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

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...

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Autores principales: Mata-Rocha, Minerva, Rangel-López, Angelica, Jimenez-Hernandez, Elva, Nuñez-Enríquez, Juan Carlos, Morales-Castillo, Blanca Angélica, Sánchez-Escobar, Norberto, Sepúlveda-Robles, Omar Alejandro, Bravata-Alcántara, Juan Carlos, Nájera-Cortés, Alan Steve, Pérez-Saldivar, María Luisa, Flores-Lujano, Janet, Duarte-Rodríguez, David Aldebarán, Oviedo de Anda, Norma Angélica, Romero Tlalolini, Maria de los Angeles, Alaez Verson, Carmen, Martín-Trejo, Jorge Alfonso, Muñoz Medina, Jose Esteban, Gonzalez-Bonilla, Cesar Raul, Hernandez Cueto, Maria de los Angeles, Bekker-Méndez, VC., Jiménez-Morales, Silvia, Medina-Sansón, Aurora, Amador-Sánchez, Raquel, Peñaloza-González, José Gabriel, Torres-Nava, José Refugio, Espinosa-Elizondo, Rosa Martha, Cortés-Herrera, Beatriz, Flores-Villegas, Luz Victoria, Merino-Pasaye, Laura Elizabeth, Gutierrez-Rivera, Maria de Lourdes, Velazquez-Aviña, Martha Margarita, Santillan-Juarez, Jessica Denisse, Gurrola-Silva, Alma, Hernández Echáurregui, Gabriela Alicia, Hidalgo-Miranda, Alfredo, Arellano Galindo, José, Rosas-Vargas, Haydeé, Mejía-Aranguré, Juan Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171364/
https://www.ncbi.nlm.nih.gov/pubmed/35685921
http://dx.doi.org/10.3389/fped.2022.837656
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author Mata-Rocha, Minerva
Rangel-López, Angelica
Jimenez-Hernandez, Elva
Nuñez-Enríquez, Juan Carlos
Morales-Castillo, Blanca Angélica
Sánchez-Escobar, Norberto
Sepúlveda-Robles, Omar Alejandro
Bravata-Alcántara, Juan Carlos
Nájera-Cortés, Alan Steve
Pérez-Saldivar, María Luisa
Flores-Lujano, Janet
Duarte-Rodríguez, David Aldebarán
Oviedo de Anda, Norma Angélica
Romero Tlalolini, Maria de los Angeles
Alaez Verson, Carmen
Martín-Trejo, Jorge Alfonso
Muñoz Medina, Jose Esteban
Gonzalez-Bonilla, Cesar Raul
Hernandez Cueto, Maria de los Angeles
Bekker-Méndez, VC.
Jiménez-Morales, Silvia
Medina-Sansón, Aurora
Amador-Sánchez, Raquel
Peñaloza-González, José Gabriel
Torres-Nava, José Refugio
Espinosa-Elizondo, Rosa Martha
Cortés-Herrera, Beatriz
Flores-Villegas, Luz Victoria
Merino-Pasaye, Laura Elizabeth
Gutierrez-Rivera, Maria de Lourdes
Velazquez-Aviña, Martha Margarita
Santillan-Juarez, Jessica Denisse
Gurrola-Silva, Alma
Hernández Echáurregui, Gabriela Alicia
Hidalgo-Miranda, Alfredo
Arellano Galindo, José
Rosas-Vargas, Haydeé
Mejía-Aranguré, Juan Manuel
author_facet Mata-Rocha, Minerva
Rangel-López, Angelica
Jimenez-Hernandez, Elva
Nuñez-Enríquez, Juan Carlos
Morales-Castillo, Blanca Angélica
Sánchez-Escobar, Norberto
Sepúlveda-Robles, Omar Alejandro
Bravata-Alcántara, Juan Carlos
Nájera-Cortés, Alan Steve
Pérez-Saldivar, María Luisa
Flores-Lujano, Janet
Duarte-Rodríguez, David Aldebarán
Oviedo de Anda, Norma Angélica
Romero Tlalolini, Maria de los Angeles
Alaez Verson, Carmen
Martín-Trejo, Jorge Alfonso
Muñoz Medina, Jose Esteban
Gonzalez-Bonilla, Cesar Raul
Hernandez Cueto, Maria de los Angeles
Bekker-Méndez, VC.
Jiménez-Morales, Silvia
Medina-Sansón, Aurora
Amador-Sánchez, Raquel
Peñaloza-González, José Gabriel
Torres-Nava, José Refugio
Espinosa-Elizondo, Rosa Martha
Cortés-Herrera, Beatriz
Flores-Villegas, Luz Victoria
Merino-Pasaye, Laura Elizabeth
Gutierrez-Rivera, Maria de Lourdes
Velazquez-Aviña, Martha Margarita
Santillan-Juarez, Jessica Denisse
Gurrola-Silva, Alma
Hernández Echáurregui, Gabriela Alicia
Hidalgo-Miranda, Alfredo
Arellano Galindo, José
Rosas-Vargas, Haydeé
Mejía-Aranguré, Juan Manuel
author_sort Mata-Rocha, Minerva
collection PubMed
description 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::ABL1p(190) 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.
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spelling pubmed-91713642022-06-08 Low Prevalence of ETV6::RUNX1 Fusion Gene in a Hispanic Population Mata-Rocha, Minerva Rangel-López, Angelica Jimenez-Hernandez, Elva Nuñez-Enríquez, Juan Carlos Morales-Castillo, Blanca Angélica Sánchez-Escobar, Norberto Sepúlveda-Robles, Omar Alejandro Bravata-Alcántara, Juan Carlos Nájera-Cortés, Alan Steve Pérez-Saldivar, María Luisa Flores-Lujano, Janet Duarte-Rodríguez, David Aldebarán Oviedo de Anda, Norma Angélica Romero Tlalolini, Maria de los Angeles Alaez Verson, Carmen Martín-Trejo, Jorge Alfonso Muñoz Medina, Jose Esteban Gonzalez-Bonilla, Cesar Raul Hernandez Cueto, Maria de los Angeles Bekker-Méndez, VC. Jiménez-Morales, Silvia Medina-Sansón, Aurora Amador-Sánchez, Raquel Peñaloza-González, José Gabriel Torres-Nava, José Refugio Espinosa-Elizondo, Rosa Martha Cortés-Herrera, Beatriz Flores-Villegas, Luz Victoria Merino-Pasaye, Laura Elizabeth Gutierrez-Rivera, Maria de Lourdes Velazquez-Aviña, Martha Margarita Santillan-Juarez, Jessica Denisse Gurrola-Silva, Alma Hernández Echáurregui, Gabriela Alicia Hidalgo-Miranda, Alfredo Arellano Galindo, José Rosas-Vargas, Haydeé Mejía-Aranguré, Juan Manuel Front Pediatr Pediatrics 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::ABL1p(190) 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. Frontiers Media S.A. 2022-05-24 /pmc/articles/PMC9171364/ /pubmed/35685921 http://dx.doi.org/10.3389/fped.2022.837656 Text en Copyright © 2022 Mata-Rocha, Rangel-López, Jimenez-Hernandez, Nuñez-Enríquez, Morales-Castillo, Sánchez-Escobar, Sepúlveda-Robles, Bravata-Alcántara, Nájera-Cortés, Pérez-Saldivar, Flores-Lujano, Duarte-Rodríguez, Oviedo de Anda, Romero Tlalolini, Alaez Verson, Martín-Trejo, Muñoz Medina, Gonzalez-Bonilla, Hernandez Cueto, Bekker-Méndez, Jiménez-Morales, Medina-Sansón, Amador-Sánchez, Peñaloza-González, Torres-Nava, Espinosa-Elizondo, Cortés-Herrera, Flores-Villegas, Merino-Pasaye, Gutierrez-Rivera, Velazquez-Aviña, Santillan-Juarez, Gurrola-Silva, Hernández Echáurregui, Hidalgo-Miranda, Arellano Galindo, Rosas-Vargas and Mejía-Aranguré. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Mata-Rocha, Minerva
Rangel-López, Angelica
Jimenez-Hernandez, Elva
Nuñez-Enríquez, Juan Carlos
Morales-Castillo, Blanca Angélica
Sánchez-Escobar, Norberto
Sepúlveda-Robles, Omar Alejandro
Bravata-Alcántara, Juan Carlos
Nájera-Cortés, Alan Steve
Pérez-Saldivar, María Luisa
Flores-Lujano, Janet
Duarte-Rodríguez, David Aldebarán
Oviedo de Anda, Norma Angélica
Romero Tlalolini, Maria de los Angeles
Alaez Verson, Carmen
Martín-Trejo, Jorge Alfonso
Muñoz Medina, Jose Esteban
Gonzalez-Bonilla, Cesar Raul
Hernandez Cueto, Maria de los Angeles
Bekker-Méndez, VC.
Jiménez-Morales, Silvia
Medina-Sansón, Aurora
Amador-Sánchez, Raquel
Peñaloza-González, José Gabriel
Torres-Nava, José Refugio
Espinosa-Elizondo, Rosa Martha
Cortés-Herrera, Beatriz
Flores-Villegas, Luz Victoria
Merino-Pasaye, Laura Elizabeth
Gutierrez-Rivera, Maria de Lourdes
Velazquez-Aviña, Martha Margarita
Santillan-Juarez, Jessica Denisse
Gurrola-Silva, Alma
Hernández Echáurregui, Gabriela Alicia
Hidalgo-Miranda, Alfredo
Arellano Galindo, José
Rosas-Vargas, Haydeé
Mejía-Aranguré, Juan Manuel
Low Prevalence of ETV6::RUNX1 Fusion Gene in a Hispanic Population
title Low Prevalence of ETV6::RUNX1 Fusion Gene in a Hispanic Population
title_full Low Prevalence of ETV6::RUNX1 Fusion Gene in a Hispanic Population
title_fullStr Low Prevalence of ETV6::RUNX1 Fusion Gene in a Hispanic Population
title_full_unstemmed Low Prevalence of ETV6::RUNX1 Fusion Gene in a Hispanic Population
title_short Low Prevalence of ETV6::RUNX1 Fusion Gene in a Hispanic Population
title_sort low prevalence of etv6::runx1 fusion gene in a hispanic population
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171364/
https://www.ncbi.nlm.nih.gov/pubmed/35685921
http://dx.doi.org/10.3389/fped.2022.837656
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