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- W4309761367 endingPage "656" @default.
- W4309761367 startingPage "647" @default.
- W4309761367 abstract "Despite recent advances in molecular therapeutics, lung cancer is still a leading cause of cancer deaths. Currently, limited targeted therapy options and acquired drug resistance present significant barriers in the treatment of patients with lung cancer. New strategies in drug development, including those that take advantage of the intracellular ubiquitin-proteasome system to induce targeted protein degradation, have the potential to advance the field of personalized medicine for patients with lung cancer. Specifically, small molecule proteolysis targeting chimeras (PROTACs), consisting of two ligands connected by a linker that bind to a target protein and an E3 ubiquitin ligase, have been developed against many cancer targets, providing promising opportunities for advanced lung cancer. In this review, we focus on the rationale for PROTAC therapy as a new targeted therapy and the current status of PROTAC development in lung cancer." @default.
- W4309761367 created "2022-11-29" @default.
- W4309761367 creator A5005862221 @default.
- W4309761367 creator A5049363820 @default.
- W4309761367 creator A5058794772 @default.
- W4309761367 creator A5084674340 @default.
- W4309761367 date "2023-03-01" @default.
- W4309761367 modified "2023-10-13" @default.
- W4309761367 title "PROTAC therapy as a new targeted therapy for lung cancer" @default.
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- W4309761367 doi "https://doi.org/10.1016/j.ymthe.2022.11.011" @default.