Evidence map›Paper›PMID 27213581›Full record

ArticleOncotarget2016

ARF1 promotes prostate tumorigenesis via targeting oncogenic MAPK signaling.

Jason E Davis, Xiayang Xie, Jianhui Guo, Wei Huang, Wen-Ming Chu, Shuang Huang, Yong Teng, Guangyu Wu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
3.1field-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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Jason E DavisDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, USA.
Xiayang XieCancer Center, Augusta University, Augusta, GA, USA.
Jianhui GuoDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, USA.
Wei HuangDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, USA.
Wen-Ming ChuCancer Biology Program, University of Hawaii Cancer Center, Honolulu, HI, USA.
Shuang HuangCancer Center, Augusta University, Augusta, GA, USA.
Yong TengCancer Center, Augusta University, Augusta, GA, USA.
Guangyu WuDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, USA.
Augusta University · USAugusta University Health · USUniversity of Hawaii System · US

Funding

ER-to-Golgi traffic and signal regulation of GPCRsR01GM076167 · NIGMS · LSU HEALTH SCIENCES CENTER · PI WU, GUANGYU · 2006 to 2013
$2.2M
NIGMS NIH HHS R01 GM076167
6 · The paper itself

Abstract

ADP-ribosylation factor 1 (ARF1) is a crucial regulator in vesicle-mediated membrane trafficking and involved in the activation of signaling molecules. However, virtually nothing is known about its function in prostate cancer. Here we have demonstrated that ARF1 expression is significantly elevated in prostate cancer cells and human tissues and that the expression levels of ARF1 correlate with the activation of mitogen-activated protein kinases (MAPK) ERK1/2. Furthermore, we have shown that overexpression and knockdown of ARF1 produce opposing effects on prostate cancer cell proliferation, anchorage-independent growth and tumor growth in mouse xenograft models and that ARF1-mediated cell proliferation can be abolished by the Raf1 inhibitor GW5074 and the MEK inhibitors U0126 and PD98059. Moreover, inhibition of ARF1 activation achieved by mutating Thr48 abolishes ARF1's abilities to activate the ERK1/2 and to promote cell proliferation. These data demonstrate that the aberrant MAPK signaling in prostate cancer is, at least in part, under the control of ARF1 and that, similar to Ras, ARF1 is a critical regulator in prostate cancer progression. These data also suggest that ARF1 may represent a key molecular target for prostate cancer therapeutics and diagnosis.

Indexed as

Gene Expression Regulation, NeoplasticMAP Kinase Signaling SystemADP-Ribosylation Factor 1AnimalsButadienesCarcinogenesisCell Line, TumorCell ProliferationDisease ProgressionFlavonoidsHumansMaleMAP Kinase Kinase 4MiceMice, SCIDMutation2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-oneADP-Ribosylation Factor 1ButadienesFlavonoidsMAP Kinase Kinase 4Nitrilesp38 Mitogen-Activated Protein KinasesU 0126ARF1cell growthprostate cancerRaf1/MEK/ERK1/2tumorigenesis

Identifiers

PMID27213581
PMCPMC5129974
OpenAlexW2403791073

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.