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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 |
Appears in Collections: | Staff Publications Elements |
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