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HIN-1、MGMT和RASSF1A启动子甲基化作为检测乳腺癌场癌化生物标志物的适用性。

Applicability of HIN-1, MGMT and RASSF1A promoter methylation as biomarkers for detecting field cancerization in breast cancer.

作者信息

Spitzwieser Melanie, Holzweber Elisabeth, Pfeiler Georg, Hacker Stefan, Cichna-Markl Margit

机构信息

Department of Analytical Chemistry, University of Vienna, Währinger Str. 38, 1090, Vienna, Austria.

Department of Obstetrics and Gynecology, Division of Gynecology and Gynecological Oncology, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.

出版信息

Breast Cancer Res. 2015 Sep 14;17(1):125. doi: 10.1186/s13058-015-0637-5.

Abstract

INTRODUCTION

It 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.

METHODS

The 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.

RESULTS

All 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).

CONCLUSIONS

Among 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.

摘要

引言

一些文章表明,遗传和表观遗传异常不仅能在肿瘤组织中发现,还能在组织学上看似正常的相邻区域发现。这种现象被形象地称为场癌化或场缺陷。场癌化被认为具有临床意义,因为它被假定为癌症局部复发的一个重要因素。由于显示这些分子异常的区域可能无法通过手术完全切除,这些变化可能导致肿瘤形成并随后转变为肿瘤。我们旨在研究六个抑癌基因的甲基化状态作为检测乳腺癌场癌化生物标志物的适用性。

方法

通过甲基化敏感的高分辨率熔解(MS-HRM)分析确定CCND2、DAPK1、GSTP1、HIN-1、MGMT和RASSF1A的启动子甲基化状态。CCND2、MGMT和RASSF1A的MS-HRM方法是内部开发的,DAPK1、GSTP1和HIN-1的引物序列已经发表。从17例乳腺癌患者的肿瘤、肿瘤相邻和肿瘤远处组织中采集活检样本。四名健康女性的正常乳腺组织作为对照。

结果

所有MS-HRM方法都证明非常敏感。检测限在0.1%至1.5%范围内,定量限在0.3%至5.3%范围内。分别有94%、82%和65%的肿瘤显示RASSF1A、HIN-1和MGMT启动子甲基化。这些启动子的甲基化状态在肿瘤远处组织中明显低于肿瘤组织。肿瘤相邻组织中RASSF1A、HIN-1和MGMT启动子的甲基化状态高于肿瘤远处组织,表明存在场癌化。发现肿瘤相邻组织中HIN-1启动子的甲基化状态与相应肿瘤中的甲基化状态密切相关(r = 0.785,p < 0.001),但与相应肿瘤远处组织中的甲基化状态无关(r = 0.312,p = 0.239)。

结论

在所研究的基因启动子中,HIN-1启动子的甲基化状态可被认为是检测场癌化最合适的生物标志物。需要进一步研究以测试其是否可用于确定手术切缘,以预防未来乳腺癌的复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e7a/4570691/c7ce2c96a297/13058_2015_637_Fig1_HTML.jpg

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