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Cancer researchers have long known that prostate cancer tends to be more common, more aggressive and more resistant to existing treatments in African-Americans than in Caucasian-Americans, but they’re only beginning to understand why. mitochondrial dysfunction and an inability to generate apoptosome formation are key factors behind higher prostate cancer incidence and poorer outcomes in African-Americans.
Many African-American men lack a key mitochondrial protein known as cytochrome c—the main protein that facilitates the formation of the desirable “death wheel” effect against cancer cells. Cytochrome c deficiency can occur in people of any race or background, but is common among people of African ancestry. Dr. Chandra and his team report in their new study that African-American males tend to have high expression of the cancer promoters c-Myc and NF-κB, leading to the inhibition of cytochrome c.
The findings shed light on why current therapeutic agents for firstline prostate cancer treatment, chiefly docetaxel, do not provide much benefit for many African-American men,” says Dr. Chandra, Professor of Oncology in the Department of Pharmacology and Therapeutics at the Buffalo-based cancer center. “But importantly, they also provide strong evidence that new therapeutic strategies can be developed to address and exploit these mechanisms.”
Inhibiting the cancer-promoting proteins c-Myc and NF-κB can restore cytochrome c in the prostate cancer cells of those with cytochrome c deficiency, thereby enhancing apoptosome production to kill prostate cancer cells. Existing drugs approved for other applications can be used to inhibit c-Myc and NF-κB. The team plans to pursue clinical trials to assess the effectiveness of this approach as treatment for prostate cancer.