANIDAD ISCIII SPAIN grantid: CB06/03/0018 – fundername: ISCIII-FIS SPAIN grantid: PI11/01661 – fundername: CONSEJERIA INNOVACION JUNTA DE ANDALUCIA ,SPAIN grantid: PI11-CTS-8181 – fundername: FPU MINISTERIO EDUCACION SPAIN grantid: 13/04211 – fundername: ; – fundername: ; grantid: PI11/01661 – fundername: ; grantid: CB06/03/0018 – fundername: ; grantid: 13/04211 – fundername: ; grantid: PI11-CTS-8181 – fundername: ; grantid: C-0029-2014 |
GroupedDBID | --- 0R~ 23N 2WC 53G 5VS 6J9 6PF 7X7 88E 8FI 8FJ AAFWJ AAJSJ AASML AAWTL AAYXX ABDBF ABUWG ACGFO ACGFS ACIHN ACMJI ACPRK ACUHS ADBBV ADRAZ ADUKV AEAQA AENEX AFKRA AFPKN AHBYD AHMBA AHYZX ALIPV ALMA_UNASSIGNED_HOLDINGS AMKLP AMTXH AOIJS BAPOH BAWUL BCNDV BENPR BFQNJ BMC BPHCQ BVXVI C6C CCPQU CITATION CS3 DIK DU5 E3Z EAD EAP EAS EBD EBLON EBS EJD EMB EMK EMOBN ESX F5P FYUFA GROUPED_DOAJ GX1 H13 HMCUK HYE IAO IHR IHW INH INR ISR ITC KQ8 M1P M48 M~E O5R O5S OK1 OVT P2P PGMZT PHGZM PHGZT PIMPY PQQKQ PROAC PSQYO RBZ RNS ROL RPM RSV SBL SOJ SV3 TR2 TUS U2A UKHRP W2D WOQ WOW XSB -A0 3V. ACRMQ ADINQ C24 CGR CUY CVF ECM EIF NPM PMFND 7X8 PPXIY 5PM PJZUB PUEGO |
ID | FETCH-LOGICAL-c597t-a327406b4dd92b1be292372c374712ac54dbe01ae0adb24b026294ba867d16f33 |
IEDL.DBID | M48 |
ISSN | 1471-2407 |
IngestDate | Wed Aug 27 01:13:39 EDT 2025 Thu Aug 21 18:22:58 EDT 2025 Fri Jul 11 11:43:51 EDT 2025 Tue Jun 17 21:46:31 EDT 2025 Tue Jun 10 20:29:07 EDT 2025 Fri Jun 27 04:22:32 EDT 2025 Thu May 22 21:19:01 EDT 2025 Wed Feb 19 02:35:03 EST 2025 Tue Jul 01 03:06:13 EDT 2025 Thu Apr 24 22:51:54 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Keywords | Obesity Epigenetic Vitamin D Global DNA methylation Colorectal cancer |
Language | English |
License | Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c597t-a327406b4dd92b1be292372c374712ac54dbe01ae0adb24b026294ba867d16f33 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ORCID | 0000-0002-6475-4704 |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.1186/s12885-018-5226-4 |
PMID | 30665376 |
PQID | 2179409630 |
PQPubID | 23479 |
PageCount | 7 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_99ba311d930d46e4937ffa4d1e359a99 pubmedcentral_primary_oai_pubmedcentral_nih_gov_6341579 proquest_miscellaneous_2179409630 gale_infotracmisc_A581425913 gale_infotracacademiconefile_A581425913 gale_incontextgauss_ISR_A581425913 gale_healthsolutions_A581425913 pubmed_primary_30665376 crossref_citationtrail_10_1186_s12885_018_5226_4 crossref_primary_10_1186_s12885_018_5226_4 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2019-01-21 |
PublicationDateYYYYMMDD | 2019-01-21 |
PublicationDate_xml | – month: 01 year: 2019 text: 2019-01-21 day: 21 |
PublicationDecade | 2010 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: London |
PublicationTitle | BMC cancer |
PublicationTitleAlternate | BMC Cancer |
PublicationYear | 2019 |
Publisher | BioMed Central Ltd BioMed Central BMC |
Publisher_xml | – name: BioMed Central Ltd – name: BioMed Central – name: BMC |
References | JP Issa (5226_CR11) 1994; 7 5226_CR9 U Hübner (5226_CR44) 2013; 51 M Pufulete (5226_CR45) 2005; 54 EE Frezza (5226_CR8) 2006; 55 CM Suter (5226_CR14) 2004; 19 D Castellano-Castillo (5226_CR27) 2018; 10 5226_CR29 T Shanmugalingam (5226_CR40) 2014; 14 5226_CR3 HS Tapp (5226_CR43) 2013; 12 5226_CR26 M Barchitta (5226_CR31) 2014; 9 5226_CR22 PG Vashi (5226_CR25) 2011; 10 M Bardou (5226_CR5) 2013; 62 JC Figueiredo (5226_CR39) 2009; 18 5226_CR24 V Nair-Shalliker (5226_CR42) 2012; 733 5226_CR41 AI Pérez-Hernández (5226_CR10) 2014; 5 JA Alegria-Torres (5226_CR15) 2011; 3 AE Harvey (5226_CR7) 2011; 1229 R Dou (5226_CR20) 2016; 115 DJ Weisenberger (5226_CR23) 2015; 24 DJ Weisenberger (5226_CR21) 2006; 38 JD Morillas (5226_CR4) 2012; 35 AJ Cox (5226_CR1) 2015; 3 J Park (5226_CR6) 2014; 10 AM Oommen (5226_CR16) 2005; 16 HD Woo (5226_CR36) 2012; 7 ES Schernhammer (5226_CR17) 2010; 59 S Ogino (5226_CR35) 2009; 15 DJ Weisenberger (5226_CR12) 2005; 33 S Riondino (5226_CR2) 2014; 20 5226_CR38 5226_CR33 5226_CR32 5226_CR13 R Cordaux (5226_CR34) 2009; 10 A Agodi (5226_CR18) 2015; 10 GM Martín-Núñez (5226_CR19) 2014; 58 C Zhuo (5226_CR37) 2015; 6 GM Martín-Núñez (5226_CR28) 2014; 9 V Turcot (5226_CR30) 2012; 4 |
References_xml | – volume: 15 start-page: 4431 year: 2009 ident: 5226_CR35 publication-title: Clin Cancer Res doi: 10.1158/1078-0432.CCR-08-3330 – volume: 16 start-page: 74 year: 2005 ident: 5226_CR16 publication-title: J Nutr Biochem doi: 10.1016/j.jnutbio.2004.08.004 – volume: 20 start-page: 5177 year: 2014 ident: 5226_CR2 publication-title: World J Gastroenterol doi: 10.3748/wjg.v20.i18.5177 – volume: 1229 start-page: 45 year: 2011 ident: 5226_CR7 publication-title: Ann N Y Acad Sci doi: 10.1111/j.1749-6632.2011.06096.x – volume: 115 start-page: 1643 year: 2016 ident: 5226_CR20 publication-title: Br J Nutr doi: 10.1017/S0007114516000696 – volume: 51 start-page: 649 year: 2013 ident: 5226_CR44 publication-title: Clin Chem Lab Med doi: 10.1515/cclm-2012-0624 – volume: 10 start-page: 30 year: 2015 ident: 5226_CR18 publication-title: Genes Nutr doi: 10.1007/s12263-015-0480-4 – ident: 5226_CR41 doi: 10.2174/0929867324666161117155325 – volume: 14 start-page: 712 year: 2014 ident: 5226_CR40 publication-title: BMC Cancer doi: 10.1186/1471-2407-14-712 – volume: 7 start-page: e34615 year: 2012 ident: 5226_CR36 publication-title: PLoS One doi: 10.1371/journal.pone.0034615 – volume: 10 start-page: 455 year: 2014 ident: 5226_CR6 publication-title: Nat Rev Endocrinol doi: 10.1038/nrendo.2014.94 – volume: 7 start-page: 536 year: 1994 ident: 5226_CR11 publication-title: Nat Genet doi: 10.1038/ng0894-536 – ident: 5226_CR3 doi: 10.1136/gutjnl-2015-310912 – volume: 38 start-page: 787 year: 2006 ident: 5226_CR21 publication-title: Nat Genet doi: 10.1038/ng1834 – volume: 10 start-page: 691 year: 2009 ident: 5226_CR34 publication-title: Nat Rev Genet doi: 10.1038/nrg2640 – volume: 33 start-page: 6823 year: 2005 ident: 5226_CR12 publication-title: Nucleic Acids Res doi: 10.1093/nar/gki987 – volume: 24 start-page: 512 year: 2015 ident: 5226_CR23 publication-title: Cancer Epidemiol Biomark Prev doi: 10.1158/1055-9965.EPI-14-1161 – volume: 58 start-page: 1528 year: 2014 ident: 5226_CR19 publication-title: Mol Nutr Food Res doi: 10.1002/mnfr.201400079 – ident: 5226_CR13 doi: 10.1093/jnci/dju195 – volume: 9 start-page: 1322 year: 2014 ident: 5226_CR28 publication-title: Epigenetics doi: 10.4161/15592294.2014.969617 – volume: 18 start-page: 1041 year: 2009 ident: 5226_CR39 publication-title: Cancer Epidemiol Biomark Prev doi: 10.1158/1055-9965.EPI-08-0926 – volume: 54 start-page: 648 year: 2005 ident: 5226_CR45 publication-title: Gut doi: 10.1136/gut.2004.054718 – volume: 55 start-page: 285 year: 2006 ident: 5226_CR8 publication-title: Gut doi: 10.1136/gut.2005.073163 – volume: 5 start-page: 65 year: 2014 ident: 5226_CR10 publication-title: Front Endocrinol (Lausanne) doi: 10.3389/fendo.2014.00065 – volume: 59 start-page: 794 year: 2010 ident: 5226_CR17 publication-title: Gut doi: 10.1136/gut.2009.183707 – ident: 5226_CR38 – volume: 9 start-page: e109478 year: 2014 ident: 5226_CR31 publication-title: PLoS One doi: 10.1371/journal.pone.0109478 – volume: 62 start-page: 933 year: 2013 ident: 5226_CR5 publication-title: Gut doi: 10.1136/gutjnl-2013-304701 – ident: 5226_CR29 doi: 10.1177/003335490912400320 – volume: 3 start-page: 207 year: 2015 ident: 5226_CR1 publication-title: Lancet Diabetes Endocrinol doi: 10.1016/S2213-8587(14)70134-2 – volume: 19 start-page: 95 year: 2004 ident: 5226_CR14 publication-title: Int J Color Dis doi: 10.1007/s00384-003-0539-3 – volume: 3 start-page: 267 year: 2011 ident: 5226_CR15 publication-title: Epigenomics doi: 10.2217/epi.11.22 – ident: 5226_CR9 doi: 10.18632/oncotarget.10998 – ident: 5226_CR24 doi: 10.1016/S0140-6736(89)91789-3 – volume: 10 start-page: 60 year: 2018 ident: 5226_CR27 publication-title: Clin Epigenetics doi: 10.1186/s13148-018-0493-0 – volume: 12 start-page: 148 year: 2013 ident: 5226_CR43 publication-title: Aging Cell doi: 10.1111/acel.12030 – ident: 5226_CR26 doi: 10.1016/j.jsbmb.2016.11.020 – ident: 5226_CR33 doi: 10.1186/1476-4598-9-125 – ident: 5226_CR32 doi: 10.1038/ijo.2014.34. – volume: 733 start-page: 50 year: 2012 ident: 5226_CR42 publication-title: Mutat Res Mol Mech Mutagen doi: 10.1016/j.mrfmmm.2012.02.005 – volume: 35 start-page: 109 year: 2012 ident: 5226_CR4 publication-title: Gastroenterol Hepatol doi: 10.1016/j.gastrohep.2012.01.002. – ident: 5226_CR22 doi: 10.1038/s41366-018-0065-6 – volume: 10 start-page: 51 year: 2011 ident: 5226_CR25 publication-title: Nutr J doi: 10.1186/1475-2891-10-51 – volume: 6 start-page: 23820 year: 2015 ident: 5226_CR37 publication-title: Oncotarget doi: 10.18632/oncotarget.4450 – volume: 4 start-page: 10 year: 2012 ident: 5226_CR30 publication-title: Clin Epigenetics doi: 10.1186/1868-7083-4-10 |
SSID | ssj0017808 |
Score | 2.3454015 |
Snippet | Visceral adipose tissue (VAT) has been identified as the essential fat depot for pathogenetic theories that associateobesity and colon cancer. LINE-1... Abstract Background Visceral adipose tissue (VAT) has been identified as the essential fat depot for pathogenetic theories that associateobesity and colon... |
SourceID | doaj pubmedcentral proquest gale pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 93 |
SubjectTerms | Adipose tissues Aged Care and treatment Colorectal cancer Colorectal Neoplasms - blood Colorectal Neoplasms - genetics Development and progression DNA Methylation Enzyme-Linked Immunosorbent Assay Epigenetic Female Global DNA methylation Humans Intra-Abdominal Fat - metabolism Long Interspersed Nucleotide Elements - genetics Male Middle Aged Multivariate Analysis Obesity Obesity - blood Obesity - genetics Risk factors Sequence Analysis, DNA Vitamin D Vitamin D - analogs & derivatives Vitamin D - blood |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3daxQxEA_SB_FF_Ha1ahRBEEI3m-xu8nhaSxXaB7XQt5CvtQt2r3T3Cn3uP96Z3dxxi6Avvl7m4DIzmZnfZeYXQt5rHMjkuWVN4CWTtdNM29Iy7TwAjKYp7UhffHRcHZ7Ib6fl6dZTX9gTNtEDT4rb09pZwXnQIg-yihLSadNYGXgUpbZ6HN2DnLcGU-n-oFa5SneYXFV7PURhhU1qimG9weQsC41k_X-G5K2cNO-X3EpABw_I_VQ50sX0ix-SO7F7RO4epbvxx-RmS9M0tV9RcLDVOS1KdnYdsGHlqh3sedvRfWq7QCc2ELp_vKD4kvT11BdHYf2q7T3-W0VtaC-WfaTDaCCK0ygUia4xUMKyR6e5pImdtX9CTg6-_Px8yNITC8wDkhiYFYBK88rJEHThuIsFFHx14QVi1cL6UgYXc25jboMrpAPEVmjprKrqwKtGiKdkp1t28TmhqgHwlmvrZQDIxyvnuPI197qBeOqkyEi-VrnxiX8cn8H4bUYcoiozWcmAlQxayciMfNx85WIi3_ib8Ce040YQebPHD8CbTPIm8y9vysgb9AIzDaFuTr9ZlIpDdNMctvFulEDujA6bc37ZVd-brz--z4Q-JKFmCXv0Ns06gKaQbmsmuTuThMPtZ8tv1-5ocAk74rq4XPWmwEgK-FPkGXk2uedm6wLv0yBzZKSeOe5MN_OVrj0bucUrqGrKWr_4H8p8Se5BHMB2PFbwXbIzXK7iKyjhBvd6PK23eOBCag priority: 102 providerName: Directory of Open Access Journals |
Title | Association between serum 25-hydroxyvitamin D and global DNA methylation in visceral adipose tissue from colorectal cancer patients |
URI | https://www.ncbi.nlm.nih.gov/pubmed/30665376 https://www.proquest.com/docview/2179409630 https://pubmed.ncbi.nlm.nih.gov/PMC6341579 https://doaj.org/article/99ba311d930d46e4937ffa4d1e359a99 |
Volume | 19 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1bi9NAFB72AuKLeLe61lEEQYibSSaXeRBp3V1WoUWqheLLMJdkt7Cbrk272Gf_uOdMprXBRXzJQ-c0MHPuOWe-Q8hrgRcyWaiC0rIk4JkWgVCJCoQ2kGCUZaIcfPFgmJ6O-edJMtkh6_FW_gDrG1M7nCc1nl-8-_lj9QEU_r1T-Dw9rMHG5tiClgcYTQR8l-yDY8pQTwf8T1Ehy92AOgb2GIsKmS9y3viKlptyaP5_2-wtp9VuqNzyUCd3yR0fWtJeIwv3yE5R3Se3Br54_oD82mIF9f1ZFCRweUmjJDhfWexouZ4u1OW0okdUVZY2cCH0aNijOGp61TTOUVi_ntYGP2dRZadXs7qgC8dBitdVKCJhoyWFZYNSNacevrV-SMYnx98-ngZ-BkNgINVYBCqGtDVMNbdWRJrpIoKIMItMjMlspEzCrS5CpopQWR1xDSldJLhWeZpZlpZx_IjsVbOqeEJoXkJ2FwpluIWckKVas9xkzIgSDK7mcYeE6yOXxgOU45yMC-kSlTyVDZckcEkilyTvkLebv1w16Bz_Iu4jHzeECKztfpjNz6TXUymEVjFjVsSh5WnBIXorS8UtK-JEKCE65AVKgWxuqW7Mg-wlOQPzJxhs45WjQHCNCrt3ztSyruWnr6MW0RtPVM5gj0b5yxBwUojH1aI8aFGC9pvW8su1OEpcwpa5qpgtaxmhqYUENQ475HEjnputx1hwA9fSIVlLcFtn016ppucOfDyFsCfJxNP_2eUzchsMAfbjBRE7IHuL-bJ4DjHcQnfJbjbJumS_fzz8Muq6LyFdp63wHPW__wZcmEVy |
linkProvider | Scholars Portal |
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=Association+between+serum+25-hydroxyvitamin+D+and+global+DNA+methylation+in+visceral+adipose+tissue+from+colorectal+cancer+patients&rft.jtitle=BMC+cancer&rft.au=Castellano-Castillo%2C+Daniel&rft.au=Morcillo%2C+Sonsoles&rft.au=Crujeiras%2C+Ana+B&rft.au=Sanchez-Alcoholado%2C+Lidia&rft.date=2019-01-21&rft.pub=BioMed+Central+Ltd&rft.issn=1471-2407&rft.eissn=1471-2407&rft.volume=19&rft.issue=1&rft_id=info:doi/10.1186%2Fs12885-018-5226-4&rft.externalDBID=ISR&rft.externalDocID=A581425913 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1471-2407&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1471-2407&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1471-2407&client=summon |