Evidence map›Paper›PMID 24872499›Full record

ArticleJournal of the Royal Society, Interface2014

Patterns in melanocytic lesions: impact of the geometry on growth and transport inside the epidermis.

Thibaut Balois, Clément Chatelain, Martine Ben Amar

Open access · hybridAbstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Signaling Pathways in Melanogenesis.International journal of molecular sciences · 2016
    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

3 authors at 2 institutions in 1 country.

Thibaut BaloisLaboratoire de Physique Statistique, Ecole Normale Supérieure, UPMC Univ Paris 06, Université Paris Diderot, CNRS, 24 rue Lhomond, Paris 75005, France Faculté de médecine, Institut Universitaire de Cancérologie, Université Pierre et Marie Curie-Paris 6, 91 Boulevard de l'hôpital, Paris 75013, France.
Clément ChatelainLaboratoire de Physique Statistique, Ecole Normale Supérieure, UPMC Univ Paris 06, Université Paris Diderot, CNRS, 24 rue Lhomond, Paris 75005, France Faculté de médecine, Institut Universitaire de Cancérologie, Université Pierre et Marie Curie-Paris 6, 91 Boulevard de l'hôpital, Paris 75013, France.
Martine Ben AmarLaboratoire de Physique Statistique, Ecole Normale Supérieure, UPMC Univ Paris 06, Université Paris Diderot, CNRS, 24 rue Lhomond, Paris 75005, France Faculté de médecine, Institut Universitaire de Cancérologie, Université Pierre et Marie Curie-Paris 6, 91 Boulevard de l'hôpital, Paris 75013, France benamar@lps.ens.fr.
Centre National de la Recherche Scientifique · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In glabrous skin, nevi and melanomas exhibit pigmented stripes during clinical dermoscopic examination. They find their origin in the basal layer geometry which periodically exhibits ridges, alternatively large (limiting ridges) and thin (intermediate ridges). However, nevus and melanoma lesions differ by the localization of the pigmented stripes along furrows or ridges of the epidermis surface. Here, we propose a biomechanical model of avascular tumour growth which takes into account this specific geometry in the epidermis where both kinds of lesions first appear. Simulations show a periodic distribution of tumour cells inside the lesion, with a global contour stretched out along the ridges. In order to be as close as possible to clinical observations, we also consider the melanin transport by the keratinocytes. Our simulations show that reasonable assumptions on melanocytic cell repartition in the ridges favour the limiting ridges of the basal compared with the intermediate ones in agreement with nevus observations but not really with melanomas. It raises the question of cell aggregation and repartition of melanocytic cells in acral melanomas and requires further biological studies of these cells in situ.

Indexed as

Models, BiologicalAnimalsCell MovementCell ProliferationCell SizeComputer SimulationEpidermisHumansMelaninsMelanocytesMelanomaNeoplasm InvasivenessSkin NeoplasmsMelaninsclinical dermatologygeometrical growth and transportpattern formationskin cancer morphologytumour multiphase model

Identifiers

PMID24872499
PMCPMC4208365
OpenAlexW2143891530

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.