Frequency of the mitochondrial DNA 4977bp deletion in oesophageal mucosa during the progression of Barrett's oesophagus

被引:18
作者
Tan, Benjamin H. L.
Skipworth, Richard J. E.
Stephens, Nathan A.
Wheelhouse, Nicholas M. [1 ]
Gilmour, Hugh [2 ]
de Beauxa, Andrew C.
Paterson-Brown, Simon
Fearon, Kenneth C. H.
Ross, James A.
机构
[1] Moredun Res Inst, Penicuik EH26 0PZ, Midlothian, Scotland
[2] Univ Edinburgh, Royal Infirm, Dept Pathol, Edinburgh EH16 4SA, Midlothian, Scotland
关键词
Barrett's oesophagus; Oesophageal cancer; Mitochondrial DNA; Sequence deletion; Biomarker; HIGH-GRADE DYSPLASIA; GASTROESOPHAGEAL-REFLUX; SOMATIC MUTATIONS; CANCER; NUCLEAR; RISK;
D O I
10.1016/j.ejca.2009.01.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: The mechanisms of the progression of Barrett's oesophagus (BO) to oesophageal adenocarcinoma (OA) are poorly understood. The frequency of the 4977bp deletion in mitochondrial DNA (mtDNA) was investigated in specimens ranging from normal oesophageal tissue to OA in order to investigate whether this deletion represents a useful biomarker of disease progression. Methods: The presence of the 4977bp deletion was screened by PCR amplification from 70 specimens in total. Results: The frequency of specimens with the 4977bp deletion increased in relation to the degree of dysplasia (8.3% in normal squamous epithelium; 15.4% in BO; 40% in low grade dysplasia (LGD); 69.2% in high-grade dysplasia and 90% in para-tumoural tissue). However, the frequency of the deletion reduced sharply in OA specimens (16.7%; p < 0.001). Conclusion: The mtDNA 4977bp deletion may be useful as a biomarker to detect the severity of dysplasia but not the presence of OA. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:736 / 740
页数:5
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