CONSTITUTIVE OVEREXPRESSION OF THE 27,000-DALTON HEAT-SHOCK PROTEIN IN LATE PASSAGE HUMAN BREAST-CANCER CELLS

We present evidence that the mechanisms controlling induction of heat shock transcription factors (HSFs) and mRNA expression of the 27,000 molecular weight heat shock protein, hsp27, are diverse in human breast cancer cells. Heat shock accumulation of hsp27 RNA is associated with the activation of HSF in MDA-MB-231 cells. We have later passage MCF-7 breast cancer cell lines with elevated, constitutive expression of hsp27 mRNA, perhaps due to hsp 27 gene amplification. Estradiol and heat shock treatment no longer affect the level of hsp27 mRNA in these cells. Heat induction of HSF is inhibited in cells overexpressing hsp27, although metal ions and amino acid analogs are still capable of activating HSE These cells will provide a useful system for characterizing alternative pathways in HSF inhibition and activation.