Evidence map›Paper›PMID 33506271›Full record

ArticleProtoplasma2021

Melanization as unfavorable factor in amelanotic melanoma cell biology.

A Skoniecka, M Cichorek, A Tyminska, I Pelikant-Malecka, J Dziewiatkowski

Open access · hybridAbstract read
In one paragraph

Article in Protoplasma, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Amelanotic Melanoma-Biochemical and Molecular Induction Pathways.International journal of molecular sciences · 2024
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. RAB3A Regulates Melanin Exocytosis and Transfer Induced by Keratinocyte-Conditioned Medium.JID innovations : skin science from molecules to population health · 2022
    Article
  12. Review
  13. 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

5 authors at 1 institution in 1 country.

A SkonieckaEmbryology Department, Medical University of Gdansk, Ul. Debinki 1 St, 80-211, Gdansk, Poland. aneta.skoniecka@gumed.edu.pl.ORCID http://orcid.org/0000-0002-2768-0531
M CichorekEmbryology Department, Medical University of Gdansk, Ul. Debinki 1 St, 80-211, Gdansk, Poland.ORCID https://orcid.org/0000-0003-2659-9130
A TyminskaEmbryology Department, Medical University of Gdansk, Ul. Debinki 1 St, 80-211, Gdansk, Poland.ORCID https://orcid.org/0000-0002-6195-1024
I Pelikant-MaleckaDepartment of Medical Laboratory Diagnostics-Biobank, Medical University of Gdansk, 80-211, Gdansk, Poland.ORCID https://orcid.org/0000-0002-4780-8256
J DziewiatkowskiDepartment of Anatomy and Neurobiology, Medical University of Gdansk, Debinki 1 St, 80-211, Gdansk, Poland.
Gdańsk Medical University · PL

Funding

Medical University of Gdansk (MN 01-0138/08)
6 · The paper itself

Abstract

The biology of three amelanotic melanoma cell lines (Ab, B16F10, and A375) of different species origin was analyzed during in vitro induced melanization in these cells. Melanin production was induced by DMEM medium characterized by a high level of L-tyrosine (a basic amino acid for melanogenesis). The biodiversity of amelanotic melanoma cells was confirmed by their different responses to melanogenesis induction; Ab hamster melanomas underwent intensive melanization, mouse B16F10 darkened slightly, while human A375 cells did not show any change in melanin content. Highly melanized Ab cells entered a cell death pathway, while slight melanization did not influence cell biology in a significant way. The rapid and high melanization of Ab cells induced apoptosis documented by phosphatidylserine externalization, caspase activation, and mitochondrial energetic state decrease. Melanoma cell type, culture medium, and time of incubation should be taken into consideration during amelanotic melanoma cell culture in vitro. L-tyrosine, as a concentration-dependent factor presented in the culture media, could stimulate some amelanotic melanoma cell lines (Ab, B16F10) to melanin production. The presence of melanin should be considered in the examination of antimelanoma compounds in vitro, because induction of melanin may interfere or be helpful in the treatment of amelanotic melanoma.

Indexed as

Melanoma, AmelanoticSkin NeoplasmsAnimalsApoptosisCell LineCricetinaeMelaninsMiceMelaninsAmelanotic melanomaApoptosisL-tyrosineMelaninMelanizationMelanoma

Identifiers

PMID33506271
PMCPMC8433105
OpenAlexW3122480181

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.