Background: A cross-sectional study was conducted to determine the prevalence of urinary schistosomiasis among primary school pupils in Wamakko Local Government, Sokoto State, Nigeria. Four hundred terminal urine samples were collected from primary school pupils and analysed using standard filtration technique. Results: Out of the 400 urine samples examined, 192 (48%) were found to be infected with Schistosoma haematobium. Males had a higher prevalence (49.49%) than females (43.93%), although statistical analysis indicated no significant association of S. haematobium infection with gender. The highest infection rate was recorded among pupils aged 4-6 years (62.82%) while the least was found among pupils aged 7-9 years; this did not attend significant level (p > 0.05). The occurrence of S. haematobium infection did not significantly associate with a source of drinking water and water contact activity (p > 0.05). Conclusion: This study indicates the presence of urinary schistosomiasis in the study area and that all pupils in the study area are equally exposed to the source of infection. Therefore, prompt intervention is highly advocated.

Protein kinase CK2 plays a critical role in cell growth, proliferation, and suppression of cell death. CK2 is overexpressed, especially in the nuclear compartment, in the majority of cancers, including prostate cancer (PCa). CK2-mediated activation of transcription factor nuclear factor kappa B (NF-κB) p65 is a key step in cellular proliferation, resulting in translocation of NF-κB p65 from the cytoplasm to the nucleus. As CK2 expression and activity are also elevated in benign prostatic hyperplasia (BPH), we sought to increase the knowledge of CK2 function in benign and malignant prostate by examination of the relationships between nuclear CK2 and nuclear NF-κB p65 protein expression. The expression level and localization of CK2α and NF-κB p65 proteins in PCa and BPH tissue specimens was determined. Nuclear CK2α and NF-κB p65 protein levels are significantly higher in PCa compared with BPH, and these proteins are positively correlated with each other in both diseases. Nuclear NF-κB p65 levels correlated with Ki-67 or with cytoplasmic NF-κB p65 expression in BPH, but not in PCa. The findings provide information that combined analysis of CK2α and NF-κB p65 expression in prostate specimens relates to the disease status. Increased nuclear NF-κB p65 expression levels in PCa specifically related to nuclear CK2α levels, indicating a possible CK2-dependent relationship in malignancy. In contrast, nuclear NF-κB p65 protein levels related to both Ki-67 and cytoplasmic NF-κB p65 levels exclusively in BPH, suggesting a potential separate impact for NF-κB p65 function in proliferation for benign disease as opposed to malignant disease.