Evidence map›Paper›PMID 30206212›Full record

ArticleCell death & disease2018

Melanoma cells resistant towards MAPK inhibitors exhibit reduced TAp73 expression mediating enhanced sensitivity to platinum-based drugs.

Elena Makino, Vanessa Gutmann, Corinna Kosnopfel, Heike Niessner, Andrea Forschner, Claus Garbe, Tobias Sinnberg, Birgit Schittek

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Trametinib-Resistant Melanoma Cells Displaying MITFInternational journal of molecular sciences · 2023
    Article
  6. Article
  7. p53 Family in Resistance to Targeted Therapy of Melanoma.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Review
  10. Targeting Genome Stability in Melanoma-A New Approach to an Old Field.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. 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

8 authors at 1 institution in 1 country.

Elena MakinoDivision of Dermatooncology, Department of Dermatology, University of Tübingen, Tübingen, Germany.
Vanessa GutmannDivision of Dermatooncology, Department of Dermatology, University of Tübingen, Tübingen, Germany.
Corinna KosnopfelDivision of Dermatooncology, Department of Dermatology, University of Tübingen, Tübingen, Germany.
Heike NiessnerDivision of Dermatooncology, Department of Dermatology, University of Tübingen, Tübingen, Germany.
Andrea ForschnerDivision of Dermatooncology, Department of Dermatology, University of Tübingen, Tübingen, Germany.
Claus GarbeDivision of Dermatooncology, Department of Dermatology, University of Tübingen, Tübingen, Germany.
Tobias SinnbergDivision of Dermatooncology, Department of Dermatology, University of Tübingen, Tübingen, Germany.
Birgit SchittekDivision of Dermatooncology, Department of Dermatology, University of Tübingen, Tübingen, Germany. birgit.schittek@med.uni-tuebingen.de.
University of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The efficacy of targeted MAPK signalling pathway inhibitors (MAPKi) in metastatic melanoma therapy is limited by the development of resistance mechanisms that results in disease relapse. This situation still requires treatment alternatives for melanoma patients with acquired resistance to targeted therapy. We found that melanoma cells, which developed resistance towards MAPKi show an enhanced susceptibility to platinum-based drugs, such as cisplatin and carboplatin. We found that this enhanced susceptibility inversely correlates with the expression level of the p53 family member TAp73. We show that the lower expression of the TAp73 isoform in MAPKi-resistant melanoma cells enhances accumulation of DNA double-strand breaks upon cisplatin and carboplatin treatment by reducing the efficiency of nucleotide excision repair. These data suggest that a subgroup of melanoma patients with acquired resistance to MAPKi treatment and low TAp73 expression can benefit from chemotherapy with platinum-based drugs as a second-line therapy.

Indexed as

Antineoplastic AgentsCarboplatinCell Line, TumorCisplatinDNA Breaks, Double-StrandedDNA RepairDrug Resistance, NeoplasmHumansMelanomaPaclitaxelProtein Kinase InhibitorsRetrospective StudiesTumor Protein p73Tumor Suppressor Protein p53Antineoplastic AgentsCarboplatinCisplatinPaclitaxelProtein Kinase InhibitorsTP53 protein, humanTumor Protein p73Tumor Suppressor Protein p53

Identifiers

PMID30206212
PMCPMC6133963
OpenAlexW2891788986

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.