Evidence map›Paper›PMID 20944652›Full record

ArticleThe Journal of investigative dermatology2011

Activated Kras alters epidermal homeostasis of mouse skin, resulting in redundant skin and defective hair cycling.

Anandaroop Mukhopadhyay, Suguna R Krishnaswami, Benjamin D-Y Yu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

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  16. Defining the origins of Ras/p53-mediated squamous cell carcinoma.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  17. Pleiotropic patterning response to activation of Shh signaling in the limb apical ectodermal ridge.Developmental dynamics : an official publication of the American Association of Anatomists · 2011
    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

3 authors at 1 institution in 1 country.

Anandaroop MukhopadhyayDivision of Dermatology, Department of Medicine, UCSD Stem Cell Program, and Institute for Genomic Medicine, University of California, San Diego, San Diego, California 92093-0869, USA.
Suguna R Krishnaswami
Benjamin D-Y Yu
University of California San Diego · US

Funding

RAS Signaling in Skin Stem Cell Proliferation and FateR01AR056667 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SEN, GEORGE L · 2009 to 2013
$1.5M
Functional Analysis of Sprouty Genes in Limb DevelopmentK08HD047674 · NICHD · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI YU, BENJAMIN DIUNG-YUEN · 2004 to 2008
$609k
NIAMS NIH HHS R01 AR056667NICHD NIH HHS K08 HD047674
6 · The paper itself

Abstract

Germline mutations in the RAS-mitogen-activated protein kinase (RAS/MAPK) pathway are associated with genodermatoses, characterized by cutaneous, cardiac, and craniofacial defects, and cancer predisposition. Whereas activating mutations in HRAS are associated with the vast majority of patients with Costello syndrome, mutations in its paralog, KRAS, are rare. To better understand the disparity among RAS paralogs in human syndromes, we generated mice that activate a gain-of-function Kras allele (Lox-Stop-Lox (LSL)-Kras(G12D)) in ectodermal tissue using two different Cre transgenic lines. Using Msx2-Cre or ligand-inducible keratin 15 (K15)-CrePR, the embryonic effects of activated Kras were bypassed and the effects of Kras(G12D) expression from its endogenous promoter were determined. We found that Kras(G12D) induced redundant skin, papillomas, shortened nails, and hair loss. Redundant skin was associated with basal keratinocyte hyperplasia and an increase in body surface area. Paradoxically, Kras(G12D) also prevented hair cycle activation. We find that Kras(G12D) blocks proliferation in the bulge region of the hair follicle, when activated through Msx2-Cre but not through K15-CrePR. These studies reveal that KRAS, although infrequently involved in RAS/MAPK syndromes, is capable of inducing multiple cutaneous features that grossly resemble human RAS/MAPK syndromes.

Indexed as

AllelesAnimalsCell CycleCell ProliferationEpidermisHairHomeostasisHyperplasiaKeratinocytesMiceMice, Inbred C57BLMice, TransgenicModels, AnimalProto-Oncogene Proteins p21(ras)SkinHras protein, mouseProto-Oncogene Proteins p21(ras)

Identifiers

PMID20944652
PMCPMC3335744
OpenAlexW2012877571

What OpenQuestion holds

Textmetadata
LicenceTDM
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.