Evidence map›Paper›PMID 38785491›Full record

ArticleCurrent oncology (Toronto, Ont.)2024

MISP Is Overexpressed in Intestinal Metaplasia and Gastric Cancer.

Tomás Vilarinho, Diana Pádua, Bruno Pereira, Patrícia Mesquita, Raquel Almeida

Abstract read
In one paragraph

Article in Current oncology (Toronto, Ont.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

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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

5 authors.

Tomás Vilarinhoi3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.
Diana Páduai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-5780-9842
Bruno Pereirai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0003-2460-6720
Patrícia Mesquitai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-4766-9831
Raquel Almeidai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.

Funding

Fundação para a Ciência e Tecnologia CEECINST/00131/2021Fundação para a Ciência e Tecnologia PTDC/BIA-CEL/0456/2021Programa Operacional Regional do Norte and co-funded by European Regional Development Fund under the project "The Porto Comprehensive Cancer Center" - Consórcio PORTO.CCC - Porto.Comprehensive Cancer Center Raquel Seruca NORTE-01-0145-FEDER-072678
6 · The paper itself

Abstract

Gastric cancer is the fifth most common cancer and the fourth cause of global cancer mortality. The identification of new biomarkers and drug targets is crucial to allow the better prognosis and treatment of patients. The mitotic spindle positioning (MISP) protein has the function of correcting mitotic spindle positioning and centrosome clustering and has been implicated in the cytokinesis and migration of cancer cells. The goal of this work was to evaluate the expression and clinical relevance of MISP in gastric cancer. MISP expression was evaluated by immunohistochemistry in a single hospital series (n = 286) of gastric adenocarcinomas and compared with normal gastric mucosa and intestinal metaplasia, a preneoplastic lesion. MISP was detected on the membrane in 83% of the cases, being overexpressed in gastric cancer compared to normal gastric mucosa (n = 10). Its expression was negatively associated with diffuse and poorly cohesive types. On the other hand, it was strongly expressed in intestinal metaplasia where it was associated with MUC2 and CDX2 expression. Furthermore, when we silenced MISP in vitro, a significant decrease in the viability of gastric carcinoma cells was observed. In conclusion, MISP is overexpressed in gastric cancer, being associated with an intestinal phenotype in gastric carcinogenesis and having a role in cellular proliferation.

Indexed as

MetaplasiaMicrofilament ProteinsStomach NeoplasmsAdenocarcinomaAgedBiomarkers, TumorCell Cycle ProteinsCell Line, TumorFemaleGastric MucosaHumansMaleMiddle AgedPhosphoproteinsBiomarkers, TumorCell Cycle ProteinsMicrofilament ProteinsMISP protein, humanPhosphoproteinsgastric cancerintestinal metaplasiaMISP

Identifiers

PMID38785491
PMCPMC11120023

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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.