𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Loss of chromosome 3 alleles and multiplication of chromosome 8 alleles in uveal melanoma

✍ Scribed by Barnhard Horsthemke; Gabriele Prescher; Reinhard Becher; Norbert Bornfeld


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
486 KB
Volume
4
Category
Article
ISSN
1045-2257

No coin nor oath required. For personal study only.

✦ Synopsis


lnstitut fur Humangenetik (B.H.), lnnere Klinik und Poliklinik (Tumorfonchung) (G.P., R.B.), and Zentrum fur Augenheilkunde (N.B.).

Univenitatsklinikum Essen, Federal Republic of Germany Uveal melanoma is the most frequent primary intraocular tumor. The etiology is unknown. Using neutral DNA polymorphisms on chromosomes 2, 3, and 8, we have detected loss of chromosome 3 alleles in 8 of 13 tumors and multiplication of chromosome 8 alleles in 6 of I I tumors. No anomalies at a locus on chromosome 2 were found in I0 of I0 tumors. These results confirm and extend previous cytogenetic findings and suggest that a tumor suppressor gene on chromosome 3 and an oncogene on chromosome 8 may be involved in the formation o r progression of this tumor. Genes Chrom Cancer 4 2 I7-22 I (1 992) @ 1992 Wiley-Liss, Inc.


πŸ“œ SIMILAR VOLUMES


Loss of chromosome 22 alleles in human s
✍ Bertrand Fontaine; Mark P. Hanson; Jean Paul Von Sattel; Robert L. Martuza; Dr J πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 453 KB

Acoustic neuromas occur either as sporadic solitary tumors in the general population or as inherited bilateral tumors typically in patients with neurofibromatosis type 2. Loss of heterozygosity for markers on the long arm of chromosome 22 has been reported in both instances, and neurofibromatosis ty

Abnormalities of chromosomes 3 and 8 in
✍ Karen Sisley; Ian G. Rennie; M. Andrew Parsons; Rhona Jacques; David W. Hammond; πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 125 KB πŸ‘ 2 views

Posterior uveal melanomas have nonrandom alterations affecting chromosomes 3, 6, and 8. Loss of chromosome 3 in uveal melanoma has been shown to act as a predictor of disease-free and overall survival. To confirm the significance of chromosome 3 loss and to extend the observations to include those o

Deletion mapping reveals two regions of
✍ M. Lisa Yaremko; Marina L. Wasylyshyn; Kristen L. Paulus; Fabrizio Michelassi; C πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 488 KB

## Abstract Colorectal carcinogenesis is associated with the accumulation of genetic changes involving both dominant oncogenes and tumor suppressor genes. Although at least four different genes have been implicated in the process, the detection of allele loss from other regions of the genome sugges

Cytogenetic findings in six posterior uv
✍ Dr. Karen Sisley; Ian G. Rennie; David W. Cottam; Anthony M. Potter; Christopher πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 391 KB

## Abstract Six posterior uveal melanomas were karyotyped after short‐term culture. One had a normal chromosome complement; the remaining five had limited chromosome changes. Involvement of chromosomes 1 and 6 was noted in two and four cases, respectively, and three ciliary body tumours demonstrate

Frequent allelic loss and homozygous del
✍ Chandramohan S. Ishwad; Michele Shuster; Ulrike BockmΓΌhl; Nalin Thakker; Punit S πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 French βš– 304 KB πŸ‘ 2 views

Frequent loss of heterozygosity on chromosome 8p in a variety of human malignancies, including head and neck cancers, has suggested the presence of a tumor suppressor gene (or genes) associated with the pathogenesis of these cancers. To test the role of genetic alterations at 8p23 in oral carcinogen

Non-random abnormalities of chromosomes
✍ Karen Sisley; David W. Cottam; Ian G. Rennie; M. Andrew Parsons; Anthony M. Pott πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 342 KB

## Abstract We present ten cases of posterior uveal melanoma which were karyotyped after short‐term culture. One tumour had a normal chromosome complement. The remaining nine tumours were cytogenetically abnormal, with chromosomes 3, 6, 8, 11, and 13 most frequently involved. Abnormalities of chrom