PROTAC as a novel anti-cancer strategy by targeting aging-related signaling

被引:0
|
作者
Peng, Yunhua [1 ,2 ]
Liu, Donghua [1 ,3 ,4 ]
Huang, Daoyuan [5 ]
Inuzuka, Hiroyuki [5 ]
Liu, Jing [1 ,3 ,4 ]
机构
[1] Xi An Jiao Tong Univ, Dept Urol, Affiliated Hosp 1, Xian 710061, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Minist Educ, Ctr Mitochondrial Biol & Med,Key Lab Biomed Inform, Xian 710049, Peoples R China
[3] Xi An Jiao Tong Univ, Key Lab Tumor Precis Med Shaanxi Prov, Affiliated Hosp 1, Xian 710061, Peoples R China
[4] Minist Educ, Key Lab Environm & Genes Related Dis, Xian 710061, Peoples R China
[5] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USA
基金
中国国家自然科学基金;
关键词
PROteolysis-TArgeting Chimera (PROTAC); Cancer therapy; Protein degradation; Senescence; CELL-CYCLE; EMBRYONIC LETHALITY; MDM2-DEFICIENT MICE; TELOMERASE; SENESCENCE; CANCER; INHIBITORS; P53; HALLMARKS; OLAPARIB;
D O I
10.1016/j.semcancer.2024.09.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aging and cancer share common cellular hallmarks, including cellular senescence, genomic instability, and abnormal cell death and proliferation, highlighting potential areas for therapeutic interventions. Recent advancements in targeted protein degradation technologies, notably Proteolysis-Targeting Chimeras (PROTACs), offer a promising approach to address these shared pathways. PROTACs leverage the ubiquitin-proteasome system to specifically degrade pathogenic proteins involved in cancer and aging, thus offering potential solutions to key oncogenic drivers and aging-related cellular dysfunction. This abstract summarizes the recent progress of PROTACs in targeting critical proteins implicated in both cancer progression and aging, and explores future perspectives in integrating these technologies for more effective cancer treatments.
引用
收藏
页码:143 / 155
页数:13
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