Research progress of TNKS as drug target / 中国药理学通报
Chinese Pharmacological Bulletin
; (12): 1206-1210, 2018.
Article
em Zh
| WPRIM
| ID: wpr-705177
Biblioteca responsável:
WPRO
ABSTRACT
TNKSs are members of poly ( ADPribose) polymera-ses, which are different from other members of the PARP family with two unique structures SAM domain and ankyrin repeat re-gion. TNKS participates in a variety of cellular function regula-tion, including telomere’ s dynamic balance, Wnt signaling pathways, glucose metabolism and spindle formation during mi-tosis. TNKS, as a very attractive drug target, regulates the sta-bility of target proteins via poly ( ADP-ribosylation). In recent years, the significant progress has been made for PARP inhibi-tors in cancer treatment. Multiple PARP inhibitors have entered different clinical evaluation stages. AstraZeneca's Olaparib, Clo-vis's Rucaparib, Merck's Niraparib come into existence in the market. This paper summarizes the recent studies of TNKS and its related inhibitors.
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Índice:
WPRIM
Idioma:
Zh
Revista:
Chinese Pharmacological Bulletin
Ano de publicação:
2018
Tipo de documento:
Article