Evidence map›Paper›PMID 25015776›Full record

ArticlePathology oncology research : POR2015

Metallothionein 3 expression in normal skin and malignant skin lesions.

Bartosz Pula, Tadeusz Tazbierski, Aleksandra Zamirska, Bozena Werynska, Andrzej Bieniek, Jacek Szepietowski, Janusz Rys, Piotr Dziegiel, Marzena Podhorska-Okolow

Open access · hybridAbstract read
In one paragraph

Article in Pathology oncology research : POR, 2015. 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
1.6field-weighted citation impact, top 19% 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, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The roles of metallothioneins in carcinogenesis.Journal of hematology & oncology · 2018
    Review
  5. Zinc and Skin Disorders.Nutrients · 2018
    Review
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 4 institutions in 1 country.

Bartosz Pula
Tadeusz Tazbierski
Aleksandra Zamirska
Bozena Werynska
Andrzej Bieniek
Jacek Szepietowski
Janusz Rys
Piotr Dziegiel
Marzena Podhorska-Okolow
University of Wrocław · PLWroclaw Medical University · PLThe Maria Sklodowska-Curie National Research Institute of Oncology · PLUniversity School of Physical Education in Wroclaw · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metallothionein-3 (MT-3) has been shown to be expressed in several malignancies and to have an impact on patients' survival in breast and urinary bladder cancer cases. However, its expression has not been determined in normal skin or in its malignant lesions. MT-3 expression was studied using immunohistochemistry in 17 cases of normal skin, 18 of actinic keratosis (AK), 39 of squamous cell carcinoma (SCC), and 23 of basal cell carcinoma (BCC). Low MT-3 expression was observed in normal skin epidermis with faint or no expression in the epidermis basal layer. Significantly higher MT-3 expression was noted in AK (P=0.007) and SCC (P<0.0001), as compared with normal skin epidermis. BCC cases were characterized by the lowest MT-3 expression of all the examined groups, which was significantly lower in comparison to normal skin epidermis, AK, and SCC (P=0.009;P<0.0001 and P<0.0001, respectively). In conclusion, MT-3 may be involved in the development of SCC.

Indexed as

AdultAgedAged, 80 and overBasal Cell CarcinomaCarcinoma, Squamous CellFemaleHumansKeratosis, ActinicMaleMetallothionein 3Middle AgedNerve Tissue ProteinsSkinSkin DiseasesSkin NeoplasmsMetallothionein 3Nerve Tissue Proteins

Identifiers

PMID25015776
PMCPMC4287679
OpenAlexW1964734417

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.