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线粒体塑形蛋白与化疗

Mitochondria-Shaping Proteins and Chemotherapy.

作者信息

Xie Longlong, Zhou Tiansheng, Xie Yujun, Bode Ann M, Cao Ya

机构信息

Hunan Children's Hospital, The Pediatric Academy of University of South China, Changsha, China.

Key Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Department of Radiology, Xiangya Hospital, Central South University, Changsha, China.

出版信息

Front Oncol. 2021 Nov 18;11:769036. doi: 10.3389/fonc.2021.769036. eCollection 2021.

DOI:10.3389/fonc.2021.769036
PMID:34868997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8637292/
Abstract

The emergence, in recent decades, of an entirely new area of "Mitochondrial dynamics", which consists principally of fission and fusion, reflects the recognition that mitochondria play a significant role in human tumorigenesis and response to therapeutics. Proteins that determine mitochondrial dynamics are referred to as "shaping proteins". Marked heterogeneity has been observed in the response of tumor cells to chemotherapy, which is associated with imbalances in mitochondrial dynamics and function leading to adaptive and acquired resistance to chemotherapeutic agents. Therefore, targeting mitochondria-shaping proteins may prove to be a promising approach to treat chemotherapy resistant cancers. In this review, we summarize the alterations of mitochondrial dynamics in chemotherapeutic processing and the antitumor mechanisms by which chemotherapy drugs synergize with mitochondria-shaping proteins. These might shed light on new biomarkers for better prediction of cancer chemosensitivity and contribute to the exploitation of potent therapeutic strategies for the clinical treatment of cancers.

摘要

近几十年来,一个全新的“线粒体动力学”领域出现了,其主要包括裂变和融合,这反映出人们认识到线粒体在人类肿瘤发生和对治疗的反应中起着重要作用。决定线粒体动力学的蛋白质被称为“塑形蛋白”。已观察到肿瘤细胞对化疗的反应存在显著异质性,这与线粒体动力学和功能的失衡有关,导致对化疗药物产生适应性和获得性耐药。因此,靶向线粒体塑形蛋白可能是治疗化疗耐药癌症的一种有前景的方法。在这篇综述中,我们总结了化疗过程中线粒体动力学的改变以及化疗药物与线粒体塑形蛋白协同作用的抗肿瘤机制。这些可能有助于揭示新的生物标志物,以更好地预测癌症化疗敏感性,并有助于开发有效的治疗策略用于癌症的临床治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c08/8637292/496974c00f35/fonc-11-769036-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c08/8637292/019721226c17/fonc-11-769036-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c08/8637292/f3aa7ab768e4/fonc-11-769036-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c08/8637292/c898e285466b/fonc-11-769036-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c08/8637292/496974c00f35/fonc-11-769036-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c08/8637292/019721226c17/fonc-11-769036-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c08/8637292/f3aa7ab768e4/fonc-11-769036-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c08/8637292/c898e285466b/fonc-11-769036-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c08/8637292/496974c00f35/fonc-11-769036-g004.jpg

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Alterations in mitochondrial morphology as a key driver of immunity and host defence.线粒体形态改变作为免疫和宿主防御的关键驱动因素。
三氧化二砷增强肝癌的免疫原性细胞死亡并诱导 cGAS-STING-IFN 通路激活。
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Long-Chain Acyl Coenzyme A Dehydrogenase, a Key Player in Metabolic Rewiring/Invasiveness in Experimental Tumors and Human Mesothelioma Cell Lines.长链酰基辅酶A脱氢酶,实验性肿瘤和人恶性间皮瘤细胞系中代谢重编程/侵袭性的关键参与者。
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Systematic identification of anticancer drug targets reveals a nucleus-to-mitochondria ROS-sensing pathway.系统鉴定抗癌药物靶点揭示了细胞核到线粒体 ROS 感应途径。
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