From colorectal cancer pattern to the characterization of individuals at risk: picture for genetic research in Latin America

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Colorectal cancer (CRC) is one of the most common cancers in Latin America and the Caribbean, with the highest rates reported for Uruguay, Brazil and Argentina. We provide a global snapshot of the CRC patterns, how screening is performed, and compared/contrasted to the genetic profile of Lynch syndr...

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Detalles Bibliográficos
Autores: Vaccaro, Carlos Alberto, López-Kostner, Francisco, Della Valle, Adriana, Palmero, Edenir Inez, Rossi, Benedito Mauro, Antelo, Marina, Solano, Angela, Carraro, Dirce Maria, Forones, Nora Manoukian, Bohorquez, Mabel, Lino-Silva, Leonardo S., Buleje, Jose, Spirandelli, Florencia, Abe-Sandes, Kiyoko, Nascimento, Ivana, Sullcahuaman, Yasser, Sarroca, Carlos, Gonzalez, Maria Laura, Herrando, Alberto Ignacio, Alvarez, Karin, Neffa, Florencia, Galvao, Henrique Camposreis, Esperon, Patricia, Golubicki, Mariano, Cisterna, Daniel, Cardoso, Florencia C., Torrezan, Giovana Tardin, Aguiar Junior, Samuel, Pimenta, Celia Aparecida Marques, da Cruz Formiga, Maria Nirvana, Santos, Erika, Sa, Caroline U., Oliveira, Edite P., Fujita, Ricardo, Spirandelli, Enrique, Jimenez, Geiner, Guindalini, Rodrigo Santa Cruz, de Azevedo, Renata Gondim Meira Velame, Bueno, Larissa Souza Mario, Nogueira, Sonia Tereza dos Santos, Torres Loarte, Mariela, Padron, Jorge, Castro-Mujica, Maria del Carmen, Sanchez del Monte, Julio, Caballero, Carmelo, Muñeton Peña, Carlos Mario, Pinto, Joseph, Barletta-Carrillo, Claudia, Gutiérrez Angulo, Melva, Piñero, Tamara, Montenegro Beltran, Paola, Ashton-Prolla, Patricia, Rodriguez, Yenni, Quispe, Richard, Rossi, Norma Teresa, Martin, Claudia, Chialina, Sergio, Kalfayan, Pablo German, Bazo-Alvarez, Juan Carlos, Recalde Cañete, Alcides, Dominguez-Barrera, Constantino, Nuñez, Lina, Da Silva, Sabrina Daniela, Balavarca, Yesilda, Wernhoff, Patrik, Plazzer, John-Paul, Moller, Pal, Hovig, Eivind, Dominguez-Valentin, Mev
Formato: artículo
Fecha de Publicación:2019
Institución:Universidad de San Martín de Porres
Repositorio:USMP-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorio.usmp.edu.pe:20.500.12727/6095
Enlace del recurso:https://hdl.handle.net/20.500.12727/6095
https://doi.org/10.1002/ijc.31920
Nivel de acceso:acceso abierto
Materia:América Latina
Neoplasias colorrectales
Síndromes neoplásicos hereditarios
Neoplasias colorrectales hereditarias sin poliposis
https://purl.org/pe-repo/ocde/ford#3.02.00
Descripción
Sumario:Colorectal cancer (CRC) is one of the most common cancers in Latin America and the Caribbean, with the highest rates reported for Uruguay, Brazil and Argentina. We provide a global snapshot of the CRC patterns, how screening is performed, and compared/contrasted to the genetic profile of Lynch syndrome (LS) in the region. From the literature, we find that only nine (20%) of the Latin America and the Caribbean countries have developed guidelines for early detection of CRC, and also with a low adherence. We describe a genetic profile of LS, including a total of 2,685 suspected families, where confirmed LS ranged from 8% in Uruguay and Argentina to 60% in Peru. Among confirmed LS, path_MLH1 variants were most commonly identified in Peru (82%), Mexico (80%), Chile (60%), and path_MSH2/EPCAM variants were most frequently identified in Colombia (80%) and Argentina (47%). Path_MSH6 and path_PMS2 variants were less common, but they showed important presence in Brazil (15%) and Chile (10%), respectively. Important differences exist at identifying LS families in Latin American countries, where the spectrum of path_MLH1 and path_MSH2 variants are those most frequently identified. Our findings have an impact on the evaluation of the patients and their relatives at risk for LS, derived from the gene affected. Although the awareness of hereditary cancer and genetic testing has improved in the last decade, it is remains deficient, with 39%–80% of the families not being identified for LS among those who actually met both the clinical criteria for LS and showed MMR deficiency.
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