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Detection of Aberrant Methylated Sept9 and Ntrk3 Genes in Sporadic Colorectal Cancer Patients As a Potential Diagnostic Biomarker Publisher



Sharif SB1, 2, 3 ; Hashemzadeh S4, 5 ; Ardehaie RM1, 2 ; Eftekharsadat A6 ; Ghojazadeh M7 ; Mehrtash AH2 ; Estiar MA8 ; Teimooritoolabi L2 ; Sakhinia E1, 5
Authors
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Authors Affiliations
  1. 1. Department of Biochemistry and Clinical Laboratory, Division of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, 5165665811, Iran
  2. 2. Department of Molecular Medicine, Pasteur Institute of Iran, Tehran, 1316943551, Iran
  3. 3. Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, 5166614731, Iran
  4. 4. Department of General & Vascular Surgery, Tabriz University of Medical Sciences, Tabriz, 5165665811, Iran
  5. 5. Tuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, 5165665811, Iran
  6. 6. Department of Pathology, Imam Reza Hospital, Tabriz University of Medical Sciences, Tabriz, 5165665811, Iran
  7. 7. Liver and Gastrointestinal Disease Research Center, Department of General and Thoracic Surgery, Tabriz University of Medical Sciences, Tabriz, 5165665811, Iran
  8. 8. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, 1471613151, Iran

Source: Oncology Letters Published:2016


Abstract

Colorectal cancer (CRC) is one of the most common malignancies, and the third leading cause of cancer mortality worldwide. Timely detection of CRC in patients with earlier stages provides the highest rate of survival. Epigenetic alterations are important in the occurrence and progression of CRC, and represent the primary modifications of cancer cells. Therefore, detection of these alterations in CRC cases are thought to hold great promise as diagnostic biomarkers. It has been shown that the SEPT9 and NTRK3 genes are aberrantly methylated and their detection can be used as biomarkers for early diagnosis of CRC. The present study analyzed promoter methylation status of these genes in CRC patients. Genomic DNA was extracted from 45 CRC and paired adjacent healthy tissues and undergone bisulfite conversion, and the methylation status of NTRK3 and SEPT9 were defined using the MS-HRM assay. Our results showed that there are statistically significant differences in methylation status of NTRK3 and specially SEPT9 between CRC and adjacent normal tissues (P<0.001). High sensitivity and specificity for a specific location in SEPT9 gene promoter as a diagnostic biomarker was observed. SEPT9 promoter hypermethylation may serve as a promising biomarker for the detection of CRC development. However, to validate the biomarker potential of NTRK3 there is a requirement for further investigation. © 2016, Spandidos Publications. All rights reserved.