Detection of LOH and mitochondrial DNA alterations in ductal lavage and nipple aspirate fluids from high-risk patients

被引:39
作者
Isaacs, C
Cavalli, LR
Cohen, Y
Pennanen, M
Shankar, LK
Freedman, M
Singh, B
Liu, M
Gallagher, A
Rone, JD
Dickson, RB
Sidransky, D
Haddad, BR
机构
[1] Georgetown Univ, Med Ctr, Inst Mol & Human Genet, Lombardi Comprehens Canc Ctr, Washington, DC 20007 USA
[2] Georgetown Univ, Dept Oncol, Washington, DC 20007 USA
[3] Georgetown Univ, Dept Surg, Washington, DC 20007 USA
[4] Georgetown Univ, Dept Radiol, Washington, DC 20007 USA
[5] Georgetown Univ, Dept Nucl Med, Washington, DC 20007 USA
[6] Georgetown Univ, Dept Pathol, Washington, DC 20007 USA
[7] Georgetown Univ, Dept Obstet & Gynecol, Washington, DC 20007 USA
[8] Johns Hopkins Univ, Dept Otolaryngol Head & Neck Surg, Baltimore, MD USA
关键词
breast cancer; ductal lavage; loss of heterozygosity; mitochondrial mutations; nipple aspirate fluid;
D O I
10.1023/B:BREA.0000018406.03679.2e
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We describe a method for the isolation of free DNA from ductal lavage (DL) and nipple aspirate fluid (NAF), and its evaluation for the presence of LOH at the BRCA1 and FHIT genes and for mitochondrial DNA ( mtDNA) mutations at the D310 marker, to improve early detection of breast cancer. We evaluated 26 DL and six NAF samples from 14 women of known BRCA1 status, who have no clinical evidence of breast tumors: nine mutation carriers and five non-carriers. LOH studies at the BRCA1 locus were possible in 19/26 DL samples, and at the FHIT locus in 16/26 samples. In 4/9 mutation carriers we found LOH at the BRCA1 allele, and in two of these we also found LOH at the FHIT allele. In one of the mutation carriers with BRCA1 LOH, invasive breast cancer was subsequently detected, and the tumor showed the same LOH as the DL. In one of the true negatives, BRCA1 and FHIT LOH were detected. The mitochondrial studies were possible in all 26 DL samples and a somatic mutation was found in 3/9 carriers, two of whom also had LOH at the BRCA1 locus, and in none of the non-carriers. mtDNA mutation evaluation was possible in 4/6 NAF samples. The NAF and DL results were concordant. One NAF sample from a BRCA1 patient showed a mtDNA mutation. Our data demonstrates the feasibility of performing molecular studies using the free DNA present in the ductal fluid, while the intact cells can be used for cytologic studies.
引用
收藏
页码:99 / 105
页数:7
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