LincROR Mediates the Suppressive Effects of Curcumin on Hepatocellular Carcinoma Through Inactivating Wnt/β-Catenin Signaling
As one of the leading causes of cancer-related death in the world, hepatocellular carcinoma (HCC) has continued to attract growing attention in recent decades. The use of traditional Chinese herbs in medicine has been practiced for thousands of years, and holds the potential of being a possible trea...
Saved in:
Published in | Frontiers in pharmacology Vol. 11; p. 847 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Frontiers Media S.A
02.07.2020
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | As one of the leading causes of cancer-related death in the world, hepatocellular carcinoma (HCC) has continued to attract growing attention in recent decades. The use of traditional Chinese herbs in medicine has been practiced for thousands of years, and holds the potential of being a possible treatment for HCC. Curcumin, a bioactive ingredient derived from Curcuma longa, exhibits anti-tumor activity in various cancers. Although the effects of Curcumin on HCC have been elucidated, the underlying mechanism remains unclear. In the present study, Curcumin was demonstrated to inhibit the proliferation of HCC cells via inducing cell cycle arrest and apoptosis. Several previously reported lncRNAs related to tumorigenesis were chosen for examination of their expression profiles, and lincROR was found to be the most down-regulated in the Curcumin-treated HCC cells. Furthermore, Curcumin was found to decrease β-catenin expression and induce the inactivation of Wnt/β-catenin signaling. Therefore, Curcumin suppressed tumor growth through a lincROR/β-catenin regulatory pattern. In conclusion, our results demonstrated that Curcumin suppressed the cell proliferation via the down-regulation of lincROR and inactivation of Wnt/β-catenin signaling, suggesting that it may be a potential anti-cancer candidate for HCC patients with activated Wnt/β-catenin signaling.As one of the leading causes of cancer-related death in the world, hepatocellular carcinoma (HCC) has continued to attract growing attention in recent decades. The use of traditional Chinese herbs in medicine has been practiced for thousands of years, and holds the potential of being a possible treatment for HCC. Curcumin, a bioactive ingredient derived from Curcuma longa, exhibits anti-tumor activity in various cancers. Although the effects of Curcumin on HCC have been elucidated, the underlying mechanism remains unclear. In the present study, Curcumin was demonstrated to inhibit the proliferation of HCC cells via inducing cell cycle arrest and apoptosis. Several previously reported lncRNAs related to tumorigenesis were chosen for examination of their expression profiles, and lincROR was found to be the most down-regulated in the Curcumin-treated HCC cells. Furthermore, Curcumin was found to decrease β-catenin expression and induce the inactivation of Wnt/β-catenin signaling. Therefore, Curcumin suppressed tumor growth through a lincROR/β-catenin regulatory pattern. In conclusion, our results demonstrated that Curcumin suppressed the cell proliferation via the down-regulation of lincROR and inactivation of Wnt/β-catenin signaling, suggesting that it may be a potential anti-cancer candidate for HCC patients with activated Wnt/β-catenin signaling. |
---|---|
AbstractList | As one of the leading causes of cancer-related death in the world, hepatocellular carcinoma (HCC) has continued to attract growing attention in recent decades. The use of traditional Chinese herbs in medicine has been practiced for thousands of years, and holds the potential of being a possible treatment for HCC. Curcumin, a bioactive ingredient derived from Curcuma longa, exhibits anti-tumor activity in various cancers. Although the effects of Curcumin on HCC have been elucidated, the underlying mechanism remains unclear. In the present study, Curcumin was demonstrated to inhibit the proliferation of HCC cells via inducing cell cycle arrest and apoptosis. Several previously reported lncRNAs related to tumorigenesis were chosen for examination of their expression profiles, and lincROR was found to be the most down-regulated in the Curcumin-treated HCC cells. Furthermore, Curcumin was found to decrease β-catenin expression and induce the inactivation of Wnt/β-catenin signaling. Therefore, Curcumin suppressed tumor growth through a lincROR/β-catenin regulatory pattern. In conclusion, our results demonstrated that Curcumin suppressed the cell proliferation via the down-regulation of lincROR and inactivation of Wnt/β-catenin signaling, suggesting that it may be a potential anti-cancer candidate for HCC patients with activated Wnt/β-catenin signaling.As one of the leading causes of cancer-related death in the world, hepatocellular carcinoma (HCC) has continued to attract growing attention in recent decades. The use of traditional Chinese herbs in medicine has been practiced for thousands of years, and holds the potential of being a possible treatment for HCC. Curcumin, a bioactive ingredient derived from Curcuma longa, exhibits anti-tumor activity in various cancers. Although the effects of Curcumin on HCC have been elucidated, the underlying mechanism remains unclear. In the present study, Curcumin was demonstrated to inhibit the proliferation of HCC cells via inducing cell cycle arrest and apoptosis. Several previously reported lncRNAs related to tumorigenesis were chosen for examination of their expression profiles, and lincROR was found to be the most down-regulated in the Curcumin-treated HCC cells. Furthermore, Curcumin was found to decrease β-catenin expression and induce the inactivation of Wnt/β-catenin signaling. Therefore, Curcumin suppressed tumor growth through a lincROR/β-catenin regulatory pattern. In conclusion, our results demonstrated that Curcumin suppressed the cell proliferation via the down-regulation of lincROR and inactivation of Wnt/β-catenin signaling, suggesting that it may be a potential anti-cancer candidate for HCC patients with activated Wnt/β-catenin signaling. As one of the leading causes of cancer-related death in the world, hepatocellular carcinoma (HCC) has continued to attract growing attention in recent decades. The use of traditional Chinese herbs in medicine has been practiced for thousands of years, and holds the potential of being a possible treatment for HCC. Curcumin, a bioactive ingredient derived from Curcuma longa, exhibits anti-tumor activity in various cancers. Although the effects of Curcumin on HCC have been elucidated, the underlying mechanism remains unclear. In the present study, Curcumin was demonstrated to inhibit the proliferation of HCC cells via inducing cell cycle arrest and apoptosis. Several previously reported lncRNAs related to tumorigenesis were chosen for examination of their expression profiles, and lincROR was found to be the most down-regulated in the Curcumin-treated HCC cells. Furthermore, Curcumin was found to decrease β-catenin expression and induce the inactivation of Wnt/β-catenin signaling. Therefore, Curcumin suppressed tumor growth through a lincROR/β-catenin regulatory pattern. In conclusion, our results demonstrated that Curcumin suppressed the cell proliferation via the down-regulation of lincROR and inactivation of Wnt/β-catenin signaling, suggesting that it may be a potential anti-cancer candidate for HCC patients with activated Wnt/β-catenin signaling. As one of the leading causes of cancer-related death in the world, hepatocellular carcinoma (HCC) has continued to attract growing attention in recent decades. The use of traditional Chinese herbs in medicine has been practiced for thousands of years, and holds the potential of being a possible treatment for HCC. Curcumin, a bioactive ingredient derived from Curcuma longa , exhibits anti-tumor activity in various cancers. Although the effects of Curcumin on HCC have been elucidated, the underlying mechanism remains unclear. In the present study, Curcumin was demonstrated to inhibit the proliferation of HCC cells via inducing cell cycle arrest and apoptosis. Several previously reported lncRNAs related to tumorigenesis were chosen for examination of their expression profiles, and lincROR was found to be the most down-regulated in the Curcumin-treated HCC cells. Furthermore, Curcumin was found to decrease β-catenin expression and induce the inactivation of Wnt/β-catenin signaling. Therefore, Curcumin suppressed tumor growth through a lincROR/β-catenin regulatory pattern. In conclusion, our results demonstrated that Curcumin suppressed the cell proliferation via the down-regulation of lincROR and inactivation of Wnt/β-catenin signaling, suggesting that it may be a potential anti-cancer candidate for HCC patients with activated Wnt/β-catenin signaling. |
Author | Zhang, Feng-wei Fu, Wei-ming Shi, Chuan-Jian Li, Yun Pan, Fei-fei Shao, Jiang Zhang, Jin-fang |
AuthorAffiliation | 2 Key Laboratory of Orthopaedics and Traumatology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, The First Clinical Medical College, Guangzhou University of Chinese Medicine , Guangzhou , China 3 School of Pharmaceutical Sciences, Southern Medical University , Guangzhou , China 1 Lingnan Medical Research Center, Guangzhou University of Chinese Medicine , Guangzhou , China 4 Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University , Guangzhou , China 5 Shenzhen Traditional Chinese Medicine Hospital, the Fourth Clinical Medical College of Guangzhou University of Chinese Medicine , Shenzhen , China |
AuthorAffiliation_xml | – name: 5 Shenzhen Traditional Chinese Medicine Hospital, the Fourth Clinical Medical College of Guangzhou University of Chinese Medicine , Shenzhen , China – name: 2 Key Laboratory of Orthopaedics and Traumatology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, The First Clinical Medical College, Guangzhou University of Chinese Medicine , Guangzhou , China – name: 1 Lingnan Medical Research Center, Guangzhou University of Chinese Medicine , Guangzhou , China – name: 4 Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University , Guangzhou , China – name: 3 School of Pharmaceutical Sciences, Southern Medical University , Guangzhou , China |
Author_xml | – sequence: 1 givenname: Jiang surname: Shao fullname: Shao, Jiang – sequence: 2 givenname: Chuan-Jian surname: Shi fullname: Shi, Chuan-Jian – sequence: 3 givenname: Yun surname: Li fullname: Li, Yun – sequence: 4 givenname: Feng-wei surname: Zhang fullname: Zhang, Feng-wei – sequence: 5 givenname: Fei-fei surname: Pan fullname: Pan, Fei-fei – sequence: 6 givenname: Wei-ming surname: Fu fullname: Fu, Wei-ming – sequence: 7 givenname: Jin-fang surname: Zhang fullname: Zhang, Jin-fang |
BookMark | eNp1kk1r3DAQhk1JaT6ae4869uKNZH3YvhTKkjYLWwJJSo9Clka7CrbkSvJCL_1R_SH9TfHuhtIUqssIzbzPaKT3vDjxwUNRvCN4QWnTXtlxq-KiwhVeYNyw-lVxRoSgZduQ6uSv_WlxmdIjnhdtWyrYm-KUVjVhpKFnxc-18_ru9g59AeNUhoTyFtD9NI4RUnI7QNfWgs4JBYuWU9TT4DwKHt3AqHLQ0PdTryJaqqidD4NCD9sYps0WrbzS2e1Udn6Dvvl89ftXuZw7-Fl_7zZe9XPibfHaqj7B5XO8KL5-un5Y3pTr28-r5cd1qRltc6mAClpT2wljuSUCalDGNIRXBHPDNLGEay24MUpbqjDhDGyr53lBgK4FvShWR64J6lGO0Q0q_pBBOXk4CHEjVcxO9yAtJ52gXUONFUxo1nWmrmqGjaC80cBm1ocja5y6AYwGn6PqX0BfZrzbyk3YyZpywnE1A94_A2L4PkHKcnBp_5LKQ5iSrFhV84o1NZ5L8bFUx5BSBPunDcFy7wJ5cIHcu0AeXDBLxD8S7fL8C2F_Gdf_X_gEosm8sA |
CitedBy_id | crossref_primary_10_1080_10408398_2021_2001785 crossref_primary_10_3389_fcell_2024_1421763 crossref_primary_10_1002_jcp_31076 crossref_primary_10_1371_journal_pone_0312417 crossref_primary_10_2174_0109298673264372230919102758 crossref_primary_10_1039_D4BM00024B crossref_primary_10_1016_j_ejphar_2021_174485 crossref_primary_10_1016_j_jff_2023_105705 crossref_primary_10_3390_cancers17030484 crossref_primary_10_1016_j_biopha_2024_117508 crossref_primary_10_3390_antiox11122352 crossref_primary_10_1166_mex_2023_2368 crossref_primary_10_3390_molecules28041623 crossref_primary_10_1002_ptr_7338 crossref_primary_10_1080_09205063_2023_2230845 crossref_primary_10_1080_10408398_2021_1968786 crossref_primary_10_4251_wjgo_v17_i1_93983 crossref_primary_10_1055_a_2499_1140 crossref_primary_10_3748_wjg_v28_i28_3535 crossref_primary_10_1016_j_jot_2022_12_003 crossref_primary_10_1155_2022_5946670 crossref_primary_10_3389_fonc_2022_831366 crossref_primary_10_1016_j_semcancer_2020_11_004 crossref_primary_10_1016_j_biopha_2022_113713 crossref_primary_10_1016_j_pbiomolbio_2021_04_001 crossref_primary_10_1016_j_medntd_2022_100192 crossref_primary_10_1186_s11658_021_00305_5 crossref_primary_10_3389_fphar_2023_1144836 crossref_primary_10_1016_j_phymed_2021_153706 crossref_primary_10_3389_fonc_2021_660712 |
Cites_doi | 10.1089/ars.2007.1769 10.1016/j.jep.2013.07.030 10.3390/molecules16064567 10.1016/j.jhep.2015.05.016 10.1073/pnas.0904715106 10.1186/s13046-019-1320-y 10.1186/s13046-019-1234-8 10.1158/0008-5472.CAN-16-2634 10.1001/jama.294.10.1255 10.1016/j.cell.2009.02.006 10.1016/S1665-2681(19)30802-6 10.1016/j.omtn.2018.03.004 10.1080/10408690490424702 10.1016/S0168-8278(00)80428-6 10.1053/j.gastro.2004.09.011 10.7150/thno.25194 10.18632/oncotarget.4154 10.1186/s13059-019-1685-4 10.4048/jbc.2013.16.2.133 10.1016/j.devcel.2009.06.016 10.1016/j.cca.2017.07.031 10.1039/C7FO01242J 10.1016/j.biopha.2019.109278 10.1016/j.devcel.2013.03.002 10.1038/cr.2012.164 10.1016/j.devcel.2013.03.020 10.1016/j.ejmech.2019.07.015 10.1038/nrg2521 10.1016/j.ygyno.2014.02.033 10.1038/ng.710 10.1038/nature08975 10.1016/S0014-5793(02)02292-5 10.1007/s00018-008-7452-4 10.1016/j.cbi.2009.06.012 10.1016/j.gene.2017.08.008 10.1007/s00018-019-03240-z 10.1038/s41388-017-0041-y 10.1038/nrc3419 |
ContentType | Journal Article |
Copyright | Copyright © 2020 Shao, Shi, Li, Zhang, Pan, Fu and Zhang. Copyright © 2020 Shao, Shi, Li, Zhang, Pan, Fu and Zhang 2020 Shao, Shi, Li, Zhang, Pan, Fu and Zhang |
Copyright_xml | – notice: Copyright © 2020 Shao, Shi, Li, Zhang, Pan, Fu and Zhang. – notice: Copyright © 2020 Shao, Shi, Li, Zhang, Pan, Fu and Zhang 2020 Shao, Shi, Li, Zhang, Pan, Fu and Zhang |
DBID | AAYXX CITATION 7X8 5PM DOA |
DOI | 10.3389/fphar.2020.00847 |
DatabaseName | CrossRef MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Open Access Journals |
DatabaseTitle | CrossRef MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Pharmacy, Therapeutics, & Pharmacology |
EISSN | 1663-9812 |
ExternalDocumentID | oai_doaj_org_article_f51b63b83df646c4bbd72740d6358ce4 PMC7351502 10_3389_fphar_2020_00847 |
GrantInformation_xml | – fundername: National Natural Science Foundation of China grantid: 81773066, 81772404 |
GroupedDBID | 53G 5VS 9T4 AAFWJ AAKDD AAYXX ACGFO ACGFS ACXDI ADBBV ADRAZ AENEX AFPKN ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BCNDV CITATION DIK EMOBN GROUPED_DOAJ GX1 HYE KQ8 M48 M~E O5R O5S OK1 P2P PGMZT RNS RPM 7X8 5PM |
ID | FETCH-LOGICAL-c439t-ae36373fb6df5f16e7eadd8152105d4c1f15cc65ddacf3a0154ef9c399e6ec763 |
IEDL.DBID | DOA |
ISSN | 1663-9812 |
IngestDate | Wed Aug 27 01:32:14 EDT 2025 Thu Aug 21 14:33:58 EDT 2025 Fri Jul 11 15:10:40 EDT 2025 Tue Jul 01 03:27:38 EDT 2025 Thu Apr 24 23:08:47 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Language | English |
License | This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c439t-ae36373fb6df5f16e7eadd8152105d4c1f15cc65ddacf3a0154ef9c399e6ec763 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors have contributed equally to this work This article was submitted to Pharmacology of Anti-Cancer Drugs, a section of the journal Frontiers in Pharmacology Reviewed by: Marina Dukhinova, Italian Institute of Technology (IIT), Italy; Alexandre Vallee, University of Poitiers, France Edited by: Ernest Palomer, University College London, United Kingdom |
OpenAccessLink | https://doaj.org/article/f51b63b83df646c4bbd72740d6358ce4 |
PMID | 32714183 |
PQID | 2427524870 |
PQPubID | 23479 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_f51b63b83df646c4bbd72740d6358ce4 pubmedcentral_primary_oai_pubmedcentral_nih_gov_7351502 proquest_miscellaneous_2427524870 crossref_primary_10_3389_fphar_2020_00847 crossref_citationtrail_10_3389_fphar_2020_00847 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2020-07-02 |
PublicationDateYYYYMMDD | 2020-07-02 |
PublicationDate_xml | – month: 07 year: 2020 text: 2020-07-02 day: 02 |
PublicationDecade | 2020 |
PublicationTitle | Frontiers in pharmacology |
PublicationYear | 2020 |
Publisher | Frontiers Media S.A |
Publisher_xml | – name: Frontiers Media S.A |
References | Golonko (B11) 2019 Zhou (B38) 2014; 133 Prasad (B30) 2009; 181 Mercer (B27) 2009; 10 Fan (B8) 2018; 482 Vallée (B35) 2019; 38 Wang (B36) 2013; 25 Basnet (B2) 2011; 16 Bosch (B4) 2004; 127 Liang (B22) 2019; 20 Hatcher (B13) 2008; 65 Suarez (B33) 2015; 14 Anastas (B1) 2013; 13 Jakubek (B15) 2019; 118 Liang (B21) 2018; 37 Liu (B24) 2017; 631 Bhan (B3) 2017; 77 Choudhuri (B7) 2002; 512 Loewer (B25) 2010; 42 Tsuda (B34) 2018; 9 Ponting (B29) 2009; 136 Cheng (B6) 2013; 25 Gupta (B12) 2010; 464 Liu (B23) 2013; 16 Lecerf (B19) 2019; 76 Joe (B17) 2004; 44 Okuda (B28) 2000; 32 Liang (B20) 2015; 6 MacDonald (B26) 2009; 17 Fu (B10) 2015; 63 Feng (B9) 2018; 11 Jemal (B16) 2005; 294 Khalil (B18) 2009; 106 Hu (B14) 2013; 149 Song (B31) 2018; 8 Strimpakos (B32) 2008; 10 Zhang (B37) 2013; 23 Chen (B5) 2019; 38 |
References_xml | – volume: 10 start-page: 511 year: 2008 ident: B32 article-title: Curcumin: preventive and therapeutic properties in laboratory studies and clinical trials publication-title: Antioxid. Redox Signal doi: 10.1089/ars.2007.1769 – volume: 149 start-page: 601 year: 2013 ident: B14 article-title: Chinese herbal medicine-derived compounds for cancer therapy: a focus on hepatocellular carcinoma publication-title: J. Ethnopharmacol. doi: 10.1016/j.jep.2013.07.030 – volume: 16 start-page: 4567 year: 2011 ident: B2 article-title: Curcumin: an anti-inflammatory molecule from a curry spice on the path to cancer treatment publication-title: Molecules doi: 10.3390/molecules16064567 – volume: 63 start-page: 886 year: 2015 ident: B10 article-title: Hotair Mediates hepatocarcigenesis through suppressing miRNA-218 expression and Activating P14 and P16 Signaling publication-title: J. Hepatol. doi: 10.1016/j.jhep.2015.05.016 – volume: 106 start-page: 11667 year: 2009 ident: B18 article-title: Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression publication-title: Proc. Natl. Acad. Sci. U.S.A. doi: 10.1073/pnas.0904715106 – volume: 38 start-page: 323 year: 2019 ident: B35 article-title: Curcumin: a therapeutic strategy in cancers by inhibiting the canonical WNT/β-catenin pathway publication-title: J. Exp. Clin. Cancer Res. doi: 10.1186/s13046-019-1320-y – volume: 38 start-page: 254 year: 2019 ident: B5 article-title: Curcumin overcome primary gefitinib resistance in non-small-cell lung cancer cells through inducing autophagy-related cell death publication-title: J. Exp. Clin. Cancer Res. doi: 10.1186/s13046-019-1234-8 – volume: 77 start-page: 3965 year: 2017 ident: B3 article-title: Long Noncoding RNA and Cancer: A New Paradigm publication-title: Cancer Res. doi: 10.1158/0008-5472.CAN-16-2634 – volume: 294 start-page: 1255 year: 2005 ident: B16 article-title: Trends in the leading causes of death in the United States 1970-2002 publication-title: JAMA doi: 10.1001/jama.294.10.1255 – volume: 136 start-page: 629 year: 2009 ident: B29 article-title: Evolution and functions of long noncoding RNAs publication-title: Cell doi: 10.1016/j.cell.2009.02.006 – volume: 14 start-page: 64 year: 2015 ident: B33 article-title: Wnt/beta-catenin signaling pathway in hepatocellular carcinomas cases from Colombia publication-title: Ann. Hepatol. doi: 10.1016/S1665-2681(19)30802-6 – volume: 11 start-page: 345 year: 2018 ident: B9 article-title: Linc-ROR promotes osteogenic differentiation of mesenchymal stem cell through functioning as a competing endogenous RNA for miR-138 and miR-145 publication-title: Mol. Ther. Nucleic Acids doi: 10.1016/j.omtn.2018.03.004 – volume: 44 start-page: 97 year: 2004 ident: B17 article-title: Biological properties of curcumin-cellular and molecular mechanisms of action publication-title: Crit. Rev. Food Sci. Nutr. doi: 10.1080/10408690490424702 – volume: 32 start-page: 225 year: 2000 ident: B28 article-title: Hepatocellular carcinoma publication-title: J. Hepatol. doi: 10.1016/S0168-8278(00)80428-6 – volume: 127 start-page: S5 year: 2004 ident: B4 article-title: Primary liver cancer: Worldwide incidence and trends publication-title: Gastroenterology doi: 10.1053/j.gastro.2004.09.011 – volume: 8 start-page: 3571 year: 2018 ident: B31 article-title: Transcription factor AP-4 promotes tumorigenic capability and activates the Wnt/beta-catenin pathway in hepatocellular carcinoma publication-title: Theranostics doi: 10.7150/thno.25194 – volume: 6 start-page: 22513 year: 2015 ident: B20 article-title: The LncRNA H19 Promotes Epithelial to Mesenchymal Transition by Functioning as ceRNA in Colorectal Cancer publication-title: Oncotarget doi: 10.18632/oncotarget.4154 – volume: 20 start-page: 84 year: 2019 ident: B22 article-title: Translation of circular RNA circβ-catenin promotes liver cancer cell growth through activation of Wnt/β-catenin pathway publication-title: Genome Biol. doi: 10.1186/s13059-019-1685-4 – volume: 16 start-page: 133 year: 2013 ident: B23 article-title: The effect of curcumin on breast cancer cells publication-title: J. Breast Cancer doi: 10.4048/jbc.2013.16.2.133 – volume: 17 start-page: 9 year: 2009 ident: B26 article-title: Wnt/beta-catenin signaling: components, mechanisms, and diseases publication-title: Dev. Cell doi: 10.1016/j.devcel.2009.06.016 – volume: 482 start-page: 224 year: 2018 ident: B8 article-title: Long noncoding RNA HOTTIP as an independent prognostic marker in cancer publication-title: Clin. Chim. Acta doi: 10.1016/j.cca.2017.07.031 – volume: 9 start-page: 705 year: 2018 ident: B34 article-title: Curcumin as a functional food-derived factor: degradation products, metabolites, bioactivity, and future perspectives publication-title: Food Funct. doi: 10.1039/C7FO01242J – volume: 118 start-page: 109278 year: 2019 ident: B15 article-title: Strategy for improved therapeutic efficiency of curcumin in the treatment of gastric cancer publication-title: BioMed. Pharmacother. doi: 10.1016/j.biopha.2019.109278 – volume: 25 start-page: 69 year: 2013 ident: B36 article-title: Endogenous miRNA sponge lincRNA-RoR regulates Oct4, Nanog, and Sox2 in human embryonic stem cell self-renewal publication-title: Dev. Cell doi: 10.1016/j.devcel.2013.03.002 – volume: 23 start-page: 340 year: 2013 ident: B37 article-title: The human long non-coding RNA-RoR is a p53 repressor in response to DNA damage publication-title: Cell Res. doi: 10.1038/cr.2012.164 – volume: 25 start-page: 1 year: 2013 ident: B6 article-title: Repressing the repressor: a lincRNA as a MicroRNA sponge in embryonic stem cell self-renewal publication-title: Dev. Cell doi: 10.1016/j.devcel.2013.03.020 – start-page: 181 year: 2019 ident: B11 article-title: Curcumin as tyrosine kinase inhibitor in cancer treatment publication-title: Eur. J. Med. Chem. doi: 10.1016/j.ejmech.2019.07.015 – volume: 10 start-page: 155 year: 2009 ident: B27 article-title: Long non-coding RNAs: insights into functions publication-title: Nat. Rev. Genet. doi: 10.1038/nrg2521 – volume: 133 start-page: 333 year: 2014 ident: B38 article-title: Linc-RNA-RoR acts as a “sponge” against mediation of the differentiation of endometrial cancer stem cells by microRNA-145 publication-title: Gynecol. Oncol. doi: 10.1016/j.ygyno.2014.02.033 – volume: 42 start-page: 1113 year: 2010 ident: B25 article-title: Large intergenic non-coding RNA-RoR modulates reprogramming of human induced pluripotent stem cells publication-title: Nat. Genet. doi: 10.1038/ng.710 – volume: 464 start-page: 1071 year: 2010 ident: B12 article-title: Long non-coding RNA HOTAIR reprograms chromatin state to promote cancer metastasis publication-title: Nature doi: 10.1038/nature08975 – volume: 512 start-page: 334 year: 2002 ident: B7 article-title: Curcumin induces apoptosis in human breast cancer cells through p53-dependent Bax induction publication-title: FEBS Lett. doi: 10.1016/S0014-5793(02)02292-5 – volume: 65 start-page: 1631 year: 2008 ident: B13 article-title: Curcumin: from ancient medicine to current clinical trials publication-title: Cell Mol. Life Sci. doi: 10.1007/s00018-008-7452-4 – volume: 181 start-page: 263 year: 2009 ident: B30 article-title: Potent growth suppressive activity of curcumin in human breast cancer cells: Modulation of Wnt/beta-catenin signaling publication-title: Chem. Biol. Interact. doi: 10.1016/j.cbi.2009.06.012 – volume: 631 start-page: 29 year: 2017 ident: B24 article-title: Curcumin suppresses proliferation and in vitro invasion of human prostate cancer stem cells by ceRNA effect of miR-145 and lncRNA-ROR publication-title: Gene doi: 10.1016/j.gene.2017.08.008 – volume: 76 start-page: 4673 year: 2019 ident: B19 article-title: The long non-coding RNA H19: an active player with multiple facets to sustain the hallmarks of cancer publication-title: Cell Mol. Life Sci. doi: 10.1007/s00018-019-03240-z – volume: 37 start-page: 1445 year: 2018 ident: B21 article-title: The LncRNA-NEF antagonized epithelial to mesenchymal transition and cancer metastasis via cis-regulating FOXA2 and inactivating Wnt/β-catenin signaling publication-title: Oncogene doi: 10.1038/s41388-017-0041-y – volume: 13 start-page: 11 year: 2013 ident: B1 article-title: WNT signalling pathways as therapeutic targets in cancer publication-title: Nat. Rev. Cancer doi: 10.1038/nrc3419 |
SSID | ssj0000399364 |
Score | 2.3894854 |
Snippet | As one of the leading causes of cancer-related death in the world, hepatocellular carcinoma (HCC) has continued to attract growing attention in recent decades.... |
SourceID | doaj pubmedcentral proquest crossref |
SourceType | Open Website Open Access Repository Aggregation Database Enrichment Source Index Database |
StartPage | 847 |
SubjectTerms | apoptosis curcumin hepatocellular carcinoma lincROR Pharmacology Wnt/β-catenin signaling |
SummonAdditionalLinks | – databaseName: Scholars Portal Journals: Open Access dbid: M48 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9NAEF5BuXBBPEV4aZFQJaSaJPuyfUAIIqqAFKhKI3qzvK80UrsusYPIhR_FD-E3MbN2GyxVnLjaHq29M7PzzXr2G0JeOF6yUmQ2SSG2J0JKlugSGWhzLfOcGeYNHk6efVLTufh4LI-3x6O7CayvTO2wn9R8dfrqx7fNG3D415hxQrwd-vOTEqk9GVZpwWp7ndyAuJSim846sB_XZYzFSrT_Kq8U7MWmSOHfw539qsm_wtD-bXKrw4_0bavwO-SaC3fJ7kFLQL3Zo0fb81T1Ht2lB1tq6s098hNST3P4-ZDOYocOV1PAfxQ7e8Zy2O-OtmzGNa08naxXZn22DLQKdApRq6lwlx_LVukEOxCF6qyE8WKfH_oh4AkJ3N8NC_o1NMPfv5IJjBBA_stygXA_LO6T-f77o8k06TowJAaASpOUjiuecq-V9dKPlUvB8GyGMX8krTBjP5bGKGltaTwvEY85nxuYaKecgaXrAdkJVXAPCYU83INViNIyLUxuteYiMzy1VrExSA7I8GLuC9PRk2OXjNMC0hTUVhG1VaC2iqitAXl5KXHeUnP849l3qM7L55BUO16oVoui89HCy7FWXGfceiWUEVpbQHdiZAGUZcaJAXl-YQwFOCHOeRlcta4LwDmpZJD7jQYk7VlJb8T-nbA8iXTeKQdMOWKP_scrPiY38aNjPTF7Qnaa1do9BdTU6GfRGf4AeXkc8w priority: 102 providerName: Scholars Portal |
Title | LincROR Mediates the Suppressive Effects of Curcumin on Hepatocellular Carcinoma Through Inactivating Wnt/β-Catenin Signaling |
URI | https://www.proquest.com/docview/2427524870 https://pubmed.ncbi.nlm.nih.gov/PMC7351502 https://doaj.org/article/f51b63b83df646c4bbd72740d6358ce4 |
Volume | 11 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1La9wwEBYlp15Kn3T7QoUSKMTsWi_bx3Rp2Ba2DWlCcxN6bhYaOWS9gVz6o_pD-ps6I2-S9aW99OKDbSFbM9L3jT36hpB3gRtmRO2LCrC9EFKywhpUoG2sbBrmWHS4OXn-Rc1OxOdTebpV6gtzwnp54H7gxlGWVnFbcx-VUE5Y6wFyxcQDUtYuZCVQwLytYCqvwYi7SvT_JSEKa8bx4syg_ifDVK4aq6ls4VCW6x9wzGGG5BbkHDwkDzZcke73z_iI3AvpMdk97MWmr_fo8d3eqdUe3aWHdzLU10_ITwgz3dHXIzrP1TjCigLXo1jFM6e-XgXaKxevaBvpdH3p1ufLRNtEZ4BQXYtf9DFFlU6x2lBqzw30l2v60E8Jd0Pgt9y0oN9TN_79q5hCDwnaf1sukNqnxVNycvDxeDorNtUWCgekpCtM4IpXPFrlo4ylChU4ma8R3yfSC1fGUjqnpPfGRW6Qe4XYOBjooIKDZeoZ2UltCs8JhZg7ggcI45kVrvHWclE7XnmvWAktR2R8M_babaTIsSLGDw0hCVpLZ2tptJbO1hqR97ctLnoZjr_c-wHNeXsfCmjnE-BWeuNW-l9uNSJvb5xBw4TDMTcptOuVBk5TSQZx3mREqoGXDHocXknLsyzdXXHgjxP24n884ktyH1865w6zV2Snu1yH18CQOvsmTwY4zkX9B3zMFcA |
linkProvider | Directory of Open Access Journals |
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=LincROR+Mediates+the+Suppressive+Effects+of+Curcumin+on+Hepatocellular+Carcinoma+Through+Inactivating+Wnt%2F%CE%B2-Catenin+Signaling&rft.jtitle=Frontiers+in+pharmacology&rft.au=Jiang+Shao&rft.au=Jiang+Shao&rft.au=Chuan-Jian+Shi&rft.au=Chuan-Jian+Shi&rft.date=2020-07-02&rft.pub=Frontiers+Media+S.A&rft.eissn=1663-9812&rft.volume=11&rft_id=info:doi/10.3389%2Ffphar.2020.00847&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_f51b63b83df646c4bbd72740d6358ce4 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1663-9812&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1663-9812&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1663-9812&client=summon |