Evidence map›Paper›PMID 25287686›Full record

ReviewAdvances in cancer research2014

The intricate role of CXCR4 in cancer.

Samit Chatterjee, Babak Behnam Azad, Sridhar Nimmagadda

Abstract readReview
In one paragraph

Review in Advances in cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 382 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
382citing papers in PubMed, 2 pooled it
83.8field-weighted citation impact, top 1% 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

382 citing papers in PubMed, 2 syntheses or guidelines pooled it, 660 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Exploration of Chemokine Receptor 4 Targeted [Molecular imaging and biology · 2026
    Article
  5. Article
  6. Article
  7. Mechanisms of breast cancer dormancy in bone metastasis.Clinical & experimental metastasis · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. [Cancer imaging : the official publication of the International Cancer Imaging Society · 2026
    Article
  14. Review
  15. Anti-myeloma activity of the CXCR4 antagonist WZ811.Journal of molecular medicine (Berlin, Germany) · 2026
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

322 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Samit ChatterjeeRussell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University, Baltimore, Maryland, USA.
Babak Behnam AzadRussell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University, Baltimore, Maryland, USA.
Sridhar NimmagaddaRussell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University, Baltimore, Maryland, USA. Electronic address: snimmag1@jhmi.edu.
Johns Hopkins University · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI ALAN KEITH MEEKER · 1985 to 2026
$208.6M
Imaging and targeting metastatic diseaseR01CA166131 · NCI · JOHNS HOPKINS UNIVERSITY · PI NIMMAGADDA, SRIDHAR · 2012 to 2016
$1.6M
NCI NIH HHS P30 CA006973NCI NIH HHS R01 CA166131NCI NIH HHS R01CA166131
6 · The paper itself

Abstract

Chemokines mediate numerous physiological and pathological processes related primarily to cell homing and migration. The chemokine CXCL12, also known as stromal cell-derived factor-1, binds the G-protein-coupled receptor CXCR4, which, through multiple divergent pathways, leads to chemotaxis, enhanced intracellular calcium, cell adhesion, survival, proliferation, and gene transcription. CXCR4, initially discovered for its involvement in HIV entry and leukocytes trafficking, is overexpressed in more than 23 human cancers. Cancer cell CXCR4 overexpression contributes to tumor growth, invasion, angiogenesis, metastasis, relapse, and therapeutic resistance. CXCR4 antagonism has been shown to disrupt tumor-stromal interactions, sensitize cancer cells to cytotoxic drugs, and reduce tumor growth and metastatic burden. As such, CXCR4 is a target not only for therapeutic intervention but also for noninvasive monitoring of disease progression and therapeutic guidance. This review provides a comprehensive overview of the biological involvement of CXCR4 in human cancers, the current status of CXCR4-based therapeutic approaches, as well as recent advances in noninvasive imaging of CXCR4 expression.

Indexed as

Antibodies, MonoclonalAnimalsGene Expression Regulation, NeoplasticHumansMolecular ImagingNeoplasmsReceptors, CXCR4Antibodies, MonoclonalReceptors, CXCR4Cancer therapyChemokine receptorChemotaxisCXCL12CXCR4 inhibitorCXCR4 tracersMetastasisMolecular imagingPET–CTTherapeutic intervention

Identifiers

PMID25287686
PMCPMC4322894
OpenAlexW1438161774

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.