Researchers at Whitehead Institute have found that the cellular survival response regulated by Heat-Shock Factor 1 (HSF1) also induces neighboring cells into supporting the malignant progression and metastasis of cancer cells, a new study published in the journal Cell reveals.
Over the past several years, researchers in the lab of Whitehead Member Susan Lindquist have been investigating the role the transcription factor HSF1 plays in supporting malignancy. In normal cells, stressful conditions, including those caused by heat, hypoxia, and toxins activate HSF1, which serves to maintain protein homeostasis and helps the cells endure tough times. Cancer cells, however, are capable of hijacking this heat-shock response to their own benefit. Two years ago, Lindquist's lab implicated HSF1 in this corruption, showing that it activates a set of genes in cancer cells quite distinct from those up-regulated in normal cells during heat-shock.
Building upon that research, the lab has now discovered that HSF1 operates not only on the cancer cells in a tumor, but also on the cells of the tumor microenvironment, or stroma. Here HSF1 drives a transcriptional program distinct from that operating in adjacent cancer cells. HSF1 activation in both cancer cells and stromal cells is a powerful, complementary combination that fuels malignant processes.
In a series of experiments, Scherz-Shouval and colleagues found clear evidence of HSF1 activation in stromal cells known as cancer-associated fibroblasts, or CAFs, in a variety of human tumors, including breast, lung, skin, esophageal, colon, and prostate cancers. Moreover, they discovered that not only does HSF1 activation in CAFs up-regulate genes supporting malignancy, it also suppresses genes that would ordinarily trigger a protective, anti-cancer immune response in surrounding tissue. Although such a synergistic dynamic may seem daunting to overcome, it may in fact actually present a real opportunity for therapeutic intervention.
"It's important to find HSF1 operating this way in the stroma," notes Scherz-Shouval. "The tumor microenviroment tends to be more genetically stable and less prone to mutation, suggesting that even if cancer cells could mutate to evade therapeutic disruption of HSF1, supportive cells in the stroma could still be susceptible."
"Although it's thought to be quite difficult to drug a transcription factor like HSF1 directly, the role of HSF1 suggests that we might be able to treat cancer more effectively by modifying the underlying tumor biology," says Luke Whitesell, an oncologist, Lindquist lab senior scientist, and a corresponding author on the latest Cell paper. "Targeting the dual role of HSF1 has the potential to change how a cancer responds to therapeutic interventions, perhaps making it less able to cope with other therapies."
Another significant finding from the research is the potential to use stromal HSF1 activation as a diagnostic and prognostic biomarker. In analysis of tumor samples from breast cancer patients, the scientists found that HSF1 activation in the stroma was associated with poor patient outcomes, including reduced disease-free survival and overall survival. Further, the researchers also found that stromal HSF1 activation in samples from patients with early-stage non-small cell lung cancer was also associated with poor outcomes.
Although the scientists emphasize that the numbers of breast and lung cancer samples studied were small, the correlation between stromal HSF1 activation and poor patient outcomes was strong enough in each case to warrant further clinical investigation. They add that an HSF1-based biomarker could help predict which patient tumors, early-stage lung in particular, are most likely to progress and might benefit from more aggressive therapy. Conversely, such information could prevent patients with less aggressive cancers from suffering the ill effects of "over-treatment" with highly toxic therapies.