Evidence map›Paper›PMID 32167697›Full record

ArticleInternational braz j urol : official journal of the Brazilian Society of Urology

Evaluation of nuclear NF-κB, transglutaminase2, and ERCC1 as predictors of platinum resistance in testicular tumors.

Alan A Azambuja, Paula Engroff, Bruna T Silva, Roberta C S Zorzetti, Fernanda B Morrone

Open access · diamondAbstract read
In one paragraph

Article in International braz j urol : official journal of the Brazilian Society of Urology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Pediatric Urology highlighted.International braz j urol : official journal of the Brazilian Society of Urology
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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 at 2 institutions in 1 country.

Alan A AzambujaPrograma de Pós-Graduação em Medicina e Ciências da Saúde, Escola de Medicina, Pontifícia Universidade Católica do Rio Grande do Sul, PUCRS e Hospital Mãe de Deus, Porto Alegre, Brasil.
Paula EngroffInstituto de Geriatria e Gerontologia, Pontifícia Universidade Católica do Rio Grande do Sul, PUCRS, Porto Alegre, Brasil.
Bruna T SilvaEscola de Medicina, Pontifícia Universidade Católica do Rio Grande do Sul, PUCRS, Porto Alegre, Brasil.
Roberta C S ZorzettiEscola de Medicina, Pontifícia Universidade Católica do Rio Grande do Sul, PUCRS, Porto Alegre, Brasil.
Fernanda B MorronePrograma de Pós-Graduação em Medicina e Ciências da Saúde, Escola de Medicina e Laboratório de Farmacologia Aplicada, Escola de Ciências da Saúde, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brasil.
Pontifícia Universidade Católica do Rio Grande do Sul · BRHospital Mãe de Deus · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTesticular germ cells tumor (TGCT) are associated with a high cure rate and are treated with platinum-based chemotherapy. However, a group of testicular cancer patients may have a very unfavorable evolution and insensitivity to the main therapeutic agent chemotherapy (CT) cisplatin. The aim of this study was to evaluate the risk of recurrence and overall survival related to the expression of nuclear factor kappa-B (NF-κB), transglutaminase 2 (TG2) and excision repair cross-complementation group 1 (ERCC1) in patients with TGCT treated with platinum combinations. PATIENTS AND

methodsA retrospective study was performed with TGCT patients treated with platinum-based chemotherapy. Immunohistochemical analysis was performed and the expression was correlated with clinical and laboratory data.

resultsFifty patients were included, the mean age was 28.4 years (18 to 45), and 76% were non-seminoma. All patients were treated with standard cisplatin, etoposide and bleomycin or cisplatin, and etoposide. Patient's analyzed immunodetection for NF-κB, TG2, and ERCC1 were positive in 76%, 54% and 42%, respectively. Multivariate analysis identified that positive expressions to ERCC1 and NF-κB are independent risk factors for higher recurrence TGCT after chemotherapy (RR 2.96 and 3.16, respectively). Patients with positive expression of ERCC1 presented a poor overall survival rate for 10-year follow (p=0.001).

conclusionsThe expression of ERCC1 and NF-κB give a worse prognosis for relapse, and only ERCC1 had an influence on the overall survival of TGCT patients treated with platinum-based chemotherapy. These may represent markers that predict poor clinical outcome and response to cisplatin.

Indexed as

Lung NeoplasmsTesticular NeoplasmsAdultAntineoplastic Combined Chemotherapy ProtocolsCisplatinDNA-Binding ProteinsDNA RepairDrug Resistance, NeoplasmEndonucleasesGTP-Binding ProteinsHumansMaleNF-kappa BPrognosisProtein Glutamine gamma Glutamyltransferase 2Retrospective StudiesCisplatinDNA-Binding ProteinsEndonucleasesERCC1 protein, humanGTP-Binding ProteinsNF-kappa BProtein Glutamine gamma Glutamyltransferase 2TransglutaminasesCisplatinTesticular Neoplasmstransglutaminase 2 [Supplementary Concept]

Identifiers

PMID32167697
PMCPMC7088506
OpenAlexW3011534908

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Registered trials

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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.