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ATP酶VCP/p97受到抑制后,蛋白质合成的微调不足以及氨基酸稳态失衡。

Inadequate fine-tuning of protein synthesis and failure of amino acid homeostasis following inhibition of the ATPase VCP/p97.

作者信息

Parzych K, Chinn T M, Chen Z, Loaiza S, Porsch F, Valbuena G N, Kleijnen M F, Karadimitris A, Gentleman E, Keun H C, Auner H W

机构信息

Department of Medicine, Centre for Haematology, Imperial College London, London W12 0NN, UK.

Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK.

出版信息

Cell Death Dis. 2015 Dec 31;6(12):e2031. doi: 10.1038/cddis.2015.373.

Abstract

The cellular mechanisms that control protein degradation may constitute a non-oncogenic cancer cell vulnerability and, therefore, a therapeutic target. Although this proposition is supported by the clinical success of proteasome inhibitors in some malignancies, most cancers are resistant to proteasome inhibition. The ATPase valosin-containing protein (VCP; p97) is an essential regulator of protein degradation in multiple pathways and has emerged as a target for cancer therapy. We found that pharmacological depletion of VCP enzymatic activity with mechanistically different inhibitors robustly induced proteotoxic stress in solid cancer and multiple myeloma cells, including cells that were insensitive, adapted, or clinically resistant to proteasome inhibition. VCP inhibition had an impact on two key regulators of protein synthesis, eukaryotic initiation factor 2α (eIF2α) and mechanistic target of rapamycin complex 1 (mTORC1), and attenuated global protein synthesis. However, a block on protein translation that was itself cytotoxic alleviated stress signaling and reduced cell death triggered by VCP inhibition. Some of the proteotoxic effects of VCP depletion depended on the eIF2α phosphatase, protein phosphatase 1 regulatory subunit 15A (PPP1R15A)/PP1c, but not on mTORC1, although there appeared to be cross-talk between them. Thus, cancer cell death following VCP inhibition was linked to inadequate fine-tuning of protein synthesis and activity of PPP1R15A/PP1c. VCP inhibitors also perturbed intracellular amino acid levels, activated eukaryotic translation initiation factor 2α kinase 4 (EIF2AK4), and enhanced cellular dependence on amino acid supplies, consistent with a failure of amino acid homeostasis. Many of the observed effects of VCP inhibition differed from the effects triggered by proteasome inhibition or by protein misfolding. Thus, depletion of VCP enzymatic activity triggers cancer cell death in part through inadequate regulation of protein synthesis and amino acid metabolism. The data provide novel insights into the maintenance of intracellular proteostasis by VCP and may have implications for the development of anti-cancer therapies.

摘要

控制蛋白质降解的细胞机制可能构成非致癌性癌细胞的脆弱点,因此可作为一个治疗靶点。尽管蛋白酶体抑制剂在某些恶性肿瘤中的临床成功支持了这一观点,但大多数癌症对蛋白酶体抑制具有抗性。含缬酪肽蛋白(VCP;p97)的ATP酶是多种途径中蛋白质降解的关键调节因子,并已成为癌症治疗的一个靶点。我们发现,使用机制不同的抑制剂对VCP酶活性进行药理学耗竭,可在实体癌和多发性骨髓瘤细胞中强烈诱导蛋白毒性应激,包括对蛋白酶体抑制不敏感、已适应或临床上具有抗性的细胞。VCP抑制对蛋白质合成的两个关键调节因子,即真核起始因子2α(eIF2α)和雷帕霉素复合物1的机制性靶点(mTORC1)产生影响,并减弱整体蛋白质合成。然而,本身具有细胞毒性的蛋白质翻译阻断减轻了应激信号,并减少了由VCP抑制引发的细胞死亡。VCP耗竭的一些蛋白毒性作用依赖于eIF2α磷酸酶、蛋白磷酸酶1调节亚基15A(PPP1R15A)/PP1c,但不依赖于mTORC1,尽管它们之间似乎存在相互作用。因此,VCP抑制后的癌细胞死亡与蛋白质合成的微调不足以及PPP1R15A/PP1c的活性有关。VCP抑制剂还扰乱了细胞内氨基酸水平,激活了真核翻译起始因子2α激酶4(EIF2AK4),并增强了细胞对氨基酸供应的依赖性,这与氨基酸稳态失衡一致。VCP抑制所观察到许多效应不同于蛋白酶体抑制或蛋白质错误折叠所引发的效应。因此,VCP酶活性的耗竭部分通过蛋白质合成和氨基酸代谢调节不足而触发癌细胞死亡。这些数据为VCP维持细胞内蛋白质稳态提供了新的见解,并可能对抗癌治疗的发展具有启示意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2820/4720905/ddbf1aebb33e/cddis2015373f1.jpg

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