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
相关论文
共 50 条
  • [1] Targeting XBP-1 as a novel anti-cancer strategy
    Koong, Albert C.
    Chauhan, Vibha
    Romero-Ramirez, Lorenzo
    CANCER BIOLOGY & THERAPY, 2006, 5 (07) : 756 - 759
  • [2] Targeting the Ubiquitin E1 as a Novel Anti-Cancer Strategy
    Xu, Wei
    Lukkarila, Julie L.
    da Silva, Sara R.
    Paiva, Stacey-Lynn
    Gunning, Patrick T.
    Schimmer, Aaron D.
    CURRENT PHARMACEUTICAL DESIGN, 2013, 19 (18) : 3201 - 3209
  • [3] Targeting ferroptosis as a potential prevention and treatment strategy for aging-related diseases
    Jiao, Taiwei
    Chen, Yiman
    Sun, Haiyan
    Yang, Lina
    PHARMACOLOGICAL RESEARCH, 2024, 208
  • [4] Targeting mTOR for Anti-Aging and Anti-Cancer Therapy
    Fu, Wencheng
    Wu, Geng
    MOLECULES, 2023, 28 (07):
  • [5] Targeting an aging-related molecule overcomes resistance to anti-PD1 treatment of cancer
    Kudo-Saito, Chie
    Imazeki, Hiroshi
    Shoji, Hirokazu
    Boku, Narikazu
    CANCER RESEARCH, 2024, 84 (07)
  • [6] Targeting the Metabolic Mevalonate Pathway as an Anti-Cancer Strategy
    Penn, L. Z.
    PANCREAS, 2017, 46 (07) : 962 - 962
  • [7] Targeting Autophagy in Aging and Aging-Related Cardiovascular Diseases
    Ren, Jun
    Zhang, Yingmei
    TRENDS IN PHARMACOLOGICAL SCIENCES, 2018, 39 (12) : 1064 - 1076
  • [8] Porcupine inhibitors: Novel and emerging anti-cancer therapeutics targeting the Wnt signaling pathway
    Shah, Karmani
    Panchal, Shivangi
    Patel, Bhumika
    PHARMACOLOGICAL RESEARCH, 2021, 167
  • [9] Role of Notch signaling in human mucoepidermoid carcinoma and combined targeting of Notch and EGFR signaling as an anti-cancer strategy
    Ni, Wei
    Chen, Zirong
    Zhou, Xin
    Yang, Rongqiang
    Kaye, Frederic
    Wu, Lizi
    CANCER RESEARCH, 2019, 79 (13)
  • [10] Development of a novel anti-cancer drug targeting for γ-glutamylcyclotransferase
    Ii, Hiromi
    Nakata, Susumu
    Taniguchi, Keiko
    Takagi, Hiroko
    Moyama, Chiami
    Kageyama, Susumu
    Yoshiki, Tatsuhiro
    CANCER SCIENCE, 2018, 109 : 1189 - 1189