Article: Up-regulation of microRNAs, miR21 and miR23a in human liver cancer cells treated with Coptidis rhizoma aqueous extract

File Download Links for fulltext
(May Require Subscription)
  • Basic View
  • Metadata View
  • XML View
TitleUp-regulation of microRNAs, miR21 and miR23a in human liver cancer cells treated with Coptidis rhizoma aqueous extract
AuthorsZhu, M1
Wang, N1
Tsao, SW2
Yuen, MF2
Feng, Y1
Wan, TSK2
Man, K2
Feng, Y
KeywordsCoptidis rhizoma aqueous extract
Hepatocellular carcinoma
MicroRNA
miR-21
miR-23a
Issue Date2011
PublisherSpandidos Publications. The Journal's web site is located at http://www.spandidos-publications.com
CitationExperimental And Therapeutic Medicine, 2011, v. 2 n. 1, p. 27-32 [How to Cite?]
DOI: http://dx.doi.org/10.3892/etm.2010.164
AbstractCoptidis rhizoma (CR; Huanglian in Chinese) has been used for the treatment of cancer in Chinese medicine, and recent studies have supported its use in cancer therapy. MicroRNAs (miRNAs) play an important role in the pathophysiology of human cancers. We examined alterations in the miRNA profile of hepatocellular carcinoma (HCC) cells after treatment with coptidis rhizoma aqueous extract (CRAE). An on-chip microarray method was used to detect alterations in the expression profile of miRNAs in human HCCMHCC97-Lcells after exposure to 175 μg/ml CRAE. Altered expression of several miRNAs was detected in the MHCC97-Lcells after treatment with 175 μg/ml CRAE. The microarray results were validated by quantitative real-time PCR(qRT-PCR). Consistent results were obtained; qRT-PCR confirmed that both miR-21 and miR-23a were significantly up-regulated. TargetScan and PicTar microRNA databases were used to predict the possible target genes of the altered miRNAs. The results showed that the altered miRNAs after CRAE treatment may serve as markers for the therapy of liver cancer. To the best of our knowledge, this is the first report on the up-regulation of miRNAs, miR21 and miR23a in human liver cancer cells treated with CRAE. Our results suggest that CRAE targets miR-21 and miR-23a in liver cancer cells supporting the potential application of CRAE in the treatment of HCC.
ISSN1792-0981
2011 Impact Factor: 0.206
DOIhttp://dx.doi.org/10.3892/etm.2010.164
ISI Accession Number IDWOS:000286365000004
Funding AgencyGrant Number
research council of the University of Hong Kong200907176140
Research Grants Council (RGC) of Hong Kong SAR, China764708M
Pong Ding Yueng Endowment Fund for Education and Research in Chinese-Western Medicine20005274
Hong Kong Government20740314
Funding Information:

The present study was financially supported by grants from the research council of the University of Hong Kong (project code, 200907176140), the Research Grants Council (RGC) of Hong Kong SAR, China (project code, 764708M), the Pong Ding Yueng Endowment Fund for Education and Research in Chinese-Western Medicine (project code, 20005274) and the Hong Kong Government-Matching Grant Scheme (4th Phase, project code, 20740314). The cell line MHCC97-L was a kind gift from the Liver Cancer Institute Fudan University, Shanghai, China. The authors would like to express thanks to Dr Ka-Yu Siu, Ms. Cindy Lee, Mr. Keith Wong and Mr. Freddy Tsang for the technical support.

ReferencesReferences in Scopus
GrantsThe role of autophagy and mitochondrial apoptosis in berberine induced hepatocellular caricinoma cell death and its underlying mechanism
DC Field
Value
dc.contributor.authorZhu, M
dc.contributor.authorWang, N
dc.contributor.authorTsao, SW
dc.contributor.authorYuen, MF
dc.contributor.authorFeng, Y
dc.contributor.authorWan, TSK
dc.contributor.authorMan, K
dc.contributor.authorFeng, Y
dc.date.accessioned2011-08-26T14:41:21Z
dc.date.available2011-08-26T14:41:21Z
dc.date.issued2011
dc.description.abstractCoptidis rhizoma (CR; Huanglian in Chinese) has been used for the treatment of cancer in Chinese medicine, and recent studies have supported its use in cancer therapy. MicroRNAs (miRNAs) play an important role in the pathophysiology of human cancers. We examined alterations in the miRNA profile of hepatocellular carcinoma (HCC) cells after treatment with coptidis rhizoma aqueous extract (CRAE). An on-chip microarray method was used to detect alterations in the expression profile of miRNAs in human HCCMHCC97-Lcells after exposure to 175 μg/ml CRAE. Altered expression of several miRNAs was detected in the MHCC97-Lcells after treatment with 175 μg/ml CRAE. The microarray results were validated by quantitative real-time PCR(qRT-PCR). Consistent results were obtained; qRT-PCR confirmed that both miR-21 and miR-23a were significantly up-regulated. TargetScan and PicTar microRNA databases were used to predict the possible target genes of the altered miRNAs. The results showed that the altered miRNAs after CRAE treatment may serve as markers for the therapy of liver cancer. To the best of our knowledge, this is the first report on the up-regulation of miRNAs, miR21 and miR23a in human liver cancer cells treated with CRAE. Our results suggest that CRAE targets miR-21 and miR-23a in liver cancer cells supporting the potential application of CRAE in the treatment of HCC.
dc.description.grantThe role of autophagy and mitochondrial apoptosis in berberine induced hepatocellular caricinoma cell death and its underlying mechanism
dc.description.grantcode101411
dc.description.naturelink_to_OA_fulltext
dc.identifier.citationExperimental And Therapeutic Medicine, 2011, v. 2 n. 1, p. 27-32 [How to Cite?]
DOI: http://dx.doi.org/10.3892/etm.2010.164
dc.identifier.doihttp://dx.doi.org/10.3892/etm.2010.164
dc.identifier.epage32
dc.identifier.hkuros191223
dc.identifier.isiWOS:000286365000004
Funding AgencyGrant Number
research council of the University of Hong Kong200907176140
Research Grants Council (RGC) of Hong Kong SAR, China764708M
Pong Ding Yueng Endowment Fund for Education and Research in Chinese-Western Medicine20005274
Hong Kong Government20740314
Funding Information:

The present study was financially supported by grants from the research council of the University of Hong Kong (project code, 200907176140), the Research Grants Council (RGC) of Hong Kong SAR, China (project code, 764708M), the Pong Ding Yueng Endowment Fund for Education and Research in Chinese-Western Medicine (project code, 20005274) and the Hong Kong Government-Matching Grant Scheme (4th Phase, project code, 20740314). The cell line MHCC97-L was a kind gift from the Liver Cancer Institute Fudan University, Shanghai, China. The authors would like to express thanks to Dr Ka-Yu Siu, Ms. Cindy Lee, Mr. Keith Wong and Mr. Freddy Tsang for the technical support.

dc.identifier.issn1792-0981
2011 Impact Factor: 0.206
dc.identifier.issue1
dc.identifier.openurl
dc.identifier.scopuseid_2-s2.0-78751622851
dc.identifier.spage27
dc.identifier.urihttp://hdl.handle.net/10722/138139
dc.identifier.volume2
dc.languageeng
dc.publisherSpandidos Publications. The Journal's web site is located at http://www.spandidos-publications.com
dc.publisher.placeGreece
dc.relation.ispartofExperimental and Therapeutic Medicine
dc.relation.referencesReferences in Scopus
dc.subjectCoptidis rhizoma aqueous extract
dc.subjectHepatocellular carcinoma
dc.subjectMicroRNA
dc.subjectmiR-21
dc.subjectmiR-23a
dc.titleUp-regulation of microRNAs, miR21 and miR23a in human liver cancer cells treated with Coptidis rhizoma aqueous extract
dc.typeArticle
Author Affiliations
  1. School of Chinese Medicine
  2. The University of Hong Kong
  3. Sun Yat-Sen University