The Role of HSP90 and TRAP1 Targets on Treatment in Hepatocellular Carcinoma
- PMID: 38684604
- DOI: 10.1007/s12033-024-01151-4
The Role of HSP90 and TRAP1 Targets on Treatment in Hepatocellular Carcinoma
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.
Keywords: Heat Shock Protein 90; Hepatocellular Carcinoma; Mitochondrial Targeting; Systems Biology; Tumor Necrosis Factor associated with Protein-1.
© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Conflict of interest statement
Declarations. Conflict of interest: The authors claim no conflict of interests.
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