The role of estradiol metabolism in urogenital schistosomiasis-induced bladder cancer

Author:

Vale Nuno1,Gouveia Maria J12,Rinaldi Gabriel34,Santos Júlio56,Santos Lúcio Lara6,Brindley Paul J3,da Costa José M Correia27

Affiliation:

1. UCIBIO/REQUIMTE, Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, Porto, Portugal

2. Center for the Study of Animal Science, ICETA, University of Porto, Porto, Portugal

3. Department of Microbiology, Immunology, & Tropical Medicine and Research Center for Neglected Diseases of Poverty, School of Medicine & Health Sciences, George Washington University, Washington, DC, USA

4. The Wellcome Trust Sanger Institute, Cambridge, UK

5. Clínica da Sagrada Esperança, Luanda, Angola

6. Experimental Pathology and Therapeutics Group, Research Center of Instituto Português de Oncologia, Porto, Portugal

7. Department of Infectious Diseases, R&D Unit, National Health Institute Doutor Ricardo Jorge (INSA), Porto, Portugal

Abstract

Urogenital schistosomiasis is a neglected tropical disease that can lead to bladder cancer. How urogenital schistosomiasis induces carcinogenesis remains unclear, although there is evidence that the human blood fluke Schistosoma haematobium, the infectious agent of urogenital schistosomiasis, releases estradiol-like metabolites. These kind of compounds have been implicated in other cancers. Aiming for enhanced understanding of the pathogenesis of the urogenital schistosomiasis-induced bladder cancer, here we review, interpret, and discuss findings of estradiol-like metabolites detected in both the parasite and in the human urine during urogenital schistosomiasis. Moreover, we predict pathways and enzymes that are involved in the production of these metabolites emphasizing their potential effects on the dysregulation of the tumor suppressor gene p53 expression during urogenital schistosomiasis. Enhanced understanding of these potential carcinogens may not only shed light on urogenital schistosomiasis-induced neoplasia of the bladder, but would also facilitate development of interventions and biomarkers for this and other infection-associated cancers at large.

Publisher

IOS Press

Subject

General Medicine

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