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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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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. |
format | Online Article Text |
id | pubmed-9171364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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