Detection and quantification of mutations in the plasma of patients with colorectal tumors

被引:941
作者
Diehl, F
Li, M
Dressman, D
He, YP
Shen, D
Szabo, S
Diaz, LA
Goodman, SN
David, KA
Juhl, H
Kinzler, KW
Vogelstein, B
机构
[1] Johns Hopkins Med Inst, Howard Hughes Med Inst, Baltimore, MD 21231 USA
[2] Johns Hopkins Med Inst, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
[3] Israelit Hosp, Canc Res Ctr, Indivumed, D-22297 Hamburg, Germany
关键词
colorectal cancer; plasma DNA; tumor suppressor gene; circulating DNA; diagnosis;
D O I
10.1073/pnas.0507904102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The early detection of cancers through analysis of circulating DNA could have a substantial impact on morbidity and mortality. To achieve this goal, it is essential to determine the number of mutant molecules present in the circulation of cancer patients and to develop methods that are sufficiently sensitive to detect these mutations. Using a modified version of a recently developed assay for this purpose, we found that patients with advanced colorectal cancers consistently contained mutant adenomatous polyposis coli (APC) DNA molecules in their plasma. The median number of APC DNA fragments in such patients was 47,800 per ml of plasma, of which 8% were mutant. Mutant APC molecules were also detected in > 60% of patients :with early, presumably curable colorectal cancers, at levels ranging from 0.01% to 1.7% of the total APC molecules. These results have implications for the mechanisms through which tumor DNA is released into the circulation and for diagnostic tests based on this phenomenon.
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页码:16368 / 16373
页数:6
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