Evidence map›Paper›PMID 25486364›Full record

ArticleCell cycle (Georgetown, Tex.)2014

Ciliary abnormalities in senescent human fibroblasts impair proliferative capacity.

Loretta Breslin, Suzanna L Prosser, Sandra Cuffe, Ciaran G Morrison

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cholangiocytes' primary cilia regulate DNA damage response and repair.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Autophagy and the hallmarks of aging.Ageing research reviews · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. Failure to reabsorb the primary cilium induces cellular senescence.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Loretta Breslina Center for Chromosome Biology; School of Natural Sciences ; National University of Ireland Galway ; Galway , Ireland.
Suzanna L Prosser
Sandra Cuffe
Ciaran G Morrison
Ollscoil na Gaillimhe – University of Galway · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Somatic cells senesce in culture after a finite number of divisions indefinitely arresting their proliferation. DNA damage and senescence increase the cellular number of centrosomes, the 2 microtubule organizing centers that ensure bipolar mitotic spindles. Centrosomes also provide the basal body from which primary cilia extend to sense and transduce various extracellular signals, notably Hedgehog. Primary cilium formation is facilitated by cellular quiescence a temporary cell cycle exit, but the impact of senescence on cilia is unknown. We found that senescent human fibroblasts have increased frequency and length of primary cilia. Levels of the negative ciliary regulator CP110 were reduced in senescent cells, as were levels of key elements of the Hedgehog pathway. Hedgehog inhibition reduced proliferation in young cells with increased cilium length accompanying cell cycle arrest suggesting a regulatory function for Hedgehog in primary ciliation. Depletion of CP110 in young cell populations increased ciliation frequencies and reduced cell proliferation. These data suggest that primary cilia are potentially novel determinants of the reduced cellular proliferation that initiates senescence.

Indexed as

Cellular SenescenceCell Cycle ProteinsCell ProliferationCells, CulturedCiliaFibroblastsHedgehog ProteinsHumansMicrotubule-Associated ProteinsPhosphoproteinsCCP110 protein, humanCell Cycle ProteinsHedgehog ProteinsMicrotubule-Associated ProteinsPhosphoproteinscentrosomeCP110CP110, centriolar coiled coil protein of 110kDaDABCO, 1,4-Diazabicyclo[2.2.2]octaneDAPI, 4′,6-diamidino-2-phenylindoleECL, enhanced chemiluminescenceFITC, Fluorescein isothiocyanateGAPDH, glyceraldehyde 3-phosphate dehydrogenaseHedgehogHh, HedgehogHMEC, human mammary epithelial cellNHDF, normal human dermal fibroblastsPLK4, Polo-like kinase 4primary ciliumreplicative senescenceSAHF, senescence-associated heterochromatin fociSA-β-gal, senescence-associated β-galactosidaseSmo, smoothened

Identifiers

PMID25486364
PMCPMC4613152
OpenAlexW2051054464

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.