TRIM65 Promotes Cervical Cancer Through Selectively Degrading p53-Mediated Inhibition of Autophagy and Apoptosis

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 c...

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Main Authors: Deng, K.-Y (Author), Guan, X.-H (Author), Huang, Q.-M (Author), Huang, X. (Author), Mao, H.-W (Author), Tan, H.-L (Author), Wang, X.-Y (Author), Wu, J. (Author), Xin, H.-B (Author), Yu, Z.-P (Author), Zhang, F. (Author)
Format: Article
Language:English
Published: Frontiers Media S.A. 2022
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Online Access:View Fulltext in Publisher
LEADER 02107nam a2200313Ia 4500
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020 |a 2234943X (ISSN) 
245 1 0 |a TRIM65 Promotes Cervical Cancer Through Selectively Degrading p53-Mediated Inhibition of Autophagy and Apoptosis 
260 0 |b Frontiers Media S.A.  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.3389/fonc.2022.853935 
520 3 |a 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. Copyright © 2022 Wang, Mao, Guan, Huang, Yu, Wu, Tan, Zhang, Huang, Deng and Xin. 
650 0 4 |a apoptosis 
650 0 4 |a autophagy 
650 0 4 |a cervical cancer 
650 0 4 |a TRIM65 
650 0 4 |a ubiquitination 
700 1 |a Deng, K.-Y.  |e author 
700 1 |a Guan, X.-H.  |e author 
700 1 |a Huang, Q.-M.  |e author 
700 1 |a Huang, X.  |e author 
700 1 |a Mao, H.-W.  |e author 
700 1 |a Tan, H.-L.  |e author 
700 1 |a Wang, X.-Y.  |e author 
700 1 |a Wu, J.  |e author 
700 1 |a Xin, H.-B.  |e author 
700 1 |a Yu, Z.-P.  |e author 
700 1 |a Zhang, F.  |e author 
773 |t Frontiers in Oncology