Evidence map›Paper›PMID 36008689›Full record

ArticleJournal of cancer research and clinical oncology2023

Tissue immunostaining of candidate prognostic proteins in metastatic and non-metastatic prostate cancer.

Érica Romão Pereira, Laís Capelasso Lucas Pinheiro, Amanda Letícia Francelino, Carlos Alberto Miqueloto, Alda Fiorina Maria Losi Guembarovski, Karen Brajão de Oliveira, Paulo Emílio Fuganti, Ilce Mara de Syllos Cólus, Roberta Losi Guembarovski

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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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 1 institution in 1 country.

Érica Romão PereiraLaboratory of Mutagenesis and Oncogenetics, Department of General Biology, Londrina State University, Londrina, PR, Brazil.
Laís Capelasso Lucas PinheiroLaboratory of Mutagenesis and Oncogenetics, Department of General Biology, Londrina State University, Londrina, PR, Brazil.
Amanda Letícia FrancelinoLaboratory of Mutagenesis and Oncogenetics, Department of General Biology, Londrina State University, Londrina, PR, Brazil.
Carlos Alberto MiquelotoLaboratory of Extracellular Matrix, Department of General Biology, Londrina State University, Londrina, PR, Brazil.
Alda Fiorina Maria Losi GuembarovskiDepartment of Pathology, Clinical and Toxicological Analysis, Londrina State University, Londrina, PR, Brazil.
Karen Brajão de OliveiraLaboratory of Molecular Genetics and Immunology, Department of Pathological Science, Londrina State University, Londrina, PR, Brazil.
Paulo Emílio FugantiCancer Hospital of Londrina - HCL, Londrina, PR, Brazil.
Ilce Mara de Syllos CólusLaboratory of Mutagenesis and Oncogenetics, Department of General Biology, Londrina State University, Londrina, PR, Brazil.
Roberta Losi GuembarovskiLaboratory of Mutagenesis and Oncogenetics, Department of General Biology, Londrina State University, Londrina, PR, Brazil. robertalosi@uel.br.ORCID http://orcid.org/0000-0002-6291-8621
Universidade Estadual de Londrina · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico Proc.308231/2017-1Coordenação de Aperfeiçoamento de Pessoal de Nível Superior Finance Code 001Fundação Araucária de Apoio ao Desenvolvimento Científico e Tecnológico do Paraná Grant 185/2014PPSUS - Fundação Araucária de Apoio ao Desenvolvimento Científico e Tecnológico do Paraná Grant 051/2021
6 · The paper itself

Abstract

purposeProstate cancer (PCa) lacks specific markers capable of distinguishing aggressive tumors from those with indolent behavior. Therefore, the aim of this study was to evaluate the immunostaining of candidate proteins (PTEN, AKT, TRPM8, and NKX3.1) through the immunohistochemistry technique (IHC) on patients with metastatic and non-metastatic PCa.

methodsTissues from 60 patients were divided into three groups categorized according to prognostic parameters: better prognosis (n = 20), worse prognosis (n = 23), and metastatic (n = 17). Immunostaining was analyzed by a pathologist and staining classifications were considered according to signal intensity: (0) no staining, (+) weak, and (++ and +++) intermediate to strong.

resultsAKT protein was associated (p = 0.012) and correlated (p = 0.014; Tau = - 0.288) with the prognostic groups. The immunostaining for TRPM8 (p = 0.010) and NKX3.1 (p = 0.003) proteins differed between malignant tumor and non-tumoral adjacent tissue as well as for proteins in cellular locations (nucleus and cytoplasm). TRPM8 was independently associated with the ISUP grade ≥ 4 (p = 0.024; OR = 8.373; 95% CI = 1.319-53.164). The NKX3.1 showed positive and predominantly strong immunostaining in all patients in both tumoral and non-tumoral adjacent tissues. All metastatic samples had positive immunostaining, with strong intensity for NKX3.1 (p = 0.021; Tau = - 0.302). In the non-metastatic group, this strong protein staining was not observed in any patients.

conclusionThis study confirmed that NKX3.1 is highly specific for prostate tissue and indicated that NKX3.1, AKT, and TRPM8 may be candidate markers for prostate cancer prognosis.

Indexed as

Homeodomain ProteinsProstatic NeoplasmsHumansMalePrognosisProto-Oncogene Proteins c-aktTranscription FactorsHomeodomain ProteinsProto-Oncogene Proteins c-aktTranscription FactorsAKTImmunohistochemistryMetastasisNKX3-1PTENTRPM8

Identifiers

PMID36008689
PMCPMC11797605
OpenAlexW4293237552

What OpenQuestion holds

Textmetadata
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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.