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USP19 Negatively Regulates p53 and Promotes Cervical Cancer Progression

Authors
Tyagi, ApoorviKarapurkar, Janardhan KeshavColaco, Jencia CarminhaSarodaya, NehaAntao, Ainsley MikeKaushal, KaminiHaq, SabaChandrasekaran, Arun PandianDas, SoumyadipSingh, VijaiHong, SeokHoSuresh, BharathiKim, KyeSeongRamakrishna, Suresh
Issue Date
Aug-2024
Publisher
Humana Press, Inc.
Keywords
Apoptosis; Deubiquitinase; Proteolysis; Knockout; Oncogenic transformation; Ubiquitination
Citation
Molecular Biotechnology, v.66, no.8, pp 2032 - 2045
Pages
14
Indexed
SCIE
SCOPUS
Journal Title
Molecular Biotechnology
Volume
66
Number
8
Start Page
2032
End Page
2045
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/204167
DOI
10.1007/s12033-023-00814-y
ISSN
1073-6085
1559-0305
Abstract
p53 is a tumor suppressor gene activated in response to cellular stressors that inhibits cell cycle progression and induces pro-apoptotic signaling. The protein level of p53 is well balanced by the action of several E3 ligases and deubiquitinating enzymes (DUBs). Several DUBs have been reported to negatively regulate and promote p53 degradation in tumors. In this study, we identified USP19 as a negative regulator of p53 protein level. We demonstrate a direct interaction between USP19 and p53 by pull down assay. The overexpression of USP19 promoted ubiquitination of p53 and reduced its protein half-life. We also demonstrate that CRISPR/Cas9-mediated knockout of USP19 in cervical cancer cells elevates p53 protein levels, resulting in reduced colony formation, cell migration, and cell invasion. Overall, our results indicate that USP19 negatively regulates p53 protein levels in cervical cancer progression.
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Ramakrishna, Suresh
GRADUATE SCHOOL OF BIOMEDICAL SCIENCE AND ENGINEERING (DEPARTMENT OF BIOMEDICAL SCIENCE)
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