DNA methylation profile of the DKK2 gene as a biomarker in patients with colorectal cancer
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.4238/gmr16039816 https://repositorio.unifesp.br/handle/11600/57147 |
Resumo: | Purpose: Epigenetic changes can be detected in precancerous lesions, suggesting that may be involved in the early stages of carcinogenesis. The methylation of specifics genes has been correlated with the outcome of many different types of cancers. This study compared the levels of DNA methylation between normal and tumor tissues from patients with colorectal cancer (CRC). Methods: Candidate genes were screened using the MethylProfiler T PCR Array System and the Dickkopf-related protein 2 (DKK2) genes were selected for study. DNA methylation of these genes was assessed by polymerase chain reaction-high-resolution melting (PCR-HRM) analysis. Results: Out of the 112 patients studied, 68 were controls with a mean age (SD)of 59.9 years (13.4) and 45 were patients with CRC with a mean age (SD) of 64.6 years (13.6). Among the patients with CRC, 25 were women, 28 were diagnosed with colon cancer and 18 were diagnosed with rectal cancer. The number of patients with Stage I, II, III, and IV of the disease, as per the TNM classification, were 2 (4.3%), 20 (43.4%), 18 (39.1%), and 2 (4.3%), respectively. Furthermore, the DKK2 gene had a higher methylation profile in the CRC tissues when compared to normal mucosa (p < 0.001), whereas the methylation profile analysis was not statistically significant when comparing the stages of the disease (p = 0.078). Conclusion: The presence of differentially methylated sequences of the DKK2 gene between the groups showed that the methylation changes of these genes could potentially be prognostic and predictive markers in CRC. |
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DNA methylation profile of the DKK2 gene as a biomarker in patients with colorectal cancerBiomarkersColorectal cancerDNA methylationEpigeneticsDKK2 genePurpose: Epigenetic changes can be detected in precancerous lesions, suggesting that may be involved in the early stages of carcinogenesis. The methylation of specifics genes has been correlated with the outcome of many different types of cancers. This study compared the levels of DNA methylation between normal and tumor tissues from patients with colorectal cancer (CRC). Methods: Candidate genes were screened using the MethylProfiler T PCR Array System and the Dickkopf-related protein 2 (DKK2) genes were selected for study. DNA methylation of these genes was assessed by polymerase chain reaction-high-resolution melting (PCR-HRM) analysis. Results: Out of the 112 patients studied, 68 were controls with a mean age (SD)of 59.9 years (13.4) and 45 were patients with CRC with a mean age (SD) of 64.6 years (13.6). Among the patients with CRC, 25 were women, 28 were diagnosed with colon cancer and 18 were diagnosed with rectal cancer. The number of patients with Stage I, II, III, and IV of the disease, as per the TNM classification, were 2 (4.3%), 20 (43.4%), 18 (39.1%), and 2 (4.3%), respectively. Furthermore, the DKK2 gene had a higher methylation profile in the CRC tissues when compared to normal mucosa (p < 0.001), whereas the methylation profile analysis was not statistically significant when comparing the stages of the disease (p = 0.078). Conclusion: The presence of differentially methylated sequences of the DKK2 gene between the groups showed that the methylation changes of these genes could potentially be prognostic and predictive markers in CRC.Univ Fed Sao Paulo, Dept Med, Oncol Grp, Gastroenterol Div, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Surg, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Med, Oncol Grp, Gastroenterol Div, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Surg, Sao Paulo, BrazilWeb of ScienceSao Paulo Research Foundation (FAPESP)Funpec-Editora2020-08-04T13:39:51Z2020-08-04T13:39:51Z2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion-application/pdfhttp://dx.doi.org/10.4238/gmr16039816Genetics And Molecular Research. Ribeirao Preto, v. 16, n. 4, p. -, 2017.10.4238/gmr16039816WOS000419067100001.pdf1676-5680https://repositorio.unifesp.br/handle/11600/57147WOS:000419067100001engGenetics And Molecular ResearchRibeirao Pretoinfo:eu-repo/semantics/openAccessSilva, T. D. [UNIFESP]Felipe, A. V. [UNIFESP]Vidigal, V. M. [UNIFESP]Saad, S. S. [UNIFESP]Forones, N. M. [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-28T03:58:23Zoai:repositorio.unifesp.br/:11600/57147Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-28T03:58:23Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
DNA methylation profile of the DKK2 gene as a biomarker in patients with colorectal cancer |
title |
DNA methylation profile of the DKK2 gene as a biomarker in patients with colorectal cancer |
spellingShingle |
DNA methylation profile of the DKK2 gene as a biomarker in patients with colorectal cancer Silva, T. D. [UNIFESP] Biomarkers Colorectal cancer DNA methylation Epigenetics DKK2 gene |
title_short |
DNA methylation profile of the DKK2 gene as a biomarker in patients with colorectal cancer |
title_full |
DNA methylation profile of the DKK2 gene as a biomarker in patients with colorectal cancer |
title_fullStr |
DNA methylation profile of the DKK2 gene as a biomarker in patients with colorectal cancer |
title_full_unstemmed |
DNA methylation profile of the DKK2 gene as a biomarker in patients with colorectal cancer |
title_sort |
DNA methylation profile of the DKK2 gene as a biomarker in patients with colorectal cancer |
author |
Silva, T. D. [UNIFESP] |
author_facet |
Silva, T. D. [UNIFESP] Felipe, A. V. [UNIFESP] Vidigal, V. M. [UNIFESP] Saad, S. S. [UNIFESP] Forones, N. M. [UNIFESP] |
author_role |
author |
author2 |
Felipe, A. V. [UNIFESP] Vidigal, V. M. [UNIFESP] Saad, S. S. [UNIFESP] Forones, N. M. [UNIFESP] |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Silva, T. D. [UNIFESP] Felipe, A. V. [UNIFESP] Vidigal, V. M. [UNIFESP] Saad, S. S. [UNIFESP] Forones, N. M. [UNIFESP] |
dc.subject.por.fl_str_mv |
Biomarkers Colorectal cancer DNA methylation Epigenetics DKK2 gene |
topic |
Biomarkers Colorectal cancer DNA methylation Epigenetics DKK2 gene |
description |
Purpose: Epigenetic changes can be detected in precancerous lesions, suggesting that may be involved in the early stages of carcinogenesis. The methylation of specifics genes has been correlated with the outcome of many different types of cancers. This study compared the levels of DNA methylation between normal and tumor tissues from patients with colorectal cancer (CRC). Methods: Candidate genes were screened using the MethylProfiler T PCR Array System and the Dickkopf-related protein 2 (DKK2) genes were selected for study. DNA methylation of these genes was assessed by polymerase chain reaction-high-resolution melting (PCR-HRM) analysis. Results: Out of the 112 patients studied, 68 were controls with a mean age (SD)of 59.9 years (13.4) and 45 were patients with CRC with a mean age (SD) of 64.6 years (13.6). Among the patients with CRC, 25 were women, 28 were diagnosed with colon cancer and 18 were diagnosed with rectal cancer. The number of patients with Stage I, II, III, and IV of the disease, as per the TNM classification, were 2 (4.3%), 20 (43.4%), 18 (39.1%), and 2 (4.3%), respectively. Furthermore, the DKK2 gene had a higher methylation profile in the CRC tissues when compared to normal mucosa (p < 0.001), whereas the methylation profile analysis was not statistically significant when comparing the stages of the disease (p = 0.078). Conclusion: The presence of differentially methylated sequences of the DKK2 gene between the groups showed that the methylation changes of these genes could potentially be prognostic and predictive markers in CRC. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017 2020-08-04T13:39:51Z 2020-08-04T13:39:51Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.4238/gmr16039816 Genetics And Molecular Research. Ribeirao Preto, v. 16, n. 4, p. -, 2017. 10.4238/gmr16039816 WOS000419067100001.pdf 1676-5680 https://repositorio.unifesp.br/handle/11600/57147 WOS:000419067100001 |
url |
http://dx.doi.org/10.4238/gmr16039816 https://repositorio.unifesp.br/handle/11600/57147 |
identifier_str_mv |
Genetics And Molecular Research. Ribeirao Preto, v. 16, n. 4, p. -, 2017. 10.4238/gmr16039816 WOS000419067100001.pdf 1676-5680 WOS:000419067100001 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Genetics And Molecular Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
- application/pdf |
dc.coverage.none.fl_str_mv |
Ribeirao Preto |
dc.publisher.none.fl_str_mv |
Funpec-Editora |
publisher.none.fl_str_mv |
Funpec-Editora |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268462136033280 |