Evidence map›Paper›PMID 41160463›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2026

Reconstructing the Origin and Demographic Expansion of the TP53 p.R337H Founder Variant in Brazil.

Emilia Modolo Pinto, João Carlos Degraf Muzzi, José Andres Yunes, Bonald Cavalcante de Figueiredo, Raul C Ribeiro, Gerard P Zambetti

Abstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 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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1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Emilia Modolo PintoDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0001-5567-000X
João Carlos Degraf MuzziPelé Pequeno Príncipe Research Institute, Curitiba, Brazil.ORCID 0000-0002-6994-5577
José Andres YunesLaboratório de Biologia da Leucemia, Centro Infantil Boldrini, Campinas, Brazil.ORCID 0000-0002-1316-3525
Bonald Cavalcante de FigueiredoPelé Pequeno Príncipe Research Institute, Curitiba, Brazil.ORCID 0000-0002-1051-2056
Raul C RibeiroDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0002-9956-5647
Gerard P ZambettiDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0002-0929-5007

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
XAF1 IN P53 SIGNALING, APOPTOSIS AND TUMOR SUPPRESSIONR01CA260175 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GERARD PAUL ZAMBETTI · 2022 to 2026
$2.1M
American Lebanese Syrian Associated Charities (ALSAC)National Cancer Institute (NCI) 5R01CA260175National Cancer Institute (NCI) CA21765NCI NIH HHS P30 CA021765NCI NIH HHS R01 CA260175Speer Charitable Trust
6 · The paper itself

Abstract

backgroundThe TP53 p.R337H variant is a well-characterized founder mutation with an unusually high prevalence in Brazil, particularly in the South and Southeast regions, where it affects approximately one in 300 individuals. It is recurrently associated with pediatric adrenocortical tumors and malignancies within the Li-Fraumeni syndrome spectrum but exhibits markedly incomplete penetrance, suggesting the influence of additional genetic and/or environmental modifiers. Although TP53 p.R337H occurs at low frequencies in the Iberian Peninsula, its origin, timing, and dissemination pattern within Brazil have remained unresolved.

methodsWe integrated population-genetic inference with historical demographic modeling to reconstruct the introduction and expansion of the TP53 p.R337H in Brazil.

resultsOur analyses support a founder effect arising from a single founding event of European origin during the early Portuguese colonization period. The subsequent geographic dissemination of the variant parallels historical population growth, particularly in southern Brazil. The striking regional enrichment can be explained without invoking multiple introduction events or complex migratory scenarios.

conclusionsThese findings clarify the evolutionary and demographic history of TP53 p.R337H in Brazil and underscore its founder effect origin during European colonization. IMPACT: This study highlights the value of integrating population genetics with historical data to elucidate the spread of medically relevant founder variants. Understanding the dissemination of TP53 p.R337H will enhance public health planning and genetic counseling strategies in Brazil. See related In the Spotlight, p. 187.

Indexed as

Founder EffectLi-Fraumeni SyndromeTumor Suppressor Protein p53BrazilHumansMutationTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID41160463
PMCPMC12666849

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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.