| Literature DB >> 32485228 |
Xiaoying Zheng1, Jianhua Ren2, Bingjun Peng3, Junling Ye1, Xinchun Wu4, Wenhui Zhao1, Yanjun Li1, Ruihui Chen1, Xue Gong1, Chengmei Bai1, Yating Wang1, Haiyun Zhao5, Yiqing Zhang6.
Abstract
Colon cancer is one of the most common types of cancer and more than 80% of colon cancer cases are associated with Wnt-β-catenin signaling activation. Metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) is a multi-functional long non-coding RNA that is overexpressed in many types of cancers, including colon cancer. In this study, MALAT1 and β-catenin were found to be overexpressed in tumor samples from 62 patients with colon cancer. A positive correlation was identified between MALAT1 levels and β-catenin protein levels in tumors. MALAT1 was found to upregulate β-catenin protein levels in HCT116 and LOVO cells without changing the mRNA expression levels. β-catenin degradation was confirmed to be upregulated in MALAT1-knockdown cells and inhibited in cells overexpressing MALAT1 overexpressing. MALAT1 was then identified as a negative regulator of GSK-3β; it did so via promotion of H3K27 trimethylation of the promoter region. In conclusion, MALAT1 is an oncogene in colon cancer, which inhibits β-catenin degradation by upregulating H3K27 trimethylation and repressing GSK-3β expression.Entities:
Keywords: Colon cancer; GSK-3β; H3K27me3; MALAT1; β-Catenin
Year: 2020 PMID: 32485228 DOI: 10.1016/j.cellsig.2020.109676
Source DB: PubMed Journal: Cell Signal ISSN: 0898-6568 Impact factor: 4.315