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Long noncoding RNA PCAT6 inhibits colon cancer cell apoptosis by regulating anti-apoptotic protein ARC expression via EZH2

Authors :
Weimei Huang
Geng Su
Xiaoxian Huang
Angru Zou
Jingfang Wu
Yunchu Yang
Yaru Zhu
Shumei Liang
Deyu Li
Feng Ma
Linlang Guo
Source :
Cell Cycle. 18:69-83
Publication Year :
2018
Publisher :
Informa UK Limited, 2018.

Abstract

Prostate cancer-associated ncRNA transcript 6 (PCAT6) is a long intergenic noncoding RNA that is involved in the progression of prostate and lung cancer, acting as a potential diagnostic and prognostic biomarker in nonsmall cell lung cancer. However, little is known about PCAT6 expression and its clinical significance in colon cancer. Here, we aimed to investigate the clinical significance of PCAT6 in colon cancer and its underlying mechanism. The expression of PCAT6 was analyzed in colon cancer tissues using public databases, and a series of in vitro and in vivo experiments was performed to investigate the biological functions of PCAT6 in colon cancer cells and the underlying mechanisms. Our results demonstrated that PCAT6 was upregulated in colon cancer tissues compared with that in noncancerous tissues, correlating with poorer clinical stages and a worse survival status. In vitro and in vivo experiments illustrated PCAT6 promoted cell growth and inhibited cell apoptosis in colon cancer. Mechanistically, PCAT6 enhanced the coenrichment of EZH2 and H3K4me3 at the apoptosis repressor with caspase recruitment domain (ARC) genomic region, promoting the transcriptional activity of ARC. Our data highlighted that PCAT6 acts as a key activator of ARC expression by forming a complex with EZH2, inhibiting cell apoptosis and contributing to colon cancer progression. These findings elucidated that PCAT6 may be a novel prognostic predictor and therapeutic target of colon cancer.

Details

ISSN :
15514005 and 15384101
Volume :
18
Database :
OpenAIRE
Journal :
Cell Cycle
Accession number :
edsair.doi.dedup.....658bbf8754d4f15acf5053ab4a7a6b73
Full Text :
https://doi.org/10.1080/15384101.2018.1558872