Karyotypic evolution of four novel mouse mammary carcinoma cell lines. Identification of marker chromosomes by fluorescence in situ hybridization

We studied the karyotypes of four different mammary carcinoma cell lines derived from a medroxyprogesterone acetate (MPA)-induced mouse mammary carcinoma using G-banding and fluorescence in situ hybridization. All the cell lines showed the same four marker chromosomes (M1-M4) as the parental tumor a...

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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01654608_v142_n1_p36_Fabris
http://hdl.handle.net/20.500.12110/paper_01654608_v142_n1_p36_Fabris
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spelling paper:paper_01654608_v142_n1_p36_Fabris2023-06-08T15:14:53Z Karyotypic evolution of four novel mouse mammary carcinoma cell lines. Identification of marker chromosomes by fluorescence in situ hybridization medroxyprogesterone acetate acrocentric chromosome animal cell article breast carcinoma cell line chromosome 1 chromosome 10 chromosome 12 chromosome 13 chromosome 16 chromosome 17 chromosome 18 chromosome 2 chromosome 3 chromosome 4 chromosome 5 chromosome 6 chromosome 8 chromosome 9 chromosome number controlled study cytogenetics diploidy fluorescence in situ hybridization hormone dependence karyotype karyotyping marker chromosome mouse nonhuman phenotype ploidy priority journal Robertsonian chromosome translocation Murinae Robertsonia We studied the karyotypes of four different mammary carcinoma cell lines derived from a medroxyprogesterone acetate (MPA)-induced mouse mammary carcinoma using G-banding and fluorescence in situ hybridization. All the cell lines showed the same four marker chromosomes (M1-M4) as the parental tumor and also acquired new markers. M1 and M2 are Robertsonian translocations between chromosomes 1 and 10 and 2 and 17. M3 is an acrocentric marker derived from chromosomes 4, 5, and 12; M4 is derived from chromosomes 6 and 8. The parental tumor disclosed a modal number of 39, with a trisomy of chromosomes 3, 4, 10, and 11 and monosomies of 9, 13, and 16. MC4-L1 and MC4-L3 lines had a chromosome number similar to that of the parental tumor in early passages, which increased to the triploid range in late passages. MC4-L5 showed a near-diploid modal number in both early and late passages. MC4-L2 cells had a high chromosome number even in early passages. To our knowledge, this is the first study in which a complete characterization of the cytogenetics of murine mammary carcinoma cell lines and of their parental tumor is described. No associations between changes in ploidy, invasiveness, or hormone dependence were found. Conversely, the presence of one exclusive marker chromosome, a translocation between chromosomes 1 and 18 (M5), in the most aggressive and in vivo hormone-independent line suggests that this rearrangement may be associated with these biologic features. The constant presence of common marker chromosomes in both the parental tumor and the derived cell lines suggests that they are involved in the maintenance of this tumor phenotype. © 2003 Elsevier Science Inc. All rights reserved. 2003 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01654608_v142_n1_p36_Fabris http://hdl.handle.net/20.500.12110/paper_01654608_v142_n1_p36_Fabris
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic medroxyprogesterone acetate
acrocentric chromosome
animal cell
article
breast carcinoma
cell line
chromosome 1
chromosome 10
chromosome 12
chromosome 13
chromosome 16
chromosome 17
chromosome 18
chromosome 2
chromosome 3
chromosome 4
chromosome 5
chromosome 6
chromosome 8
chromosome 9
chromosome number
controlled study
cytogenetics
diploidy
fluorescence in situ hybridization
hormone dependence
karyotype
karyotyping
marker chromosome
mouse
nonhuman
phenotype
ploidy
priority journal
Robertsonian chromosome translocation
Murinae
Robertsonia
spellingShingle medroxyprogesterone acetate
acrocentric chromosome
animal cell
article
breast carcinoma
cell line
chromosome 1
chromosome 10
chromosome 12
chromosome 13
chromosome 16
chromosome 17
chromosome 18
chromosome 2
chromosome 3
chromosome 4
chromosome 5
chromosome 6
chromosome 8
chromosome 9
chromosome number
controlled study
cytogenetics
diploidy
fluorescence in situ hybridization
hormone dependence
karyotype
karyotyping
marker chromosome
mouse
nonhuman
phenotype
ploidy
priority journal
Robertsonian chromosome translocation
Murinae
Robertsonia
Karyotypic evolution of four novel mouse mammary carcinoma cell lines. Identification of marker chromosomes by fluorescence in situ hybridization
topic_facet medroxyprogesterone acetate
acrocentric chromosome
animal cell
article
breast carcinoma
cell line
chromosome 1
chromosome 10
chromosome 12
chromosome 13
chromosome 16
chromosome 17
chromosome 18
chromosome 2
chromosome 3
chromosome 4
chromosome 5
chromosome 6
chromosome 8
chromosome 9
chromosome number
controlled study
cytogenetics
diploidy
fluorescence in situ hybridization
hormone dependence
karyotype
karyotyping
marker chromosome
mouse
nonhuman
phenotype
ploidy
priority journal
Robertsonian chromosome translocation
Murinae
Robertsonia
description We studied the karyotypes of four different mammary carcinoma cell lines derived from a medroxyprogesterone acetate (MPA)-induced mouse mammary carcinoma using G-banding and fluorescence in situ hybridization. All the cell lines showed the same four marker chromosomes (M1-M4) as the parental tumor and also acquired new markers. M1 and M2 are Robertsonian translocations between chromosomes 1 and 10 and 2 and 17. M3 is an acrocentric marker derived from chromosomes 4, 5, and 12; M4 is derived from chromosomes 6 and 8. The parental tumor disclosed a modal number of 39, with a trisomy of chromosomes 3, 4, 10, and 11 and monosomies of 9, 13, and 16. MC4-L1 and MC4-L3 lines had a chromosome number similar to that of the parental tumor in early passages, which increased to the triploid range in late passages. MC4-L5 showed a near-diploid modal number in both early and late passages. MC4-L2 cells had a high chromosome number even in early passages. To our knowledge, this is the first study in which a complete characterization of the cytogenetics of murine mammary carcinoma cell lines and of their parental tumor is described. No associations between changes in ploidy, invasiveness, or hormone dependence were found. Conversely, the presence of one exclusive marker chromosome, a translocation between chromosomes 1 and 18 (M5), in the most aggressive and in vivo hormone-independent line suggests that this rearrangement may be associated with these biologic features. The constant presence of common marker chromosomes in both the parental tumor and the derived cell lines suggests that they are involved in the maintenance of this tumor phenotype. © 2003 Elsevier Science Inc. All rights reserved.
title Karyotypic evolution of four novel mouse mammary carcinoma cell lines. Identification of marker chromosomes by fluorescence in situ hybridization
title_short Karyotypic evolution of four novel mouse mammary carcinoma cell lines. Identification of marker chromosomes by fluorescence in situ hybridization
title_full Karyotypic evolution of four novel mouse mammary carcinoma cell lines. Identification of marker chromosomes by fluorescence in situ hybridization
title_fullStr Karyotypic evolution of four novel mouse mammary carcinoma cell lines. Identification of marker chromosomes by fluorescence in situ hybridization
title_full_unstemmed Karyotypic evolution of four novel mouse mammary carcinoma cell lines. Identification of marker chromosomes by fluorescence in situ hybridization
title_sort karyotypic evolution of four novel mouse mammary carcinoma cell lines. identification of marker chromosomes by fluorescence in situ hybridization
publishDate 2003
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01654608_v142_n1_p36_Fabris
http://hdl.handle.net/20.500.12110/paper_01654608_v142_n1_p36_Fabris
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