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https://www.arca.fiocruz.br/handle/icict/15494
COLORECTAL CANCER DNA METHYLATION PATTERNS FROM PATIENTS IN MANAUS, BRAZIL
Author
Almeida, Fabiana Greyce Oliveira
Aquino, Priscila Ferreira de
Souza, Afonso Duarte Leão de
Souza, Antonia Queiroz Lima de
Vinhote, Sonia do Carmo
Mac-Cormick, Thaís Messias
Silva Marcelo Soares da Mota
Chalub, Sidney Raimundo Silva
Fischer, Juliana de Saldanha da Gama
Carvalho, Paulo Costa
Carvalho, Maria da Gloria da Costa
Aquino, Priscila Ferreira de
Souza, Afonso Duarte Leão de
Souza, Antonia Queiroz Lima de
Vinhote, Sonia do Carmo
Mac-Cormick, Thaís Messias
Silva Marcelo Soares da Mota
Chalub, Sidney Raimundo Silva
Fischer, Juliana de Saldanha da Gama
Carvalho, Paulo Costa
Carvalho, Maria da Gloria da Costa
Affilliation
Federal University of Amazonas. Institute of Exact Sciences. Laboratory of Chromatography and Mass Spectrometry. Manaus, AM, Brazil.
Oswaldo Cruz Fundation. Instituto Leonidas e Maria Deane. Manaus, AM, Brazil.
Amazon State University. High School of Health. Manaus, AM, Brazil.
Federal University of Rio de Janeiro. Department of Pathology. Laboratory of Molecular Pathology. Rio de Janeiro, RJ, Brazil.
Oncology Control Center Foundation of Amazon State. Department of Abdominal Surgery. Manaus, AM, Brazil.
Oswaldo Cruz Fundation. Carlos Chagas Institute. Laboratory of Proteomics and Protein Engineering. Curitiba, PR, Brazil.
Oswaldo Cruz Fundation. Instituto Leonidas e Maria Deane. Manaus, AM, Brazil.
Amazon State University. High School of Health. Manaus, AM, Brazil.
Federal University of Rio de Janeiro. Department of Pathology. Laboratory of Molecular Pathology. Rio de Janeiro, RJ, Brazil.
Oncology Control Center Foundation of Amazon State. Department of Abdominal Surgery. Manaus, AM, Brazil.
Oswaldo Cruz Fundation. Carlos Chagas Institute. Laboratory of Proteomics and Protein Engineering. Curitiba, PR, Brazil.
Abstract
Background
DNA methylation is commonly linked with the silencing of the gene expression for many tumor suppressor genes. As such, determining DNA methylation patterns should aid, in times to come, in the diagnosis and personal treatment for various types of cancers. Here, we analyzed the methylation pattern from five colorectal cancer patients from the Amazon state in Brazil for four tumor suppressor genes, viz.: DAPK, CDH1, CDKN2A, and TIMP2 by employing a polymerase chain reaction (PCR) specific to methylation. Efforts in the study of colorectal cancer are fundamental as it is the third most of highest incidence in the world.
Results
Tumor biopsies were methylated in 1/5 (20 %), 2/5 (40 %), 4/5 (80 %), and 4/5 (80 %) for CDH1, CDKN2A, DAPK, and TIMP2 genes, respectively. The margin biopsies were methylated in 3/7 (43 %), 2/7 (28 %), 7/7 (100 %), and 6/7 (86 %) for CDH1, CDKN2A, DAPK, and TIMP2, respectively.
Conclusions
Our findings showed DAPK and TIMP2 to be methylated in most samples from both tumor tissues and adjacent non-neoplastic margins; thus presenting distinct methylation patterns. This emphasizes the importance of better understanding of the relation of these patterns with cancer in the context of different populations.
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