The involvement of the familial breast-ovarian cancer gene (BRCA1) in the m
olecular pathogenesis of breast cancer among Indian women is unknown. We ha
ve used a set of microsatellite polymorphisms to examine the frequency of a
llele loss at the BRCA1 region on chromosome 17q21, in a panel of 80 human
breast tumours. Tumour and blood leukocyte/normal tissue DNA from a series
of 80 patients with primary breast cancer was screened by PCR-amplified mic
rosatellite length polymorphisms to detect deletions at three polymorphic B
RCA1 loci. PCR-allelotype was valuable in examining allele losses from arch
ival and small tumour samples. Loss of alleles at BRCA1 in the patient set,
confirmed a noteworthy role of this gene in the molecular pathogenesis of
breast cancer and was in accordance with its well-documented tumour suppres
sive function.