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Tumor suppressor Parkin induces p53-mediated cell cycle arrest in human lung and colorectal cancer cells.

Authors :
Kim, Sung
Kim, Sung
Cho, Yoonjung
Kim, Yoon
Jung, Byung Chul
Kim, Sung
Kim, Sung
Cho, Yoonjung
Kim, Yoon
Jung, Byung Chul
Source :
BMB Reports; vol 56, iss 10
Publication Year :
2023

Abstract

Dysregulation of the E3 ubiquitin ligase Parkin has been linked to various human cancers, indicating that Parkin is a tumor suppressor protein. However, the mechanisms of action of Parkin remain unclear to date. Thus, we aimed to elucidate the mechanisms of action of Parkin as a tumor suppressor in human lung and colorectal cancer cells. Results showed that Parkin overexpression reduced the viability of A549 human lung cancer cells by inducing G2/M cell cycle arrest. In addition, Parkin caused DNA damage and ATM (Ataxia telangiectasia mutated) activation, which subsequently led to p53 activation. It also induced the p53-mediated upregulation of p21 and downregulation of cyclin B1. Moreover, Parkin suppressed the proliferation of HCT-15 human colorectal cancer cells by a mechanism similar to that in A549 lung cancer cells. Taken together, our results suggest that the tumor-suppressive effects of Parkin on lung and colorectal cancer cells are mediated by DNA damage/p53 activation/cyclin B1 reduction/cell cycle arrest. [BMB Reports 2023; 56(10): 557-562].

Details

Database :
OAIster
Journal :
BMB Reports; vol 56, iss 10
Notes :
application/pdf, BMB Reports vol 56, iss 10
Publication Type :
Electronic Resource
Accession number :
edsoai.on1410326292
Document Type :
Electronic Resource