TRIM65 Promotes Cervical Cancer Through Selectively Degrading p53-Mediated Inhibition of Autophagy and Apoptosis.
TRIM65 Promotes Cervical Cancer Through Selectively Degrading p53-Mediated Inhibition of Autophagy and Apoptosis.
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TRIM65 通过选择性降解 p53 介导的自噬和细胞凋亡抑制促进宫颈癌
DOI:
10.3389/fonc.2022.853935
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发表时间:
2022
影响因子:
4.7
通讯作者:
Xin HB
中科院分区:
文献类型:
--
作者:
Wang XY;Mao HW;Guan XH;Huang QM;Yu ZP;Wu J;Tan HL;Zhang F;Huang X;Deng KY;Xin HB
Tripartite motif containing 65 (TRIM65) is an E3 ubiquitin ligase that has been implicated in a variety of cellular processes as well as tumor progression, but its biological role and the underlying mechanism in cervical cancer is unclear. Here, we reported that TRIM65 expression in human cervical cancer tissues was significantly higher than that in the adjacent normal cervical tissues, and TRIM65 knockdown enhanced autophagic flux and cell apoptosis, but not cell cycle, to dramatically inhibit the proliferation and migration of cervical cancer cells. Furthermore, our experiments showed that TRIM65 exhibited oncogenic activities via directly targeting p53, a tumor suppressor and a common upsteam regulator between autophagy and apoptosis, promoting ubiquitination and proteasomal degradation of p53. Taken together, our studies demonstrated that TRIM65 knockdown promotes cervical cancer cell death through enhancing autophagy and apoptosis, suggesting that TRIM65 may be a potential therapeutic target for cervical cancer clinically.
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DOI:
10.1083/jcb.201503023
发表时间:
2015-09-14
期刊:
The Journal of cell biology
影响因子:
--
作者:
Kimura T;Jain A;Choi SW;Mandell MA;Schroder K;Johansen T;Deretic V
通讯作者:
Deretic V
影响因子:
8
作者:
Chen, Daici;Li, Yichen;Wang, Lei
通讯作者:
Wang, Lei
DOI:
10.1084/jem.20160592
发表时间:
2017-02
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Lang X;Tang T;Jin T;Ding C;Zhou R;Jiang W
通讯作者:
Jiang W
DOI:
10.1007/s10495-021-01667-z
发表时间:
2021-06
期刊:
Apoptosis : an international journal on programmed cell death
影响因子:
--
作者:
Li M
通讯作者:
Li M
影响因子:
13.3
作者:
Han T;Guo M;Gan M;Yu B;Tian X;Wang JB
通讯作者:
Wang JB