Evidence map›Paper›PMID 30123066›Full record

ArticleInternational journal of biological sciences2018

Topical Application of Tat-Rac1 Promotes Cutaneous Wound Healing in Normal and Diabetic Mice.

Bin Fan, Tao Wang, Li Bian, Zhe Jian, Dongyan D Wang, Fulun Li, Fanglong Wu, Tao Bai, Gongyi Zhang, Nik Muller and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

13 authors at 5 institutions in 2 countries.

Bin FanDepartment of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
Tao WangDepartment of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
Li BianDepartment of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
Zhe JianDepartment of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
Dongyan D WangDepartment of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
Fulun LiDepartment of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
Fanglong WuDepartment of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
Tao BaiDepartment of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
Gongyi ZhangDepartment of Biomedical Research, National Jewish Health, CO, USA.
Nik MullerDepartment of Ophthalmology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
Barry HolwerdaMolecular Throughput Inc., Las Vegas, NV89118, USA.
Gangwen HanDepartment of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
Xiao-Jing WangDepartment of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
University of Colorado Denver · USUniversity of Colorado Anschutz Medical Campus · USFirst Affiliated Hospital of Kunming Medical University · CNPeking University International Hospital · CNXijing Hospital · CN

Funding

Effects of Altering TGF Beta Signaling on Wound HealingR01AR061792 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI WANG, XIAO-JING · 2011 to 2015
$1.9M
NIAMS NIH HHS R01 AR061792
6 · The paper itself

Abstract

The endogenous small GTPase, Rac1, plays a critical role during normal skin wound healing. It remains to be determined whether endogenous Rac1 can be appropriately activated in chronic wounds; if not, whether exogenous Rac1 has therapeutic effects on wound healing. Here we show that Rac1 protein levels were lower in wounds of db/db diabetic mice than wounds in wild type mice during the healing process. To assess the therapeutic potential of exogenous Rac1 in wound healing, we produced a Tat-Rac1 fusion protein that enters into cells through protein transduction. Tat-Rac1 increased proliferation and migration of keratinocytes and dermal fibroblasts

Indexed as

AnimalsBlotting, WesternCell MovementCell ProliferationCells, CulturedFibroblastsHumansKeratinocytesMicerac1 GTP-Binding ProteinSkintat Gene Products, Human Immunodeficiency VirusWound Healingrac1 GTP-Binding Proteintat Gene Products, Human Immunodeficiency Virusdiabetic woundsRac1Tat-Rac1wound healing

Identifiers

PMID30123066
PMCPMC6097474
OpenAlexW2853199050

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.