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长链非编码RNA PVT1通过表观遗传调控LATS2表达促进非小细胞肺癌细胞增殖。

Long Noncoding RNA PVT1 Promotes Non-Small Cell Lung Cancer Cell Proliferation through Epigenetically Regulating LATS2 Expression.

作者信息

Wan Li, Sun Ming, Liu Guo-Jian, Wei Chen-Chen, Zhang Er-Bao, Kong Rong, Xu Tong-Peng, Huang Ming-De, Wang Zhao-Xia

机构信息

Department of Oncology, Second Affiliated Hospital, Nanjing Medical University, Nanjing, People's Republic of China. Department of Oncology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, People's Republic of China.

Department of Biochemistry and Molecular Biology, Nanjing Medical University, Nanjing, People's Republic of China.

出版信息

Mol Cancer Ther. 2016 May;15(5):1082-94. doi: 10.1158/1535-7163.MCT-15-0707. Epub 2016 Feb 23.

DOI:10.1158/1535-7163.MCT-15-0707
PMID:26908628
Abstract

Long noncoding RNAs (lncRNA) are a novel class of transcripts with no protein coding capacity, but with diverse functions in cancer cell proliferation, apoptosis, and metastasis. The lncRNA PVT1 is 1,716 nt in length and located in the chr8q24.21 region, which also contains the myelocytomatosis (MYC) oncogene. Previous studies demonstrated that MYC promotes PVT1 expression in primary human cancers. However, the expression pattern and potential biologic function of PVT1 in non-small cell lung cancer (NSCLC) is still unclear. Here, we found that PVT1 was upregulated in 105 human NSCLC tissues compared with normal samples. High expression of PVT1 was associated with a higher tumor-node-metastasis stage and tumor size, as well as poorer overall survival. Functional analysis revealed that knockdown of PVT1 inhibited NSCLC cell proliferation and induced apoptosis both in vitro and in vivo RNA immunoprecipitation and chromatin immunoprecipitation assays demonstrated that PVT1 recruits EZH2 to the large tumor suppressor kinase 2 (LATS2) promoter and represses LATS2 transcription. Furthermore, ectopic expression of LATS2 increased apoptosis and repressed lung adenocarcinoma cell proliferation by regulating the Mdm2-p53 pathway. Taken together, our findings indicated that PVT1/EZH2/LATS2 interactions might serve as new target for lung adenocarcinoma diagnosis and therapy. Mol Cancer Ther; 15(5); 1082-94. ©2016 AACR.

摘要

长链非编码RNA(lncRNA)是一类新的转录本,不具备蛋白质编码能力,但在癌细胞增殖、凋亡和转移中具有多种功能。lncRNA PVT1长度为1716个核苷酸,位于8号染色体q24.21区域,该区域还包含原癌基因髓细胞瘤(MYC)。先前的研究表明,MYC在原发性人类癌症中促进PVT1的表达。然而,PVT1在非小细胞肺癌(NSCLC)中的表达模式和潜在生物学功能仍不清楚。在此,我们发现与正常样本相比,PVT1在105例人类NSCLC组织中上调。PVT1的高表达与更高的肿瘤-淋巴结-转移分期和肿瘤大小相关,以及总体生存率较差。功能分析显示,敲低PVT1在体外和体内均抑制NSCLC细胞增殖并诱导凋亡。RNA免疫沉淀和染色质免疫沉淀试验表明,PVT1招募EZH2至大肿瘤抑制激酶2(LATS2)启动子并抑制LATS2转录。此外,LATS2的异位表达通过调节Mdm2-p53途径增加凋亡并抑制肺腺癌细胞增殖。综上所述,我们的研究结果表明,PVT1/EZH2/LATS2相互作用可能作为肺腺癌诊断和治疗的新靶点。《分子癌症治疗》;15(5);1082 - 1094。©2016美国癌症研究协会。

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