Please use this identifier to cite or link to this item: https://doi.org/10.18632/oncotarget.7391
Title: Characterization of novel low passage primary and metastatic colorectal cancer cell lines
Authors: Boot, A 
Van Eendenburg, J
Crobach, S
Ruano, D
Speetjens, F
Calame, J
Oosting, J
Morreau, H
Van Wezel, T
Keywords: oxaliplatin
transcriptome
tumor marker
adult
aged
antineoplastic activity
Article
cancer genetics
cell mutant
colorectal cancer cell line
controlled study
copy number alteration
copy number variation
drug resistance
female
gene expression profiling
genetics
genome
genomics
human
human cell
human tissue
liver metastasis
male
metastatic colorectal cancer
middle aged
mutational analysis
signal transduction
transcriptomics
very elderly
colorectal tumor
DNA methylation
gene expression regulation
genetics
high throughput sequencing
human genome
liver tumor
mutation
pathology
procedures
secondary
tumor cell culture
Adult
Aged
Aged, 80 and over
Biomarkers, Tumor
Colorectal Neoplasms
DNA Methylation
Female
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
Genome, Human
High-Throughput Nucleotide Sequencing
Humans
Liver Neoplasms
Male
Middle Aged
Mutation
Transcriptome
Tumor Cells, Cultured
Issue Date: 2016
Citation: Boot, A, Van Eendenburg, J, Crobach, S, Ruano, D, Speetjens, F, Calame, J, Oosting, J, Morreau, H, Van Wezel, T (2016). Characterization of novel low passage primary and metastatic colorectal cancer cell lines. Oncotarget 7 (12) : 14499-14509. ScholarBank@NUS Repository. https://doi.org/10.18632/oncotarget.7391
Rights: Attribution 4.0 International
Abstract: In vitro models are essential to understanding the molecular characteristics of colorectal cancer (CRC) and the testing of therapies for CRC. Many efforts to establish and characterize primary CRC cell lines have been published, most describing a small number of novel cell lines. However, there remains a lack of a large panel of uniformly established and characterized cell lines. To this end we established 20 novel CRC cell lines, of which six were derived from liver metastases. Genetic, genomic and transcriptomic profiling was performed in order to characterize these new cell lines. All data are made publically available upon publication. By combining mutation profiles with CNA and gene expression profiles, we generated an overall profile of the alterations in the major CRC-related signaling pathways. The combination of mutation profiles with genome, transcriptome and methylome data means that these low passage cell lines are among the best characterized of all CRC cell lines. This will allow researchers to select model cell lines appropriate to specific experiments, facilitating the optimal use of these cell lines as in vitro models for CRC. All cell lines are available for further research.
Source Title: Oncotarget
URI: https://scholarbank.nus.edu.sg/handle/10635/179935
ISSN: 19492553
DOI: 10.18632/oncotarget.7391
Rights: Attribution 4.0 International
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