Evidence map›Paper›PMID 25963887›Full record

ReviewCancer letters2015

Conditioning solid tumor microenvironment through inflammatory chemokines and S100 family proteins.

Mohd W Nasser, Mohamad Elbaz, Dinesh K Ahirwar, Ramesh K Ganju

Open access · greenAbstract readReview
In one paragraph

Review in Cancer letters, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Review
  7. Current approaches in glioblastoma multiforme immunotherapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. AllergoOncology: Role of immune cells and immune proteins.Clinical and translational allergy · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
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

4 authors at 1 institution in 1 country.

Mohd W NasserDepartment of Pathology, Comprehensive Cancer Center, The Ohio State Medical Center, Columbus, OH, USA. Electronic address: mohd.nasser@osumc.edu.
Mohamad ElbazDepartment of Pathology, Comprehensive Cancer Center, The Ohio State Medical Center, Columbus, OH, USA.
Dinesh K AhirwarDepartment of Pathology, Comprehensive Cancer Center, The Ohio State Medical Center, Columbus, OH, USA.
Ramesh K GanjuDepartment of Pathology, Comprehensive Cancer Center, The Ohio State Medical Center, Columbus, OH, USA.
The Ohio State University · US

Funding

Role of Slit in CXCR4-Mediated Breast Cancer MetastasisR01CA109527 · NCI · OHIO STATE UNIVERSITY · PI GANJU, RAMESH K. · 2005 to 2019
$2.6M
Role of S100A7 in breast cancer progression and metastasisR01CA153490 · NCI · OHIO STATE UNIVERSITY · PI GANJU, RAMESH K. · 2011 to 2014
$1.2M
Synthetic cannabinoids as novel therapeutic strategies against non-small cell lunR21CA163010 · NCI · OHIO STATE UNIVERSITY · PI GANJU, RAMESH K. · 2011 to 2012
$365k
NCI NIH HHS CA153490NCI NIH HHS CA163010NCI NIH HHS R01 CA109527NCI NIH HHS R01 CA153490NCI NIH HHS R21 CA163010
6 · The paper itself

Abstract

Recently, there has been growing attention to the role of the tumor microenvironment (TME) in cancer growth, metastasis and emergence of chemotherapy resistance. Stromal and tumor cells make up the TME and interact with each other through a complex cross-talk manner. This interaction is facilitated by a variety of growth factors, cytokines, chemokines and S100 proteins. In this review, we focus on chemokines and their cognate receptors in regulating the tumorigenic process. Chemokines are cytokines that have chemotactic potential. Chemokine receptors are expressed on tumor cells and stromal cells. Chemokines and their cognate receptors modulate tumor growth and metastasis in a paracrine and autocrine manner. They play a major role in the modulation of stromal cell recruitment, angiogenic potential, cancer cell proliferation, survival, adhesion, invasion and metastasis to distant sites. In addition, a new class of calcium binding family S100 proteins has been getting attention as they play significant roles in tumor progression and metastasis by modulating TME. Here, we highlight recent developments regarding the inflammatory chemokine/S100 protein systems in the TME. We also focus on how chemokines/S100 proteins, through their role in the TME, modulate cancer cell ability to grow, proliferate, invade and metastasize to different organs. This review highlights the possibility of using the chemokine/chemokine receptor axis as a promising strategy in cancer therapy, the current difficulties in achieving this goal, and how it could be overcome for successful future therapeutic intervention.

Indexed as

Tumor MicroenvironmentAnimalsAnti-Inflammatory AgentsAntineoplastic AgentsChemokinesHumansInflammation MediatorsMolecular Targeted TherapyNeoplasmsReceptors, ChemokineS100 ProteinsSignal TransductionAnti-Inflammatory AgentsAntineoplastic AgentsChemokinesInflammation MediatorsReceptors, ChemokineS100 ProteinsChemokinesS100 proteinsTumor microenvironment

Identifiers

PMID25963887
PMCPMC11707611
OpenAlexW2114217747

What OpenQuestion holds

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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.