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

被引:3
|
作者
Jung, Byung Chul [1 ,2 ]
Kim, Sung Hoon [2 ,3 ]
Cho, Yoonjung [2 ,4 ]
Kim, Yoon Suk [2 ]
机构
[1] Univ Calif Berkeley, Dept Nutr Sci & Toxicol, Berkeley, CA 94720 USA
[2] Yonsei Univ, Coll Software & Digital Healthcare Convergence, Dept Biomed Lab Sci, Wonju 26493, South Korea
[3] Korea Nazarene Univ, Dept Biomed Lab Sci, Cheonan 31172, South Korea
[4] Natl Forens Serv, Forens DNA Div, Wonju 26460, South Korea
关键词
Cell cycle arrest; Cyclin B1; DNA damage; p53; Parkin; APOPTOSIS; P53; DEGRADATION; MULTIPLE; DEATH;
D O I
10.5483/BMBRep.2023-0134
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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]
引用
收藏
页码:557 / 562
页数:6
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