Literature DB >> 27107655

Changes of heterogeneous cell populations in the Ishikawa cell line during long-term culture: Proposal for an in vitro clonal evolution model of tumor cells.

Fumio Kasai1, Noriko Hirayama2, Midori Ozawa2, Masashi Iemura2, Arihiro Kohara2.   

Abstract

Genomic changes in tumor cell lines can occur during culture, leading to differences between cell lines carrying the same name. In this study, genome profiles between low and high passages were investigated in the Ishikawa 3-H-12 cell line (JCRB1505). Cells contained between 43 and 46 chromosomes and the modal number changed from 46 to 45 during culture. Cytogenetic analysis revealed that a translocation t(9;14), observed in all metaphases, is a robust marker for this cell line. Single-nucleotide polymorphism microarrays showed a heterogeneous copy number in the early passages and distinct profiles at late passages. These results demonstrate that cell culture can lead to elimination of ancestral clones by sequential selection, resulting in extensive replacement with a novel clone. Our observations on Ishikawa cells in vitro are different from the in vivo heterogeneity in which ancestral clones are often retained during tumor evolution and suggest a model for in vitro clonal evolution.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cell culture passage; Cell line authentication; Chromosome rearrangements; Genome instability; Tumor heterogeneity

Mesh:

Year:  2016        PMID: 27107655     DOI: 10.1016/j.ygeno.2016.04.003

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  18 in total

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8.  Homologue-specific chromosome sequencing characterizes translocation junctions and permits allelic assignment.

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Journal:  DNA Res       Date:  2018-08-01       Impact factor: 4.458

9.  A Combination of Species Identification and STR Profiling Identifies Cross-contaminated Cells from 482 Human Tumor Cell Lines.

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10.  Kasumi leukemia cell lines: characterization of tumor genomes with ethnic origin and scales of genomic alterations.

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