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广泛的检测中通用突变型 p53 挽救化合物的特性。

Characterization of the generic mutant p53-rescue compounds in a broad range of assays.

机构信息

Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.

Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Cancer Cell. 2024 Mar 11;42(3):325-327. doi: 10.1016/j.ccell.2024.01.008. Epub 2024 Feb 22.

DOI:10.1016/j.ccell.2024.01.008
PMID:38402608
Abstract

Dozens of compounds that rescue tumor-associated mutant p53 have been reported. Xiao et al. perform 10 assays to evaluate effectiveness of the mutant p53-rescue compounds side-by-side but do not detect reliable rescue in any assay for the evaluated compounds, except for ATO and its analog PAT.

摘要

据报道,有数十种化合物可挽救肿瘤相关的突变型 p53。Xiao 等人进行了 10 项测定来评估这些突变型 p53 挽救化合物的效果,但除了 ATO 和其类似物 PAT 之外,在所有评估的化合物中,没有任何一项测定能可靠地挽救突变型 p53。

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引用本文的文献

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Nat Rev Cancer. 2025 May 16. doi: 10.1038/s41568-025-00825-8.
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Heterogeneity of TP53 mutations necessitates differentiation with p53-rescue therapies.TP53突变的异质性使得有必要通过p53挽救疗法进行区分。
Nat Rev Cancer. 2025 May 16. doi: 10.1038/s41568-025-00826-7.
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Pharmacological rescue of mutant p53 triggers spontaneous tumor regression via immune responses.突变型p53的药理学挽救通过免疫反应触发肿瘤自发消退。
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Cabozantinib selectively induces proteasomal degradation of p53 somatic mutant Y220C and impedes tumor growth.卡博替尼选择性诱导p53体细胞突变体Y220C的蛋白酶体降解并抑制肿瘤生长。
J Biol Chem. 2025 Feb;301(2):108167. doi: 10.1016/j.jbc.2025.108167. Epub 2025 Jan 8.
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Deep CRISPR mutagenesis characterizes the functional diversity of TP53 mutations.深度CRISPR诱变揭示了TP53突变的功能多样性。
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