Evidence map›Paper›PMID 28777946›Full record

ArticleCell stem cell2017

Engineered Epidermal Progenitor Cells Can Correct Diet-Induced Obesity and Diabetes.

Jiping Yue, Xuewen Gou, Yuanyuan Li, Barton Wicksteed, Xiaoyang Wu

Open access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Charting Endocrine Progenitors Across Species and Organs.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  7. CRISPR-Cas9‒Based Genomic Engineering in Keratinocytes: From Technology to Application.JID innovations : skin science from molecules to population health · 2022
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  11. NThe EMBO journal · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Jiping YueBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Xuewen GouBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Yuanyuan LiBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Barton WicksteedDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.
Xiaoyang WuBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA. Electronic address: xiaoyangwu@uchicago.edu.
University of Chicago · USUniversity of Illinois Chicago · US

Funding

TRANSGENIC COREP60DK020595 · NIDDK · UNIVERSITY OF CHICAGO · PI BELL, GRAEME I · 1985 to 2012
$25.5M
Pilot and Feasibility ProgramP30DK020595 · NIDDK · UNIVERSITY OF CHICAGO · PI Matthew J Brady · 2013 to 2026
$20.9M
Development of epidermal progenitor cell-based therapy for regenerative medicineR01OD023700 · OD · UNIVERSITY OF CHICAGO · PI WU, XIAOYANG · 2017 to 2021
$2.4M
Coordinated cytoskeletal dynamics in skin somatic stem cells - Resubmission 01R01AR063630 · NIAMS · UNIVERSITY OF CHICAGO · PI WU, XIAOYANG · 2013 to 2017
$1.7M
NIAMS NIH HHS R01 AR063630NIDDK NIH HHS P30 DK020595NIDDK NIH HHS P60 DK020595NIH HHS R01 OD023700
6 · The paper itself

Abstract

Somatic gene therapy is a promising approach for treating otherwise terminal or debilitating diseases. The human skin is a promising conduit for genetic engineering, as it is the largest and most accessible organ, epidermal autografts and tissue-engineered skin equivalents have been successfully deployed in clinical applications, and skin epidermal stem/progenitor cells for generating such grafts are easy to obtain and expand in vitro. Here, we develop skin grafts from mouse and human epidermal progenitors that were engineered by CRISPR-mediated genome editing to controllably release GLP-1 (glucagon-like peptide 1), a critical incretin that regulates blood glucose homeostasis. GLP-1 induction from engineered mouse cells grafted onto immunocompetent hosts increased insulin secretion and reversed high-fat-diet-induced weight gain and insulin resistance. Taken together, these results highlight the clinical potential of developing long-lasting, safe, and versatile gene therapy approaches based on engineering epidermal progenitor cells.

Indexed as

Genetic EngineeringAnimalsBlood GlucoseBody WeightCRISPR-Cas SystemsDiabetes Mellitus, Type 2Diet, High-FatEpidermisGene EditingGene Transfer TechniquesGlucagon-Like Peptide 1HomeostasisHumansMiceObesitySkin TransplantationBlood GlucoseGlucagon-Like Peptide 1CRISPRcutaneous gene therapydiabetesepidermal progenitor cellsobesity

Identifiers

PMID28777946
PMCPMC5555372
OpenAlexW2742507319

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.