Evidence map›Paper›PMID 20162608›Full record

ArticleInternational journal of cancer2010

Overlapping and distinct role of CXCR7-SDF-1/ITAC and CXCR4-SDF-1 axes in regulating metastatic behavior of human rhabdomyosarcomas.

Katarzyna Grymula, Maciej Tarnowski, Marcin Wysoczynski, Justyna Drukala, Frederic G Barr, Janina Ratajczak, Magdalena Kucia, Mariusz Z Ratajczak

Expression of concernOpen access · bronzeAbstract read
In one paragraph

Article in International journal of cancer, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It carries an expression of concern. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. CXCL12-CXCR4/CXCR7 Axis in Cancer: from Mechanisms to Clinical Applications.International journal of biological sciences · 2023
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Katarzyna GrymulaStem Cell Institute at James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
Maciej Tarnowski
Marcin Wysoczynski
Justyna Drukala
Frederic G Barr
Janina Ratajczak
Magdalena Kucia
Mariusz Z Ratajczak
James Graham Brown Foundation · USUniversity of Louisville · USJagiellonian University · PLUniversity of Pennsylvania · US

Funding

PROJ 12: STEM CELL-BASED VACCINE FOR CANCER PROPHYLAXISP20RR018733 · NCRR · UNIVERSITY OF LOUISVILLE · PI TRENT, JOHN O · 2003 to 2011
$18.9M
Novel mechanisms involving complement cascade in stem cell traffickingR01DK074720 · NIDDK · UNIVERSITY OF LOUISVILLE · PI RATAJCZAK, MARIUSZ Z · 2007 to 2020
$4.1M
T(2--13) OF ALVEOLAR RHABDOMYOSARCOMAR01CA064202 · NCI · UNIVERSITY OF PENNSYLVANIA · PI BARR, FREDERIC G · 1994 to 2007
$3.1M
COG studies of gene amplification in rhabdomyosarcomaR01CA104896 · NCI · UNIVERSITY OF PENNSYLVANIA · PI BARR, FREDERIC G · 2005 to 2009
$1.8M
The CXCR4-SDF-1 Axis in Metastatic RhabdomyosarcomaR01CA106281 · NCI · UNIVERSITY OF LOUISVILLE · PI RATAJCZAK, MARIUSZ Z · 2005 to 2009
$1.3M
NCI NIH HHS R01 CA064202NCI NIH HHS R01 CA104896NCI NIH HHS R01 CA106281NCI NIH HHS R01 CA64202NCRR NIH HHS P20 RR018733NCRR NIH HHS P20RR018733NIDDK NIH HHS R01 DK074720
6 · The paper itself

Abstract

We have demonstrated that the α-chemokine stromal-derived factor (SDF)-1-CXCR4 axis plays an important role in rhabdomyosarcoma (RMS) metastasis. With the recent description of CXCR7, a new receptor for SDF-1 that also binds the interferon-inducible T-cell α chemoattractant (ITAC) chemokine, we became interested in the role of the CXCR7-SDF-1/ITAC axis in RMS progression. To address this issue, we evaluated 6 highly metastatic alveolar (A)RMS and 3 less metastatic embryonal (E)RMS cell lines and found that all these cell lines express CXCR7. Although CXCR4 was expressed at a much higher level by highly metastatic ARMS lines, CXCR7 was present at a high level on ERMS lines. We also noticed that CXCR7 expression on RMS cells was downregulated in hypoxic conditions. More importantly, the CXCR7 receptor on RMS cell lines was functional after stimulation with ITAC and SDF-1 as evidenced by mitogen-activated protein kinase (MAPK)p42/44 and AKT phosphorylation as well as CXCR7 internalization, chemotaxis, cell motility and adhesion assays. Similarly to CXCR4, signaling from activated CXCR7 was not associated with increased RMS proliferation or cell survival. Moreover, CXCR7(+) RMS cells responded to SDF-1 and I-TAC in the presence of CXCR4 antagonists (T140, AMD3100). Furthermore, while intravenous injection of RMS cells with overexpressed CXCR7 resulted in increased seeding efficiency of tumor cells to bone marrow, CXCR7 downregulation showed the opposite effect. In conclusion, the CXCR7-SDF-1/ITAC axis is involved in the progression of RMS; targeting of the CXCR4-SDF-1 axis alone without simultaneous blockage of CXCR7 will be an inefficient strategy for inhibiting SDF-1-mediated prometastatic responses of RMS cells.

Indexed as

AnimalsBenzylaminesCell AdhesionCell Growth ProcessesCell Line, TumorCell MovementChemokine CXCL11Chemokine CXCL12CyclamsDown-RegulationEndothelial CellsFibronectinsHeterocyclic CompoundsHumansMatrix MetalloproteinasesMiceACKR3 protein, humanBenzylaminesChemokine CXCL11Chemokine CXCL12CXCL11 protein, humanCXCL12 protein, humanCXCR4 protein, humanCyclamsFibronectinsHeterocyclic CompoundsMatrix MetalloproteinasesOligopeptidesPertussis ToxinplerixaforReceptors, CXCRReceptors, CXCR4T140 peptideTissue Inhibitor of Metalloproteinases

Identifiers

PMID20162608
PMCPMC2907445
OpenAlexW2059053280

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.