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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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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 |
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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 |
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