Evidence map›Paper›PMID 29371916›Full record

ArticleOncotarget2017

The IL-17B-IL-17 receptor B pathway promotes resistance to paclitaxel in breast tumors through activation of the ERK1/2 pathway.

Emilie Laprevotte, Stéphanie Cochaud, Stanislas du Manoir, Marion Lapierre, Cécile Dejou, Marion Philippe, Jérome Giustiniani, Kathryn A Frewer, Andrew J Sanders, Wen G Jiang and 7 more

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 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

24 citing papers in PubMed, 52 citations in OpenAlex.

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  7. IL25American journal of cancer research · 2023
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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

17 authors at 7 institutions in 2 countries.

Emilie LaprevotteOREGA Biotech, Ecully, F-69130 France.
Stéphanie CochaudOREGA Biotech, Ecully, F-69130 France.
Stanislas du ManoirIRCM, INSERM, Université de Montpellier, ICM, Montpellier, F-34298 France.
Marion LapierreIRCM, INSERM, Université de Montpellier, ICM, Montpellier, F-34298 France.
Cécile DejouOREGA Biotech, Ecully, F-69130 France.
Marion PhilippeOREGA Biotech, Ecully, F-69130 France.
Jérome GiustinianiInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 976, Université Paris Diderot, Sorbonne Paris Cité, Laboratoire Immunologie Dermatologie and Oncologie, Paris, F-75475 France.
Kathryn A FrewerCardiff China Medical Research Collaborative, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK.
Andrew J SandersCardiff China Medical Research Collaborative, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK.
Wen G JiangCardiff China Medical Research Collaborative, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK.
Henri-Alexandre MichaudIRCM, INSERM, Université de Montpellier, ICM, Montpellier, F-34298 France.
Pierre-Emmanuel ColomboDépartement de chirurgie oncologique, Institut Régional du Cancer de Montpellier, Université de Montpellier, Montpellier, F-34298 France.
Armand BensussanInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 976, Université Paris Diderot, Sorbonne Paris Cité, Laboratoire Immunologie Dermatologie and Oncologie, Paris, F-75475 France.
Gilles AlbericiOREGA Biotech, Ecully, F-69130 France.
Jérémy BastidOREGA Biotech, Ecully, F-69130 France.
Jean-François EliaouIRCM, INSERM, Université de Montpellier, ICM, Montpellier, F-34298 France.
Nathalie BonnefoyIRCM, INSERM, Université de Montpellier, ICM, Montpellier, F-34298 France.
OREGA Biotech (France) · FRCardiff University · GBUniversité de Montpellier · FRInserm · FRInstitut de Recherche en Cancérologie de Montpellier · FRSorbonne Paris Cité · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin 17B (IL-17B) is a pro-inflammatory cytokine that belongs to the IL-17 cytokines family and binds to IL-17 receptor B (IL-17RB). Here we found that high expression of IL-17B and IL-17RB is associated with poor prognosis in patients with breast cancer and that IL-17B expression upregulation is specifically associated with poorer survival in patients with basal-like breast cancer. We thus focused on IL-17B role in breast cancer by using luminal and triple negative (TN)/basal-like tumor cell lines. We found that IL-17B induces resistance to conventional chemotherapeutic agents.

Indexed as

breast cancerchemoresistanceinterleukin-17interleukin-17Bpaclitaxel

Identifiers

PMID29371916
PMCPMC5768333
OpenAlexW2775028758

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.