Evidence map›Paper›PMID 28596572›Full record

ArticleScientific reports2017

Inhibition of androgen receptor promotes CXC-chemokine receptor 7-mediated prostate cancer cell survival.

James J Hoy, Georgios Kallifatidis, Diandra K Smith, Bal L Lokeshwar

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  7. The power of heteronemin in cancers.Journal of biomedical science · 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

4 authors at 2 institutions in 1 country.

James J HoySheila and David Fuente Graduate Program in Cancer Biology, University of Miami-Miller School of Medicine, Miami, FL, USA.
Georgios KallifatidisGeorgia Cancer Center, Augusta University, Augusta, GA, USA.
Diandra K SmithGeorgia Cancer Center, Augusta University, Augusta, GA, USA.
Bal L LokeshwarGeorgia Cancer Center, Augusta University, Augusta, GA, USA. blokeshwar@augusta.edu.
Augusta University Health · USCharlie Norwood VA Medical Center · US

Funding

Chemoprevention of Prostate Cancer by Allspice Derived Polyphenol: EricifolinR01CA156776 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LOKESHWAR, BAL L · 2011 to 2016
$1.6M
Role of chemokine Receptor CXCR7 in prostate cancer progressionI01BX001517 · VA · MIAMI VA HEALTH CARE SYSTEM · PI LOKESHWAR, BAL L · 2012 to 2015
–
BLRD VA I01 BX001517NCI NIH HHS R01 CA156776
6 · The paper itself

Abstract

The atypical C-X-C chemokine receptor 7 (CXCR7) has been implicated in supporting aggressive cancer phenotypes in several cancers including prostate cancer. However, the mechanisms driving overexpression of this receptor in cancer are poorly understood. This study investigates the role of androgen receptor (AR) in regulating CXCR7. Androgen deprivation or AR inhibition significantly increased CXCR7 expression in androgen-responsive prostate cancer cell lines, which was accompanied by enhanced epidermal growth factor receptor (EGFR)-mediated mitogenic signaling, promoting tumor cell survival through an androgen-independent signaling program. Using multiple approaches we demonstrate that AR directly binds to the CXCR7 promoter, suppressing transcription. Clustered regularly interspaced short palindromic repeats (CRISPR) directed Cas9 nuclease-mediated gene editing of CXCR7 revealed that prostate cancer cells depend on CXCR7 for proliferation, survival and clonogenic potential. Loss of CXCR7 expression by CRISPR-Cas9 gene editing resulted in a halt of cell proliferation, severely impaired EGFR signaling and the onset of cellular senescence. Characterization of a mutated CXCR7-expressing LNCaP cell clone showed altered intracellular signaling and reduced spheroid formation potential. Our results demonstrate that CXCR7 is a potential target for adjuvant therapy in combination with androgen deprivation therapy (ADT) to prevent androgen-independent tumor cell survival.

Indexed as

Androgen Receptor AntagonistsCell Line, TumorCell ProliferationCell SurvivalHumansMaleProstatic NeoplasmsReceptors, AndrogenReceptors, CXCRACKR3 protein, humanAndrogen Receptor AntagonistsReceptors, AndrogenReceptors, CXCR

Identifiers

PMID28596572
PMCPMC5465216
OpenAlexW2621319673

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.