NIOSHTIC-2 Publications Search
Detection of three novel translocation and specific common chromosomal break sites in malignant melanoma by spectral karyotyping.
Sargent-LM; Nelson-MA; Lowry-DT; Senft-JR; Jefferson-AM; Ariza-ME; Reynolds-SH
Genes Chromosomes Cancer 2001 Sep; 32(1):18-25
Chromosomal aberrations in malignant melanoma cells have been reported using standard chromosome banding analysis and comparative genomic hybridization. To identify marker chromosomes and translocations that are difficult to characterize by standard banding analysis, 15 early passage malignant melanoma cell lines were examined using spectral karyotyping. All 15 tumor cell lines had lost all or part of 1p and 10q. Losses of material on chromosome arms 4p (12/15), 6q (12/15), 9p (15/15), 12p (13/15), 12q (13/15), 13q (11/15), and 19q (14/15) were the next most frequent events. Gain of chromosome arms 1q (11/15), 6p (13/15), and 20q11 (14/15) was also observed. Interestingly, we identified translocations der(12)t(12;20)(q15;q11), der(19)t(10;19)(q23;q13), and der(12)t(12;19)(q13;q13) in 4/15 tumors. Three recurring translocations involving four of the most frequent break points were detected. The identification of recurring translocations and unique chromosome break points in melanoma will aid in the identification of the genes that are important in the neoplastic process.
Chromosome-damage; Chromosome-disorders; Cancer; Genes; Tumors
Dr. Linda M. Sargent, 1095 Willowdale Road, MS-3014, Morgantown, WV 26505
Issue of Publication
Genes Chromosomes and Cancer
Page last reviewed: April 12, 2019
Content source: National Institute for Occupational Safety and Health Education and Information Division