Evidence map›Paper›PMID 40476566›Full record

ArticleCancer research communications2025

Genetic Ancestry, Intrinsic Tumor Subtypes, and Breast Cancer Survival in Latin American Women.

Daniela Alves da Quinta, Darío Rocha, Cristian Yáñez, Renata Binato, Sheila Coelho Soares-Lima, Xiaosong Huang, Daiana Ganiewich, Valentina A Zavala, Monica Sans, Alejandra Lopez-Vazquez and 23 more

Abstract read
In one paragraph

Article in Cancer research communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed.

  1. Article
  2. Article
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

33 authors.

Daniela Alves da Quinta *Laboratorio de Terapia Molecular y Celular, Fundación Instituto Leloir-CONICET, Ciudad de Buenos Aires, Argentina.ORCID 0009-0007-4592-9402
Darío Rocha *Universidad Nacional de Córdoba, Facultad de Ciencias Exactas, Físicas y Naturales, Córdoba, Argentina.ORCID 0000-0002-6000-3874
Cristian YáñezPrograma de Genética Humana, ICBM, Facultad de Medicina, Universidad de Chile, Santiago, Chile.ORCID 0009-0002-0856-0654
Renata BinatoInstituto Nacional de Câncer, Rio de Janeiro, Brazil.ORCID 0000-0001-7590-0335
Sheila Coelho Soares-LimaInstituto Nacional de Câncer, Rio de Janeiro, Brazil.ORCID 0000-0002-6742-3708
Xiaosong HuangGenome Center, College of Biological Sciences, University of California Davis, Davis, California.ORCID 0000-0003-0627-1509
Daiana GaniewichLaboratorio de Terapia Molecular y Celular, Fundación Instituto Leloir-CONICET, Ciudad de Buenos Aires, Argentina.ORCID 0009-0006-0285-9910
Valentina A ZavalaDepartment of Public Health Sciences, University of California, Davis, Davis, California.ORCID 0000-0003-2040-1760
Monica SansHospital de Clinicas Manuel Quintela, Universidad de la República, Montevideo, Uruguay.ORCID 0000-0002-1564-8761
Alejandra Lopez-VazquezUniversidad de Sonora, Hermosillo, Mexico.ORCID 0000-0001-7405-2530
Jael QuinteroUniversidad de Sonora, Hermosillo, Mexico.ORCID 0000-0002-7471-6269
Olivia ValenzuelaUniversidad de Sonora, Hermosillo, Mexico.ORCID 0000-0002-4456-2107
Antonio Quintero-RamosUniversidad de Guadalajara, Guadalajara, Mexico.ORCID 0000-0001-5963-9712
Alicia Del Toro-ArreolaUniversidad de Guadalajara, Guadalajara, Mexico.ORCID 0000-0002-1994-9027
Mauricio CerdaIntegrative Biology Program, Instituto de Ciencias Biomedicas (ICBM), Centro de Informática Mádica y Telemedicina, Facultad de Medicina, Universidad de Chile, Santiago, Chile.ORCID 0000-0003-3447-1815
Katherine MarcelainDepartamento de Oncología Básico Clínico and Centro para la Prevención y el Control del Cáncer (CeCAN), Facultad de Medicina, Universidad de Chile, Santiago, Chile.ORCID 0000-0003-4018-6623
Susanne CrocamoInstituto Nacional de Câncer, Rio de Janeiro, Brazil.ORCID 0000-0002-5463-5517
Maria Aparecida NagaiInstituto de Cancer de São Paulo, São Paulo, Brazil.ORCID 0000-0002-0728-4937
Dirce M CarraroAC Camargo Cancer Center, São Paulo, Brazil.ORCID 0000-0001-5667-1418
Marcia Maria Chiquitelli MarquesHospital de Cancer de Barretos, Barretos, Brazil.ORCID 0000-0001-5616-6710
Jorge GómezHealth Sciences Center, Texas A&M University, Bryan, Texas.ORCID 0000-0001-9506-7408
Nora ArtagaveytiaHospital de Clinicas Manuel Quintela, Universidad de la República, Montevideo, Uruguay.ORCID 0000-0001-8798-7941
Adrian Daneri-NavarroUniversidad de Guadalajara, Guadalajara, Mexico.ORCID 0000-0002-8206-749X
Bettina G MüllerInstituto Nacional del Cáncer, Santiago de Chile, Chile.ORCID 0000-0002-8589-5725
Javier RetamalesGrupo Oncológico Cooperativo Chileno de Investigación, Santiago de Chile, Chile.ORCID 0000-0001-7051-0362
Carlos VelazquezUniversidad de Sonora, Hermosillo, Mexico.ORCID 0000-0002-3728-7848
Elmer A FernándezFundación para el Progreso de la Medicina, ScireLab, Córdoba, Argentina.ORCID 0000-0002-4711-8634
Osvaldo L PodhajcerLaboratorio de Terapia Molecular y Celular, Fundación Instituto Leloir-CONICET, Ciudad de Buenos Aires, Argentina.ORCID 0000-0002-6512-8553
Eliana AbdelhayInstituto Nacional de Câncer, Rio de Janeiro, Brazil.ORCID 0000-0001-5166-0832
Ricardo A VerdugoPrograma de Genética Humana, ICBM, Facultad de Medicina, Universidad de Chile, Santiago, Chile.ORCID 0000-0001-5668-5449
LACRN Investigators
Andrea S Llera *Laboratorio de Terapia Molecular y Celular, Fundación Instituto Leloir-CONICET, Ciudad de Buenos Aires, Argentina.ORCID 0000-0002-0089-0061
Laura Fejerman *Instituto Nacional de Câncer, Rio de Janeiro, Brazil.ORCID 0000-0003-3179-1151

Funding

Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI KC KENT LLOYD · 2002 to 2026
$84.9M
Latin America Genomics of Breast Cancer Risk Study (LAGENO-BCR)R01CA286650 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Julie Dutil, Laura Fejerman · 2024 to 2026
$2.5M
Biological implications of breast cancer protective variants in Latin Americanwomen with high Indigenous American ancestryR01CA204797 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FEJERMAN, LAURA · 2016 to 2020
$1.9M
Her2 status of breast cancer in diverse populations: improving genetic prediction and understanding molecular correlatesR01CA273313 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Laura Fejerman · 2023 to 2026
$1.8M
NCI NIH HHS P30 CA093373NCI NIH HHS R01 CA204797NCI NIH HHS R01 CA273313NCI NIH HHS R01 CA286650
6 · The paper itself

Abstract

This study investigates the relationship between genetic ancestry, breast cancer subtypes, and survival outcomes among 951 locally advanced breast cancer cases from Argentina, Brazil, Chile, Mexico, and Uruguay, participating in the Molecular Profile of Breast Cancer Study. Array-based genotyping and ADMIXTURE analysis were used for genetic ancestry evaluation. Breast cancer subtypes were defined by IHC and the gene expression-based PAM50 algorithm. The distribution of genetic ancestry, including European, Indigenous American (IA), African (AFR), and East Asian components, revealed a heterogeneous genetic admixture across countries, with the highest IA ancestry observed in Chile (30.9%) and Mexico (30.8%). Testing the relationship between genetic ancestry and breast cancer subtypes demonstrated that a 10% increase in European ancestry was significantly associated with a 14% decrease in the odds of developing HER2-enriched breast cancer, after adjustment by age, nodal status, and the AFR component (adj. P = 0.021, luminal A as reference). Accordingly, a 10% increase in IA ancestry was associated with a 21% increase in the probability of having HER2-enriched breast cancer (adj. P = 0.022). IA ancestry also significantly increased overall survival after adjustment by age, nodal status, and AFR ancestry, although this result is controversial and may be affected by the size and heterogeneity of the Molecular Profile Breast Cancer Study cohort. Our research confirms previous findings of a high prevalence of HER2-dependent breast tumors among Hispanic/Latina women and strengthens the hypotheses of the existence of either population-specific genetic variant(s) or of other ancestry-correlated factors that impact HER2 expression in breast cancer consistently across different Latin American regions. SIGNIFICANCE: The evidence in this work supports the idea that factors linked to genetic ancestry influence the prevalence of breast cancer subtypes in Latin America, potentially affecting treatment needs in the region.

Indexed as

Breast NeoplasmsAdultAgedBiomarkers, TumorCentral American PeopleErb-b2 Receptor Tyrosine KinasesFemaleHumansLatin AmericaMiddle AgedSouth American PeopleBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID40476566
PMCPMC12223717

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