Evidence map›Paper›PMID 28147314›Full record

ArticleOncotarget2017

The antiangiogenic role of the pro-inflammatory cytokine interleukin-31.

Shiri Davidi, Ella Fremder, Tal Kan, Ziv Raviv, Michael Timaner, Nathan Karin, Dov Hershkovitz, Ami Arohneim, Yuval Shaked

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Impact ofOncology research · 2026
    Article
  2. Review
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  4. Article
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  6. Emerging roles for the IL-6 family of cytokines in pancreatic cancer.Clinical science (London, England : 1979) · 2020
    Review
  7. IL-31 induces antitumor immunity in breast carcinoma.Journal for immunotherapy of cancer · 2020
    Article
  8. Article
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  12. Review
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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

9 authors at 1 institution in 1 country.

Shiri DavidiCell Biology and Cancer Science, Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Ella FremderCell Biology and Cancer Science, Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Tal KanCell Biology and Cancer Science, Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Ziv RavivCell Biology and Cancer Science, Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Michael TimanerCell Biology and Cancer Science, Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Nathan KarinDepartment of Immunology, Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Dov HershkovitzDepartment of Pathology, Rambam Medical Center, Haifa, Israel.
Ami ArohneimCell Biology and Cancer Science, Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Yuval ShakedCell Biology and Cancer Science, Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Rambam Health Care Campus · IL

Funding

European Research Council 260633
6 · The paper itself

Abstract

Pro-inflammatory cytokines in the tumor microenvironment are known for their ability to either inhibit or promote cancer progression. Here we evaluated the role of Interleukin-31 (IL31), a protein belonging to the pro-inflammatory IL-6 cytokine family which has been characterized in autoimmune disease, in tumorigenesis. We show that IL31 and its receptor, IL31RA, are highly expressed in various human and mouse cancer cell lines, as well as in tumor specimens from cancer patients. MC38 murine colon carcinoma cells depleted of IL31 exhibit an increase in invasive and migratory properties in vitro, effects that are reversed by supplementing the cells with exogenous IL31. In vivo, IL31-depleted MC38 tumor cells implanted to mice grow faster than control tumors. In contrast, MC38 tumor-bearing mice infused with recombinant IL31, exhibit a significant reduction in tumor growth than control mice. Furthermore, IL31 infusion reduces the number of metastatic lesions in the lungs of mice bearing 4T1 murine metastatic breast carcinoma. Lastly, injecting tumor-bearing, chemotherapy-treated mice with a long-lived IL31-IgG fusion protein reduces tumor growth, angiogenesis and pulmonary metastasis to a greater extent than when chemotherapy is used alone. The IL31 anti-tumor activity is explained, in part, by the anti-angiogenic effects demonstrated both in vitro and in vivo highlighting the potential use of IL31 as an anti-cancer drug.

Indexed as

AnimalsCell Line, TumorFemaleHumansInterleukinsMiceMice, Inbred C57BLMice, Inbred NODMice, SCIDNeoplasmsNeovascularization, PathologicTumor MicroenvironmentIL31 protein, humanInterleukinsangiogenesiscancer therapyhost responsemetastasis

Identifiers

PMID28147314
PMCPMC5369974
OpenAlexW2582312689

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.