Evidence map›Paper›PMID 20663859›Full record

ArticleMolecular cancer research : MCR2010

Epigenetic upregulation of urokinase plasminogen activator promotes the tropism of mesenchymal stem cells for tumor cells.

Sai Murali Krishna Pulukuri, Bharathi Gorantla, Venkata Ramesh Dasari, Christopher S Gondi, Jasti S Rao

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

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  17. Mesenchymal stem cells in the pathogenesis and therapy of breast cancer.Journal of mammary gland biology and neoplasia · 2010
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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

5 authors at 2 institutions in 1 country.

Sai Murali Krishna PulukuriDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria, IL 61605, USA.
Bharathi Gorantla
Venkata Ramesh Dasari
Christopher S Gondi
Jasti S Rao
Illinois College · USUniversity of Illinois Urbana-Champaign · US

Funding

Cath B and uPAR si RNA constructs regressed glioma growthR01CA116708 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI O'BRYAN, JOHN P · 2005 to 2014
$2.9M
Role of uPA and uPAR in Human Glioma InvasivenessR01CA075557 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI RAO, JASTI S. · 1998 to 2009
$2.3M
Inhibition of matrix proteases to sensitize medulloblastoma cells to radiationR01CA138409 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GARTEL, ANDREI L · 2009 to 2013
$1.6M
NCI NIH HHS CA116708NCI NIH HHS CA138409NCI NIH HHS CA75557NCI NIH HHS R01 CA075557NCI NIH HHS R01 CA116708NCI NIH HHS R01 CA138409
6 · The paper itself

Abstract

A major obstacle for the effective treatment of cancer is the invasive capacity of the tumor cells. Previous studies have shown the capability of mesenchymal stem cells (MSC) to target these disseminated tumor cells and to serve as therapeutic delivery vehicles. However, the molecular mechanisms that would enhance the migration of MSCs toward tumor areas are not well understood. In particular, very little is known about the role that epigenetic mechanisms play in cell migration and tropism of MSCs. In this study, we investigated whether histone deacetylation was involved in the repression of urokinase plasminogen activator (uPA) expression in MSCs derived from umbilical cord blood (CB) and bone marrow (BM). Induction of uPA expression by histone deacetylase inhibitors trichostatin A and sodium butyrate was observed in CB- and BM-derived MSCs examined. In vitro migration assays showed that induction of uPA expression by histone deacetylase inhibitors in CB- and BM-derived MSCs significantly enhanced tumor tropism of these cells. Furthermore, overexpression of uPA in CB-MSCs induced migration capacity toward human cancer cells in vitro. In addition, our results showed that uPA-uPAR knockdown in PC3 prostate cancer cells significantly inhibited tumor-specific migration of uPA-overexpressing MSCs. These results have significant implications for the development of MSC-mediated, tumor-selective gene therapies.

Indexed as

Epigenesis, GeneticAcetylationBlotting, WesternBreast NeoplasmsCell LineCell MovementChromatin ImmunoprecipitationFemaleFluorescent Antibody TechniqueHistone Deacetylase InhibitorsHistonesHumansKidneyMaleMesenchymal Stem CellsPromoter Regions, GeneticHistone Deacetylase InhibitorsHistonesRNA, MessengerRNA, Small InterferingUrokinase-Type Plasminogen Activator

Identifiers

PMID20663859
PMCPMC2923682
OpenAlexW2171791800

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.