Evidence map›Paper›PMID 17353358›Full record

ArticleThe Journal of cell biology2007

Critical requirement for cell cycle inhibitors in sustaining nonproliferative states.

Deborah Pajalunga, Alessia Mazzola, Anna Maria Salzano, Maria Grazia Biferi, Gabriele De Luca, Marco Crescenzi

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Therapeutic targeting of replicative immortality.Seminars in cancer biology · 2015
    Review
  10. Proliferation of Multiple Cell Types in the Skeletal Muscle Tissue Elicited by Acute p21 Suppression.Molecular therapy : the journal of the American Society of Gene Therapy · 2015
    Article
  11. Article
  12. Increased expression of p21WAF1/CIP1 in kidney proximal tubules mediates fibrosis.American journal of physiology. Renal physiology · 2015
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Scratch2 prevents cell cycle re-entry by repressing miR-25 in postmitotic primary neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  19. Article
  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

6 authors at 1 institution in 1 country.

Deborah PajalungaDepartment of Environment and Primary Prevention, Istituto Superiore di Sanità, 00161 Roma, Italy.
Alessia Mazzola
Anna Maria Salzano
Maria Grazia Biferi
Gabriele De Luca
Marco Crescenzi
Istituto Superiore di Sanità · IT

Funding

Telethon GGP05006
6 · The paper itself

Abstract

In adult vertebrates, most cells are not in the cell cycle at any one time. Physiological nonproliferation states encompass reversible quiescence and permanent postmitotic conditions such as terminal differentiation and replicative senescence. Although these states appear to be attained and maintained quite differently, they might share a core proliferation-restricting mechanism. Unexpectedly, we found that all sorts of nonproliferating cells can be mitotically reactivated by the sole suppression of histotype-specific cyclin-dependent kinase (cdk) inhibitors (CKIs) in the absence of exogenous mitogens. RNA interference-mediated suppression of appropriate CKIs efficiently triggered DNA synthesis and mitosis in established and primary terminally differentiated skeletal muscle cells (myotubes), quiescent human fibroblasts, and senescent human embryo kidney cells. In serum-starved fibroblasts and myotubes alike, cell cycle reactivation was critically mediated by the derepression of cyclin D-cdk4/6 complexes. Thus, both temporary and permanent growth arrest must be actively maintained by the constant expression of CKIs, whereas the cell cycle-driving cyclins are always present or can be readily elicited. In principle, our findings could find wide application in biotechnology and tissue repair whenever cell proliferation is limiting.

Indexed as

Cell ProliferationAnimalsCell CycleCell DifferentiationCells, CulturedCellular SenescenceCyclin D3Cyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin-Dependent Kinase Inhibitor ProteinsCyclinsDNA ReplicationHumansMiceMuscle Fibers, SkeletalRNA InterferenceCCND3 protein, humanCcnd3 protein, mouseCyclin D3Cyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin-Dependent Kinase Inhibitor ProteinsCyclins

Identifiers

PMID17353358
PMCPMC2064055
OpenAlexW2140891814

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.