Evidence map›Paper›PMID 28057752›Full record

ArticleThe Journal of biological chemistry2017

Forkhead Box Protein 1 (FoxO1) Inhibits Accelerated β Cell Aging in Pancreas-specific SMAD7 Mutant Mice.

Xiangwei Xiao, Congde Chen, Ping Guo, Ting Zhang, Shane Fischbach, Joseph Fusco, Chiyo Shiota, Krishna Prasadan, Henry Dong, George K Gittes

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 23 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

10 authors at 3 institutions in 2 countries.

Xiangwei XiaoDivisions of Pediatric Surgery. Electronic address: xiangwei.xiao@chp.edu.
Congde ChenDivisions of Pediatric Surgery; Department of Pediatric Surgery, Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou 325000, China.
Ping GuoDivisions of Pediatric Surgery; Department of Orthopedic Surgery, University of Texas Health Sciences Center, Houston, Texas 77054.
Ting ZhangImmunogenetics, Department of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15224.
Shane FischbachDivisions of Pediatric Surgery.
Joseph FuscoDivisions of Pediatric Surgery.
Chiyo ShiotaDivisions of Pediatric Surgery.
Krishna PrasadanDivisions of Pediatric Surgery.
Henry DongImmunogenetics, Department of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15224.
George K GittesDivisions of Pediatric Surgery. Electronic address: gittesgk@upmc.edu.
Children's Hospital of Pittsburgh · USSecond Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical University · CNThe University of Texas Health Science Center at Houston · US

Funding

Fox01 in Beta-Cell CompensationR01DK098437 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DONG, HENGJIANG HENRY · 2014 to 2017
$1.4M
Pancreatic Intra-Islet DuctsR01DK098196 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GITTES, GEORGE K. · 2013 to 2014
$667k
NIDDK NIH HHS R01 DK098196NIDDK NIH HHS R01 DK098437
6 · The paper itself

Abstract

The mechanisms underlying the effects of exocrine dysfunction on the development of diabetes remain largely unknown. Here we show that pancreatic depletion of SMAD7 resulted in age-dependent increases in β cell dysfunction with accelerated glucose intolerance, followed by overt diabetes. The accelerated β cell dysfunction and loss of proliferation capacity, two features of β cell aging, appeared to be non-cell-autonomous, secondary to the adjacent exocrine failure as a "bystander effect." Increased Forkhead box protein 1 (FoxO1) acetylation and nuclear retention was followed by progressive FoxO1 loss in β cells that marked the onset of diabetes. Moreover, forced FoxO1 expression in β cells prevented β cell dysfunction and loss in this model. Thus, we present a model of accelerated β cell aging that may be useful for studying the mechanisms underlying β cell failure in diabetes. Moreover, we provide evidence highlighting a critical role of FoxO1 in maintaining β cell identity in the context of SMAD7 failure.

Indexed as

AnimalsCell ProliferationCellular SenescenceDiabetes MellitusForkhead Box Protein O1Insulin-Secreting CellsMaleMiceMice, KnockoutMice, SCIDMutationPancreasProtein TransportSmad7 ProteinForkhead Box Protein O1Foxo1 protein, mouseSmad7 ProteinSmad7 protein, mouseAgingcell proliferationdiabetesFoxO1SMAD7TGFβtype 2 diabetesβ cell

Identifiers

PMID28057752
PMCPMC5336177
OpenAlexW2568752519

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.