Evidence map›Paper›PMID 21563192›Full record

ArticleThe Prostate2012

EMMPRIN regulates cytoskeleton reorganization and cell adhesion in prostate cancer.

Haining Zhu, Jun Zhao, Beibei Zhu, Joanne Collazo, Jozsef Gal, Ping Shi, Li Liu, Anna-Lena Ström, Xiaoning Lu, Richard O McCann and 2 more

Abstract read
In one paragraph

Article in The Prostate, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Arf6-driven endocytic recycling of CD147 determines HCC malignant phenotypes.Journal of experimental & clinical cancer research : CR · 2019
    Article
  5. Review
  6. Article
  7. EMMPRIN and ADAM12 in prostate cancer: preliminary results of a prospective study.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
  8. Prostate cancer relevant antigens and enzymes for targeted drug delivery.Journal of controlled release : official journal of the Controlled Release Society · 2014
    Review
  9. Article
  10. Article
  11. CCL2 disrupts the adherens junction: implications for neuroinflammation.Laboratory investigation; a journal of technical methods and pathology · 2012
    Article
  12. Article
  13. Article
  14. Article
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 1 institution in 1 country.

Haining ZhuDepartment of Molecular and Cellular Biochemistry, College of Medicine, University of Kentucky, Lexington, Kentucky, USA.
Jun Zhao
Beibei Zhu
Joanne Collazo
Jozsef Gal
Ping Shi
Li Liu
Anna-Lena Ström
Xiaoning Lu
Richard O McCann
Michal Toborek
Natasha Kyprianou
University of Kentucky · US

Funding

Vascular Mechanisms of PCB-Induced Brain MetastasesP42ES007380 · NIEHS · UNIVERSITY OF KENTUCKY · PI PENNELL, KELLY G · 1997 to 2024
$47.8M
UNDERSTANDING THE MOLECULAR BASIS OF EPIGENETIC TRANSCRIPTIONAL SILENCINGP20RR020171 · NCRR · UNIVERSITY OF KENTUCKY · PI RODGERS, DAVID W · 2004 to 2011
$16.5M
TGF-Beta Signaling Effectors in Prostate Growth Regulation/Tumor ProgressionR01DK083761 · NIDDK · UNIVERSITY OF KENTUCKY · PI KYPRIANOU, NATASHA · 2010 to 2013
$1.3M
Exercise-mediated protection against brain metastasesR01CA133257 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TOBOREK, MICHAL · 2010 to 2014
$1.2M
TGF BETA SIGNAL TRANSDUCTION IN PROSTATE CANCERR01DK053525 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI KYPRIANOU, NATASHA · 1997 to 2005
$843k
NCI NIH HHS R01CA133257NCRR NIH HHS 1P20RR020171NCRR NIH HHS P20 RR020171NIDDK NIH HHS R01 DK053525NIDDK NIH HHS R01DK053525NIDDK NIH HHS R01 DK083761NIEHS NIH HHS P42ES07380
6 · The paper itself

Abstract

backgroundProteins on cell surface play important roles during cancer progression and metastasis via their ability to mediate cell-to-cell interactions and navigate the communication between cells and the microenvironment.

methodsIn this study a targeted proteomic analysis was conducted to identify the differential expression of cell surface proteins in human benign (BPH-1) versus malignant (LNCaP and PC-3) prostate epithelial cells. We identified EMMPRIN (extracellular matrix metalloproteinase inducer) as a key candidate and shRNA functional approaches were subsequently applied to determine the role of EMMPRIN in prostate cancer cell adhesion, migration, invasion as well as cytoskeleton organization.

resultsEMMPRIN was found to be highly expressed on the surface of prostate cancer cells compared to BPH-1 cells, consistent with a correlation between elevated EMMPRIN and metastasis found in other tumors. No significant changes in cell proliferation, cell cycle progression, or apoptosis were detected in EMMPRIN knockdown cells compared to the scramble controls. Furthermore, EMMPRIN silencing markedly decreased the ability of PC-3 cells to form filopodia, a critical feature of invasive behavior, while it increased expression of cell-cell adhesion and gap junction proteins.

conclusionsOur results suggest that EMMPRIN regulates cell adhesion, invasion, and cytoskeleton reorganization in prostate cancer cells. This study identifies a new function for EMMPRIN as a contributor to prostate cancer cell-cell communication and cytoskeleton changes towards metastatic spread, and suggests its potential value as a marker of prostate cancer progression to metastasis.

Indexed as

AdenocarcinomaBasiginCell AdhesionCell Line, TumorCell MembraneCytoskeletonDisease ProgressionHumansMaleNeoplasm InvasivenessProstateProstatic NeoplasmsTumor Cells, CulturedBasigin

Identifiers

PMID21563192
PMCPMC3158271
OpenAlexW2068957073

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.