Evidence map›Paper›PMID 28468774›Full record

ArticleMolecular cancer therapeutics2017

Synergy between Androgen Receptor Antagonism and Inhibition of mTOR and HER2 in Breast Cancer.

Michael A Gordon, Nicholas C D'Amato, Haihua Gu, Beatrice Babbs, Julia Wulfkuhle, Emanuel F Petricoin, Isela Gallagher, Ting Dong, Kathleen Torkko, Bolin Liu and 2 more

Open access · bronzeAbstract 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. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 59 citations in OpenAlex.

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  15. Modulating the Activity of Androgen Receptor for Treating Breast Cancer.International journal of molecular sciences · 2022
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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

12 authors at 3 institutions in 2 countries.

Michael A GordonDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Nicholas C D'AmatoDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Haihua GuDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Beatrice BabbsDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Julia WulfkuhleCenter for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, Virginia.
Emanuel F PetricoinCenter for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, Virginia.
Isela GallagherCenter for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, Virginia.
Ting DongCenter for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, Virginia.
Kathleen TorkkoDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Bolin LiuDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Anthony EliasDivision of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Jennifer K RicherDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado. jennifer.richer@ucdenver.edu.
University of Colorado Anschutz Medical Campus · USGeorge Mason University · USWenzhou Medical University · CN

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
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 P30 CA046934NCI NIH HHS R01 CA187733
6 · The paper itself

Abstract

The androgen receptor (AR) is widely expressed in breast cancer, and evidence suggests dependence on AR signaling for growth and survival. AR antagonists such as enzalutamide and seviteronel have shown success in preclinical models and clinical trials of prostate cancer and are currently being evaluated in breast cancer. Reciprocal regulation between AR and the HER2/PI3K/mTOR pathway may contribute to resistance to HER2- and mTOR-targeted therapies; thus, dual inhibition of these pathways may synergistically inhibit breast cancer growth. HER2

Indexed as

Androgen Receptor AntagonistsAnimalsAntineoplastic Combined Chemotherapy ProtocolsApoptosisCell Line, TumorCell ProliferationDrug Resistance, NeoplasmErb-b2 Receptor Tyrosine KinasesEverolimusFemaleHumansMiceReceptors, AndrogenTOR Serine-Threonine KinasesTrastuzumabTriple Negative Breast NeoplasmsAndrogen Receptor AntagonistsAR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesEverolimusMTOR protein, humanReceptors, AndrogenTOR Serine-Threonine KinasesTrastuzumab

Identifiers

PMID28468774
PMCPMC5517319
OpenAlexW2610242496

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.