Title Expression, regulation and roles of miR-26a and MEG3 in tongue squamous cell carcinoma
Authors Jia, Ling-Fei
Wei, Su-Bi
Gan, Ye-Hua
Guo, Yong
Gong, Kai
Mitchelson, Keith
Cheng, Jing
Yu, Guang-Yan
Affiliation Peking Univ, Dept Oral & Maxillofacial Surg, Sch & Hosp Stomatol, Beijing 100081, Peoples R China.
Tsinghua Univ, Med Syst Biol Res Ctr, Beijing 100084, Peoples R China.
Peking Univ, Mol Biol Lab, Sch & Hosp Stomatol, Beijing 100081, Peoples R China.
Tsinghua Univ, Sch Life Sci, State Key Lab Biomembrane & Membrane Biotechnol, Beijing 100084, Peoples R China.
Peking Univ, Dept Oral & Maxillofacial Surg, Sch & Hosp Stomatol, 22 Zhongguancun Ave South, Beijing 100081, Peoples R China.
Keywords miR-26a
lncRNA
MEG3
DNMT3B
squamous cell carcinoma
LONG NONCODING RNA
HEPATOCELLULAR-CARCINOMA
MICRORNA EXPRESSION
BREAST-CANCER
LIVER-CANCER
EZH2
APOPTOSIS
PATHWAY
GROWTH
GENE
Issue Date 2014
Publisher international journal of cancer
Citation INTERNATIONAL JOURNAL OF CANCER.2014,135,(10),2282-2293.
Abstract MicroRNA miR-26a and long noncoding RNA (lncRNA) MEG3 gene have been independently reported to be tumor suppressor genes in various cancers, but neither has been previously associated with tongue squamous cell carcinoma (TSCC). We report here that miR-26a and lncRNA MEG3 gene expression were both strongly reduced in TSCC compared with levels in matched nonmalignant tissues, and combined low expression levels of both miR-26a and MEG3 emerged as an independent prognostic factor for poor clinical outcome in TSCC patients. Assays in the human TSCC cell lines SCC-15 and CAL27 showed that miR-26a targets the DNA methyltransferase 3B transcript and that its inhibition may result in the upregulation of MEG3, providing a plausible link between the observed reduction of miR-26a and MEG3 in TSCC tissue. Furthermore, the overexpression of miR-26a or MEG3 in SCC-15 and CAL27 cells inhibited cell proliferation and cell cycle progression, and promoted cell apoptosis. Considering the poor prognostic outcomes associated with reduced miR-26a and MEG3, our findings imply that these factors likely play important antitumor effects in TSCC pathogenesis. Furthermore, they represent potential prognostic biomarkers for stratification of TSCC patients.
URI http://hdl.handle.net/20.500.11897/190094
ISSN 0020-7136
DOI 10.1002/ijc.28667
Indexed SCI(E)
PubMed
Appears in Collections: 口腔医院

Web of Science®


170

Checked on Last Week

Scopus®



Checked on Current Time

百度学术™


0

Checked on Current Time

Google Scholar™





License: See PKU IR operational policies.