Evidence map›Paper›PMID 28507054›Full record

ArticleMolecular cancer research : MCR2017

Glutamine Transporters Are Targets of Multiple Oncogenic Signaling Pathways in Prostate Cancer.

Mark A White, Chenchu Lin, Kimal Rajapakshe, Jianrong Dong, Yan Shi, Efrosini Tsouko, Ratna Mukhopadhyay, Diana Jasso, Wajahat Dawood, Cristian Coarfa and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
2.9field-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

62 citing papers in PubMed, 95 citations in OpenAlex.

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2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Mark A WhiteCenter for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, Texas.
Chenchu LinCenter for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, Texas.
Kimal RajapaksheDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Jianrong DongDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Yan ShiCenter for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, Texas.
Efrosini TsoukoCenter for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, Texas.
Ratna MukhopadhyayCenter for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, Texas.
Diana JassoCenter for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, Texas.
Wajahat DawoodCenter for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, Texas.
Cristian CoarfaDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Daniel E FrigoCenter for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, Texas. frigo@uh.edu.
Baylor College of Medicine · US

Funding

Genetic & Metabolic Dissection of the CaMKKbeta Signaling Axis in Prostate CancerR01CA184208 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI FRIGO, DANIEL EDWARD · 2015 to 2019
$1.9M
Androgen Receptor- and Myc-Mediated Glutamine Metabolism in Prostate CancerR21CA191009 · NCI · UNIVERSITY OF HOUSTON · PI FRIGO, DANIEL EDWARD · 2015 to 2016
$372k
NCI NIH HHS R01 CA184208NCI NIH HHS R21 CA191009
6 · The paper itself

Abstract

Despite the known importance of androgen receptor (AR) signaling in prostate cancer, the processes downstream of AR that drive disease development and progression remain poorly understood. This knowledge gap has thus limited the ability to treat cancer. Here, it is demonstrated that androgens increase the metabolism of glutamine in prostate cancer cells. This metabolism was required for maximal cell growth under conditions of serum starvation. Mechanistically, AR signaling promoted glutamine metabolism by increasing the expression of the glutamine transporters

Indexed as

Amino Acid Transport System ASCCarcinogenesisCarrier ProteinsCell Line, TumorCell ProliferationDatasets as TopicGene Expression Regulation, NeoplasticGlutamineHumansMaleMechanistic Target of Rapamycin Complex 1Minor Histocompatibility AntigensProstatic NeoplasmsProto-Oncogene Proteins c-mycPTEN PhosphohydrolaseSignal TransductionAmino Acid Transport System ASCCarrier ProteinsGlutamineglutamine transport proteinsMechanistic Target of Rapamycin Complex 1Minor Histocompatibility AntigensMTOR protein, humanMYC protein, humanProto-Oncogene Proteins c-mycPTEN PhosphohydrolasePTEN protein, humanSLC1A4 protein, humanSLC1A5 protein, humanTCF20 protein, humanTOR Serine-Threonine KinasesTranscription Factors

Identifiers

PMID28507054
PMCPMC5685160
OpenAlexW2614594790

What OpenQuestion holds

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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.