Evidence map›Paper›PMID 26573802›Full record

ArticleCancer research2015

miR-124 and Androgen Receptor Signaling Inhibitors Repress Prostate Cancer Growth by Downregulating Androgen Receptor Splice Variants, EZH2, and Src.

Xu-Bao Shi, Ai-Hong Ma, Lingru Xue, Meimei Li, Hao G Nguyen, Joy C Yang, Clifford G Tepper, Regina Gandour-Edwards, Christopher P Evans, Hsing-Jien Kung and 1 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04188275 (CIRCULATING MICRO-RNA), which is not on this map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.9field-weighted citation impact, top 9% 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.

NCT04188275 unknown statusnot on this mapstarted 2018, after this paper: background citation

CIRCULATING MICRO-RNA (miRNA) AND AR-V7 MUTATIONAL STATUS IN METASTATIC CASTRATION-RESISTANT PROSTATE CANCER (CRPC): PRIMERA+ STUDY (PROSTATE CANCER INNOVATING MARKERS OF EXPECTED RESPONSE TO AGONIST LHRH+ ANDROGEN RECEPTOR INHIBITION

TypeobservationalSponsorAzienda Ospedaliero-Universitaria CareggiRan2018 to 2022Enrolled46ConditionsD011471, D064129, D035683, D009360ArmsPeriodic ARV7 and miRNA evaluation
3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 71 citations in OpenAlex.

  1. Trial
  2. Review
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  8. The mFrontiers in immunology · 2023
    Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Androgen Receptor-Related Non-coding RNAs in Prostate Cancer.Frontiers in cell and developmental biology · 2021
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

11 authors at 2 institutions in 1 country.

Xu-Bao ShiDepartment of Urology, School of Medicine, University of California at Davis, Sacramento, California. ralph.devere-white@ucdmc.ucdavis.edu xbshi@ucdavis.edu.
Ai-Hong MaDepartment of Urology, School of Medicine, University of California at Davis, Sacramento, California.
Lingru XueDepartment of Urology, School of Medicine, University of California at Davis, Sacramento, California.
Meimei LiDepartment of Urology, School of Medicine, University of California at Davis, Sacramento, California.
Hao G NguyenDepartment of Urology, University of California, San Francisco, California.
Joy C YangDepartment of Urology, School of Medicine, University of California at Davis, Sacramento, California.
Clifford G TepperDepartment of Biochemistry and Molecular Medicine, School of Medicine, University of California at Davis, Sacramento, California. UC Davis Comprehensive Cancer Center, University of California at Davis, Sacramento, California.
Regina Gandour-EdwardsDepartment of Pathology, School of Medicine, University of California at Davis, Sacramento, California.
Christopher P EvansDepartment of Urology, School of Medicine, University of California at Davis, Sacramento, California. UC Davis Comprehensive Cancer Center, University of California at Davis, Sacramento, California.
Hsing-Jien KungDepartment of Biochemistry and Molecular Medicine, School of Medicine, University of California at Davis, Sacramento, California. UC Davis Comprehensive Cancer Center, University of California at Davis, Sacramento, California.
Ralph W deVere WhiteDepartment of Urology, School of Medicine, University of California at Davis, Sacramento, California. UC Davis Comprehensive Cancer Center, University of California at Davis, Sacramento, California. ralph.devere-white@ucdmc.ucdavis.edu xbshi@ucdavis.edu.
University of California, Davis · USUniversity of California, San Francisco · US

Funding

Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI Laura Marcu · 2002 to 2026
$84.9M
Tyrosine Kinases and Prostate CancerR01CA165263 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KUNG, HSING-JIEN · 2012 to 2016
$1.7M
Identification and characterization of the functional role of miRNA in prostate cR01CA136597 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DEVERE WHITE, RALPH W. · 2010 to 2013
$1.1M
NCI NIH HHS P30 CA093373NCI NIH HHS R01 CA136597NCI NIH HHS R01CA136597NCI NIH HHS R01 CA165263
6 · The paper itself

Abstract

miR-124 targets the androgen receptor (AR) transcript, acting as a tumor suppressor to broadly limit the growth of prostate cancer. In this study, we unraveled the mechanisms through which miR-124 acts in this setting. miR-124 inhibited proliferation of prostate cancer cells in vitro and sensitized them to inhibitors of androgen receptor signaling. Notably, miR-124 could restore the apoptotic response of cells resistant to enzalutamide, a drug approved for the treatment of castration-resistant prostate cancer. We used xenograft models to examine the effects of miR-124 in vivo when complexed with polyethylenimine-derived nanoparticles. Intravenous delivery of miR-124 was sufficient to inhibit tumor growth and to increase tumor cell apoptosis in combination with enzalutamide. Mechanistic investigations revealed that miR-124 directly downregulated AR splice variants AR-V4 and V7 along with EZH2 and Src, oncogenic targets that have been reported to contribute to prostate cancer progression and treatment resistance. Taken together, our results offer a preclinical rationale to evaluate miR-124 for cancer treatment.

Indexed as

AnimalsCell Line, TumorDown-RegulationEnhancer of Zeste Homolog 2 ProteinGene Expression Regulation, NeoplasticHumansMaleMiceMicroRNAsPolycomb Repressive Complex 2Prostatic NeoplasmsProtein IsoformsReceptors, AndrogenSignal Transductionsrc-Family KinasesXenograft Model Antitumor AssaysEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanMicroRNAsMIRN124 microRNA, humanPolycomb Repressive Complex 2Protein IsoformsReceptors, Androgensrc-Family Kinases

Identifiers

PMID26573802
PMCPMC4681619
OpenAlexW2177175549

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.