Evidence map›Paper›PMID 31915130›Full record

ArticleCancer research2020

Tumor Cell-Derived IL1β Promotes Desmoplasia and Immune Suppression in Pancreatic Cancer.

Shipra Das, Beny Shapiro, Emily A Vucic, Sandra Vogt, Dafna Bar-Sagi

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04581343 (A Phase 1B Study to Determine the Safety and Tolerability and Confirm the Dose of Canakinumab and Spartalizumab in Combination With Nab-paclitaxel and Gemcitabine for Patients With Metastatic Pancreatic Cancer), which is not on this map. Cited by 243 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
243citing papers in PubMed, 2 pooled it
17.7field-weighted citation impact, top 1% 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.

NCT04581343 phase1completednot on this map

A Phase 1B Study to Determine the Safety and Tolerability and Confirm the Dose of Canakinumab and Spartalizumab in Combination With Nab-paclitaxel and Gemcitabine for Patients With Metastatic Pancreatic Cancer

TypeinterventionalSponsorPancreatic Cancer Action NetworkRan2020 to 2023Enrolled10ConditionsMetastatic Pancreatic Ductal AdenocarcinomaArmsCanakinumab injection, spartalizumab, nab-paclitaxel, gemcitabine
3 · Its place in the literature

Who cites it

243 citing papers in PubMed, 2 syntheses or guidelines pooled it, 360 citations in OpenAlex.

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  20. Progress in Designing Cytokine Antagonist Antibodies for Cancer Therapy.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review

183 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

5 authors at 1 institution in 1 country.

Shipra DasDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, New York.
Beny ShapiroDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, New York.ORCID 0000-0002-1067-3458
Emily A VucicDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, New York.
Sandra VogtDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, New York.
Dafna Bar-SagiDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, New York. dafna.bar-sagi@nyulangone.org.
New York University · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Oncogenic Ras-induced macropinocytosis: A new paradigm for metabolic adaptationR35CA210263 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BAR-SAGI, DAFNA · 2016 to 2022
$6.6M
Training Program in Cell BiologyT32GM136542 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SMITH, SUSAN · 2020 to 2024
$3.0M
Genome Integrity Training ProgramT32GM115313 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SMITH, SUSAN · 2015 to 2019
$927k
NCI NIH HHS P30 CA016087NCI NIH HHS R35 CA210263NIGMS NIH HHS T32 GM115313NIGMS NIH HHS T32 GM136542
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDA) is an aggressive malignancy typified by a highly stromal and weakly immunogenic tumor microenvironment that promotes tumor evolution and contributes to therapeutic resistance. Here, we demonstrate that PDA tumor cell-derived proinflammatory cytokine IL1β is essential for the establishment of the protumorigenic PDA microenvironment. Tumor cell-derived IL1β promoted the activation and secretory phenotype of quiescent pancreatic stellate cells and established an immunosuppressive milieu mediated by M2 macrophages, myeloid-derived suppressor cells, CD1d

Indexed as

AnimalsAntineoplastic Agents, ImmunologicalCarcinogenesisCarcinoma, Pancreatic DuctalCD8-Positive T-LymphocytesCell Line, TumorDisease Models, AnimalDrug SynergismEpithelial CellsFemaleHumansInflammasomesInterleukin-1betaLymphocytes, Tumor-InfiltratingMiceMice, TransgenicAntineoplastic Agents, ImmunologicalIL1B protein, humanIL1B protein, mouseInflammasomesInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanNlrp3 protein, mousePDCD1 protein, humanProgrammed Cell Death 1 ReceptorTLR4 protein, humanTlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID31915130
PMCPMC7302116
OpenAlexW2999401147

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.