DNA copy number losses at 1p32-pter in monozygotic twins concordant for breast cancer.

el-Rifai W, Tarmo L, Hemmer S, Försti A, Pedersen N, Lichtenstein P, Ahlbom A, Söderberg M, Knuutila S, Hemminki K
Cancer Genet Cytogenet. 1999 112 (2): 169-72

PMID: 10686947 · DOI:10.1016/s0165-4608(98)00274-x

To find similarities that may possibly indicate novel mutations, we performed comparative genomic hybridization (CGH) analysis following degenerate oligonucleotide primed polymerase chain reaction (PCR) for DNA obtained from unique material of breast cancer that developed in monozygotic twin-pairs. Polymerase chain reaction amplification was successful in 12 samples for 11 patients, including 3 pairs. Six samples exhibited DNA copy number changes. Gains (76%) were more frequent than losses (24%). Gains or high-level amplifications in 8q were present in all but 1 of the abnormal cases. Frequent gains were detected with a minimal common overlapping region at 5p (4 cases), at 1q25-qter (3 cases), and at 20q12-qter (2 cases). The most frequent loss, detected in half of the abnormal cases, was at 1p32-pter. One twin-pair showed similar changes in 4 chromosomal locations involving loss of 1p32-pter and gains in 1q25-qter, 5, and 8q.

MeSH Terms (10)

Base Sequence Breast Neoplasms Chromosome Deletion Chromosomes, Human, Pair 1 Diseases in Twins DNA, Neoplasm DNA Primers Humans Polymerase Chain Reaction Twins, Monozygotic

Connections (1)

This publication is referenced by other Labnodes entities: