Discovery of the cereblon-recruiting tubulin PROTACs effective in overcoming Taxol resistance in vitro and in vivo.

Eur J Med Chem

School of Pharmaceutical Sciences, and Institute of Drug Discovery & Development, Zhengzhou University, 100 Kexue Avenue, Zhengzhou, Henan, 450001, China. Electronic address:

Published: February 2024

AI Article Synopsis

  • Overexpression of β3-tubulin in tumors contributes to resistance against microtubule-targeting drugs.
  • Researchers developed W13, the first PROTAC designed to target tubulin, by linking a CRBN ligand to the drug CA-4, maintaining CA-4’s effectiveness.
  • W13 effectively degrades α/β/β3-tubulin in cancer cell lines and shows promising antitumor activity against lung cancer in xenograft studies, indicating its potential as a treatment for NSCLC related to β3-tubulin overexpression.

Article Abstract

Overexpression of β3-tubulin is a common occurrence in human tumors and is associated with resistance to microtubule-targeting agents. PROTAC strategy has demonstrated significant potential in overcoming drug resistance. Herein, we report the discovery of W13 as the first PROTAC against tubulin, which was created by connecting a CRBN ligand to the widely recognized microtubule-destabilizing agent CA-4. Notably, it retains the inhibitory activity of the parental CA-4 and further exhibits substantial degradation of α/β/β3-tubulin in both A549 and A549/Taxol cell lines. The degradation of tubulin was subsequently verified to be mediated by the ubiquitin-proteasome system. Importantly, tumor xenograft research clearly showed W13's promising antitumor activity against human lung cancer. Taken together, the discovery of W13 demonstrated the practicality and feasibility of PROTAC targeting tubulin, hence establishing a potential therapeutic approach for treating NSCLC caused by the overexpression of β3-tubulin.

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Source
http://dx.doi.org/10.1016/j.ejmech.2023.116067DOI Listing

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