Abstract

IntroductionIt has been shown in some articles that genetic and epigenetic abnormalities cannot only be found in tumor tissues but also in adjacent regions that appear histologically normal. This phenomenon is metaphorically called field cancerization or field defect. Field cancerization is regarded as clinically significant because it is assumed to be an important factor in local recurrence of cancer. As the field showing these molecular abnormalities may not be removed completely by surgery, these changes might lead to neoplasms and subsequent transformation to a tumor. We aimed to investigate the applicability of the methylation status of six tumor suppressor genes as biomarkers for detecting field cancerization in breast cancer.MethodsThe promoter methylation status of CCND2, DAPK1, GSTP1, HIN-1, MGMT and RASSF1A was determined by methylation-sensitive high-resolution melting (MS-HRM) analysis. MS-HRM methods for CCND2, MGMT and RASSF1A were developed in-house, primer sequences for DAPK1, GSTP1 and HIN-1 have already been published. Biopsy samples were taken from tumor, tumor-adjacent and tumor-distant tissue from 17 breast cancer patients. Normal breast tissues of four healthy women served as controls.ResultsAll MS-HRM methods proved to be very sensitive. LODs were in the range from 0.1 to 1.5 %, LOQs ranged from 0.3 to 5.3 %. A total of 94 %, 82 % and 65 % of the tumors showed methylation of RASSF1A, HIN-1 and MGMT promoters, respectively. The methylation status of these promoters was significantly lower in tumor-distant tissues than in tumor tissues. Tumor-adjacent tissues showed higher methylation status of RASSF1A, HIN-1 and MGMT promoters than tumor-distant tissues, indicating field cancerization. The methylation status of the HIN-1 promoter in tumor-adjacent tissues was found to correlate strongly with that in the corresponding tumors (r = 0.785, p < 0.001), but not with that in the corresponding tumor-distant tissues (r = 0.312, p = 0.239).ConclusionsAmong the gene promoters investigated, the methylation status of the HIN-1 promoter can be considered the best suitable biomarker for detecting field cancerization. Further investigation is needed to test whether it can be used for defining surgical margins in order to prevent future recurrence of breast cancer.

Highlights

  • It has been shown in some articles that genetic and epigenetic abnormalities cannot only be found in tumor tissues and in adjacent regions that appear histologically normal

  • Further investigation is needed to test whether it can be used for defining surgical margins in order to prevent future recurrence of breast cancer

  • Validation of the methylation-sensitive high-resolution melting (MS-HRM) methods MS-HRM methods for cyclin D2 (CCND2), methylguanineDNA methyltransferase (MGMT) and Ras association domain family member 1 (RASSF1A) were developed in-house, primer sequences for death-associated protein kinase 1 (DAPK1), glutathione S-transferase P1 (GSTP1) and high in normal1 (HIN-1) were taken from previously published articles

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Summary

Introduction

It has been shown in some articles that genetic and epigenetic abnormalities cannot only be found in tumor tissues and in adjacent regions that appear histologically normal. This phenomenon is metaphorically called field cancerization or field defect. We aimed to investigate the applicability of the methylation status of six tumor suppressor genes as biomarkers for detecting field cancerization in breast cancer. Epigenetic alterations, in changes in the DNA methylation pattern, are known to play a crucial role in carcinogenesis. CpG islands are present in promoter regions and first exons of genes that regulate important cell functions [3].

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