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热休克蛋白90(HSP90)和肿瘤坏死因子受体相关蛋白1(TRAP1)靶点在肝细胞癌治疗中的作用

The Role of HSP90 and TRAP1 Targets on Treatment in Hepatocellular Carcinoma.

作者信息

Praveen Kumar P K, Sundar Harini, Balakrishnan Kamalavarshini, Subramaniam Sakthivel, Ramachandran Hemalatha, Kevin M, Michael Gromiha M

机构信息

Department of Biotechnology, Sri Venkateswara College of Engineering, Pennalur, Sriperumbudur Tk, Tamil Nadu, 602117, India.

Department of Biotechnology, Bhupat and Jyoti Mehta School of Biosciences, Indian Institute of Technology Madras, Chennai, 600036, India.

出版信息

Mol Biotechnol. 2025 Apr;67(4):1367-1381. doi: 10.1007/s12033-024-01151-4. Epub 2024 Apr 29.

Abstract

Hepatocellular Carcinoma (HCC) is the predominant form of liver cancer and arises due to dysregulation of the cell cycle control machinery. Heat Shock Protein 90 (HSP90) and mitochondrial HSP90, also referred to as TRAP1 are important critical chaperone target receptors for early diagnosis and targeting HCC. Both HSP90 and TRAP1 expression was found to be higher in HCC patients. Hence, the importance of HSP90 and TRAP1 inhibitors mechanism and mitochondrial targeted delivery of those inhibitors function is widely studied. This review also focuses on importance of protein-protein interactions of HSP90 and TRAP1 targets and association of its interacting proteins in various pathways of HCC. To further elucidate the mechanism, systems biology approaches and computational biology approach studies are well explored in the association of inhibition of herbal plant molecules with HSP90 and its mitochondrial type in HCC.

摘要

肝细胞癌(HCC)是肝癌的主要形式,由细胞周期调控机制失调引起。热休克蛋白90(HSP90)和线粒体热休克蛋白90(也称为TRAP1)是早期诊断和靶向HCC的重要关键伴侣靶受体。研究发现,HSP90和TRAP1在HCC患者中的表达均较高。因此,人们广泛研究了HSP90和TRAP1抑制剂的作用机制以及这些抑制剂的线粒体靶向递送功能。本综述还着重探讨了HSP90和TRAP1靶点的蛋白质-蛋白质相互作用的重要性及其相互作用蛋白在HCC各种通路中的关联。为了进一步阐明其机制,在草药植物分子抑制与HCC中HSP90及其线粒体类型的关联方面,系统生物学方法和计算生物学方法的研究得到了充分探索。

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