Evidence map›Paper›PMID 26894854›Full record

ArticleOncotarget2016

Characterization of novel low passage primary and metastatic colorectal cancer cell lines.

Arnoud Boot, Jaap van Eendenburg, Stijn Crobach, Dina Ruano, Frank Speetjens, Jan Calame, Jan Oosting, Hans Morreau, Tom van Wezel

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Frontiers in genetics · 2025
    Review
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  8. Review
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  10. Allelic Switching ofInternational journal of genomics · 2019
    Article
  11. Article
  12. Application ofOncotarget · 2017
    Article
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Arnoud BootDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Jaap van EendenburgDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Stijn CrobachDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Dina RuanoDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Frank SpeetjensDepartment of Clinical Oncology, Leiden University Medical Center, Leiden, The Netherlands.
Jan CalameDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Jan OostingDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Hans MorreauDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Tom van WezelDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Leiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Gene Expression Regulation, NeoplasticGenome, HumanTranscriptomeAdultAgedAged, 80 and overBiomarkers, TumorColorectal NeoplasmsDNA MethylationFemaleGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansLiver NeoplasmsMaleMiddle AgedBiomarkers, Tumorchemosensitivitycolorectal cancer cell linecopy number profilinggene expressionnext generation sequencing

Identifiers

PMID26894854
PMCPMC4924731
OpenAlexW2289762324

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.