TIPE1 promotes cervical cancer progression by repression of p53 acetylation and is associated with poor cervical cancer outcome.
Acetylation
Animals
Apoptosis
Biomarkers, Tumor
/ genetics
Cell Proliferation
Disease Progression
Female
Gene Expression Regulation, Neoplastic
Humans
Intracellular Signaling Peptides and Proteins
/ genetics
Mice
Mice, Inbred BALB C
Mice, Nude
Prognosis
Survival Rate
Tumor Cells, Cultured
Tumor Suppressor Protein p53
/ genetics
Uterine Cervical Neoplasms
/ genetics
Xenograft Model Antitumor Assays
Journal
Carcinogenesis
ISSN: 1460-2180
Titre abrégé: Carcinogenesis
Pays: England
ID NLM: 8008055
Informations de publication
Date de publication:
10 06 2019
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
592-599Informations de copyright
© The Author(s) 2018. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.