The characteristics and roles of β-TrCP1/2 in carcinogenesis

被引:49
作者
Bi, Yanli [1 ,2 ]
Cui, Danrui [1 ,2 ]
Xiong, Xiufang [2 ,3 ]
Zhao, Yongchao [1 ,2 ]
机构
[1] Zhejiang Univ, Sch Med, Key Lab Combined Multiorgan Transplantat, Minist Publ Hlth,Affiliated Hosp 1, Hangzhou, Peoples R China
[2] Zhejiang Univ, Sch Med, Inst Translat Med, Hangzhou, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Canc Inst, Hangzhou, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
CRL; Cullin‐ RING ligase; F‐ box protein; SCF; tumorigenesis; β ‐ TrCP; I-KAPPA-B; F-BOX PROTEIN; TRCP-UBIQUITIN LIGASE; CULLIN-RING LIGASES; BETA-TRCP; MEDIATED DEGRADATION; MESSENGER-RNA; DEPENDENT DEGRADATION; CELL-PROLIFERATION; DNA-REPLICATION;
D O I
10.1111/febs.15585
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
beta-transducin repeat-containing protein (beta-TrCP), one of the well-characterized F-box proteins, acts as a substrate receptor and constitutes an active SCF beta-TrCP E3 ligase with a scaffold protein CUL1, a RING protein RBX1, and an adaptor protein SKP1. beta-TrCP plays a critical role in the regulation of various physiological and pathological processes, including signal transduction, cell cycle progression, cell migration, DNA damage response, and tumorigenesis, by governing burgeoning amounts of key regulators for ubiquitination and proteasomal degradation. Given that a variety of beta-TrCP substrates are well-known oncoproteins and tumor suppressors, and dysregulation of beta-TrCP is frequently identified in human cancers, beta-TrCP plays a vital role in carcinogenesis. In this review, we first briefly introduce the characteristics of beta-TrCP1, beta-TrCP2, and SCF beta-TrCP ubiquitin ligase, and then discuss SCF beta-TrCP ubiquitin ligase regulated biological processes by targeting its substrates for degradation. Moreover, we summarize the regulation of beta-TrCP1 and beta-TrCP2 at multiple layers and further discuss the various roles of beta-TrCP1 and beta-TrCP2 in human cancer, functioning as either an oncoprotein or a tumor suppressor in a manner dependent of cellular context. Finally, we provide novel insights for future perspectives on the potential of targeting beta-TrCP1 and beta-TrCP2 for cancer therapy.
引用
收藏
页码:3351 / 3374
页数:24
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