HSP70 Multi-Functionality in Cancer

被引:222
作者
Albakova, Zarema [1 ,2 ]
Armeev, Grigoriy A. [1 ]
Kanevskiy, Leonid M. [2 ]
Kovalenko, Elena, I [2 ]
Sapozhnikov, Alexander M. [1 ,2 ]
机构
[1] Lomonosov Moscow State Univ, Dept Biol, Moscow 119192, Russia
[2] Russian Acad Sci, Dept Immunol, Shemyakin & Ovchinnikov Inst Bioorgan Chem, Moscow 117997, Russia
基金
俄罗斯科学基金会;
关键词
HSP70; cancer; immunotherapy; apoptosis; authophagy; senescence; metastasis; exosomes; HEAT-SHOCK-PROTEIN; SMALL-MOLECULE INHIBITOR; ADENOSINE-DERIVED INHIBITORS; NUCLEOTIDE-BINDING DOMAIN; TRANSCRIPTION FACTOR HSF1; ANTIGEN-PRESENTING CELLS; C-TERMINAL DOMAIN; HEAT-SHOCK-PROTEIN-70; HSP70; EXTRACELLULAR HSP70; INDUCED APOPTOSIS;
D O I
10.3390/cells9030587
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The 70-kDa heat shock proteins (HSP70s) are abundantly present in cancer, providing malignant cells selective advantage by suppressing multiple apoptotic pathways, regulating necrosis, bypassing cellular senescence program, interfering with tumor immunity, promoting angiogenesis and supporting metastasis. This direct involvement of HSP70 in most of the cancer hallmarks explains the phenomenon of cancer "addiction" to HSP70, tightly linking tumor survival and growth to the HSP70 expression. HSP70 operates in different states through its catalytic cycle, suggesting that it can multi-function in malignant cells in any of these states. Clinically, tumor cells intensively release HSP70 in extracellular microenvironment, resulting in diverse outcomes for patient survival. Given its clinical significance, small molecule inhibitors were developed to target different sites of the HSP70 machinery. Furthermore, several HSP70-based immunotherapy approaches were assessed in clinical trials. This review will explore different roles of HSP70 on cancer progression and emphasize the importance of understanding the flexibility of HSP70 nature for future development of anti-cancer therapies.
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页数:26
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