Recurrent alterations of the short arm of chromosome 3 define a tumor suppressor region in rat mammary tumor cells

Cytogenetic alterations associated with different stages in carcinogenesis can be distinguished in cultured human or rodent cells transformed by carcinogenic agents. Three tumorigenic rat mammary epithelial cell lines transformed in vitro with 7,12,-dimethylbenz[a]anthracene alone or in combination...

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Veröffentlicht in:Carcinogenesis (New York) 1999-10, Vol.20 (10), p.2033-2036
Hauptverfasser: Popescu, Nicholas C., Greiner, John W.
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description Cytogenetic alterations associated with different stages in carcinogenesis can be distinguished in cultured human or rodent cells transformed by carcinogenic agents. Three tumorigenic rat mammary epithelial cell lines transformed in vitro with 7,12,-dimethylbenz[a]anthracene alone or in combination with 12-O-tetradecanoylphorbol-13-acetate were examined cytogenetically. Non-random alterations consisting of translocations involving the short arm of chromosome 3 and trisomy of chromosomes 14 and X were identified in all three lines. Deletion and inversion of chromosome 1 with the breakpoint at band 1q22 and a duplication 1q 32–43 and trisomy of chromosome 2 were observed in two cell lines. The accumulation of structural alterations and chromosome imbalances during the process of cell immortalization and acquisition of tumorigenicity are required for normal rat mammary cells to become malignant. Unbalanced translocations of chromosome 3 resulting in loss of the short arm had the breakpoint at 3p11. This site is a hotspot of breakage and recombination in various rat tumors and may represent a region of tumor suppressor gene critical to the development of rat mammary tumors, as well as other types of tumors.
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Three tumorigenic rat mammary epithelial cell lines transformed in vitro with 7,12,-dimethylbenz[a]anthracene alone or in combination with 12-O-tetradecanoylphorbol-13-acetate were examined cytogenetically. Non-random alterations consisting of translocations involving the short arm of chromosome 3 and trisomy of chromosomes 14 and X were identified in all three lines. Deletion and inversion of chromosome 1 with the breakpoint at band 1q22 and a duplication 1q 32–43 and trisomy of chromosome 2 were observed in two cell lines. The accumulation of structural alterations and chromosome imbalances during the process of cell immortalization and acquisition of tumorigenicity are required for normal rat mammary cells to become malignant. Unbalanced translocations of chromosome 3 resulting in loss of the short arm had the breakpoint at 3p11. 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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects 12-dimethylbenz[a]anthracene
12-O-tetradecanoylphorbol-13-acetate
7,12-dimethylbenz(a)anthracene
Animal tumors. Experimental tumors
Animals
Biological and medical sciences
Cell Line, Transformed
chromosome 1
chromosome 14
chromosome 2
chromosome 3
Chromosome Aberrations
DMBA
Experimental genital and mammary tumors
FBS
Female
fetal bovine serum
Genes, Tumor Suppressor
Humans
Karyotyping
LOH
loss of heterozygosity
Mammary Neoplasms, Experimental - chemically induced
Mammary Neoplasms, Experimental - genetics
Medical sciences
N-nitroso-N-methylurea
NMU
NOR
nucleolar organizer regions
Rats
Rats, Sprague-Dawley
TPA
Tumor Cells, Cultured
Tumors
title Recurrent alterations of the short arm of chromosome 3 define a tumor suppressor region in rat mammary tumor cells
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