Evidence map›Paper›PMID 42088651›Full record

ArticleFrontiers in reproductive health2026

TP53 codon 47 and 72 polymorphisms show no association with HPV in Zimbabwean women living with HIV and histologically confirmed cervical and vulvar disease.

Oppah Kuguyo, Margaret Pascoe, Eugenie Lohmann, Takudzwa Magwaku, Diana L T Mukuku, Ardele Mandiriri, Nyarai Soko, Collet Dandara, Rudo Makunike Mutasa, Megan Fitzpatrick and 4 more

Abstract read
In one paragraph

Article in Frontiers in reproductive health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Oppah KuguyoDivision of Human Genetics, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Margaret PascoeNewlands Clinic, Harare, Zimbabwe.
Eugenie LohmannEarly Detection and Prevention Research, International Agency for Research on Cancer, Lyon, France.
Takudzwa MagwakuDepartment of Biochemistry and Biotechnology, Faculty of Science, University of Zimbabwe, Harare, Zimbabwe.
Diana L T MukukuMedical Microbiology Unit, University of Zimbabwe Faculty of Health Sciences, Harare, Zimbabwe.
Ardele MandiririNewlands Clinic, Harare, Zimbabwe.
Nyarai SokoDivision of Human Genetics, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Collet DandaraDivision of Human Genetics, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Rudo Makunike MutasaDepartment of Histopathology, University of Zimbabwe Faculty of Health Sciences, Harare, Zimbabwe.
Megan FitzpatrickDepartment of Pathology, University of Wisconsin, Madison, WI, United States.
Joel PalefskyDepartment of Medicine, UCSF School of Medicine, San Francisco, CA, United States.
Trine RoungeDepartment of Research, Cancer Registry of Norw,aY, Oslo, Norway.
Zvavahera Mike ChirenjeDepartment of Obstetrics and Gynaecology, University of Zimbabwe Faculty of Health Sciences, Harare, Zimbabwe.
Racheal S Dube MandishoraEarly Detection and Prevention Research, International Agency for Research on Cancer, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Interaction between HIV and human papillomavirus (HPV) increases the risk of HPV persistence. However, a few studies have explored the interplay between host genetic factors and HPV in women living with HIV (WLWH). We report on a study investigating the role of TP53 mutations among HPV DNA-positive cervical and vulvar tissue from Zimbabwean WLWH. Methods: This cross-sectional study recruited 102 WLWH aged over 18 years, with histologically confirmed vulvar ( Results: The histological classifications had the following proportions: cervical intraepithelial neoplasia (CIN)1: 10%, CIN2: 4.5%, CIN3: 82%, and cervical cancer: 3.4%. Vulvar disease was classified as: vulvar intraepithelial neoplasia (VIN)3: 84.6%, and vulvar cancer (15.4%). HPV16 prevalence was 40% and 64% in vulvar tissue. Codon 72G and codon 47 T alleles had frequencies of 34.1% and 2.9% in cervical tissue, and 29.2% and 4.2% in vulvar tissue, respectively. There was no significant association between TP53 codon 72 and 47 mutations, and HPV genotypes ( Discussion and Conclusion: These findings underscore the need to conduct further research to identify other genetic variants within the TP53 gene that may contribute to the role of TP53 in HPV susceptibility that has been previously reported in other studies.

Indexed as

cervical cancerCINHIVHIV opportunistic infectionsHPVSub-Saharan AfricaVINvulvar cancer

Identifiers

PMID42088651
PMCPMC13136159

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.