Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast
โ Scribed by Nikos Pandis; Yuesheng Jin; Janusz Limon; Georgia Bardi; Ingrid Idvall; Nils Mandahl; Felix Mitelman; Dr. Sverre Heim
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 387 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1045-2257
No coin nor oath required. For personal study only.
โฆ Synopsis
Interstitial deletions of the short arm of chromosome 3 were found in short-term cultures of five breast carcinomas (of 41 breast cancers with clonal aberrations analyzed by us during the same period). They were the only clonal structural change in three tumors; in the remaining two, the clone with 3p-coexisted with seemingly unrelated clones that had other structural and numerical aberrations. The dleletions were identical, del(3)(p I2p I4), in four cases. The fifth tumor seemed t o have a smaller deletion, interpreted as del(3)(p I 3p 14). Our findings constitute karyotypic evidence that 3p deletions are relatively common in breast carcinomas and concur with the molecular genetic detection of loss of heterozygosity in this chromosome arm. The fact that the deletions were found as solitary changes indicates that loss of genetic information from 3p loci is an early, possibly primary, event in tumorigenesis. Genes Chrom Cancer 6:/51-155 (1993) 0 1993 Wiley-Liss, Inc.
๐ SIMILAR VOLUMES
Deletions in the short arm of chromosome 3 have long been known to be common in many tumor types, including carcinomas of the lung and kidney. Small interstitial deletions of the proximal-central region of 3p, with band 3p14 as a minimal common deleted segment, have recently been shown to occur in a
Little is known about the biology of Merkel cell carcinoma (MCC), also called small cell carcinoma of the skin. MCC has similarities with small cell lung cancer (SCLC): both are neuroendocrine malignancies with early metastasis t o distant sites and a poor prognosis. Small cell lung cancer biopsies
## Abstract A male patient with a de novo proximal interstitial deletion of the short arm of chromosome 1 (46XY), del(1)(p13p22.3) is described with multiple anomalies and developmental delay. This patient's clinical manifestations are compared to previously reported patients with deletions of chro
Previous cytogenetic investigations have revealed frequent deletions and ocher unbalanced structural rearrangements of 3p in human malignant mesothelioma, We have performed a restriction fragment length polymorphism analysis by using the polymerase chain reaction and primer sets for seven DNA marker