马拉特1
连环素
癌症研究
癌基因
结直肠癌
基因敲除
下调和上调
Wnt信号通路
腺癌
癌症
转移
生物
化学
长非编码RNA
医学
内科学
细胞凋亡
信号转导
细胞周期
细胞生物学
基因
生物化学
作者
Xiaoying Zheng,Jianhua Ren,Bingjun Peng,Jun-Ling Ye,Xinchun Wu,Wenhui Zhao,Yanjun Li,Ruihui Chen,Xue Gong,Chengmei Bai,Yating Wang,Haiyun Zhao,Yiqing Zhang
标识
DOI:10.1016/j.cellsig.2020.109676
摘要
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.
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