Mitochondrial Protein Linked to Development of Prostate Cancer

In a prior study, investigators at The Wistar Institute (Philadelphia, PA, USA) genetically engineered a line of mice with the gene for TRAP1 protein "knocked out" to determine what impact it may have on disease. They found that these mice lived longer and experienced fewer age-related illnesses than did normal animals.

In the current study, the investigators created a line of mice that overexpressed the TRAP1 gene. Furthermore, these animals also lacked one copy of the important tumor suppressor gene PTEN. At least one copy of PTEN is deleted in about 40% of cases of prostate cancer and is often found in more aggressive tumors, so mice without this gene more accurately simulate the behavior of the disease.

The investigators reported in the October 17, 2016, online edition of the Journal of Biological Chemistry that combination of increased TRAP1 coupled with the loss of PTEN resulted in the development of aggressive, early-onset invasive prostate cancer. The mice also displayed increased tumor cell proliferation, inhibition of apoptosis, and increased epithelial cell invasion.

"In our prior study, while we had evidence that hinted at TRAP1's role in tumor growth, we lacked the direct evidence we needed to define the role of this protein in prostate cancer development," said senior author Dr. Dario C. Altieri, president and CEO of The Wistar Institute. "As we better understand the role of mitochondria in cancer, it's important to thoroughly study the roles of the proteins involved in helping tumors receive the energy they desire for survival. What is exciting about these findings is the fact that we believe TRAP1 is a druggable target. We are continuing to advance our promising research and development program aimed at targeting the mitochondria in tumors."

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The Wistar Institute