Evidence map›Paper›PMID 25073103›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2014

Activated FoxM1 attenuates streptozotocin-mediated β-cell death.

Maria L Golson, Matthew F Maulis, Jennifer C Dunn, Greg Poffenberger, Jonathan Schug, Klaus H Kaestner, Maureen A Gannon

Open access · bronzeAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. FOXM1 cooperates with ERα to regulate functional β-cell mass.American journal of physiology. Endocrinology and metabolism · 2025
    Article
  2. Pharmaceuticals (Basel, Switzerland) · 2024
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. In vivo Antihyperglycemic and Antidyslipidemic Effects of L-Tartaric Acid.Cardiovascular & hematological disorders drug targets · 2022
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Opposing effects of prostaglandin EMolecular metabolism · 2017
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. High-fat diet-induced β-cell proliferation occurs prior to insulin resistance in C57Bl/6J male mice.American journal of physiology. Endocrinology and metabolism · 2015
    Article
  18. 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

7 authors at 2 institutions in 1 country.

Maria L GolsonTennessee Valley Healthcare System Department of Veteran Affairs (M.L.G., M.F.M., J.C.D., G.P., M.A.G.), Nashville, Tennessee 37212; Department of Medicine, Division of Diabetes, Endocrinology, and Metabolism (M.L.G., M.F.M., J.C.D., G.P., M.A.G.), and Departments of Cell and Developmental Biology (M.A.G.) and Molecular Physiology and Biophysics (M.A.G.), Vanderbilt University Medical Center, Nashville, Tennessee 37232; and Department of Genetics and Institute for Diabetes, Obesity and Metabolism (J.S., K.H.K.), University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania 19104.
Matthew F Maulis
Jennifer C Dunn
Greg Poffenberger
Jonathan Schug
Klaus H Kaestner
Maureen A Gannon
VA Tennessee Valley Healthcare System · USUniversity of Pennsylvania · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
VIRAL VECTOR COREP30DK019525 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI MITCHELL A. LAZAR · 1986 to 2026
$48.3M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI OWEN P MCGUINNESS · 2012 to 2026
$29.3M
TRANSGENIC MOUSE/ ES CELL SHARES RESOURCESP60DK020593 · NIDDK · VANDERBILT UNIVERSITY · PI MCGUINNESS, OWEN P · 1986 to 2011
$28.1M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Kevin L Schey · 1989 to 2026
$19.6M
VANTAGE:Consolidation to create the Vanderbilt Technologies for Advanced GenomicsG20RR030956 · NCRR · VANDERBILT UNIVERSITY · PI PIETENPOL, JENNIFER A · 2010 to 2010
$8.7M
Integrated Biological Systems Training in OncologyT32CA119925 · NCI · VANDERBILT UNIVERSITY · PI Vivian Gama, William Patrick Tansey · 2008 to 2026
$7.6M
Regulation of adult pancreatic beta cell replicationI01BX000990 · VA · VETERANS HEALTH ADMINISTRATION · PI GANNON, MAUREEN A · 2011 to 2014
–
BLRD VA I01 BX000990NCI NIH HHS 5T32 CA119925NCI NIH HHS P30 CA068485NCI NIH HHS P30 CA58645NCI NIH HHS P30 CA68485NCI NIH HHS T32 CA119925NCRR NIH HHS G20 RR030956NEI NIH HHS P30 EY008126NEI NIH HHS P30 EY08126NIDDK NIH HHS DK20593NIDDK NIH HHS P30 DK019525NIDDK NIH HHS P30 DK020593
6 · The paper itself

Abstract

The forkhead box transcription factor FoxM1, a positive regulator of the cell cycle, is required for β-cell mass expansion postnatally, during pregnancy, and after partial pancreatectomy. Up-regulation of full-length FoxM1, however, is unable to stimulate increases in β-cell mass in unstressed mice or after partial pancreatectomy, probably due to the lack of posttranslational activation. We hypothesized that expression of an activated form of FoxM1 could aid in recovery after β-cell injury. We therefore derived transgenic mice that inducibly express an activated version of FoxM1 in β-cells (RIP-rtTA;TetO-hemagglutinin (HA)-Foxm1(Δ)(NRD) mice). This N-terminally truncated form of FoxM1 bypasses 2 posttranslational controls: exposure of the forkhead DNA binding domain and targeted proteasomal degradation. Transgenic mice were subjected to streptozotocin (STZ)-induced β-cell ablation to test whether activated FoxM1 can promote β-cell regeneration. Mice expressing HA-FoxM1(ΔNRD) displayed decreased ad libitum-fed blood glucose and increased β-cell mass. β-Cell proliferation was actually decreased in RIP-rtTA:TetO-HA-Foxm1(NRD) mice compared with that in RIP-rtTA mice 7 days after STZ treatment. Unexpectedly, β-cell death was decreased 2 days after STZ treatment. RNA sequencing analysis indicated that activated FoxM1 alters the expression of extracellular matrix and immune cell gene profiles, which may protect against STZ-mediated death. These studies highlight a previously underappreciated role for FoxM1 in promoting β-cell survival.

Indexed as

AnimalsCell CycleCell DeathCell ProliferationCell SurvivalDiabetes MellitusFemaleForkhead Box Protein M1Forkhead Transcription FactorsImmune SystemInsulin-Secreting CellsMaleMiceMice, Inbred C57BLMice, TransgenicRegenerationForkhead Box Protein M1Forkhead Transcription FactorsFoxm1 protein, mouseStreptozocin

Identifiers

PMID25073103
PMCPMC4154244
OpenAlexW1973396248

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.