<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Sepulveda-Robles O</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The distribution of &lt;i>RUNX1-RUNXT1&lt;/i>, &lt;i>PML-RARA&lt;/i>, &lt;i>CBFB-MYH11&lt;/i>, &lt;i>BCR-ABL1&lt;sup>p210&lt;/sup>&lt;/i> , and &lt;i>KMT2A-MLLT3&lt;/i> in the pediatric population with acute myeloid leukemia (AML) in many countries of Latin America is largely unknown. Therefore, we aimed to investigate the frequency of these fusion genes in children with &lt;i>de novo&lt;/i> AML from Mexico City, which has one of the highest incidence rates of acute leukemia in the world. Additionally, we explored their impact in mortality during the first year of treatment.&lt;h4>Methods&lt;/h4>We retrospectively analyzed the presence of &lt;i>RUNX1-RUNXT1&lt;/i>, &lt;i>PML-RARA&lt;/i>, &lt;i>CBFB-MYH11&lt;/i>, &lt;i>BCR-ABL1&lt;sup>p210&lt;/sup>&lt;/i> , and &lt;i>KMT2A-MLLT3&lt;/i> by RT-PCR among 77 patients (&lt;18 years) diagnosed with &lt;i>de novo&lt;/i></pubmed_abstract><journal>Frontiers in pediatrics</journal><pagination>946690</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9702800</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Analytical study of &lt;i>RUNX1-RUNXT1&lt;/i>, &lt;i>PML-RARA&lt;/i>, &lt;i>CBFB-MYH11&lt;/i>, &lt;i>BCR-ABL1&lt;sup>p210&lt;/sup>&lt;/i> , and &lt;i>KMT2-MLLT3&lt;/i> in Mexican children with acute myeloid leukemia: A multicenter study of the Mexican interinstitutional group for the identification of the causes of childhood leukemia (MIGICCL).</pubmed_title><pmcid>PMC9702800</pmcid><pubmed_authors>Flores-Villegas LV</pubmed_authors><pubmed_authors>Perez-Saldivar ML</pubmed_authors><pubmed_authors>Rosas-Vargas H</pubmed_authors><pubmed_authors>Torres-Nava JR</pubmed_authors><pubmed_authors>Mata-Rocha M</pubmed_authors><pubmed_authors>Bekker-Mendez VC</pubmed_authors><pubmed_authors>Morales-Castillo BA</pubmed_authors><pubmed_authors>Santillan-Juarez JD</pubmed_authors><pubmed_authors>Medina-Sanson A</pubmed_authors><pubmed_authors>Najera-Cortes AS</pubmed_authors><pubmed_authors>Velazquez-Avina MM</pubmed_authors><pubmed_authors>Nunez-Enriquez JC</pubmed_authors><pubmed_authors>Flores-Lujano J</pubmed_authors><pubmed_authors>Bravata-Alcantara JC</pubmed_authors><pubmed_authors>Dominguez-Catzin V</pubmed_authors><pubmed_authors>Orozco-Ruiz D</pubmed_authors><pubmed_authors>De Ita M</pubmed_authors><pubmed_authors>Gomez-Flores E</pubmed_authors><pubmed_authors>Jimenez-Hernandez E</pubmed_authors><pubmed_authors>Sepulveda-Robles O</pubmed_authors><pubmed_authors>Merino-Pasaye LE</pubmed_authors><pubmed_authors>Mejia-Arangure JM</pubmed_authors><pubmed_authors>Amador-Sanchez R</pubmed_authors><pubmed_authors>Sanchez-Escobar N</pubmed_authors><pubmed_authors>Penaloza-Gonzalez JG</pubmed_authors><pubmed_authors>Solis-Labastida KA</pubmed_authors><pubmed_authors>Jimenez-Morales S</pubmed_authors><pubmed_authors>Martin-Trejo JA</pubmed_authors><pubmed_authors>Espinosa-Elizondo RM</pubmed_authors><pubmed_authors>Rangel-Lopez A</pubmed_authors><pubmed_authors>Gonzalez-Avila AI</pubmed_authors></additional><is_claimable>false</is_claimable><name>Analytical study of &lt;i>RUNX1-RUNXT1&lt;/i>, &lt;i>PML-RARA&lt;/i>, &lt;i>CBFB-MYH11&lt;/i>, &lt;i>BCR-ABL1&lt;sup>p210&lt;/sup>&lt;/i> , and &lt;i>KMT2-MLLT3&lt;/i> in Mexican children with acute myeloid leukemia: A multicenter study of the Mexican interinstitutional group for the identification of the causes of childhood leukemia (MIGICCL).</name><description>&lt;h4>Background&lt;/h4>The distribution of &lt;i>RUNX1-RUNXT1&lt;/i>, &lt;i>PML-RARA&lt;/i>, &lt;i>CBFB-MYH11&lt;/i>, &lt;i>BCR-ABL1&lt;sup>p210&lt;/sup>&lt;/i> , and &lt;i>KMT2A-MLLT3&lt;/i> in the pediatric population with acute myeloid leukemia (AML) in many countries of Latin America is largely unknown. Therefore, we aimed to investigate the frequency of these fusion genes in children with &lt;i>de novo&lt;/i> AML from Mexico City, which has one of the highest incidence rates of acute leukemia in the world. Additionally, we explored their impact in mortality during the first year of treatment.&lt;h4>Methods&lt;/h4>We retrospectively analyzed the presence of &lt;i>RUNX1-RUNXT1&lt;/i>, &lt;i>PML-RARA&lt;/i>, &lt;i>CBFB-MYH11&lt;/i>, &lt;i>BCR-ABL1&lt;sup>p210&lt;/sup>&lt;/i> , and &lt;i>KMT2A-MLLT3&lt;/i> by RT-PCR among 77 patients (&lt;18 years) diagnosed with &lt;i>de novo&lt;/i></description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-03T22:44:22.35Z</modification><creation>2025-04-21T14:27:56.196Z</creation></dates><accession>S-EPMC9702800</accession><cross_references><pubmed>36452349</pubmed><doi>10.3389/fped.2022.946690</doi></cross_references></HashMap>