Evidence map›Paper›PMID 28120820›Full record

ArticleNature communications2017

DNA copy number changes define spatial patterns of heterogeneity in colorectal cancer.

Soulafa Mamlouk, Liam Harold Childs, Daniela Aust, Daniel Heim, Friederike Melching, Cristiano Oliveira, Thomas Wolf, Pawel Durek, Dirk Schumacher, Hendrik Bläker and 18 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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

69 citing papers in PubMed, 1 synthesis or guideline pooled it, 130 citations in OpenAlex.

  1. Pooled it
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  12. Digestive cancers: mechanisms, therapeutics and management.Signal transduction and targeted therapy · 2025
    Review
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9 more citing papers are in PubMed but not listed here.

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

28 authors at 9 institutions in 1 country.

Soulafa MamloukInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Liam Harold ChildsKnowledge Management in Bioinformatics, Humboldt University of Berlin, Berlin 10099, Germany.
Daniela AustGerman Cancer Consortium (DKTK), Heidelberg 69120, Germany.
Daniel HeimInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Friederike MelchingInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Cristiano OliveiraInstitute of Pathology, University of Heidelberg, Heidelberg 69120, Germany.
Thomas WolfGerman Cancer Consortium (DKTK), Heidelberg 69120, Germany.
Pawel DurekExperimental Rheumatology, German Rheumatism Research Centre, Berlin 10117, Germany.
Dirk SchumacherInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Hendrik BläkerInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Moritz von WinterfeldInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Bastian GastlInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Kerstin MöhrInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Andrea MenneInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Silke ZeugnerInstitute for Pathology, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden 01307, Germany.
Torben RedmerInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Dido LenzeInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Sascha TierlingDepartment of Genetics/Epigenetics, FR8.3 Life Sciences, Saarland University, Saarbrücken 66123, Germany.
Markus MöbsInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Wilko WeichertGerman Cancer Consortium (DKTK), Heidelberg 69120, Germany.
Gunnar FolprechtUniversity Hospital Carl Gustav Carus, University Cancer Center/Medical Dpt. I, Dresden 01307, Germany.
Eric BlancCore Unit Bioinformatics, Berlin Institute of Health, Berlin 10117, Germany.
Dieter BeuleCore Unit Bioinformatics, Berlin Institute of Health, Berlin 10117, Germany.
Reinhold SchäferInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Markus MorkelInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Frederick KlauschenInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Ulf LeserKnowledge Management in Bioinformatics, Humboldt University of Berlin, Berlin 10099, Germany.
Christine SersInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Charité - Universitätsmedizin Berlin · DEGerman Cancer Research Center · DEDeutschen Konsortium für Translationale Krebsforschung · DEHeidelberg University · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DEHumboldt-Universität zu Berlin · DEUniversity Hospital Carl Gustav Carus · DEGerman Rheumatism Research Centre · DESaarland University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic heterogeneity between and within tumours is a major factor determining cancer progression and therapy response. Here we examined DNA sequence and DNA copy-number heterogeneity in colorectal cancer (CRC) by targeted high-depth sequencing of 100 most frequently altered genes. In 97 samples, with primary tumours and matched metastases from 27 patients, we observe inter-tumour concordance for coding mutations; in contrast, gene copy numbers are highly discordant between primary tumours and metastases as validated by fluorescent in situ hybridization. To further investigate intra-tumour heterogeneity, we dissected a single tumour into 68 spatially defined samples and sequenced them separately. We identify evenly distributed coding mutations in APC and TP53 in all tumour areas, yet highly variable gene copy numbers in numerous genes. 3D morpho-molecular reconstruction reveals two clusters with divergent copy number aberrations along the proximal-distal axis indicating that DNA copy number variations are a major source of tumour heterogeneity in CRC.

Indexed as

Adenomatous Polyposis Coli ProteinAdultAgedAged, 80 and overColorectal NeoplasmsDNA Copy Number VariationsDNA Mutational AnalysisFemaleGene DosageHigh-Throughput Nucleotide SequencingHumansIn Situ Hybridization, FluorescenceMaleMiddle AgedMutationTumor Suppressor Protein p53Adenomatous Polyposis Coli ProteinAPC protein, humanTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID28120820
PMCPMC5288500
OpenAlexW2582545871

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.