Related Experiment Video
Updated: Dec 27, 2025

Intracellular Refolding Assay
Published on: January 24, 2012
HSP70 Multi-Functionality in Cancer
Zarema Albakova1,2, Grigoriy A Armeev1, Leonid M Kanevskiy2
1Department of Biology, Lomonosov Moscow State University, 119192 Moscow, Russia.
Abstract:
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.
Insights
Heat shock proteins (HSP70s) are crucial for cancer survival, promoting tumor growth and metastasis. Targeting HSP70 offers a promising strategy for developing novel anti-cancer therapies.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- 70-kDa heat shock proteins (HSP70s) are overexpressed in various cancers.
- HSP70s confer a survival advantage to malignant cells by inhibiting apoptosis and promoting other cancer hallmarks.
Purpose of the Study:
- To review the multifaceted roles of HSP70 in cancer progression.
- To highlight the therapeutic potential of targeting HSP70.
Main Methods:
- Literature review of HSP70 functions in cancer.
- Analysis of HSP70's involvement in cancer hallmarks.
- Overview of current and emerging HSP70-targeted therapies.
Main Results:
- HSP70 suppresses apoptosis, regulates necrosis, bypasses senescence, impacts tumor immunity, and promotes angiogenesis and metastasis.
- Cancer cells exhibit a strong dependence on HSP70 for survival and growth.
- Extracellular HSP70 release influences patient survival outcomes.
Conclusions:
- HSP70 is a critical regulator of multiple cancer hallmarks, explaining cancer's "addiction" to this protein.
- Understanding HSP70's dynamic nature is key for developing effective anti-cancer strategies.
- Targeting HSP70 through small molecule inhibitors and immunotherapy shows therapeutic promise.
More Related Videos
08:29Ex Vivo Treatment Response of Primary Tumors and/or Associated Metastases for Preclinical and Clinical Development of Therapeutics
Published on: October 2, 2014
10:18From a 2DE-Gel Spot to Protein Function: Lesson Learned From HS1 in Chronic Lymphocytic Leukemia
Published on: October 19, 2014
Related Concept Videos
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Interactions Between Signaling Pathways
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
Adaptive Mechanisms in Cancer Cells
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
Cancer Stem Cells and Tumor Maintenance
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
Abnormal Proliferation
Multipotency of Hematopoietic Stem Cells