Evidence map›Paper›PMID 28428441›Full record

ArticleMolecular cancer therapeutics2017

Selective Glucocorticoid Receptor Modulators (SGRMs) Delay Castrate-Resistant Prostate Cancer Growth.

Jacob Kach, Tiha M Long, Phillip Selman, Eva Y Tonsing-Carter, Maria A Bacalao, Ricardo R Lastra, Larischa de Wet, Shane Comiskey, Marc Gillard, Calvin VanOpstall and 5 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03863145 (Open Label, Multicenter, Phase 1 Study to Evaluate the Maximum Tolerated Dose of Orally Administered CB-03-10 With Dose Expansion Phase, in Subjects With Advanced Solid Tumors), which is not on this map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.3field-weighted citation impact, top 4% 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.

NCT03863145 early_phase1unknown statusnot on this mapstarted 2022, after this paper: background citation

Open Label, Multicenter, Phase 1 Study to Evaluate the Maximum Tolerated Dose of Orally Administered CB-03-10 With Dose Expansion Phase, in Subjects With Advanced Solid Tumors

TypeinterventionalSponsorCosmo Technologies LtdRan2022 to 2026Enrolled90ConditionsAdvanced Refractory Solid Tumors, Subjects Considered Likely to Respond to CB-03-10ArmsCB-03-10
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 50 citations in OpenAlex.

  1. Phase I/II Trial of Enzalutamide and Mifepristone, a Glucocorticoid Receptor Antagonist, for Metastatic Castration-Resistant Prostate Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Trial
  2. Article
  3. Article
  4. Review
  5. The Bidirectional Interaction Between NF-Journal of immunology research · 2025
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Reciprocal and Autonomous Glucocorticoid and Androgen Receptor Activation in Salivary Duct Carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
  19. Article
  20. Review
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

15 authors at 1 institution in 1 country.

Jacob KachDepartment of Medicine, The University of Chicago, Chicago, Illinois.
Tiha M LongDepartment of Medicine, The University of Chicago, Chicago, Illinois.
Phillip SelmanDepartment of Medicine, The University of Chicago, Chicago, Illinois.
Eva Y Tonsing-CarterDepartment of Medicine, The University of Chicago, Chicago, Illinois.
Maria A BacalaoDepartment of Medicine, The University of Chicago, Chicago, Illinois.
Ricardo R LastraDepartment of Anatomical Pathology, The University of Chicago, Chicago, Illinois.
Larischa de WetDepartment of Surgery, The University of Chicago, Chicago, Illinois.
Shane ComiskeyDepartment of Medicine, The University of Chicago, Chicago, Illinois.
Marc GillardDepartment of Surgery, The University of Chicago, Chicago, Illinois.
Calvin VanOpstallDepartment of Surgery, The University of Chicago, Chicago, Illinois.
Diana C WestDepartment of Medicine, The University of Chicago, Chicago, Illinois.
Wen-Ching ChanCenter for Research Informatics, The University of Chicago, Chicago, Illinois.
Donald Vander GriendDepartment of Surgery, The University of Chicago, Chicago, Illinois.
Suzanne D ConzenDepartment of Medicine, The University of Chicago, Chicago, Illinois.
Russell Z SzmulewitzDepartment of Medicine, The University of Chicago, Chicago, Illinois. rszmulew@medicine.bsd.uchicago.edu.
University of Chicago · US

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI MARK W. LINGEN · 1985 to 2026
$122.1M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Targeting FOXA1-downstream pathways: a novel therapeutic strategy for castration-resistant prostate cancerP50CA180995 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A., HUSSAIN, MAHA H · 2015 to 2025
$19.9M
Multi-Disciplinary Training Grant in Cancer ResearchT32CA009594 · NCI · UNIVERSITY OF CHICAGO · PI KAY F MACLEOD, Scott A. Oakes · 1989 to 2026
$11.5M
Glucocorticoid receptor-mediated survival signaling in breast cancerR01CA089208 · NCI · UNIVERSITY OF CHICAGO · PI CONZEN, SUZANNE DANIELA · 2002 to 2016
$3.0M
NCATS NIH HHS UL1 TR000430NCI NIH HHS P30 CA014599NCI NIH HHS P50 CA180995NCI NIH HHS R01 CA089208NCI NIH HHS T32 CA009594
6 · The paper itself

Abstract

Increased glucocorticoid receptor (GR) expression and activity following androgen blockade can contribute to castration-resistant prostate cancer (CRPC) progression. Therefore, we hypothesized that GR antagonism will have therapeutic benefit in CRPC. However, the FDA-approved nonselective, steroidal GR antagonist, mifepristone, lacks GR specificity, reducing its therapeutic potential. Here, we report that two novel nonsteroidal and highly selective GR modulators (SGRM), CORT118335 and CORT108297, have the ability to block GR activity in prostate cancer and slow CRPC progression. In contrast to mifepristone, these novel SGRMs did not affect androgen receptor (AR) signaling, but potently inhibited GR transcriptional activity. Importantly, SGRMs decreased GR-mediated tumor cell viability following AR blockade.

Indexed as

AnimalsBenzamidesCell Line, TumorCell ProliferationCell SurvivalGene Expression Regulation, NeoplasticHumansMaleMice, NudeNitrilesPhenylthiohydantoinProstatic Neoplasms, Castration-ResistantReceptors, AndrogenReceptors, GlucocorticoidSignal TransductionSmall Molecule LibrariesBenzamidesenzalutamideNitrilesPhenylthiohydantoinReceptors, AndrogenReceptors, GlucocorticoidSmall Molecule Libraries

Identifiers

PMID28428441
PMCPMC5544558
OpenAlexW2605930901

What OpenQuestion holds

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Registered trials

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.