Evidence map›Paper›PMID 32207043›Full record

ReviewCellular oncology (Dordrecht, Netherlands)2020

CXCL-10: a new candidate for melanoma therapy?

Hossein Bagheri, Mohammad Hossein Pourhanifeh, Maryam Derakhshan, Maryam Mahjoubin-Tehran, Faezeh Ghasemi, Shabnam Mousavi, Rouhollah Rafiei, Kazem Abbaszadeh-Goudarzi, Hamid Reza Mirzaei, Hamed Mirzaei

Abstract readReview
In one paragraph

Review in Cellular oncology (Dordrecht, Netherlands), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

38 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
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  7. Therapeutic Significance of NLRP3 Inflammasome in Cancer: Friend or Foe?International journal of molecular sciences · 2024
    Review
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  20. Targeting CXCL9/10/11-CXCR3 axis: an important component of tumor-promoting and antitumor immunity.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    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

10 authors at 9 institutions in 1 country.

Hossein BagheriDepartment of Biotechnology, Faculty of Medicine, Arak University of Medical Sciences, Arak, Iran.
Mohammad Hossein PourhanifehHalal Research Center of IRI, FDA, Tehran, Iran.
Maryam DerakhshanDepartment of Pathology, Isfahan University of Medical Sciences, Isfahan, Iran.
Maryam Mahjoubin-TehranStudent Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran.
Faezeh GhasemiBlood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.
Shabnam MousaviDepartment of Chemical Engineering, Islamic Azad University, Science and Research Branch, Tehran, Iran.
Rouhollah RafieiDepartment of Chemical Engineering, Islamic Azad University, Science and Research Branch, Tehran, Iran.
Kazem Abbaszadeh-GoudarziCellular and Molecular Research Center, Department of Biochemistry and Nutrition, Sabzevar University of Medical Sciences, Sabzevar, Iran.
Hamid Reza MirzaeiDepartment of Medical Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. h-mirzaei@tums.ac.ir.
Hamed MirzaeiResearch Center for Biochemistry and Nutrition in Metabolic Diseases, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, I.R., Iran. h.mirzaei2002@gmail.com.
Islamic Azad University, Science and Research Branch · IRArak University of Medical Sciences · IRHigh Institute for Education and Research in Transfusion Medicine · IRIsfahan University of Medical Sciences · IRKashan University of Medical Sciences · IRMashhad University of Medical Sciences · IRNiroo Research Institute · IRSabzevar University of Medical Sciences · IRTehran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMelanoma is a malignancy that stems from melanocytes and is defined as the most dangerous skin malignancy in terms of metastasis and mortality rates. CXC motif chemokine 10 (CXCL10), also known as interferon gamma-induced protein-10 (IP-10), is a small cytokine-like protein secreted by a wide variety of cell types. CXCL10 is a ligand of the CXC chemokine receptor-3 (CXCR3) and is predominantly expressed by T helper cells (Th cells), cytotoxic T lymphocytes (CTLs), dendritic cells, macrophages, natural killer cells (NKs), as well as some epithelial and cancer cells. Similar to other chemokines, CXCL10 plays a role in immunomodulation, inflammation, hematopoiesis, chemotaxis and leukocyte trafficking.

conclusionsRecent studies indicate that the CXCL10/CXCR3 axis may act as a double-edged sword in terms of pro- and anti-cancer activities in a variety of tissues and cells, especially in melanoma cells and their microenvironments. Most of these activities arise from the CXCR3 splice variants CXCR3-A, CXCR3-B and CXCR3-Alt. In this review, we discuss the pro- and anti-cancer properties of CXCL10 in various types of tissues and cells, particularly melanoma cells, including its potential as a therapeutic target.

Indexed as

Antineoplastic AgentsCarcinogenesisChemokine CXCL10HumansMelanomaModels, BiologicalReceptors, CXCR3Antineoplastic AgentsChemokine CXCL10Receptors, CXCR3Cancer therapyChemokineCXCL10CXCR3ImmunomodulationMelanoma

Identifiers

PMID32207043
PMCPMC12990686
OpenAlexW3012894904

What OpenQuestion holds

Textmetadata
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.