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Molecular Insights into the Role of Exosomes in Health Disparity of Prostate Cancer
Prostate cancer (PCa) is the second leading cause of morbidity among older men in the States. The morbidity and mortality rates of PCa are more likely to be twice in in African Americans (AA) than in Caucasian Americans (CA) men. Owing to multiple factors contribute to such disparities; it remains unclear whether the high incidence and mortality rates of PCa among AA men are triggered by genetic and epigenetic factors. The molecular mechanisms underlying these biological factors have yet to be fully elucidated. Exosomes are cell-derived extracellular bodies secreted by normal and tumor cells to promote cell-cell communications. Exosomes acting as a biological cargo and shuttle various molecules, including microRNAs, mRNAs, lipids, DNA and proteins to recipient cells. Our goal here is to illustrate the role of exosomes contributing to different biological activities, especially aggressive behavior of cancer cells and poor clinical outcomes of PCa in AA patients. We discussed the need for discovering new biomarkers used in diagnosis and prognosis of PCa. This followed by unravelling the association between exosomes and induction of different signaling pathways to promote survival, cell proliferation, invasion, metastasis and escape the immune response with a special focus on cancer disparities among AA men. This review warrants more studies to build on these recent findings for future understanding of the role of PCa-associated exosomes in promoting PCa aggressiveness in AA and other cancer disparities. Adopting such exosomal findings in cancer and other chronic diseases might help to eliminate morbidity and mortality disparities among US minorities
Androgen Metabolism Genes in Prostate Cancer Health Disparities
For men in the United States, prostate cancer is common, and newly diagnosed cases of prostate cancer outnumber those of all other cancer types. For prostate cancer, there are racial disparities between Caucasian Americans and African Americans. Androgens and androgen metabolism may be involved in these disparities as well as in the initiation and progression of prostate cancer. Here, we analyzed, in the Cancer Genome Atlas (TCGA) database, the mRNA expression of genes involved in androgen metabolism in prostate cancer based on the patient’s race. The results revealed that expressions of UGT2B15 and CYP3A5 are higher but that SRD5A2, CYP17A1, HSD3B2, and AKR1C3 are lower in African American prostate cancers than in those of Caucasian Americans. These genes may relate to the racial disparities associated with prostate cancer. However, the evidence require validation and functional analysis