Evidence map›Paper›PMID 20393555›Full record

ArticleNature2010

Genome remodelling in a basal-like breast cancer metastasis and xenograft.

Li Ding, Matthew J Ellis, Shunqiang Li, David E Larson, Ken Chen, John W Wallis, Christopher C Harris, Michael D McLellan, Robert S Fulton, Lucinda L Fulton and 59 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 668 papers.

0numbers the graph read from it
0cells of the map it votes in
668citing papers in PubMed
59.3field-weighted citation impact, top 1% 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

668 citing papers in PubMed, 1,162 citations in OpenAlex.

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  16. Patient-Derived Xenografts of Breast Cancer.Advances in experimental medicine and biology · 2025
    Review
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  18. Review
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  20. Review

608 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

69 authors at 7 institutions in 2 countries.

Li DingThe Genome Center at Washington University, St Louis, Missouri 63108, USA.
Matthew J Ellis
Shunqiang Li
David E Larson
Ken Chen
John W Wallis
Christopher C Harris
Michael D McLellan
Robert S Fulton
Lucinda L Fulton
Rachel M Abbott
Jeremy Hoog
David J Dooling
Daniel C Koboldt
Heather Schmidt
Joelle Kalicki
Qunyuan Zhang
Lei Chen
Ling Lin
Michael C Wendl
Joshua F McMichael
Vincent J Magrini
Lisa Cook
Sean D McGrath
Tammi L Vickery
Elizabeth Appelbaum
Katherine Deschryver
Sherri Davies
Therese Guintoli
Li Lin
Robert Crowder
Yu Tao
Jacqueline E Snider
Scott M Smith
Adam F Dukes
Gabriel E Sanderson
Craig S Pohl
Kim D Delehaunty
Catrina C Fronick
Kimberley A Pape
Jerry S Reed
Jody S Robinson
Jennifer S Hodges
William Schierding
Nathan D Dees
Dong Shen
Devin P Locke
Madeline E Wiechert
James M Eldred
Josh B Peck
Benjamin J Oberkfell
Justin T Lolofie
Feiyu Du
Amy E Hawkins
Michelle D O'Laughlin
Kelly E Bernard
Mark Cunningham
Glendoria Elliott
Mark D Mason
Dominic M Thompson
Jennifer L Ivanovich
Paul J Goodfellow
Charles M Perou
George M Weinstock
Rebecca Aft
Mark Watson
Timothy J Ley
Richard K Wilson
Elaine R Mardis
New York Genome Center · USBreast Cancer Research Foundation · USUniversity Hospitals Seidman Cancer Center · USCancer Research And Biostatistics · USStatistical Service · CYUNC Lineberger Comprehensive Cancer CenterWashington University in St. Louis · US

Funding

Large Scale Genome SequencingU54HG003079 · NHGRI · WASHINGTON UNIVERSITY · PI DUTCHER, SUSAN K · 2004 to 2016
$445.7M
AMERICAN COLLEGE OF SURGEONS ONCOLOGY TRIALS GROUPU10CA076001 · NCI · DUKE UNIVERSITY · PI BERTAGNOLLI, MONICA M · 1998 to 2013
$62.1M
Washington University Institute of Clinical and Translational Sciences (UL1)UL1RR024992 · NCRR · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2007 to 2011
$45.4M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
SPORE IN BREAST CANCERP50CA068438 · NCI · DUKE UNIVERSITY · PI LYERLY, HERBERT KIM · 1995 to 2007
$14.3M
Biological Breast Cancer Classification by qRT-PCRU01CA114722 · NCI · WASHINGTON UNIVERSITY · PI ELLIS, MATTHEW J · 2005 to 2009
$8.7M
NCATS NIH HHS UL1 TR000448NCI NIH HHS P50 CA068438NCI NIH HHS U01 CA114722NCI NIH HHS U10 CA076001NCRR NIH HHS UL1 RR024992NHGRI NIH HHS U54 HG003079
6 · The paper itself

Abstract

Massively parallel DNA sequencing technologies provide an unprecedented ability to screen entire genomes for genetic changes associated with tumour progression. Here we describe the genomic analyses of four DNA samples from an African-American patient with basal-like breast cancer: peripheral blood, the primary tumour, a brain metastasis and a xenograft derived from the primary tumour. The metastasis contained two de novo mutations and a large deletion not present in the primary tumour, and was significantly enriched for 20 shared mutations. The xenograft retained all primary tumour mutations and displayed a mutation enrichment pattern that resembled the metastasis. Two overlapping large deletions, encompassing CTNNA1, were present in all three tumour samples. The differential mutation frequencies and structural variation patterns in metastasis and xenograft compared with the primary tumour indicate that secondary tumours may arise from a minority of cells within the primary tumour.

Indexed as

Neoplasm TransplantationAdultalpha CateninBrain NeoplasmsBreast NeoplasmsDisease ProgressionDNA Copy Number VariationsDNA Mutational AnalysisFemaleGene FrequencyGenome, HumanGenomicsHumansMutationTranslocation, GeneticTransplantation, Heterologousalpha CateninCTNNA1 protein, human

Identifiers

PMID20393555
PMCPMC2872544
OpenAlexW2147354890

What OpenQuestion holds

Textmetadata
LicenceTDM
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.