Evidence map›Paper›PMID 40430005›Full record

ArticleInternational journal of molecular sciences2025

A Pilot Study: Contrasting Genomic Profiles of Lung Adenocarcinoma Between Patients of European and Latin American Ancestry.

Bertha Rueda-Zarazua, Humberto Gutiérrez, Humberto García-Ortiz, Lorena Orozco, Gustavo Ramírez-Martínez, Luis Jiménez-Alvarez, Francina V Bolaños-Morales, Joaquín Zuñiga, Federico Ávila-Moreno, Jorge Melendez-Zajgla

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
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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

10 authors.

Bertha Rueda-ZarazuaPosgrado en Ciencias Biológicas, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico.
Humberto GutiérrezInstituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.
Humberto García-OrtizLaboratorio de Inmunogenómica y Enfermedades Metabólicas, Instituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.ORCID 0000-0002-0453-980X
Lorena OrozcoLaboratorio de Inmunogenómica y Enfermedades Metabólicas, Instituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.
Gustavo Ramírez-MartínezLaboratorio de Inmunología y Genética, Instituto Nacional de Enfermedades Respiratorias, Mexico City 14080, Mexico.ORCID 0000-0001-5157-0677
Luis Jiménez-AlvarezLaboratorio de Inmunología y Genética, Instituto Nacional de Enfermedades Respiratorias, Mexico City 14080, Mexico.
Francina V Bolaños-MoralesSubdirección de Cirugía, Instituto Nacional de Enfermedades Respiratorias, Mexico City 14080, Mexico.
Joaquín ZuñigaLaboratorio de Inmunología y Genética, Instituto Nacional de Enfermedades Respiratorias, Mexico City 14080, Mexico.ORCID 0000-0002-7143-0281
Federico Ávila-MorenoLung Diseases and Functional Epigenomics Laboratory (LUDIFE), Biomedicine Research Unit (UBIMED), Facultad de Estudios Superiores-Iztacala, Universidad Nacional Autónoma de México, Tlalnepantla 54090, Mexico.ORCID 0000-0002-0252-7899
Jorge Melendez-ZajglaLaboratorio de Genómica Funcional del Cáncer, Instituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.ORCID 0000-0002-2209-1607

Funding

Consejo Nacional de Humanidades, Ciencias y Tecnologías A1-S-8462_2
6 · The paper itself

Abstract

Lung cancer remains as the leading cause of cancer mortality worldwide. However, while current evidence suggests the existence of genomic differences between populations, indicating different risk factors associated with population-level genetic backgrounds, most studies have concentrated on populations of European ancestry, and more research is needed on non-European populations. We analyzed whole-exome sequencing data from 25 Mexican lung adenocarcinoma patients and compared them with a TCGA-PanCancer cohort enriched with patients of European ancestry as reference. Clinically relevant germline variants in cancer susceptibility genes are more frequent in our cohort (32% vs. 6.4%) than in the reference. Several mutational signatures (SBS32, SBS85, SBS12, SBS19) occurred at significantly higher frequencies in the Mexican cohort compared to the reference (

Indexed as

Adenocarcinoma of LungLung NeoplasmsWhite PeopleAdultAgedExome SequencingFemaleGenetic Predisposition to DiseaseGenomicsHumansLatin AmericaMaleMexicoMiddle AgedMutationPilot Projectsexomegenomic profilelung adenocarcinomaMexicoNSCLC

Identifiers

PMID40430005
PMCPMC12111962

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Registered trials

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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.