Evidence map›Paper›PMID 31932493›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

Diverse

Yingming Li, Rendong Yang, Christine M Henzler, Yeung Ho, Courtney Passow, Benjamin Auch, Suzanne Carreira, Daniel Nava Rodrigues, Claudia Bertan, Tae Hyun Hwang and 9 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

60 citing papers in PubMed, 83 citations in OpenAlex.

  1. Evolution of AR and Non-AR Alterations in ctDNA of Patients with Metastatic Prostate Cancer Treated in the Phase III Alliance A031201 Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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  14. Osteoblast-Derived ECM1 Promotes Anti-Androgen Resistance in Bone Metastatic Prostate Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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  18. Androgen receptor and estrogen receptor variants in prostate and breast cancers.The Journal of steroid biochemistry and molecular biology · 2024
    Review
  19. Article
  20. Stat5 induces androgen receptor (Science advances · 2024
    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

19 authors at 9 institutions in 3 countries.

Yingming LiMasonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Rendong YangMasonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Christine M HenzlerMinnesota Supercomputing Institute, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0003-4566-2211
Yeung HoMasonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Courtney PassowUniversity of Minnesota Genomics Center, University of Minnesota, Minneapolis, Minnesota.
Benjamin AuchUniversity of Minnesota Genomics Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0003-3125-5797
Suzanne CarreiraThe Institute for Cancer Research, London, United Kingdom.
Daniel Nava RodriguesThe Institute for Cancer Research, London, United Kingdom.
Claudia BertanThe Institute for Cancer Research, London, United Kingdom.
Tae Hyun HwangDepartment of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
David A QuigleyHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, California.
Ha X DangMcDonnell Genome Institute, Washington University in St. Louis, St. Louis, Missouri.
Colm MorrisseyDepartment of Urology, University of Washington, Seattle, Washington.
Michael FraserComputational Biology Program, Ontario Institute for Cancer Research, Toronto, Ontario.ORCID 0000-0002-9303-9363
Stephen R PlymateDivision of Gerontology, Geriatric Medicine, University of Washington, Seattle, Washington.
Christopher A MaherMcDonnell Genome Institute, Washington University in St. Louis, St. Louis, Missouri.
Felix Y FengHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, California.
Johann S de BonoThe Institute for Cancer Research, London, United Kingdom.
Scott M DehmMasonic Cancer Center, University of Minnesota, Minneapolis, Minnesota. dehm@umn.edu.ORCID 0000-0002-7827-5579
University of Minnesota · USCancer Research UK · GBJames S. McDonnell Foundation · USUniversity of California, San Francisco · USUniversity of Washington · USCleveland Clinic Lerner College of Medicine · USOntario Institute for Cancer Research · CARoyal Marsden NHS Foundation Trust · GBUniversity of Minnesota System · US

Funding

TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI John Kyung Lee · 2002 to 2026
$58.1M
Steroid Metabolism in Castration-Resistant Prostate CancerP01CA163227 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Henry W. Long · 2013 to 2026
$25.0M
AR Gene Rearrangements and AR Signaling in Prostate CancerR01CA174777 · NCI · UNIVERSITY OF MINNESOTA · PI Scott M. Dehm · 2013 to 2026
$4.9M
Mechanisms for the Transition to Castrate Resistant Prostate CancerI01BX000585 · VA · VA PUGET SOUND HEALTHCARE SYSTEM · PI PLYMATE, STEPHEN R. · 2009 to 2013
–
Targeting the Metabolome in Androgen Receptor-driven Castration-resistant Prostate CancerI01BX003324 · VA · VA PUGET SOUND HEALTHCARE SYSTEM · PI PLYMATE, STEPHEN R. · 2016 to 2024
–
BLRD VA I01 BX000585BLRD VA I01 BX003324NCI NIH HHS P01 CA163227NCI NIH HHS P50 CA097186NCI NIH HHS R01 CA174777
6 · The paper itself

Abstract

purposeProstate cancer is the second leading cause of male cancer deaths. Castration-resistant prostate cancer (CRPC) is a lethal stage of the disease that emerges when endocrine therapies are no longer effective at suppressing activity of the androgen receptor (AR) transcription factor. The purpose of this study was to identify genomic mechanisms that contribute to the development and progression of CRPC. EXPERIMENTAL

designWe used whole-genome and targeted DNA-sequencing approaches to identify mechanisms underlying CRPC in an aggregate cohort of 272 prostate cancer patients. We analyzed structural rearrangements at the genome-wide level and carried out a detailed structural rearrangement analysis of the

results

conclusions

Indexed as

Gene RearrangementAndrogen Receptor AntagonistsBenzamidesBiomarkers, TumorCell Line, TumorDrug Resistance, NeoplasmHumansMaleNeoplasm MetastasisNitrilesPhenylthiohydantoinProspective StudiesProstatic Neoplasms, Castration-ResistantReceptors, AndrogenWhole Genome SequencingAndrogen Receptor AntagonistsAR protein, humanBenzamidesBiomarkers, TumorenzalutamideNitrilesPhenylthiohydantoinReceptors, Androgen

Identifiers

PMID31932493
PMCPMC7165042
OpenAlexW3000411451

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.