p62 functions as an oncogene in colorectal cancer through inhibiting apoptosis and promoting cell proliferation by interacting with the vitamin D receptor

p62 functions as an oncogene in colorectal cancer through inhibiting apoptosis and promoting cell proliferation by interacting with the vitamin D receptor
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p62 通过与维生素 D 受体相互作用抑制细胞凋亡并促进细胞增殖,在结直肠癌中发挥癌基因的作用

DOI:
10.1111/cpr.12585
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发表时间:
2019-02
期刊:
影响因子:
8.5
通讯作者:
Dong Lei
Dong Lei
中科院分区:
生物学1区
文献类型:
--
作者:
Zhang Jing;Yang Suzhen;Xu Bing;Wang Ting;Zheng Ying;Liu Fei;Ren Fenggang;Jiang Jiong;Shi Haitao;Zou Baicang;Lu Xiaolan;Lu Shemin;Dong Lei

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p62在癌症中的作用存在争议。有证据表明,p62在不同的癌症中表达上调,并促进肿瘤生长,如肝癌和肺癌。然而,最近的一项研究表明,p62在肝星状细胞(hsc)中的下调促进了肝细胞癌(HCC)的发展。p62在结直肠癌(CRC)中是如何调控的仍不清楚。在这项研究中,我们旨在探讨p62在结直肠癌中的作用和分子机制。
The role of p62 in cancer is controversial. Evidence has shown that p62 is upregulated in different cancers and promotes tumour growth, such as in liver cancer and lung cancer. However, a recent study showed that the downregulation of p62 in hepatic stellate cells (HSCs) promotes hepatocellular carcinoma (HCC) development. How p62 is regulated in colorectal cancer (CRC) remains largely unknown. In this study, we aimed to investigate the roles and molecular mechanisms of p62 in CRC.
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