Quantitation of circulating DNA in the serum of breast cancer patients by real-time PCR

被引:0
作者
S Gal
C Fidler
Y M D Lo
M Taylor
C Han
J Moore
A L Harris
J S Wainscoat
机构
[1] University of Oxford,Nuffield Department of Clinical Laboratory Sciences
[2] John Radcliffe Hospital,Department of Chemical Pathology
[3] Headington,undefined
[4] The Chinese University of Hong-Kong,undefined
[5] Prince of Wales Hospital,undefined
[6] Shatin,undefined
[7] Cancer Research UK,undefined
[8] Medical Oncology Unit,undefined
[9] Churchill Hospital,undefined
[10] Cancer Research UK,undefined
[11] Molecular Oncology Laboratory,undefined
[12] University of Oxford,undefined
[13] Institute of Molecular Medicine,undefined
[14] John Radcliffe Hospital,undefined
[15] Headington,undefined
来源
British Journal of Cancer | 2004年 / 90卷
关键词
serum; circulating DNA; breast cancer; real-time PCR;
D O I
暂无
中图分类号
学科分类号
摘要
The purpose of this study was to quantify the level of serum DNA in different groups of primary breast cancer patients and in healthy controls using real-time quantitative PCR in order to determine whether such measurements have diagnostic or prognostic value. A total of 96 serum samples of patients with primary breast cancer before surgery (with positive or negative lymph nodes and with high or low relapse-free survival) as well as 24 healthy controls were analysed. DNA concentrations in the serum of the patients differed significantly from the concentration of serum DNA in the controls (medians were 221 and 63 ng ml−1, respectively, P<0.001 M–W test). However, no statistically significant difference was observed between the patient groups (P=0.87, M–W test). The serum DNA levels were elevated independently of the size of primary tumour or lymph node metastases. The overall survival of patients with serum DNA concentrations >221 ng ml−1 was better than patients with serum DNA concentration ⩽221 ng ml−1 (Kaplan–Meier, P=0.028).
引用
收藏
页码:1211 / 1215
页数:4
相关论文
共 143 条
[1]  
Beau-Faller M(2003)Plasma DNA microsatellite panel as sensitive and tumor-specific marker in lung cancer patients Int J Cancer 105 361-370
[2]  
Gaub MP(1999)Detecting tumor-related alterations in plasma or serum DNA of patients diagnosed with breast cancer Clin Cancer Res 5 2297-2303
[3]  
Schneider A(1996)Microsatellite alterations in plasma DNA of small cell lung cancer patients Nat Med 2 1033-1035
[4]  
Ducrocq X(2000)Microsatellite alterations and TP53 mutations in plasma DNA of small-cell lung cancer patients: follow-up study and prognostic significance Ann Oncol 11 1097-1104
[5]  
Massard G(1973)The occurrence of single-stranded DNA in the serum of patients with systemic lupus erythematosus and other diseases J Clin Invest 52 198-204
[6]  
Gasser B(1977)Free DNA in the serum of cancer patients and the effect of therapy Cancer Res 37 646-650
[7]  
Chenard MP(2001)Increased maternal plasma fetal DNA concentrations in women who eventually develop preeclampsia Clin Chem 47 137-139
[8]  
Kessler R(2000)Plasma DNA as a prognostic marker in trauma patients Clin Chem 46 319-323
[9]  
Anker P(1998)Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis Am J Hum Genet 62 768-775
[10]  
Stroun M(2002)Predominant hematopoietic origin of cell-free DNA in plasma and serum after sex-mismatched bone marrow transplantation Clin Chem 48 421-427