Cargando…

High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population

PURPOSE: Medulloblastomas are the most common primary malignant brain tumors in children. They are divided into molecular subgroups: WNT-activated, SHH-Activated, TP53 mutant or wild type, and non-WNT/non-SHH (Groups 3 and 4). WNT-activated medulloblastomas are usually caused by mutations in the CTN...

Descripción completa

Detalles Bibliográficos
Autores principales: Moreno, Daniel Antunes, Bonatelli, Murilo, Antoniazzi, Augusto Perazzolo, de Paula, Flávia Escremim, Leal, Leticia Ferro, Garcia, Felipe Antônio de Oliveira, de Paula, André Escremim, Teixeira, Gustavo Ramos, Santana, Iara Viana Vidigal, Saggioro, Fabiano, Neder, Luciano, Valera, Elvis Terci, Scrideli, Carlos Alberto, Stavale, João, Malheiros, Suzana Maria Fleury, Lima, Matheus, Hajj, Glaucia Noeli Maroso, Garcia-Rivello, Hernan, Christiansen, Silvia, Nunes, Susana, Gil-da-Costa, Maria João, Pinheiro, Jorge, Martins, Flavia Delgado, Junior, Carlos Almeida, Mançano, Bruna Minniti, Reis, Rui Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10513896/
https://www.ncbi.nlm.nih.gov/pubmed/37746264
http://dx.doi.org/10.3389/fonc.2023.1237170
_version_ 1785108614639255552
author Moreno, Daniel Antunes
Bonatelli, Murilo
Antoniazzi, Augusto Perazzolo
de Paula, Flávia Escremim
Leal, Leticia Ferro
Garcia, Felipe Antônio de Oliveira
de Paula, André Escremim
Teixeira, Gustavo Ramos
Santana, Iara Viana Vidigal
Saggioro, Fabiano
Neder, Luciano
Valera, Elvis Terci
Scrideli, Carlos Alberto
Stavale, João
Malheiros, Suzana Maria Fleury
Lima, Matheus
Hajj, Glaucia Noeli Maroso
Garcia-Rivello, Hernan
Christiansen, Silvia
Nunes, Susana
Gil-da-Costa, Maria João
Pinheiro, Jorge
Martins, Flavia Delgado
Junior, Carlos Almeida
Mançano, Bruna Minniti
Reis, Rui Manuel
author_facet Moreno, Daniel Antunes
Bonatelli, Murilo
Antoniazzi, Augusto Perazzolo
de Paula, Flávia Escremim
Leal, Leticia Ferro
Garcia, Felipe Antônio de Oliveira
de Paula, André Escremim
Teixeira, Gustavo Ramos
Santana, Iara Viana Vidigal
Saggioro, Fabiano
Neder, Luciano
Valera, Elvis Terci
Scrideli, Carlos Alberto
Stavale, João
Malheiros, Suzana Maria Fleury
Lima, Matheus
Hajj, Glaucia Noeli Maroso
Garcia-Rivello, Hernan
Christiansen, Silvia
Nunes, Susana
Gil-da-Costa, Maria João
Pinheiro, Jorge
Martins, Flavia Delgado
Junior, Carlos Almeida
Mançano, Bruna Minniti
Reis, Rui Manuel
author_sort Moreno, Daniel Antunes
collection PubMed
description PURPOSE: Medulloblastomas are the most common primary malignant brain tumors in children. They are divided into molecular subgroups: WNT-activated, SHH-Activated, TP53 mutant or wild type, and non-WNT/non-SHH (Groups 3 and 4). WNT-activated medulloblastomas are usually caused by mutations in the CTNNB1 gene (85%–90%), and most remaining cases of CTNNB1 wild type are thought to be caused by germline mutations in APC. So far, the frequencies of CTNNB1 have been reported mainly in North American and European populations. The aim of this study was to report the frequency of CTNNB1 mutations in WNT-activated medulloblastomas in a Latin-Iberian population and correlate with their clinicopathological characteristics. METHODS: A total of 266 medulloblastomas from seven different institutions from Brazil (n=211), Portugal (n=38), and Argentina (n=17) were evaluated. Following RNA and DNA isolation from formalin-fixed, paraffin-embedded (FFPE) tumor tissues, the molecular classification and CTNNB1 mutation analysis were performed by nCounter and Sanger sequencing, respectively. RESULTS: WNT-activated medulloblastomas accounted for 15% (40/266) of the series. We observed that 73% of WNT-activated medulloblastomas harbored CTNNB1 mutations. CTNNB1 wild-type cases (27%) were more prevalent in female individuals and suggested to be associated with a worse outcome. Among the CTNNB1 wild-type cases, the available analysis of family history revealed two cases with familiar adenomatous polyposis, harboring APC germline variants. CONCLUSION: We observed a lower incidence of CTNNB1 mutations in WNT-activated medulloblastomas in our Latin-Iberian cohort compared to frequencies previously described in other populations. Considering that CTNNB1 wild-type cases may exhibit APC germline mutations, our study suggests a higher incidence (~30%) of hereditary WNT-activated medulloblastomas in the Latin-Iberian population.
format Online
Article
Text
id pubmed-10513896
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-105138962023-09-22 High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population Moreno, Daniel Antunes Bonatelli, Murilo Antoniazzi, Augusto Perazzolo de Paula, Flávia Escremim Leal, Leticia Ferro Garcia, Felipe Antônio de Oliveira de Paula, André Escremim Teixeira, Gustavo Ramos Santana, Iara Viana Vidigal Saggioro, Fabiano Neder, Luciano Valera, Elvis Terci Scrideli, Carlos Alberto Stavale, João Malheiros, Suzana Maria Fleury Lima, Matheus Hajj, Glaucia Noeli Maroso Garcia-Rivello, Hernan Christiansen, Silvia Nunes, Susana Gil-da-Costa, Maria João Pinheiro, Jorge Martins, Flavia Delgado Junior, Carlos Almeida Mançano, Bruna Minniti Reis, Rui Manuel Front Oncol Oncology PURPOSE: Medulloblastomas are the most common primary malignant brain tumors in children. They are divided into molecular subgroups: WNT-activated, SHH-Activated, TP53 mutant or wild type, and non-WNT/non-SHH (Groups 3 and 4). WNT-activated medulloblastomas are usually caused by mutations in the CTNNB1 gene (85%–90%), and most remaining cases of CTNNB1 wild type are thought to be caused by germline mutations in APC. So far, the frequencies of CTNNB1 have been reported mainly in North American and European populations. The aim of this study was to report the frequency of CTNNB1 mutations in WNT-activated medulloblastomas in a Latin-Iberian population and correlate with their clinicopathological characteristics. METHODS: A total of 266 medulloblastomas from seven different institutions from Brazil (n=211), Portugal (n=38), and Argentina (n=17) were evaluated. Following RNA and DNA isolation from formalin-fixed, paraffin-embedded (FFPE) tumor tissues, the molecular classification and CTNNB1 mutation analysis were performed by nCounter and Sanger sequencing, respectively. RESULTS: WNT-activated medulloblastomas accounted for 15% (40/266) of the series. We observed that 73% of WNT-activated medulloblastomas harbored CTNNB1 mutations. CTNNB1 wild-type cases (27%) were more prevalent in female individuals and suggested to be associated with a worse outcome. Among the CTNNB1 wild-type cases, the available analysis of family history revealed two cases with familiar adenomatous polyposis, harboring APC germline variants. CONCLUSION: We observed a lower incidence of CTNNB1 mutations in WNT-activated medulloblastomas in our Latin-Iberian cohort compared to frequencies previously described in other populations. Considering that CTNNB1 wild-type cases may exhibit APC germline mutations, our study suggests a higher incidence (~30%) of hereditary WNT-activated medulloblastomas in the Latin-Iberian population. Frontiers Media S.A. 2023-09-04 /pmc/articles/PMC10513896/ /pubmed/37746264 http://dx.doi.org/10.3389/fonc.2023.1237170 Text en Copyright © 2023 Moreno, Bonatelli, Antoniazzi, de Paula, Leal, Garcia, de Paula, Teixeira, Santana, Saggioro, Neder, Valera, Scrideli, Stavale, Malheiros, Lima, Hajj, Garcia-Rivello, Christiansen, Nunes, Gil-da-Costa, Pinheiro, Martins, Junior, Mançano and Reis 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 Oncology
Moreno, Daniel Antunes
Bonatelli, Murilo
Antoniazzi, Augusto Perazzolo
de Paula, Flávia Escremim
Leal, Leticia Ferro
Garcia, Felipe Antônio de Oliveira
de Paula, André Escremim
Teixeira, Gustavo Ramos
Santana, Iara Viana Vidigal
Saggioro, Fabiano
Neder, Luciano
Valera, Elvis Terci
Scrideli, Carlos Alberto
Stavale, João
Malheiros, Suzana Maria Fleury
Lima, Matheus
Hajj, Glaucia Noeli Maroso
Garcia-Rivello, Hernan
Christiansen, Silvia
Nunes, Susana
Gil-da-Costa, Maria João
Pinheiro, Jorge
Martins, Flavia Delgado
Junior, Carlos Almeida
Mançano, Bruna Minniti
Reis, Rui Manuel
High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population
title High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population
title_full High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population
title_fullStr High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population
title_full_unstemmed High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population
title_short High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population
title_sort high frequency of wnt-activated medulloblastomas with ctnnb1 wild type suggests a higher proportion of hereditary cases in a latin-iberian population
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10513896/
https://www.ncbi.nlm.nih.gov/pubmed/37746264
http://dx.doi.org/10.3389/fonc.2023.1237170
work_keys_str_mv AT morenodanielantunes highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT bonatellimurilo highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT antoniazziaugustoperazzolo highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT depaulaflaviaescremim highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT lealleticiaferro highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT garciafelipeantoniodeoliveira highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT depaulaandreescremim highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT teixeiragustavoramos highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT santanaiaravianavidigal highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT saggiorofabiano highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT nederluciano highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT valeraelvisterci highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT scridelicarlosalberto highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT stavalejoao highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT malheirossuzanamariafleury highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT limamatheus highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT hajjglaucianoelimaroso highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT garciarivellohernan highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT christiansensilvia highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT nunessusana highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT gildacostamariajoao highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT pinheirojorge highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT martinsflaviadelgado highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT juniorcarlosalmeida highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT mancanobrunaminniti highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation
AT reisruimanuel highfrequencyofwntactivatedmedulloblastomaswithctnnb1wildtypesuggestsahigherproportionofhereditarycasesinalatiniberianpopulation