The roles of E3 ubiquitin ligases in cancer progression and targeted therapy.
The roles of E3 ubiquitin ligases in cancer progression and targeted therapy.
复制标题
E3 泛素连接酶在癌症进展和靶向治疗中的作用。
DOI:
10.1002/ctm2.1204
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发表时间:
2023-03
影响因子:
10.6
通讯作者:
中科院分区:
文献类型:
--
作者:
Ubiquitination is one of the most important post‐translational modifications which plays a significant role in conserving the homeostasis of cellular proteins. In the ubiquitination process, ubiquitin is conjugated to target protein substrates for degradation, translocation or activation, dysregulation of which is linked to several diseases including various types of cancers. E3 ubiquitin ligases are regarded as the most influential ubiquitin enzyme owing to their ability to select, bind and recruit target substrates for ubiquitination. In particular, E3 ligases are pivotal in the cancer hallmarks pathways where they serve as tumour promoters or suppressors. The specificity of E3 ligases coupled with their implication in cancer hallmarks engendered the development of compounds that specifically target E3 ligases for cancer therapy. In this review, we highlight the role of E3 ligases in cancer hallmarks such as sustained proliferation via cell cycle progression, immune evasion and tumour promoting inflammation, and in the evasion of apoptosis. In addition, we summarise the application and the role of small compounds that target E3 ligases for cancer treatment along with the significance of targeting E3 ligases as potential cancer therapy. E3 ubiquitin ligases are important players in cellular processes by ubiquitinating substrate proteins in disease progression such as cancer. Owing to this, scientists attempt to identify safe and bioavailable compounds targeting E3 ligases. In this review, we summarise the roles of E3 ligases in cancer‐related pathways, highlight the application and clinical significance of small molecule inhibitors and discuss further directions .
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影响因子:
16.6
作者:
Alabi S;Jaime-Figueroa S;Yao Z;Gao Y;Hines J;Samarasinghe KTG;Vogt L;Rosen N;Crews CM
通讯作者:
Crews CM
影响因子:
8
作者:
Bognar MK;Vincendeau M;Erdmann T;Seeholzer T;Grau M;Linnemann JR;Ruland J;Scheel CH;Lenz P;Ott G;Lenz G;Hauck SM;Krappmann D
通讯作者:
Krappmann D
影响因子:
8
作者:
Argentini, M;Barboule, N;Wasylyk, B
通讯作者:
Wasylyk, B
影响因子:
32.4
作者:
Bertrand, Mathieu J. M.;Doiron, Karine;Saleh, Maya
通讯作者:
Saleh, Maya
影响因子:
4.8
作者:
Brenke, Jara K.;Popowicz, Grzegorz M.;Hadian, Kamyar
通讯作者:
Hadian, Kamyar