The immunohistochemical investigation of p53 and c-MYC proteins in prostate cancer patients with associated HPV and TV parasite
Abstract
Prostate cancer is a complicated disease motivated via genetic and environmental factors, consisting of viral and parasitic infections. This look at investigated the immunohistochemical expression patterns of the c-MYC and p53 oncoproteins in prostate most cancers sufferers with and without human papillomavirus (HPV) and Trichomonas vaginalis co-contamination. The effects revealed substantial differences in c-MYC and p53 expression ranges most of the affected person organizations. In HPV and Trichomonas vaginalis co-infected instances, both c-MYC and p53 expression rankings have been notably higher compared to HPV-inflamed, Trichomonas vaginalis-infected, and normal cases. This shows a ability synergistic effect of the co-contamination in promoting the upregulation of these oncogenes, that are implicated in prostate most cancers development. Interestingly, HPV-infected cases exhibited substantially higher c-MYC expression in comparison to Trichomonas vaginalis-inflamed and normal instances, indicating that HPV infection alone may be associated with accelerated c-MYC expression and doubtlessly contribute to prostate most cancers chance. In comparison, Trichomonas vaginalis-infected cases confirmed drastically better p53 expression but lower c-MYC expression, suggesting a capability tumor-suppressor function of Trichomonas vaginalis infection. These findings spotlight the aberrant expression of c-MYC and p53 oncoproteins in prostate most cancers sufferers, specifically people with viral and parasitic co-infections. Further studies is wanted to elucidate the perfect mechanisms underlying those adjustments and discover their potential healing implications.
Fields of Study & Subjects
Prostate Cancer Treatment and Research
Cervical Cancer and HPV Research
Prostate Cancer Diagnosis and Treatment
Publication details
- Journal / source
- AIP conference proceedings
- Volume
- 3415
- Pages
- 020042–020042
- Publication date
- 1 January 2026
- Language
- EN