Evidence map›Paper›PMID 25732306›Full record

ArticleThe Journal of experimental medicine2015

Targeting IL-17B-IL-17RB signaling with an anti-IL-17RB antibody blocks pancreatic cancer metastasis by silencing multiple chemokines.

Heng-Hsiung Wu, Wendy W Hwang-Verslues, Wen-Hsin Lee, Chun-Kai Huang, Pei-Chi Wei, Chia-Lin Chen, Jin-Yuh Shew, Eva Y-H P Lee, Yung-Ming Jeng, Yu-Wen Tien and 2 more

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
5.7field-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

97 citing papers in PubMed, 164 citations in OpenAlex.

  1. CD4Cell death & disease · 2022
    Trial
  2. Article
  3. IL-17B protects against uropathogenicMicrobiology spectrum · 2026
    Article
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37 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Heng-Hsiung WuGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Wendy W Hwang-VersluesGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Wen-Hsin LeeGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Chun-Kai HuangGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Pei-Chi WeiGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Chia-Lin ChenGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Jin-Yuh ShewGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Eva Y-H P LeeDepartment of Biological Chemistry, University of California, Irvine, Irvine, CA 92697.
Yung-Ming JengDepartment of Pathology and Department of Surgery, National Taiwan University Hospital, Taipei 10617, Taiwan.
Yu-Wen TienDepartment of Pathology and Department of Surgery, National Taiwan University Hospital, Taipei 10617, Taiwan.
Che MaGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Wen-Hwa LeeGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan Graduate Institute of Clinical Medicine, China Medical University, Taichung 40402, Taiwan whlee@uci.edu.
Genomics Research Center, Academia Sinica · TWNational Taiwan University Hospital · TWPediatrics and Genetics · USUniversity of California, Irvine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer has an extremely high mortality rate due to its aggressive metastatic nature. Resolving the underlying mechanisms will be crucial for treatment. Here, we found that overexpression of IL-17B receptor (IL-17RB) strongly correlated with postoperative metastasis and inversely correlated with progression-free survival in pancreatic cancer patients. Consistently, results from ex vivo experiments further validated that IL-17RB and its ligand, IL-17B, plays an essential role in pancreatic cancer metastasis and malignancy. Signals from IL-17B-IL-17RB activated CCL20/CXCL1/IL-8/TFF1 chemokine expressions via the ERK1/2 pathway to promote cancer cell invasion, macrophage and endothelial cell recruitment at primary sites, and cancer cell survival at distant organs. Treatment with a newly derived monoclonal antibody against IL-17RB blocked tumor metastasis and promoted survival in a mouse xenograft model. These findings not only illustrate a key mechanism underlying the highly aggressive characteristics of pancreatic cancer but also provide a practical approach to tackle this disease.

Indexed as

AnimalsAntibodies, MonoclonalChemokinesDisease-Free SurvivalFemaleGene Expression Regulation, NeoplasticHumansInterleukin-17MaleMice, SCIDMiddle AgedPancreatic NeoplasmsReceptors, Interleukin-17Signal TransductionXenograft Model Antitumor AssaysAntibodies, MonoclonalChemokinesInterleukin-17Receptors, Interleukin-17

Identifiers

PMID25732306
PMCPMC4354366
OpenAlexW2136292231

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.