Evidence map›Paper›PMID 33082357›Full record

ArticleScientific reports2020

Targeting interleukin-17 receptor B enhances gemcitabine sensitivity through downregulation of mucins in pancreatic cancer.

Lung-Hung Tsai, Kai-Wen Hsu, Cheng-Ming Chiang, Hsiu-Ju Yang, Yu-Huei Liu, Shun-Fa Yang, Pei-Hua Peng, Wei-Chung Cheng, Heng-Hsiung Wu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Integrated Transcriptomic Analysis ofInternational journal of molecular sciences · 2026
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  9. Construction and Verification of a Hypoxia-Stemness-Based Gene Signature for Risk Stratification in Esophageal Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2021
    Article
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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 4 institutions in 2 countries.

Lung-Hung TsaiResearch Center for Cancer Biology, China Medical University, No. 91, Hsueh-Shih Road, North District, Taichung, Taiwan.
Kai-Wen HsuResearch Center for Cancer Biology, China Medical University, No. 91, Hsueh-Shih Road, North District, Taichung, Taiwan.
Cheng-Ming ChiangDepartment of Pharmacology, and Department of Biochemistry, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX, 75390, USA.
Hsiu-Ju YangResearch Center for Cancer Biology, China Medical University, No. 91, Hsueh-Shih Road, North District, Taichung, Taiwan.
Yu-Huei LiuGraduate Institute of Integrated Medicine, China Medical University, Taichung, Taiwan.
Shun-Fa YangInstitute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Pei-Hua PengCancer Genome Research Center, Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan.
Wei-Chung ChengResearch Center for Cancer Biology, China Medical University, No. 91, Hsueh-Shih Road, North District, Taichung, Taiwan.
Heng-Hsiung WuResearch Center for Cancer Biology, China Medical University, No. 91, Hsueh-Shih Road, North District, Taichung, Taiwan. henghsiungwu@mail.cmu.edu.tw.
China Medical University · TWChang Gung Memorial Hospital · TWChung Shan Medical University · TWThe University of Texas Southwestern Medical Center · US

Funding

Opposing Functions of BRD4 Isoforms in Breast CancerR01CA251698 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI CHIANG, CHENG-MING · 2020 to 2024
$2.3M
NCI NIH HHS R01 CA251698NIH HHS 1RO1CA251698-01
6 · The paper itself

Abstract

Pancreatic cancer is the fourth leading cause of death worldwide due to its poorest prognoses with a 7% 5-year survival rate. Eighty percent of pancreatic cancer patients relapse after chemotherapy and develop early metastasis and drug resistance. Resistance to nucleoside analog gemcitabine frequently used in first-line therapy is an urgent issue in pancreatic cancer treatment. Expression of mucin (MUC) glycoproteins has been shown to enhance chemoresistance via increased cell stemness. Here we show interlukine-17 receptor B (IL-17RB) expression is positively correlated with MUC1 and MUC4 expression in pancreatic cancer cells and tumor tissue. Moreover, IL-17RB transcriptionally up-regulates expression of MUC1 and MUC4 to enhance cancer stem-like properties and resistance to gemcitabine. These results suggest IL-17RB can be a potential target for pancreatic cancer therapy. Indeed, treatment with IL-17RB-neutralizing antibody has a synergistic effect in combination with gemcitabine for killing pancreatic cancer cells. Altogether, these findings provide feasible applications for IL-17RB-targeting therapy in pancreatic cancer treatment.

Indexed as

Antibodies, BlockingAntineoplastic AgentsAntineoplastic Agents, ImmunologicalDeoxycytidineDown-RegulationDrug ResistanceDrug SynergismDrug Therapy, CombinationGemcitabineHumansMolecular Targeted TherapyMucinsNeoplastic Stem CellsPancreatic NeoplasmsReceptors, Interleukin-17Tumor Cells, CulturedAntibodies, BlockingAntineoplastic AgentsAntineoplastic Agents, ImmunologicalDeoxycytidineGemcitabineIL17RB protein, humanMucinsReceptors, Interleukin-17

Identifiers

PMID33082357
PMCPMC7576602
OpenAlexW3094158910

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.