Evidence map›Paper›PMID 29340907›Full record

ReviewHormones & cancer2018

Harnessing a Different Dependency: How to Identify and Target Androgen Receptor-Positive Versus Quadruple-Negative Breast Cancer.

Jessica L Christenson, Jane B Trepel, Haythem Y Ali, Sunmin Lee, Joel R Eisner, Edwina S Baskin-Bey, Anthony D Elias, Jennifer K Richer

Abstract readReview
In one paragraph

Review in Hormones & cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Drug Repurposing for Triple-Negative Breast Cancer.Journal of personalized medicine · 2020
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Male breast cancer: a disease distinct from female breast cancer.Breast cancer research and treatment · 2019
    Review
  19. 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

8 authors at 4 institutions in 1 country.

Jessica L ChristensonDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Jane B TrepelCenter for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Haythem Y AliHenry Ford Medical Group, Brownstown, MI, USA.ORCID 0000-0002-9702-9541
Sunmin LeeCenter for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Joel R EisnerInnocrin Pharmaceuticals Inc., Durham, NC, USA.
Edwina S Baskin-BeyInnocrin Pharmaceuticals Inc., Durham, NC, USA.
Anthony D EliasDepartment of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA. anthony.elias@ucdenver.edu.
Jennifer K RicherDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA. jennifer.richer@ucdenver.edu.
University of Colorado Anschutz Medical Campus · USInnocrin Pharmaceuticals (United States) · USNational Cancer Institute · USFord Motor Company (United States) · US

Funding

Signal Transduction Events and the Regulation of Cell GrowthZICSC006743 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI TREPEL, JANE B · 2009 to 2023
$13.8M
Training Program in Cancer BiologyT32CA190216 · NCI · UNIVERSITY OF COLORADO DENVER · PI Craig T. Jordan · 2016 to 2026
$3.5M
Androgen Receptor and Intersecting Pathways Critical to Breast Cancer SubtypesR01CA187733 · NCI · UNIVERSITY OF COLORADO DENVER · PI RICHER-MOUCHANTAT, JENNIFER · 2015 to 2019
$1.9M
NCI NIH HHS CA187733-01A1NCI NIH HHS R01 CA187733NCI NIH HHS T32 CA190216
6 · The paper itself

Abstract

The androgen receptor (AR) is a promising therapeutic target for a subset of triple-negative breast cancers (TNBCs) in which AR is expressed. However, the mechanistic action of AR and the degree to which primary and metastatic tumors depend on AR, both before and after conventional treatment, remain to be defined. We discuss preclinical and clinical data for AR+ TNBC, the difficulties in monitoring AR protein levels, new methods for determining AR status, the influence of AR on "stemness" in the context of TNBC, the role of combined inhibition of sex steroid production and AR, and the role of AR in regulation of the immune system. Although the exact role of AR in subsets of TNBC is still being characterized, new therapies that target AR and the production of androgens may provide additional options for patients with TNBC for whom chemotherapy is currently the sole treatment option.

Indexed as

Androgen Receptor AntagonistsAnimalsAntineoplastic AgentsCarcinogenesisClinical Trials as TopicFemaleGene Expression Regulation, NeoplasticGonadal Steroid HormonesHumansMolecular Targeted TherapyReceptors, AndrogenTriple Negative Breast NeoplasmsAndrogen Receptor AntagonistsAntineoplastic AgentsGonadal Steroid HormonesReceptors, Androgen

Identifiers

PMID29340907
PMCPMC5864529
OpenAlexW2783620485

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.