Increased chromosome 20 copy number detected by fluorescent in situ hybridization (FISH) in malignant melanoma

Persistent Link:
http://hdl.handle.net/10150/278562
Title:
Increased chromosome 20 copy number detected by fluorescent in situ hybridization (FISH) in malignant melanoma
Author:
Barks, James Harold, 1966-
Issue Date:
1996
Publisher:
The University of Arizona.
Rights:
Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
Abstract:
DNA amplification is an important mechanism of tumor progression that allows cancer cells to up-regulate expression of critical genes such as oncogenes. Recent studies using comparative genomic hybridization revealed increased DNA copies on chromosome 20q in seven melanoma cell lines and eight archival metastatic melanoma lesions. We performed FISH analysis of metaphase spreads in 13 melanoma cell lines and nine primary melanoma specimens using a variety of probes specific for chromosome 20. All 13 cell lines (100%) and 8/9 primary tumors (89%) showed extra copies of chromosome 20 relative to tumor ploidy. Additionally, 6/14 cell lines (43%) and 2/8 primary tumors (25%) showed translocated chromosome 20 material. Cytological evidence for gene amplification was found in one of the 13 cell lines with an add(20)(p13). These data suggest that over-representation of a gene(s) important for melanoma pathogenesis occurs on the chromosome 20 long arm.
Type:
text; Thesis-Reproduction (electronic)
Keywords:
Biology, Molecular.; Biology, Genetics.; Health Sciences, Oncology.
Degree Name:
M.Sc.
Degree Level:
masters
Degree Program:
Graduate College; Genetics
Degree Grantor:
University of Arizona
Advisor:
Nelson, Mark A.

Full metadata record

DC FieldValue Language
dc.language.isoen_USen_US
dc.titleIncreased chromosome 20 copy number detected by fluorescent in situ hybridization (FISH) in malignant melanomaen_US
dc.creatorBarks, James Harold, 1966-en_US
dc.contributor.authorBarks, James Harold, 1966-en_US
dc.date.issued1996en_US
dc.publisherThe University of Arizona.en_US
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en_US
dc.description.abstractDNA amplification is an important mechanism of tumor progression that allows cancer cells to up-regulate expression of critical genes such as oncogenes. Recent studies using comparative genomic hybridization revealed increased DNA copies on chromosome 20q in seven melanoma cell lines and eight archival metastatic melanoma lesions. We performed FISH analysis of metaphase spreads in 13 melanoma cell lines and nine primary melanoma specimens using a variety of probes specific for chromosome 20. All 13 cell lines (100%) and 8/9 primary tumors (89%) showed extra copies of chromosome 20 relative to tumor ploidy. Additionally, 6/14 cell lines (43%) and 2/8 primary tumors (25%) showed translocated chromosome 20 material. Cytological evidence for gene amplification was found in one of the 13 cell lines with an add(20)(p13). These data suggest that over-representation of a gene(s) important for melanoma pathogenesis occurs on the chromosome 20 long arm.en_US
dc.typetexten_US
dc.typeThesis-Reproduction (electronic)en_US
dc.subjectBiology, Molecular.en_US
dc.subjectBiology, Genetics.en_US
dc.subjectHealth Sciences, Oncology.en_US
thesis.degree.nameM.Sc.en_US
thesis.degree.levelmastersen_US
thesis.degree.disciplineGraduate Collegeen_US
thesis.degree.disciplineGeneticsen_US
thesis.degree.grantorUniversity of Arizonaen_US
dc.contributor.advisorNelson, Mark A.en_US
dc.identifier.proquest1382626en_US
dc.identifier.bibrecord.b34373512en_US
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