TY - JOUR
T1 - The role of estradiol metabolism in urogenital schistosomiasis-induced bladder cancer
AU - Vale, Nuno
AU - Gouveia, Maria J.
AU - Rinaldi, Gabriel
AU - Santos, Júlio
AU - Santos, Lúcio Lara
AU - Brindley, Paul J.
AU - da Costa, José M.Correia
N1 - Publisher Copyright:
© 2017, © The Author(s) 2017.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - 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.
AB - 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.
KW - bladder
KW - estrogen-DNA adduct
KW - estrogen-like metabolites
KW - Schistosoma haematobium
KW - squamous cell carcinoma
KW - urogenital schistosomiasis
KW - Reactive Oxygen Species/metabolism
KW - Humans
KW - Schistosomiasis haematobia/parasitology
KW - Tumor Suppressor Protein p53/metabolism
KW - Estradiol/metabolism
KW - Cell Transformation, Neoplastic/pathology
KW - Animals
KW - Urinary Bladder/pathology
KW - Urinary Bladder Neoplasms/metabolism
KW - DNA Adducts/genetics
KW - Schistosoma haematobium/metabolism
UR - http://www.scopus.com/inward/record.url?scp=85016923437&partnerID=8YFLogxK
U2 - 10.1177/1010428317692247
DO - 10.1177/1010428317692247
M3 - Review Article
C2 - 28345469
AN - SCOPUS:85016923437
SN - 1010-4283
VL - 39
JO - Tumor Biology
JF - Tumor Biology
IS - 3
ER -