Evidence map›Paper›PMID 31059696›Full record

ArticleThe Journal of investigative dermatology2019

Local Inhibition of MEK/Akt Prevents Cellular Growth in Human Congenital Melanocytic Nevi.

Thomas Rouillé, Selim Aractingi, Natacha Kadlub, Sylvie Fraitag, Alexandre How-Kit, Antoine Daunay, Mikael Hivelin, Philippe Moguelet, Arnaud Picard, Romain H Fontaine and 1 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in The Journal of investigative dermatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Novel insights into the pathogenesis and treatment of NRAS mutant melanoma.Expert review of precision medicine and drug development · 2021
    Article
  11. Disorders Caused by Genetic Mosaicism.Deutsches Arzteblatt international · 2020
    Review
  12. Can Combination MEK and Akt Inhibition Slay the Giant Congenital Nevus?The Journal of investigative dermatology · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Thomas RouilléSaint-Antoine Research Center, INSERM UMRS_938, Paris, France; Sorbonne Université, Paris, France.
Selim AractingiSaint-Antoine Research Center, INSERM UMRS_938, Paris, France; Université Paris-Descartes, Paris, France; AP-HP, Hôpital Cochin, Department of Dermatology, Paris, France.
Natacha KadlubUniversité Paris-Descartes, Paris, France; AP-HP, Hôpital Necker-Enfants-Malades, Department of Maxillofacial and Plastic Surgery, Paris, France.
Sylvie FraitagAP-HP, Hôpital Necker-Enfants-Malades, Department of Pathology, Paris, France.
Alexandre How-KitLaboratory for Functional Genomics, Fondation Jean Dausset-CEPH, Paris, France.
Antoine DaunayLaboratory for Functional Genomics, Fondation Jean Dausset-CEPH, Paris, France.
Mikael HivelinUniversité Paris-Descartes, Paris, France; AP-HP, Hôpital Européen Georges-Pompidou, Department of Plastic Surgery, Paris, France.
Philippe MogueletAP-HP, Hôpital Tenon, Department of Pathology, Paris, France.
Arnaud PicardUniversité Paris-Descartes, Paris, France; AP-HP, Hôpital Necker-Enfants-Malades, Department of Maxillofacial and Plastic Surgery, Paris, France.
Romain H FontaineSaint-Antoine Research Center, INSERM UMRS_938, Paris, France; Sorbonne Université, Paris, France.
Sarah GuéganSaint-Antoine Research Center, INSERM UMRS_938, Paris, France; Université Paris-Descartes, Paris, France; AP-HP, Hôpital Cochin, Department of Dermatology, Paris, France. Electronic address: sarah.guegan.bart@gmail.com.
Délégation Paris 5 · FRFondation Jean Dausset-CEPH · FRInserm · FRHôpital Necker-Enfants Malades · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The management of large congenital melanocytic nevi (lCMN) is based exclusively on iterative surgical procedures in the absence of validated medical therapy. The aim of our study was to develop an intra-lesional medical treatment for lCMN. Seventeen patients harboring NRAS-mutated lCMN were included. Nevocytes obtained from lCMN displayed an overactivation of mitogen-activated protein kinase and phosphoinositide 3-kinase (Akt) pathways. Mitogen-activated protein kinase/extracellular signal-regulated kinase (MEK) and Akt inhibitors reduced the nevosphere diameter in sphere-forming assays, as well as cell viability and proliferation in in vitro assays. Standardized lCMN explants were then cultured ex vivo with the same inhibitors, which induced a decrease in MelanA+ and Sox10+ cells in both epidermis and dermis. Finally, intradermal injections of these inhibitors were administered within standardized lCMN xenografts in Rag2

Indexed as

AnimalsAntineoplastic AgentsCell ProliferationChildChild, PreschoolFemaleGTP PhosphohydrolasesHumansInfantInjections, IntradermalInjections, IntralesionalMaleMART-1 AntigenMelanocytesMembrane ProteinsMiceAntineoplastic AgentsGTP PhosphohydrolasesMART-1 AntigenMembrane ProteinsMitogen-Activated Protein Kinase KinasesMLANA protein, humanNRAS protein, humanProto-Oncogene Proteins c-aktSOX10 protein, humanSOXE Transcription Factors

Identifiers

PMID31059696
OpenAlexW2943702285

What OpenQuestion holds

Textmetadata
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.