Evidence map›Paper›PMID 23493571›Full record

ArticleDiabetes2013

Cytoplasmic-nuclear trafficking of G1/S cell cycle molecules and adult human β-cell replication: a revised model of human β-cell G1/S control.

Nathalie M Fiaschi-Taesch, Jeffrey W Kleinberger, Fatimah G Salim, Ronnie Troxell, Rachel Wills, Mansoor Tanwir, Gabriella Casinelli, Amy E Cox, Karen K Takane, Harish Srinivas and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 55 citations in OpenAlex.

  1. β-Cell Regeneration Is Driven by Pancreatic Plasticity.Advances in anatomy, embryology, and cell biology · 2024
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Islet Regeneration: Endogenous and Exogenous Approaches.International journal of molecular sciences · 2021
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Akt/p27International journal of endocrinology · 2018
    Article
  19. Review
  20. 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

12 authors at 1 institution in 1 country.

Nathalie M Fiaschi-TaeschDivision of Endocrinology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA. nmt2@pitt.edu
Jeffrey W Kleinberger
Fatimah G Salim
Ronnie Troxell
Rachel Wills
Mansoor Tanwir
Gabriella Casinelli
Amy E Cox
Karen K Takane
Harish Srinivas
Donald K Scott
Andrew F Stewart
University of Pittsburgh · US

Funding

Multi-Disciplinary Approaches to Driving Therapeutic Human Beta Cell ReplicationU01DK089538 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STEWART, ANDREW F. · 2010 to 2014
$3.6M
Pancreatic Islet Growth Factors: Transgenic and Viral ModelingR01DK055023 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STEWART, ANDREW F. · 1998 to 2015
$3.5M
The Role of Myc in ChREBP-dependent, Glucose-stimulated Gene ExpressionR56DK065149 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SCOTT, DONALD K. · 2010 to 2010
$183k
NIDDK NIH HHS R01 DK055023NIDDK NIH HHS R-01 DK55023NIDDK NIH HHS R56 DK065149NIDDK NIH HHS U-01 DK 089538NIDDK NIH HHS U01 DK089538
6 · The paper itself

Abstract

Harnessing control of human β-cell proliferation has proven frustratingly difficult. Most G1/S control molecules, generally presumed to be nuclear proteins in the human β-cell, are in fact constrained to the cytoplasm. Here, we asked whether G1/S molecules might traffic into and out of the cytoplasmic compartment in association with activation of cell cycle progression. Cdk6 and cyclin D3 were used to drive human β-cell proliferation and promptly translocated into the nucleus in association with proliferation. In contrast, the cell cycle inhibitors p15, p18, and p19 did not alter their location, remaining cytoplasmic. Conversely, p16, p21, and p27 increased their nuclear frequency. In contrast once again, p57 decreased its nuclear frequency. Whereas proliferating β-cells contained nuclear cyclin D3 and cdk6, proliferation generally did not occur in β-cells that contained nuclear cell cycle inhibitors, except p21. Dynamic cytoplasmic-nuclear trafficking of cdk6 was confirmed using green fluorescent protein-tagged cdk6 and live cell imaging. Thus, we provide novel working models describing the control of cell cycle progression in the human β-cell. In addition to known obstacles to β-cell proliferation, cytoplasmic-to-nuclear trafficking of G1/S molecules may represent an obstacle as well as a therapeutic opportunity for human β-cell expansion.

Indexed as

AdolescentAdultAnimalsCell Cycle ProteinsCell DivisionCell Line, TumorCell NucleusCell ProliferationChildCytoplasmFemaleG1 PhaseHumansInsulin-Secreting CellsMaleMiddle AgedCell Cycle Proteins

Identifiers

PMID23493571
PMCPMC3712040
OpenAlexW2157699156

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.