Detection of SNCA and FBN1 Methylation in the Stool as a Biomarker for Colorectal Cancer

Aim. We examined the methylation status of SNCA and FBN1 genes in patients' paired tissue and stool samples for detection of colorectal cancer (CRC). Patients and Methods. 89 DNA tissue samples (normal/cancer) and corresponding stool samples were analyzed in our study. In addition, 30 stool sa...

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Main Authors: Li, Wen-han, Zhang, Hao, Guo, Qi, Wu, Xuan-di, Xu, Zi-sen, Dang, Cheng-xue, Xia, Peng, Song, Yong-chun
Format: Online
Language:English
Published: Hindawi Publishing Corporation 2015
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4353443/
id pubmed-4353443
recordtype oai_dc
spelling pubmed-43534432015-03-23 Detection of SNCA and FBN1 Methylation in the Stool as a Biomarker for Colorectal Cancer Li, Wen-han Zhang, Hao Guo, Qi Wu, Xuan-di Xu, Zi-sen Dang, Cheng-xue Xia, Peng Song, Yong-chun Research Article Aim. We examined the methylation status of SNCA and FBN1 genes in patients' paired tissue and stool samples for detection of colorectal cancer (CRC). Patients and Methods. 89 DNA tissue samples (normal/cancer) and corresponding stool samples were analyzed in our study. In addition, 30 stool samples were collected as healthy controls. Results. The methylation level of those samples was measured by methylation-specific polymerase chain reaction (MSP). The result shows that compared with the paired controls, both SNCA and FBN1 were significantly hypermethylated in CRC patients in tissue samples (P < 0.001). In the stool samples, hypermethylated SNCA and FBN1 were detected to be significantly higher than that in normal stool samples (P < 0.001). The combined sensitivity of at least one positive among the two markers in stool samples was 84.3%, with a specificity of 93.3%. In addition, our experiment suggested that the positive rates of SNCA and FBN1 in Dukes A stage were significantly higher than that of FOBT (P = 0.039; P = 0.006, resp.). Conclusion. We concluded that methylation testing of SNCA and FBN1 genes in stool sample may offer a good alternative in a simple, promising, and noninvasive detection of colorectal cancer. Hindawi Publishing Corporation 2015 2015-02-23 /pmc/articles/PMC4353443/ /pubmed/25802477 http://dx.doi.org/10.1155/2015/657570 Text en Copyright © 2015 Wen-han Li et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Li, Wen-han
Zhang, Hao
Guo, Qi
Wu, Xuan-di
Xu, Zi-sen
Dang, Cheng-xue
Xia, Peng
Song, Yong-chun
spellingShingle Li, Wen-han
Zhang, Hao
Guo, Qi
Wu, Xuan-di
Xu, Zi-sen
Dang, Cheng-xue
Xia, Peng
Song, Yong-chun
Detection of SNCA and FBN1 Methylation in the Stool as a Biomarker for Colorectal Cancer
author_facet Li, Wen-han
Zhang, Hao
Guo, Qi
Wu, Xuan-di
Xu, Zi-sen
Dang, Cheng-xue
Xia, Peng
Song, Yong-chun
author_sort Li, Wen-han
title Detection of SNCA and FBN1 Methylation in the Stool as a Biomarker for Colorectal Cancer
title_short Detection of SNCA and FBN1 Methylation in the Stool as a Biomarker for Colorectal Cancer
title_full Detection of SNCA and FBN1 Methylation in the Stool as a Biomarker for Colorectal Cancer
title_fullStr Detection of SNCA and FBN1 Methylation in the Stool as a Biomarker for Colorectal Cancer
title_full_unstemmed Detection of SNCA and FBN1 Methylation in the Stool as a Biomarker for Colorectal Cancer
title_sort detection of snca and fbn1 methylation in the stool as a biomarker for colorectal cancer
description Aim. We examined the methylation status of SNCA and FBN1 genes in patients' paired tissue and stool samples for detection of colorectal cancer (CRC). Patients and Methods. 89 DNA tissue samples (normal/cancer) and corresponding stool samples were analyzed in our study. In addition, 30 stool samples were collected as healthy controls. Results. The methylation level of those samples was measured by methylation-specific polymerase chain reaction (MSP). The result shows that compared with the paired controls, both SNCA and FBN1 were significantly hypermethylated in CRC patients in tissue samples (P < 0.001). In the stool samples, hypermethylated SNCA and FBN1 were detected to be significantly higher than that in normal stool samples (P < 0.001). The combined sensitivity of at least one positive among the two markers in stool samples was 84.3%, with a specificity of 93.3%. In addition, our experiment suggested that the positive rates of SNCA and FBN1 in Dukes A stage were significantly higher than that of FOBT (P = 0.039; P = 0.006, resp.). Conclusion. We concluded that methylation testing of SNCA and FBN1 genes in stool sample may offer a good alternative in a simple, promising, and noninvasive detection of colorectal cancer.
publisher Hindawi Publishing Corporation
publishDate 2015
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4353443/
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