Evidence map›Paper›PMID 29907594›Full record

ArticleMolecular cancer therapeutics2018

Repositioning Dopamine D2 Receptor Agonist Bromocriptine to Enhance Docetaxel Chemotherapy and Treat Bone Metastatic Prostate Cancer.

Yang Yang, Kenza Mamouni, Xin Li, Yanhua Chen, Sravan Kavuri, Yuhong Du, Haian Fu, Omer Kucuk, Daqing Wu

Abstract read
In one paragraph

Article in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

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  11. Targeting treatment options for castration-resistant prostate cancer.American journal of clinical and experimental urology · 2021
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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

9 authors at 2 institutions in 3 countries.

Yang YangDepartment of Otorhinolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Kenza MamouniMolecular Oncology and Biomarkers Program, Georgia Cancer Center, Augusta, Georgia.
Xin LiMolecular Oncology and Biomarkers Program, Georgia Cancer Center, Augusta, Georgia.
Yanhua ChenMolecular Oncology and Biomarkers Program, Georgia Cancer Center, Augusta, Georgia.
Sravan KavuriDepartment of Pathology, Medical College of Georgia, Augusta University, Augusta, Georgia.
Yuhong DuDepartment of Pharmacology and Emory Chemical Biology Discovery Center, Emory University School of Medicine, Atlanta, Georgia.
Haian FuDepartment of Pharmacology and Emory Chemical Biology Discovery Center, Emory University School of Medicine, Atlanta, Georgia.
Omer KucukDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia.
Daqing WuMolecular Oncology and Biomarkers Program, Georgia Cancer Center, Augusta, Georgia. dwu@augusta.edu.
Augusta University · USEmory University · US

Funding

Targeting chemoresistant prostate cancer with novel EED inhibitorsR01CA256058 · NCI · CLARK ATLANTA UNIVERSITY · PI DAQING WU · 2022 to 2026
$2.1M
Novel small-molecule targeted therapy for prostate cancerR41CA206725 · NCI · METCURE THERAPEUTICS, LLC · PI WU, DAQING · 2016 to 2016
$225k
Small-molecule therapy for metastatic prostate cancerR41CA217491 · NCI · METCURE THERAPEUTICS, LLC · PI WU, DAQING · 2017 to 2017
$225k
A Dietary Supplement As Adjunct Therapy In Castration-Resistant Prostate CancerR41CA186498 · NCI · METCURE THERAPEUTICS, LLC · PI WU, DAQING · 2015 to 2015
$161k
NCI NIH HHS R01 CA256058NCI NIH HHS R41 CA186498NCI NIH HHS R41 CA206725NCI NIH HHS R41 CA217491
6 · The paper itself

Abstract

Docetaxel resistance remains a major obstacle in the treatment of prostate cancer bone metastasis. In this study, we demonstrate that the dopamine D2 receptor (DRD2) agonist bromocriptine effectively enhances docetaxel efficacy and suppresses skeletal growth of prostate cancer in preclinical models. DRD2 is ubiquitously expressed in prostate cancer cell lines and significantly reduced in prostate cancer tissues with high Gleason score. Bromocriptine has weak to moderate cytotoxicity in prostate cancer cells, but effectively induces cell-cycle arrest. At the molecular level, bromocriptine inhibits the expression of c-Myc, E2F-1, and survivin and increases the expression of p53, p21, and p27. Intriguingly, bromocriptine markedly reduces androgen receptor levels, partially through Hsp90-mediated protein degradation. The combination of bromocriptine and docetaxel demonstrates enhanced

Indexed as

Drug RepositioningXenograft Model Antitumor AssaysAnimalsAntineoplastic Combined Chemotherapy ProtocolsBone NeoplasmsBromocriptineCell Cycle CheckpointsCell Line, TumorCell SurvivalDocetaxelDopamine AgonistsDrug SynergismHumansMaleMice, NudeProstatic NeoplasmsBromocriptineDocetaxelDopamine AgonistsReceptors, Dopamine D2

Identifiers

PMID29907594
PMCPMC6125160
OpenAlexW2807716198

What OpenQuestion holds

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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.