Association of human papillomavirus 16 and 18 with ovarian cancer risk: Insights from a meta‑analysis.

HPV 16 HPV 18 meta-analysis ovarian neoplasms

Journal

Oncology letters
ISSN: 1792-1082
Titre abrégé: Oncol Lett
Pays: Greece
ID NLM: 101531236

Informations de publication

Date de publication:
Dec 2024
Historique:
received: 17 07 2024
accepted: 22 08 2024
medline: 2 10 2024
pubmed: 2 10 2024
entrez: 2 10 2024
Statut: epublish

Résumé

Ovarian cancer (OC) presents a global health challenge, with well-documented genetic aspects. However, to the best of our knowledge, the role of human papillomavirus (HPV) types 16 and 18 in OC remains unclear. The present meta-analysis assessed the prevalence of HPV in OC across 43 studies and included a comparative meta-analysis of 19 case-control studies to determine the association of HPV with OC risk. Subgroup analyses were performed based on geographic regions and histopathological types to explore heterogeneity, and publication bias was evaluated using funnel plots and statistical tests of asymmetry. The pooled prevalence of HPV was found to be 10% (95% CI, 5-18) and 7% (95% CI, 3-15) specifically for HPV 16/18. Case-control studies indicated an odds ratio (OR) of 4.92 (95% CI, 1.96-12.53) for HPV 16/18, with higher pooled prevalence rates of 17% for all HPV genotypes and 13% for HPV 16/18. Notably, Asian countries exhibited the highest HPV prevalence and OR in OC. These findings support the involvement of HPV, particularly HPV 16 and 18, in increasing the risk of OC, emphasizing the need for further research to confirm these associations and explore potential mechanisms.

Identifiants

pubmed: 39355783
doi: 10.3892/ol.2024.14689
pii: OL-28-6-14689
pmc: PMC11443309
doi:

Types de publication

Journal Article

Langues

eng

Pagination

556

Informations de copyright

Copyright: © 2024 Le et al.

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

Auteurs

Tan Minh Le (TM)

Department of Biomedical Science, Graduate School, Kyungpook National University, Daegu 41944, Republic of Korea.

Hong Duc Thi Nguyen (HDT)

Department of Biomedical Science, Graduate School, Kyungpook National University, Daegu 41944, Republic of Korea.

Junghwan Cho (J)

Clinical Omics Institute, Kyungpook National University, Daegu 41405, Republic of Korea.

Nora Jee-Young Park (NJ)

Clinical Omics Institute, Kyungpook National University, Daegu 41405, Republic of Korea.
Department of Pathology, Kyungpook National University Chilgok Hospital, Daegu 41404, Republic of Korea.

Hyung Soo Han (HS)

Department of Biomedical Science, Graduate School, Kyungpook National University, Daegu 41944, Republic of Korea.
Clinical Omics Institute, Kyungpook National University, Daegu 41405, Republic of Korea.
Department of Physiology, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea.

Gun Oh Chong (GO)

Clinical Omics Institute, Kyungpook National University, Daegu 41405, Republic of Korea.
Department of Obstetrics and Gynecology, Kyungpook National University Chilgok Hospital, Daegu 41404, Republic of Korea.

Incheol Seo (I)

Department of Immunology, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea.

Classifications MeSH