Evidence map›Paper›PMID 26689911›Full record

ArticlePloS one2015

Inflammasome Modulation by Chemotherapeutics in Malignant Mesothelioma.

Catherine Westbom, Joyce K Thompson, Alan Leggett, Maximilian MacPherson, Stacie Beuschel, Harvey Pass, Pamela Vacek, Arti Shukla

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04732455 (Intravenous Lidocaine Infusion Versus Oral Duloxetine For The Prevention And Treatment Of Chemotherapy Induced Peripheral Neuropathy Among Breast Cancer Patients), which is not on this map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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.

NCT04732455 nacompletednot on this mapstarted 2021, after this paper: background citation

Intravenous Lidocaine Infusion Versus Oral Duloxetine For The Prevention And Treatment Of Chemotherapy Induced Peripheral Neuropathy Among Breast Cancer Patients

TypeinterventionalSponsorGamal Mohamed Taha AbouelmagdRan2021 to 2022Enrolled60ConditionsPeripheral Neuropathy, Chemotherapy-induced Peripheral Neuropathy, Breast CancerArmsLidocaine in Saline, Duloxetine 30 MG, Normal saline
3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. Caspase-1 in cancer and inflammatory diseases: a potential therapeutic target.Apoptosis : an international journal on programmed cell death · 2026
    Review
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  12. New prospects of cancer therapy based on pyroptosis and pyroptosis inducers.Apoptosis : an international journal on programmed cell death · 2024
    Review
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  15. 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

8 authors at 3 institutions in 1 country.

Catherine WestbomDepartment of Pathology and Laboratory Medicine, University of Vermont College of Medicine, Burlington, VT, United States of America.
Joyce K ThompsonDepartment of Pathology and Laboratory Medicine, University of Vermont College of Medicine, Burlington, VT, United States of America.
Alan LeggettDepartment of Pathology and Laboratory Medicine, University of Vermont College of Medicine, Burlington, VT, United States of America.
Maximilian MacPhersonDepartment of Pathology and Laboratory Medicine, University of Vermont College of Medicine, Burlington, VT, United States of America.
Stacie BeuschelDepartment of Pathology and Laboratory Medicine, University of Vermont College of Medicine, Burlington, VT, United States of America.
Harvey PassDepartment of Cardiothoracic Surgery, New York University School of Medicine, New York, New York, United States of America.
Pamela VacekDepartment of Medical Biostatistics, University of Vermont College of Medicine, Burlington, VT, United States of America.
Arti ShuklaDepartment of Pathology and Laboratory Medicine, University of Vermont College of Medicine, Burlington, VT, United States of America.
University of Vermont · USNew York University · USUniversity of Vermont Medical Center · US

Funding

Inflammasomes in pathogenesis of mesotheliomaR01ES021110 · NIEHS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI SHUKLA, ARTI · 2012 to 2016
$1.7M
NIEHS NIH HHS R01 ES021110
6 · The paper itself

Abstract

Malignant mesothelioma (MM) is a fatal disease in dire need of therapy. The role of inflammasomes in cancer is not very well studied, however, literature supports both pro-and anti-tumorigenic effects of inflammasomes on cancer depending upon the type of cancer. Asbestos is a causative agent for MM and we have shown before that it causes inflammasome priming and activation in mesothelial cells. MM tumor cells/tissues showed decreased levels of inflammasome components like NLRP3 and caspase-1 as compared to human mesothelial cells or normal tissue counterpart of tumor. Based on our preliminary findings we hypothesized that treatment of MMs with chemotherapeutic drugs may elevate the levels of NLRP3 and caspase-1 resulting in increased cell death by pyroptosis while increasing the levels of IL-1β and other pro-inflammatory molecules. Therefore, a combined strategy of chemotherapeutic drug and IL-1R antagonist may play a beneficial role in MM therapy. To test our hypothesis we used two human MM tumor cell lines (Hmeso, H2373) and two chemotherapeutic drugs (doxorubicin, cisplatin). Through a series of experiments we showed that both chemotherapeutic drugs caused increases in NLRP3 levels, caspase-1 activation, pyroptosis and pro-inflammatory molecules released from MM cells. In vivo studies using SCID mice and Hmeso cells showed that tumors were smaller in combined treatment group of cisplatin and IL-1R antagonist (Anakinra) as compared to cisplatin alone or untreated control groups. Taken together our study suggests that chemotherapeutic drugs in combination with IL-1R antagonist may have a beneficial role in MM treatment.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsCarrier ProteinsCaspase 1Cell Line, TumorCisplatinDoxorubicinFeedback, PhysiologicalHumansInflammasomesInterleukin-18Interleukin-1betaInterleukin 1 Receptor Antagonist ProteinLung NeoplasmsMaleMesotheliomaCarrier ProteinsCaspase 1CisplatinDoxorubicinIL18 protein, humanInflammasomesInterleukin-18Interleukin-1betaInterleukin 1 Receptor Antagonist ProteinNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanReceptors, Interleukin-1

Identifiers

PMID26689911
PMCPMC4687055
OpenAlexW2210572357

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.