Evidence map›Paper›PMID 24345765›Full record

ArticleTranslational research : the journal of laboratory and clinical medicine2014

Adult tissue sources for new β cells.

Robert J Nichols, Connie New, Justin P Annes

Abstract read
In one paragraph

Article in Translational research : the journal of laboratory and clinical medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Repurposing cAMP-modulating medications to promote β-cell replication.Molecular endocrinology (Baltimore, Md.) · 2014
    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

3 authors.

Robert J NicholsDepartment of Genetics, Stanford University, Stanford, Calif.
Connie NewDepartment of Medicine, Stanford University Medical School, Stanford, Calif.
Justin P AnnesDepartment of Medicine, Stanford University Medical School, Stanford, Calif. Electronic address: jannes@stanford.edu.

Funding

INSTITUTIONAL TRAINING GRANT IN GENOME SCIENCET32HG000044 · NHGRI · STANFORD UNIVERSITY · PI MICHAEL P. SNYDER · 1995 to 2026
$32.2M
Pancreatic Beta-Cell Regeneration: Expanding the functional MassK08DK084206 · NIDDK · STANFORD UNIVERSITY · PI ANNES, JUSTIN PIERCE · 2009 to 2013
$788k
Interrogating the Role of Adenosine Kinase in Islet Beta-CellsR03DK098143 · NIDDK · STANFORD UNIVERSITY · PI ANNES, JUSTIN PIERCE · 2013 to 2014
$157k
NHGRI NIH HHS T32 HG000044NIDDK NIH HHS K08 DK084206NIDDK NIH HHS R03 DK098143
6 · The paper itself

Abstract

The diabetes pandemic incurs extraordinary public health and financial costs that are projected to expand for the foreseeable future. Consequently, the development of definitive therapies for diabetes is a priority. Currently, a wide spectrum of therapeutic strategies-from implantable insulin delivery devices to transplantation-based cell replacement therapy, to β-cell regeneration-focus on replacing the lost insulin-producing capacity of individuals with diabetes. Among these, β-cell regeneration remains promising but heretofore unproved. Indeed, recent experimental work has uncovered surprising biology that underscores the potential therapeutic benefit of β-cell regeneration. These studies have elucidated a variety of sources for the endogenous production of new β cells from existing cells. First, β cells, long thought to be postmitotic, have demonstrated the potential for regenerative capacity. Second, the presence of pancreatic facultative endocrine progenitor cells has been established. Third, the malleability of cellular identity has availed the possibility of generating β cells from other differentiated cell types. Here, we review the exciting developments surrounding endogenous sources of β-cell production and consider the potential of realizing a regenerative therapy for diabetes from adult tissues.

Indexed as

AdultAnimalsCell TransplantationDiabetes MellitusHumansInsulin-Secreting Cells

Identifiers

PMID24345765
PMCPMC3976738

What OpenQuestion holds

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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.