Evidence map›Paper›PMID 34757537›Full record

ArticleJournal of cancer research and clinical oncology2022

Protein expression of prognostic genes in primary melanoma and benign nevi.

T Gambichler, J Elfering, T Meyer, S Bruckmüller, E Stockfleth, M Skrygan, H U Käfferlein, T Brüning, K Lang, D Wagener and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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

13 authors at 3 institutions in 1 country.

T Gambichler *Skin Cancer Center, Department of Dermatology, Ruhr-University Bochum, Bochum, Germany. t.gambichler@klinikum-bochum.de.ORCID http://orcid.org/0000-0001-7862-3695
J ElferingSkin Cancer Center, Department of Dermatology, Ruhr-University Bochum, Bochum, Germany.
T MeyerSkin Cancer Center, Department of Dermatology, Ruhr-University Bochum, Bochum, Germany.
S BruckmüllerSkin Cancer Center, Department of Dermatology, Ruhr-University Bochum, Bochum, Germany.
E StockflethSkin Cancer Center, Department of Dermatology, Ruhr-University Bochum, Bochum, Germany.
M SkryganSkin Cancer Center, Department of Dermatology, Ruhr-University Bochum, Bochum, Germany.
H U KäfferleinInstitute for Prevention and Occupational Medicine of the German Social Accident Insurances, Ruhr-University Bochum (IPA), Bochum, Germany.
T BrüningInstitute for Prevention and Occupational Medicine of the German Social Accident Insurances, Ruhr-University Bochum (IPA), Bochum, Germany.
K LangInstitute for Prevention and Occupational Medicine of the German Social Accident Insurances, Ruhr-University Bochum (IPA), Bochum, Germany.
D WagenerPathology/Labor Lademannbogen MVZ GmbH, Hamburg, Germany.
S SchröderPathology/Labor Lademannbogen MVZ GmbH, Hamburg, Germany.
M NickSkin Cancer Center, Department of Dermatology, Ruhr-University Bochum, Bochum, Germany.
L Susok *Skin Cancer Center, Department of Dermatology, Ruhr-University Bochum, Bochum, Germany.
Ruhr University Bochum · DEInstitute for Prevention and Occupational Medicine · DEUniversity Hospitals of the Ruhr-University of Bochum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate the protein expression characteristics of genes employed in a recently introduced prognostic gene expression assay for patients with cutaneous melanoma (CM).

methodsWe studied 37 patients with CM and 10 with benign (melanocytic) nevi (BN). Immunohistochemistry of primary tumor tissue was performed for eight proteins: COL6A6, DCD, GBP4, KLHL41, KRT9, PIP, SCGB1D2, SCGB2A2.

resultsThe protein expression of most markers investigated was relatively low (e.g., DCD, KRT9, SCGB1D2) and predominantly cytoplasmatic in melanocytes and keratinocytes. COL6A6, GBP4, and KLHL41 expression was significantly enhanced in CM when compared to BN. DCD protein expression was significantly correlated with COL6A6, GBP4, and KLHL41. GBP4 was positively correlated with KLHL41 and inversely correlated with SCGB2B2. The latter was also inversely correlated with serum S100B levels at time of initial diagnosis. The presence of SCGB1D2 expression was significantly associated with ulceration of the primary tumor. KRT9 protein expression was significantly more likely found in acral lentiginous melanoma. The presence of DCD expression was less likely associated with superficial spreading melanoma subtype but significantly associated with non-progressive disease. The absence of SCGB2A2 expression was significantly more often observed in patients who did not progress to stage III or IV.

conclusionsThe expression levels observed were relatively low but differed in part with those found in BN. Even though we detected some significant correlations between the protein expression levels and clinical parameters (e.g., CM subtype, course of disease), there was no major concordance with the protective or risk-associated functions of the corresponding genes included in a recently introduced prognostic gene expression assay.

Indexed as

MelanomaNevus, PigmentedSkin NeoplasmsCutaneous Malignant MelanomaHumansPrognosisSecretoglobinsSCGB1D2 protein, humanSecretoglobinsBiomarkerCutaneous melanomaGene expressionMelaGenixPrognostic assayProtein expression

Identifiers

PMID34757537
PMCPMC9470607
OpenAlexW3212616667

What OpenQuestion 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 OpenQuestion graph.