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通过与汉黄芩素衍生物偶联的靶向JWA的铂(IV)前药破坏单链断裂修复以对抗铂耐药性。

Disruption of SSBs repair to combat platinum resistance via the JWA-targeted Pt(IV) prodrug conjugated with a wogonin derivative.

作者信息

Wang Xing, Li Leyi, Pei Sinan, Zhu Qian, Chen Feihong

机构信息

Pharmaceutical Research Center and School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China.

Pharmaceutical Research Center and School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China;, Email:

出版信息

Pharmazie. 2020 Mar 20;75(2):94-101. doi: 10.1691/ph.2020.9815.

Abstract

An octahedral Pt (IV) prodrug, Cis-wog, containing a wogonin derivative as a bioactive axial ligand was designed and prepared to suppress DDR (DNA damage repair)-related proteins. biological studies indicated that a Pt (IV) prodrug with axially functional groups (Cis-wog) showed cytotoxicity superior to cisplatin and reversed its resistance against two pairs of cisplatin sensitive and resistant cell lines. Further mechanistic research revealed that the powerful antitumor activity of Cis-wog resulted from its suppression of JWA and its multi-interaction with XRCC1 to repair DNA single strand breaks (SSBs) caused by the introduction of wogonin. It is concluded that Cis-wog is a promising cytotoxic agent, which could be used for enhancing the antitumor activity of its corresponding Pt(II)-based drugs and reversing cisplatin resistance via decaying JWA-mediated SSBs repair pathways and inducing apoptosis.

摘要

设计并制备了一种八面体铂(IV)前药Cis-wog,其含有汉黄芩素衍生物作为生物活性轴向配体,用于抑制DNA损伤修复(DDR)相关蛋白。生物学研究表明,具有轴向官能团的铂(IV)前药(Cis-wog)显示出优于顺铂的细胞毒性,并逆转了其对两对顺铂敏感和耐药细胞系的抗性。进一步的机制研究表明,Cis-wog强大的抗肿瘤活性源于其对JWA的抑制作用以及与XRCC1的多重相互作用,以修复由汉黄芩素引入导致的DNA单链断裂(SSB)。得出的结论是,Cis-wog是一种有前景的细胞毒性药物,可用于增强其相应铂(II)类药物的抗肿瘤活性,并通过衰减JWA介导的SSB修复途径和诱导凋亡来逆转顺铂耐药性。

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