Comparative genomic hybridization reveals complex genetic changes in primary breast cancer tumors and their cell lines

Marcelo L. Larramendy, Tamara Lushnikova, Anna Maria Björkqvist, Ignacio I. Wistuba, Arvind K. Virmani, Narayan Shivapurkar, Adi F. Gazdar, Sakari Knuutila

Research output: Contribution to journalArticlepeer-review

71 Scopus citations

Abstract

DNA copy number changes were characterized by comparative genomic hybridization (CGH) in 18 breast cancer cell lines. In 5 of these, the results were comparable with those from the primary tumors of which the cell lines were established. All of the cell lines showed extensive DNA copy number changes, with a mean of 16.3 ± 1.1 aberrations per sample (range 7-26). All of the cell lines had a gain at 8q22-qter. Other common gains of DNA sequences occurred at 1q31-32 (89%), 20q12-q13.2 (83%), 8q13 (72%), 3q26.1-qter (67%), 17q21-qter (67%) 5p14 (61%), 6p22 (56%), and 22pter-qter (50%). High-level amplifications were observed in all cell lines; the most frequent minimal common regions were 8q24.1 (89%), 20q12 (61%), 1q41 (39%), and 20p11.2 (28%). Losses were observed less frequently than gains and the minimal common regions of the most frequent losses were Xq11-q12 (56%), Xp11.2-pter (50%), 13q21 (50%), 8p12-pter (44%), 4p13-p14 (39%), 6q15-q22 (39%), and 18q11.2-qter (33%). Although the cell lines showed more DNA copy number changes than the primary tumors, all aberrations, except one found in a primary tumor, were always present in the corresponding cell line. High-level amplifications found both in primary tumors and cell lines were at 1q, 8q, 17q, and 20q. The DNA copy number changes detected in these cell lines can be valuable in investigation of tumor progression in vitro and for a more detailed mapping and isolation of genes implicated in breast cancer. Copyright (C) 2000 Elsevier Science Inc.

Original languageEnglish (US)
Pages (from-to)132-138
Number of pages7
JournalCancer Genetics and Cytogenetics
Volume119
Issue number2
DOIs
StatePublished - Jun 2000

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

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