Patrón de metilación génico en el cáncer de mama

Background: Genomic DNA methylation, mutations and allelic deletions explain the inactivation of genes involved in cell proliferation and cell cycle control mechanisms. Aim: To analyze the methylation pattern of important genes related to different carcinogenic mechanisms in patients with breast can...

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Autores principales: Roa S,Juan Carlos, Anabalón R,Leonardo, Tapia E,Oscar, Martínez S,Javier, Araya O,Juan Carlos, Villaseca H,Miguel, Guzmán G,Pablo, Roa E,Iván
Lenguaje:Spanish / Castilian
Publicado: Sociedad Médica de Santiago 2004
Materias:
P16
Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872004000900007
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spelling oai:scielo:S0034-988720040009000072005-11-22Patrón de metilación génico en el cáncer de mamaRoa S,Juan CarlosAnabalón R,LeonardoTapia E,OscarMartínez S,JavierAraya O,Juan CarlosVillaseca H,MiguelGuzmán G,PabloRoa E,Iván Breast neoplasms CDKN2A protein DNA probes Genes P16 Background: Genomic DNA methylation, mutations and allelic deletions explain the inactivation of genes involved in cell proliferation and cell cycle control mechanisms. Aim: To analyze the methylation pattern of important genes related to different carcinogenic mechanisms in patients with breast cancer and the relationship with its biological behavior. Material and methods: Seventy fresh-frozen breast cancer samples were selected. The methylation specific PCR (MSP) test was used to analyze promoter methylation status for genes CDKN2A (p16), hMLH1, APC, CDH1 (Cadherin E) and FHIT. Results: We found methylation in at least one of the genes studied in 88% of cases and in 3 or more genes in 40.5% of cases. The frequencies of promoter hypermethylation of CDKN2A, hMLH1, APC, CDH1 and FHIT were 41.4%, 11.4%, 52.9%, 70% y 42.9%, respectively. We found a relationship between CDKN2A methylation and better survival (p=0.002). CDH1 methylation and poor histological differentiation (p=0.007), hMLH1 methylation and non-Mapuche ethnicity (p=0.03), APC methylation and larger tumor size (p <0.05), FHIT methylation and lack of estrogen receptor IHC expression (p <0.05). Conclusions: The high frequency of promoter methylation in patients with breast cancer confirms its role in breast carcinogenesis. The finding of alterations in the methylation pattern of genes studied and its association with prognostic factors is a helpful tool in the search of new criteria for clinical and therapeutic decision making (Rev Méd Chile 2004; 132: 1069-77)info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.132 n.9 20042004-09-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872004000900007es10.4067/S0034-98872004000900007
institution Scielo Chile
collection Scielo Chile
language Spanish / Castilian
topic Breast neoplasms
CDKN2A protein
DNA probes
Genes
P16
spellingShingle Breast neoplasms
CDKN2A protein
DNA probes
Genes
P16
Roa S,Juan Carlos
Anabalón R,Leonardo
Tapia E,Oscar
Martínez S,Javier
Araya O,Juan Carlos
Villaseca H,Miguel
Guzmán G,Pablo
Roa E,Iván
Patrón de metilación génico en el cáncer de mama
description Background: Genomic DNA methylation, mutations and allelic deletions explain the inactivation of genes involved in cell proliferation and cell cycle control mechanisms. Aim: To analyze the methylation pattern of important genes related to different carcinogenic mechanisms in patients with breast cancer and the relationship with its biological behavior. Material and methods: Seventy fresh-frozen breast cancer samples were selected. The methylation specific PCR (MSP) test was used to analyze promoter methylation status for genes CDKN2A (p16), hMLH1, APC, CDH1 (Cadherin E) and FHIT. Results: We found methylation in at least one of the genes studied in 88% of cases and in 3 or more genes in 40.5% of cases. The frequencies of promoter hypermethylation of CDKN2A, hMLH1, APC, CDH1 and FHIT were 41.4%, 11.4%, 52.9%, 70% y 42.9%, respectively. We found a relationship between CDKN2A methylation and better survival (p=0.002). CDH1 methylation and poor histological differentiation (p=0.007), hMLH1 methylation and non-Mapuche ethnicity (p=0.03), APC methylation and larger tumor size (p <0.05), FHIT methylation and lack of estrogen receptor IHC expression (p <0.05). Conclusions: The high frequency of promoter methylation in patients with breast cancer confirms its role in breast carcinogenesis. The finding of alterations in the methylation pattern of genes studied and its association with prognostic factors is a helpful tool in the search of new criteria for clinical and therapeutic decision making (Rev Méd Chile 2004; 132: 1069-77)
author Roa S,Juan Carlos
Anabalón R,Leonardo
Tapia E,Oscar
Martínez S,Javier
Araya O,Juan Carlos
Villaseca H,Miguel
Guzmán G,Pablo
Roa E,Iván
author_facet Roa S,Juan Carlos
Anabalón R,Leonardo
Tapia E,Oscar
Martínez S,Javier
Araya O,Juan Carlos
Villaseca H,Miguel
Guzmán G,Pablo
Roa E,Iván
author_sort Roa S,Juan Carlos
title Patrón de metilación génico en el cáncer de mama
title_short Patrón de metilación génico en el cáncer de mama
title_full Patrón de metilación génico en el cáncer de mama
title_fullStr Patrón de metilación génico en el cáncer de mama
title_full_unstemmed Patrón de metilación génico en el cáncer de mama
title_sort patrón de metilación génico en el cáncer de mama
publisher Sociedad Médica de Santiago
publishDate 2004
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872004000900007
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