Evidence map›Paper›PMID 36428530›Full record

ArticleBiomedicines2022

In Model, In Vitro and In Vivo Killing Efficacy of Antitumor Peptide RDP22 on MUG-Mel2, a Patient Derived Cell Line of an Aggressive Melanoma Metastasis.

Maximiliane Wußmann, Florian Kai Groeber-Becker, Sabrina Riedl, Dina Alihodzic, Daniel Padaric, Lisa Gerlitz, Alexander Stallinger, Bernadette Liegl-Atzwanger, Dagmar Zweytick, Beate Rinner

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 58% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

10 authors at 4 institutions in 2 countries.

Maximiliane WußmannTranslational Center Regenerative Therapies TLC-RT, Fraunhofer Institute for Silicate Research ISC, Neunerplatz 2, 97080 Würzburg, Germany.
Florian Kai Groeber-BeckerTranslational Center Regenerative Therapies TLC-RT, Fraunhofer Institute for Silicate Research ISC, Neunerplatz 2, 97080 Würzburg, Germany.
Sabrina RiedlInstitute of Molecular Biosciences, University of Graz, Humboldtstrasse 50/III, A-8010 Graz, Austria.ORCID 0000-0002-2608-0753
Dina AlihodzicInstitute of Molecular Biosciences, University of Graz, Humboldtstrasse 50/III, A-8010 Graz, Austria.
Daniel PadaricInstitute of Molecular Biosciences, University of Graz, Humboldtstrasse 50/III, A-8010 Graz, Austria.
Lisa GerlitzInstitute of Molecular Biosciences, University of Graz, Humboldtstrasse 50/III, A-8010 Graz, Austria.
Alexander StallingerDivision of Biomedical Research, Medical University of Graz, Stiftingtalstrasse 24, A-8010 Graz, Austria.
Bernadette Liegl-AtzwangerDiagnostic and Research Institute of Pathology, Medical University of Graz, Neue Stiftingtalstrasse 6, A-8010 Graz, Austria.ORCID 0000-0003-2229-5535
Dagmar ZweytickInstitute of Molecular Biosciences, University of Graz, Humboldtstrasse 50/III, A-8010 Graz, Austria.ORCID 0000-0002-4766-7713
Beate RinnerBioTechMed-Graz, Mozartgasse 12/II, A-8010 Graz, Austria.
University of Graz · ATMedical University of Graz · ATFraunhofer Institute for Silicate Research · DEUniversitätsklinikum Würzburg · DE

Funding

Austrian Research Promotion Agency 855671Federal Ministry of Education and Research of Germany 031L0156
6 · The paper itself

Abstract

The host defense derived peptide was assessed in different model systems with increasing complexity employing the highly aggressive NRAS mutated melanoma metastases cell line MUG-Mel2. Amongst others, fluorescence microscopy and spectroscopy, as well as cell death studies were applied for liposomal, 2D and 3D in vitro models including tumor spheroids without or within skin models and in vivo mouse xenografts. Summarized, MUG-Mel2 cells were shown to significantly expose the negatively charged lipid phosphatidylserine on their plasma membranes, showing they are successfully targeted by RDP22. The peptide was able to induce cell death in MUG-Mel2 2D and 3D cultures, where it was able to kill tumor cells even inside the core of tumor spheroids or inside a melanoma organotypic model. In vitro studies indicated cell death by apoptosis upon peptide treatment with an LC

Indexed as

antitumor peptidemelanoma metastasesNRAS mutationphosphatidylserinetumor model systems

Identifiers

PMID36428530
PMCPMC9687695
OpenAlexW4309457399

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.