Expression of inducible Hsp70 enhances the proliferation of MCF-7 breast cancer cells and protects against the cytotoxic effects of hyperthermia

• Published in: Cell stress & chaperones Vol. 6; no. 4; pp. 316 - 325
• Main Authors: Barnes, J. A., Dix, D. J., Collins, B. W., Luft, C., Allen, J. W.
• Format: Journal Article
• Language: English
• Published: Netherlands Cell Stress Society International 01.10.2001
• Subjects: Breast Neoplasms - metabolism; Breast Neoplasms - pathology; Cell culture techniques; Cell cycle; Cell Division; Cell growth; Cell lines; Cultured cells; Cytoprotection; Doubling time; Female; Gene Expression Regulation; Heat shock proteins; Hot Temperature; HSP70 Heat-Shock Proteins - genetics; HSP70 Heat-Shock Proteins - metabolism; Humans; Original; Original s; Radiocarbon; Shock heating; Tetracyclines - pharmacology; Tumor Cells, Cultured
• ISSN: 1355-8145; 1466-1268
• DOI: 10.1379/1466-1268(2001)006<0316:EOIHET>2.0.CO;2

Heat shock proteins (Hsps) are ubiquitous proteins that are induced following exposure to sublethal heat shock, are highly conserved during evolution, and protect cells from damage through their function as molecular chaperones. Some cancers demonstrate elevated levels of Hsp70, and their expression has been associated with cell proliferation, disease prognosis, and resistance to chemotherapy. In this study, we developed a tetracycline-regulated gene expression system to determine the specific effects of inducible Hsp70 on cell growth and protection against hyperthermia in MCF-7 breast cancer cells. MCF-7 cells expressing high levels of Hsp70 demonstrated a significantly faster doubling time (39 hours) compared with nonoverexpressing control cells (54 hours). The effect of elevated Hsp70 on cell proliferation was characterized further by 5-bromo-2′deoxyuridine labeling, which demonstrated a higher number of second and third division metaphases in cells at 42 and 69 hours, respectively. Estimates based on cell cycle analysis and mean doubling time indicated that Hsp70 may be exerting its growth-stimulating effect on MCF-7 cells primarily by shortening of the G0/G1 and S phases of the cell cycle. In addition to the effects on cell growth, we found that elevated levels of Hsp70 were sufficient to confer a significant level of protection against heat in MCF-7 cells. The results of this study support existing evidence linking Hsp70 expression with cell growth and cytoprotection in human cancer cells.