TIPE1 promotes cervical cancer progression by repression of p53 acetylation and is associated with poor cervical cancer outcome.


Journal

Carcinogenesis
ISSN: 1460-2180
Titre abrégé: Carcinogenesis
Pays: England
ID NLM: 8008055

Informations de publication

Date de publication:
10 06 2019
Historique:
received: 08 04 2018
revised: 19 10 2018
accepted: 13 11 2018
pubmed: 18 11 2018
medline: 26 2 2020
entrez: 17 11 2018
Statut: ppublish

Résumé

Previous studies have shown that TIPE1 inhibits tumor proliferation and metastasis in certain cancers; however, increased expression of TIPE1 is observed in cervical cancer cell lines and tissues, indicating it might exert a distinctive role in cervical cancer. Cell and xenograft tumorigenicity assays showed that TIPE1 facilitates cervical cancer progression in this study. Further investigation demonstrated that TIPE1 binds to p53 and impairs its activity via inhibition of its acetylation. In addition, TIPE1 promoted cell proliferation and suppressed cisplatin susceptibility in a p53-dependent manner, indicating that TIPE1 facilitates cervical cancer progression primarily through the p53 pathway. TIPE1 expression in clinical samples also demonstrated that its upregulation predicts poor prognosis in patients with cervical cancer. Taken together, the results of this study showed that TIPE1 serves as an oncogene by restricting p53 activity in the development of cervical cancer, suggesting that TIPE1 will provide a new potential target for cervical cancer therapy and can be used as a biomarker to predict patient prognosis.

Identifiants

pubmed: 30445600
pii: 5183606
doi: 10.1093/carcin/bgy163
doi:

Substances chimiques

Biomarkers, Tumor 0
Intracellular Signaling Peptides and Proteins 0
TNFAIP8L1 protein, human 0
TP53 protein, human 0
Tumor Suppressor Protein p53 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

592-599

Informations de copyright

© The Author(s) 2018. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Auteurs

Peiqing Zhao (P)

Department of Gynecologic Oncology, The Fourth Affiliated Hospital of Jiangsu University, Zhenjiang, China.
Center of Translational Medicine, Zibo Central Hospital, Zibo, China.

Xiaoming Pang (X)

Center of Translational Medicine, Zibo Central Hospital, Zibo, China.

Jie Jiang (J)

Department of Clinical Laboratory, Yantai Affiliated Hospital of Binzhou Medical University, Yantai, China.

Lianqing Wang (L)

Center of Translational Medicine, Zibo Central Hospital, Zibo, China.

Xiaolan Zhu (X)

Department of Gynecologic Oncology, The Fourth Affiliated Hospital of Jiangsu University, Zhenjiang, China.

Yingchun Yin (Y)

Center of Translational Medicine, Zibo Central Hospital, Zibo, China.

Qiaoli Zhai (Q)

Center of Translational Medicine, Zibo Central Hospital, Zibo, China.

Xinxin Xiang (X)

Center of Translational Medicine, Zibo Central Hospital, Zibo, China.

Fan Feng (F)

Department of Gynecologic Oncology, The Fourth Affiliated Hospital of Jiangsu University, Zhenjiang, China.

Wenlin Xu (W)

Department of Gynecologic Oncology, The Fourth Affiliated Hospital of Jiangsu University, Zhenjiang, China.

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Classifications MeSH