SRGAP2通过调节线粒体复合体I活性来控制结直肠癌的化疗敏感性。

IF 4.3 3区 生物学
Human Cell Pub Date : 2022-11-01 Epub Date: 2022-09-05 DOI:10.1007/s13577-022-00781-7
Yongqin Tang, Guijun Liu, Yanhan Jia, Tao Sun
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引用次数: 1

摘要

线粒体呼吸和代谢在结直肠癌(CRC)的发生发展中起着重要作用。在这项研究中,我们在CRC细胞的线粒体中发现了一个SLIT-ROBO Rho gtpase激活蛋白2 (SRGAP2)的功能池,它是CRC化学敏感性的重要调节因子。我们发现,与正常结肠细胞相比,结直肠癌细胞中的SRGAP2水平升高。线粒体SRGAP2的缺失导致线粒体呼吸显著减少,并使结直肠癌细胞对化疗药物强烈敏感。在机制上,SRGAP2物理上与线粒体复合体I相互作用,并积极调节其活性。特别是,SRGAP2丢失后的化学增敏作用通过复合物I抑制剂的处理得到了表型。因此,我们的研究结果表明SRGAP2是CRC化疗敏感性的关键调节因子,确定SRGAP2是提高CRC化疗疗效的有希望的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SRGAP2 controls colorectal cancer chemosensitivity via regulation of mitochondrial complex I activity.

Mitochondrial respiration and metabolism play an important role in the occurrence and development of colorectal cancer (CRC). In this study, we identified a functional pool of SLIT-ROBO Rho GTPase-activating protein 2 (SRGAP2) in the mitochondria of CRC cells as an important regulator of CRC chemosensitivity. We found that SRGAP2 levels were increased in CRC cells in comparison to normal colorectal cells. Loss of mitochondrial SRGAP2 led to significant decrease in mitochondrial respiration and strongly sensitized the CRC cells to chemotherapy drugs. Mechanistically, SRGAP2 physically interacts with mitochondrial complex I and positively modulates its activity. In particular, chemosensitization upon SRGAP2 loss was phenocopied by the treatment of complex I inhibitor. Thus, our results demonstrate that SRGAP2 functions as a key regulator of CRC chemosensitivity, identifying SRGAP2 as a promising therapeutic target to enhance the efficacy of chemotherapy in CRC.

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来源期刊
Human Cell
Human Cell 生物-细胞生物学
CiteScore
6.60
自引率
2.30%
发文量
176
期刊介绍: Human Cell is the official English-language journal of the Japan Human Cell Society. The journal serves as a forum for international research on all aspects of the human cell, encompassing not only cell biology but also pathology, cytology, and oncology, including clinical oncology. Embryonic stem cells derived from animals, regenerative medicine using animal cells, and experimental animal models with implications for human diseases are covered as well. Submissions in any of the following categories will be considered: Research Articles, Cell Lines, Rapid Communications, Reviews, and Letters to the Editor. A brief clinical case report focusing on cellular responses to pathological insults in human studies may also be submitted as a Letter to the Editor in a concise and short format. Not only basic scientists but also gynecologists, oncologists, and other clinical scientists are welcome to submit work expressing new ideas or research using human cells.
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