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This study investigates the prevalence of beta (β) and gamma (γ) human papillomavirus (HPV) types in cervical and anal samples from women living with HIV and examines their association with alpha (α) HPV and cytological lesions. Cervical and anal swabs were collected from 138 women. Detection of β- and γ-HPV types were performed using bead-based assays, and data analysis included only samples with adequate DNA quality, as confirmed by β-globin amplification. The analysis revealed higher rates of β-HPV in anal samples (51.7%) compared to cervical samples (30.3%), with β-1 species being predominant in both sites. Furthermore, γ-HPV types were more prevalent in anal samples (36.5%) than in cervical site (16.9%), with γ-10 being the most frequently detected species. Concordance between cervical and anal samples for specific β-HPV types (κ = 0.20, 95% CI: 0.03-0.36) and γ-HPV types (κ = 0.17, 95% CI: 0.003-0.36) was poor. Co-infections with both β- and γ-HPV types in cervical samples was significantly associated with co-infection at the anal site (OR 7.7; 95% CI: 1.44-38.25; p = 0.01). There was no statistically significant association (p > 0.05) between β-HPV positivity and neoplastic precancerous lesions (LSIL or HSIL) at either the cervical or anal site. Similarly, γ-HPV positivity showed no significant association (p > 0.05) with cytological abnormalities in cervical or anal samples. In conclusion, while the prevalence of β- and γ-HPV types is higher in the anal region among HIV-positive women, the absence of a strong association with neoplastic lesions underscores their limited oncogenic potential compared to high-risk α-HPV types.
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http://dx.doi.org/10.1002/jmv.70518 | DOI Listing |
HIV-induced gut microbiota dysbiosis perpetuates mucosal barrier disruption and systemic inflammation despite antiretroviral therapy (ART), creating a tumor-permissive microenvironment. This review synthesizes evidence linking HIV-associated microbial alterations to oncogenesis through three convergent metabolic axes: (1) butyrate deficiency impairing epithelial energy metabolism and anti-tumor immunity; (2) tryptophan metabolism dysregulation compromising gut barrier integrity via depletion and -mediated phenylethylamine overproduction; and (3) vitamin B biosynthesis defects disrupting DNA repair and Th1/Th2 balance. Comparative profiling across HIV-associated malignancies-non-Hodgkin lymphoma, cervical cancer, hepatocellular carcinoma, and lung cancer-reveals conserved dysbiotic signatures: depletion of anti-inflammatory taxa (, ) and expansion of pro-inflammatory genera (, ).
View Article and Find Full Text PDFHigh-risk human papillomavirus (HPV) infections are the etiology of approximately 5% of all cancers worldwide, including cervical, anal, and oropharyngeal malignancies. HPV E6 is a multifunctional oncoprotein that drives tumorigenesis and is best known for bridging the ubiquitin ligase E6AP (UBE3A) and p53 into a complex that leads to proteasome mediated destruction of p53. We developed small molecule inhibitors that covalently bind to cysteine-51 (Cys-51) in HPV16 E6.
View Article and Find Full Text PDFBMC Womens Health
September 2025
Department of Gynecology, Liaoning Cancer Hospital & Institute, Cancer Hospital of Dalian University of Technology, Cancer Hospital of China Medical University, Shenyang, Liaoning, 110042, China.
Cancer Med
September 2025
Departamento de Ciências da Saúde Pública e Forenses e Educação Médica, Faculdade de Medicina, Universidade do Porto, Porto, Portugal.
Background: A Radiotherapy Service (RS) started working in the Maputo Central Hospital (MCH), Mozambique, in August 2019. Here we describe its first 5 years of activity.
Methods: A total of 810 patients who underwent external radiotherapy between August 2019 and December 2023 were considered for the analysis.
Anal Methods
September 2025
School of Materials Science and Engineering, Xiangtan University, Xiangtan 411105, PR China.
Cervical cancer is the fourth most common cancer among women worldwide. Human papillomavirus type 16 (HPV16) is one of the common biomarkers which cause cervical cancer. In this work, an electrochemical sensor based on a triblock polyadenine-based probe (TPP) and copper nanoclusters (CuNCs) was constructed for the rapid, sensitive and selective detection of HPV16.
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