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Dual Role of p21 in the Progression of Cancer and Its Treatment

Authors
Parveen, AmnaAkash, Muhammad Sajid HamidRehman, KanwalKyunn, Whang Wan
Issue Date
2016
Publisher
BEGELL HOUSE INC
Keywords
p21; p53; cancer treatment; cyclin-dependent kinases
Citation
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, v.26, no.1, pp 49 - 62
Pages
14
Journal Title
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION
Volume
26
Number
1
Start Page
49
End Page
62
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/8685
DOI
10.1615/CritRevEukaryotGeneExpr.v26.i1.60
ISSN
1045-4403
2162-6502
Abstract
Cancer develops due to an imbalance between cell proliferation and cell death. Various mechanisms of carcinogenesis as well as of novel anticancer agents that could be targeted for the treatment of cancer have been proposed by different studies. Among these, p21 is recognized as a potent cyclin-dependent kinase inhibitor that facilitates cell-cycle arrest by interacting with different stimuli such as p53, DNA repair process, CDK, E2F1, MYC, PCNA, STAT3 AP4, proteasomes, K1F, CDX2, and ER-alpha. p21 acts both as a tumor-suppressor gene and an inhibitor of apoptosis by interacting with various molecules and transition factors. In this review, we discuss the complex role of p21 in the development of cancer and as a target in its treatment. We conclude that, in the future, the tumor-suppressor activity of p21 should be the focus of a novel treatment strategies, which may lead to the devolvement of new and selective anti-cancer agents for the targeted therapy of cancers.
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Whang, Wan Kyunn
대학원 (글로벌혁신신약학과)
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