Evidence map›Paper›PMID 38990306›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2024

Celecoxib inhibits NLRP1 inflammasome pathway in MDA-MB-231 Cells.

Ege Arzuk, Derviş Birim, Güliz Armağan

Erratum issuedAbstract read
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Ege ArzukDepartment of Pharmaceutical Toxicology, Faculty of Pharmacy, Ege University, Bornova, 35040, Izmir, Turkey. ege.arzuk@ege.edu.tr.
Derviş BirimDepartment of Biochemistry, Faculty of Pharmacy, Ege University, Bornova, Izmir, Turkey.
Güliz ArmağanDepartment of Biochemistry, Faculty of Pharmacy, Ege University, Bornova, Izmir, Turkey.

Funding

Ege University Research Foundation (BAP) 22969
6 · The paper itself

Abstract

NLRP1 is predominantly overexpressed in breast cancer tissue, and the evaluated activation of NLRP1 inflammasome is associated with tumor growth, angiogenesis, and metastasis. Therefore, targeting NLRP1 activation could be a crucial strategy in anticancer therapy. In this study, we investigated the hypothesis that NLRP1 pathway may contribute to the cytotoxic effects of celecoxib and nimesulide in MDA-MB-231 cells. First of all, IC

Indexed as

Caspase 1CelecoxibInflammasomesInterleukin-1betaNLR ProteinsAdaptor Proteins, Signal TransducingAntineoplastic AgentsApoptosis Regulatory ProteinsBreast NeoplasmsCell Line, TumorCell SurvivalFemaleHumansMDA-MB-231 CellsSignal TransductionSulfonamidesAdaptor Proteins, Signal TransducingAntineoplastic AgentsApoptosis Regulatory ProteinsCaspase 1CelecoxibIL1B protein, humanInflammasomesInterleukin-1betanimesulideNLRP1 protein, humanNLR ProteinsSulfonamidesAnticancer drugCelecoxibCOX-2NLRP1 inflammasomeTriple-negative breast cancer

Identifiers

PMID38990306
PMCPMC11522188

What Socratic 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 Socratic graph.