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Elraglusib 通过直接破坏微管诱导细胞毒性,而不依赖于 GSK3 抑制。

Elraglusib Induces Cytotoxicity via Direct Microtubule Destabilization Independently of GSK3 Inhibition.

机构信息

Division of Cellular Medicine, School of Medicine, University of Dundee, Dundee, United Kingdom.

Division of Molecular, Cell and Developmental Biology, School of Life Sciences, University of Dundee, Dundee, United Kingdom.

出版信息

Cancer Res Commun. 2024 Nov 1;4(11):3013-3024. doi: 10.1158/2767-9764.CRC-24-0408.

Abstract

Elraglusib was designed as a GSK3 inhibitor and is currently in clinical trials for several cancers. We show conclusively that the target of elraglusib that leads to cytotoxicity is MTs and not GSK3. This has significant implications for ongoing clinical trials of the compound and will help in understanding off-target side effects, inform future clinical trial design, and facilitate the development of biomarkers to predict response.

摘要

Elraglusib 被设计为 GSK3 抑制剂,目前正在针对多种癌症进行临床试验。我们明确表明,导致细胞毒性的 elraglusib 的靶标是 MTs 而不是 GSK3。这对正在进行的化合物临床试验具有重要意义,并将有助于了解非靶标副作用,为未来临床试验设计提供信息,并促进生物标志物的开发以预测反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c25a/11586712/56a34ae77479/crc-24-0408_f1.jpg

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