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散发性结直肠癌中RASSF6水平降低及其体内外抗肿瘤作用

Decreased level of RASSF6 in sporadic colorectal cancer and its anti-tumor effects both in vitro and in vivo.

作者信息

Chen Erfei, Yang Fangfang, He Hongjuan, Lei Lei, Liu Ruitao, Du Le, Dong Jing, Wang Meng, Yang Jin

机构信息

School of Life Sciences, Northwest University, Xi'an, P.R. China.

Institute of Preventive Genomic Medicine, Xi'an, P.R. China.

出版信息

Oncotarget. 2016 Apr 12;7(15):19813-23. doi: 10.18632/oncotarget.7852.

Abstract

Ras-association domain family protein 6 (RASSF6) is a member of tumor suppressor RASSFs family with a wide range of function from RAS interaction, Hippo signaling involvement to cell cycle and apoptosis regulation. RASSF6 is reported inactivated in various types of cancer. However, whether RASSF6 is associated with colorectal cancer and the underlying mechanisms have yet to be investigated. In our previous exome sequencing study, we found a somatic loss-of-function (LoF) mutation in RASSF6 in one sporadic colorectal cancer (sCRC) patient, and two missense mutations in deep sequencing group of sCRC samples, implying the possibility that RASSF6 may be involved in the pathogenesis of sCRC. In this study, we demonstrate that RASSF6 acts as a tumor suppressor in colon cancer cells. Decreased level of RASSF6 was observed in adenocarcinoma compared to normal tissues, especially in advanced tumor cases. Further experiments showed exogenous introduction of RASSF6 into LoVo cells suppressed cell proliferation, migration, invasion, and induced apoptosis in vitro as well as tumor growth in vivo. In contrast, knockdown of RASSF6 in HT-29 cells showed the opposite effects. Taken together, our results suggest, in addition to epigenetics changes, functional somatic mutations may also contribute to the downregulation of RASSF6 and further participate in the pathogenesis of sCRC. RASSF6 may serve as a novel candidate against tumor growth for sCRC.

摘要

Ras 关联结构域家族蛋白 6(RASSF6)是肿瘤抑制因子 RASSFs 家族的成员,具有从 RAS 相互作用、参与 Hippo 信号传导到细胞周期和凋亡调控等广泛功能。据报道,RASSF6 在多种类型的癌症中失活。然而,RASSF6 是否与结直肠癌相关及其潜在机制尚待研究。在我们之前的外显子组测序研究中,我们在一名散发性结直肠癌(sCRC)患者的 RASSF6 中发现了一个体细胞功能丧失(LoF)突变,并且在 sCRC 样本的深度测序组中发现了两个错义突变,这意味着 RASSF6 可能参与 sCRC 发病机制的可能性。在本研究中,我们证明 RASSF6 在结肠癌细胞中起肿瘤抑制作用。与正常组织相比,腺癌中观察到 RASSF6 水平降低,尤其是在晚期肿瘤病例中。进一步的实验表明,将 RASSF6 外源性导入 LoVo 细胞可在体外抑制细胞增殖、迁移、侵袭并诱导凋亡,在体内也可抑制肿瘤生长。相反,在 HT - 29 细胞中敲低 RASSF6 则显示出相反的效果。综上所述,我们的结果表明,除了表观遗传学变化外,功能性体细胞突变也可能导致 RASSF6 的下调,并进一步参与 sCRC 的发病机制。RASSF6 可能是 sCRC 肿瘤生长的一种新型抗癌候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c454/4991420/2a6f1cb72796/oncotarget-07-19813-g001.jpg

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