Evidence map›Paper›PMID 26087337›Full record

ReviewCurrent opinion in endocrinology, diabetes, and obesity2015

Pancreatic islet cell development and regeneration.

Anthony I Romer, Lori Sussel

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in endocrinology, diabetes, and obesity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Islet Regeneration: Endogenous and Exogenous Approaches.International journal of molecular sciences · 2021
    Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Drug Delivery System in the Treatment of Diabetes Mellitus.Frontiers in bioengineering and biotechnology · 2020
    Review
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

2 authors at 1 institution in 1 country.

Anthony I RomerDepartment of Genetics and Development, Columbia University, New York, New York, USA.
Lori Sussel
Columbia University · US

Funding

Hormones: Molecular Mechanism of Action and FunctionsT32DK007328 · NIDDK · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI KOUSTENI, STAVROULA · 1986 to 2025
$7.8M
Regulation of Pancreatic Islet Cell FateR01DK082590 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LORI SUSSEL · 2009 to 2026
$7.3M
Epigenetic events underlying Type I diabetesDP3DK094400 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHRISTIANO, ANGELA M, CLYNES, RAPHAEL A. · 2011 to 2011
$6.6M
Regulation of exocrine pancreas formationR01DK087711 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SUSSEL, LORI · 2010 to 2014
$1.7M
The role of Gata 4 in exocrine pancreas developmentR01DK064146 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI SUSSEL, LORI · 2003 to 2007
$1.3M
NeuroD function during Beta cell development and in mouse models of diabetesF32DK103506 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ROMER, ANTHONY ISTVAN · 2014 to 2016
$111k
NIDDK NIH HHS DP3 DK094400NIDDK NIH HHS F32 DK103506NIDDK NIH HHS R01 DK064146NIDDK NIH HHS R01 DK082590NIDDK NIH HHS R01 DK087711NIDDK NIH HHS T32 DK007328
6 · The paper itself

Abstract

purpose of reviewThis review will discuss recent advances in understanding mouse and human pancreatic islet cell development, novel concepts related to β cell dysfunction and improved approaches for replenishing β cells to treat diabetes. RECENT

findingsConsiderable knowledge about pancreatic islet development and function has been gained using model systems with subsequent validation in human tissues. Recently, several rodent studies have revealed that differentiated adult islet cells retain remarkable plasticity and can be converted to other islet cell types by perturbing their transcription factor profiles. Furthermore, significant advances have been made in the generation of β-like cells from stem cell populations. Therefore, the generation of functionally mature β cells by the in-situ conversion of non-β cell populations or by the directed differentiation of human pluripotent stem cells could represent novel mechanisms for replenishing β cells in diabetic patients. SUMMARY: The overall conservation between mouse and human pancreatic development, islet physiology and etiology of diabetes encourages the translation of novel β cell replacement therapies to humans. Further deciphering the molecular mechanisms that direct islet cell regeneration, plasticity and function could improve and expand the β cell replacement strategies for treating diabetes.

Indexed as

AnimalsCell DifferentiationCell TransdifferentiationHumansInsulin-Secreting CellsPluripotent Stem CellsRegeneration

Identifiers

PMID26087337
PMCPMC4660868
OpenAlexW2403999012

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.