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Low Prevalence of ETV6::RUNX1 Fusion Gene in a Hispanic Population

Authors :
Minerva Mata-Rocha
Angelica Rangel-López
Elva Jimenez-Hernandez
Juan Carlos Nuñez-Enríquez
Blanca Angélica Morales-Castillo
Norberto Sánchez-Escobar
Omar Alejandro Sepúlveda-Robles
Juan Carlos Bravata-Alcántara
Alan Steve Nájera-Cortés
María Luisa Pérez-Saldivar
Janet Flores-Lujano
David Aldebarán Duarte-Rodríguez
Norma Angélica Oviedo de Anda
Maria de los Angeles Romero Tlalolini
Carmen Alaez Verson
Jorge Alfonso Martín-Trejo
Jose Esteban Muñoz Medina
Cesar Raul Gonzalez-Bonilla
Maria de los Angeles Hernandez Cueto
VC. Bekker-Méndez
Silvia Jiménez-Morales
Aurora Medina-Sansón
Raquel Amador-Sánchez
José Gabriel Peñaloza-González
José Refugio Torres-Nava
Rosa Martha Espinosa-Elizondo
Beatriz Cortés-Herrera
Luz Victoria Flores-Villegas
Laura Elizabeth Merino-Pasaye
Maria de Lourdes Gutierrez-Rivera
Martha Margarita Velazquez-Aviña
Jessica Denisse Santillan-Juarez
Alma Gurrola-Silva
Gabriela Alicia Hernández Echáurregui
Alfredo Hidalgo-Miranda
José Arellano Galindo
Haydeé Rosas-Vargas
Juan Manuel Mejía-Aranguré
Source :
Frontiers in Pediatrics, Vol 10 (2022)
Publication Year :
2022
Publisher :
Frontiers Media S.A., 2022.

Abstract

ETV6::RUNX1 is a genetic rearrangement of good prognosis in children with acute lymphoblastic leukemia (ALL). In Mexico, its prevalence is low in comparison with Caucasian populations. We developed a novel TaqMan one-step RT-qPCR approach to assess the prevalence of four genetic rearrangements in a cohort of Hispanic children with ALL from Mexico City. The prevalence of common fusion gene transcripts was as follows: TCF3::PBX1 7.7%; BCR::ABL1p190 3.3%; and KMT2A::AFF1 2.8%, and ETV6::RUNX1was observed with low prevalence (10.5%) in comparison to that reported for developed countries. This is consistent with previous findings on Mexican children with ALL and similar to those reported on children from Hispanic populations. The confirmation of a low prevalence of ETV6::RUNX1 in children of a Hispanic origin represents an advancement in the description of genetic factors of ALL in these populations.

Details

Language :
English
ISSN :
22962360
Volume :
10
Database :
Directory of Open Access Journals
Journal :
Frontiers in Pediatrics
Publication Type :
Academic Journal
Accession number :
edsdoj.00a901f63259496a808f2388ff248bba
Document Type :
article
Full Text :
https://doi.org/10.3389/fped.2022.837656