Evidence map›Paper›PMID 27771887›Full record

ReviewPathology oncology research : POR2017

Macrophage Migration Inhibitory Factor (MIF): Biological Activities and Relation with Cancer.

Camila Cristina Guimarães Nobre, Josélio Maria Galvão de Araújo, Thales Allyrio Araújo de Medeiros Fernandes, Ricardo Ney Oliveira Cobucci, Daniel Carlos Ferreira Lanza, Vânia Sousa Andrade, José Veríssimo Fernandes

Abstract readReview
PubMed Publisher
In one paragraph

Review in Pathology oncology research : POR, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

93 citing papers in PubMed, 162 citations in OpenAlex.

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33 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

7 authors at 3 institutions in 1 country.

Camila Cristina Guimarães NobrePostgraduate Program in Parasite Biology, Department of Microbiology and Parasitology, Federal University of Rio Grande do Norte, CEP, Natal, RN, 59072-970, Brazil.
Josélio Maria Galvão de AraújoPostgraduate Program in Parasite Biology, Department of Microbiology and Parasitology, Federal University of Rio Grande do Norte, CEP, Natal, RN, 59072-970, Brazil.
Thales Allyrio Araújo de Medeiros FernandesDepartment of Biomedical Sciences, University of Rio Grande do Norte State, CEP, Mossoró, RN, 59607-360, Brazil. thalesallyrio@yahoo.com.br.
Ricardo Ney Oliveira CobucciPostgraduate Program in Parasite Biology, Department of Microbiology and Parasitology, Federal University of Rio Grande do Norte, CEP, Natal, RN, 59072-970, Brazil.
Daniel Carlos Ferreira LanzaDepartment of Biochemisty, Federal University of Rio Grande do Norte, CEP, Natal, RN, 59072-970, Brazil.
Vânia Sousa AndradePostgraduate Program in Parasite Biology, Department of Microbiology and Parasitology, Federal University of Rio Grande do Norte, CEP, Natal, RN, 59072-970, Brazil.
José Veríssimo FernandesPostgraduate Program in Parasite Biology, Department of Microbiology and Parasitology, Federal University of Rio Grande do Norte, CEP, Natal, RN, 59072-970, Brazil. veris@cb.ufrn.br.
Universidade Federal do Rio Grande do Norte · BRUniversidade do Estado do Rio Grande do Norte · BRUniversidade Potiguar · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophage migration inhibitory factor (MIF) emerged in recent years as an important inflammation mediator, playing a prominent role in the pathogenesis of various types of malignant neoplasm. MIF is a glycoprotein that presents a wide spectrum of biological activities and exerts a complex interaction with various cellular signaling pathways, causing imbalance of homeostasis. Experimental and clinical studies show that high levels of MIF are found in almost all types of human cancers and are implicated in seemingly all stages of development of the tumors. The production of MIF is triggered through an autocrine signal emitted by tumor cells, and stimulates the production of cytokines, chemokines, and growth as well as angiogenic factors that lead to growth of the tumor, increasing its aggressiveness and metastatic potential. MIF is produced by virtually all types of human body cells, in response to stress caused by different factors, leading to pathological conditions such as chronic inflammation and immunomodulation with suppression of immune surveillance and of immune response against tumors, angiogenesis, and carcinogenesis. In this review, we present recent advances on the biological activity of MIF, the signaling pathways with which it is involved and their role in tumorigenesis.

Indexed as

AnimalsCarcinogenesisHumansImmunomodulationInflammationMacrophage Migration-Inhibitory FactorsNeoplasmsMacrophage Migration-Inhibitory FactorsInflammationMacrophage migration inhibitory factorNeoplasmsTumorigenesis

Identifiers

PMID27771887
OpenAlexW2537739770

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.