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Small Molecules Blocking the Assembly of TCAB1 and Telomerase Complexes: Lead Discovery and Biological Activity.
Zuo, Haojie; Ru, Yiming; Gao, Xiuxiu; Chen, Hui; Yan, Yaoyao; Ma, Xiaodong; Liu, Xinhua; Wang, Yang.
Afiliación
  • Zuo H; School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China.
  • Ru Y; School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China.
  • Gao X; School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China.
  • Chen H; School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China.
  • Yan Y; School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China.
  • Ma X; School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China.
  • Liu X; Department of Medicinal Chemistry, Anhui Academy of Chinese Medicine, Hefei 230012, China.
  • Wang Y; School of Pharmacy, Anhui Medical University, Hefei 230032, China.
ACS Med Chem Lett ; 15(8): 1205-1212, 2024 Aug 08.
Article en En | MEDLINE | ID: mdl-39140071
ABSTRACT
The vast majority of tumor cells maintain the length of the telomeres through a telomerase-dependent maintenance mechanism, allowing for unlimited proliferation. TCAB1 is indispensable for the correct assembly of telomerase complexes and the delivery of telomerase to the telomere. Therefore, this study aimed to explore small molecules capable of interfering with the assembly of TCAB1 and the telomerase complex as novel efficient telomerase inhibitors. Through virtual screening, biological evaluation, and the confirmation of target engagement, the potential ligands of TCAB1 effectively inhibiting telomerase activity were discovered. Among them, compound 9 exhibited telomerase inhibitory activity at a two-digit nanomolar level (IC50 = 0.03 µM), which was dramatically enhanced in comparison with the previously reported telomerase inhibitors. This research, based on the blockage of telomerase assembly through disturbing TCAB1, provides a novel strategy and a potential target for telomerase inhibitor discovery.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Med Chem Lett Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Med Chem Lett Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos