Evidence map›Paper›PMID 20194624›Full record

ArticleMolecular and cellular biology2010

p27kip1 controls cell morphology and motility by regulating microtubule-dependent lipid raft recycling.

Barbara Belletti, Ilenia Pellizzari, Stefania Berton, Linda Fabris, Katarina Wolf, Francesca Lovat, Monica Schiappacassi, Sara D'Andrea, Milena S Nicoloso, Sara Lovisa and 6 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.9field-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

40 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. p27International journal of molecular sciences · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Role of p27Oncotarget · 2018
    Review
  10. Article
  11. Review
  12. Article
  13. p27eLife · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. p27kip1 controls H-Ras/MAPK activation and cell cycle entry via modulation of MT stability.Proceedings of the National Academy of Sciences of the United States of America · 2015
    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

16 authors at 5 institutions in 2 countries.

Barbara BellettiDivision of Experimental Oncology 2, Centro di Riferimento Oncologico, National Cancer Institute, Via Franco Gallini, 2, 33081 Aviano, Italy.
Ilenia Pellizzari
Stefania Berton
Linda Fabris
Katarina Wolf
Francesca Lovat
Monica Schiappacassi
Sara D'Andrea
Milena S Nicoloso
Sara Lovisa
Maura Sonego
Paola Defilippi
Andrea Vecchione
Alfonso Colombatti
Peter Friedl
Gustavo Baldassarre
Centro di Riferimento Oncologico · ITAzienda Ospedaliera Sant'Andrea · ITRadboud University Medical Center · NLRadboud University Nijmegen · NLUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

p27(kip1) (p27) is an inhibitor of cyclin/cyclin-dependent kinase complexes, whose nuclear loss indicates a poor prognosis in various solid tumors. When located in the cytoplasm, p27 binds Op18/stathmin (stathmin), a microtubule (MT)-destabilizing protein, and restrains its activity. This leads to MT stabilization, which negatively affects cell migration. Here, we demonstrate that this p27 function also influences morphology and motility of cells immersed in three-dimensional (3D)matrices. Cells lacking p27 display a decrease in MT stability, a rounded shape when immersed in 3D environments, and a mesenchymal-amoeboid conversion in their motility mode. Upon cell contact to extracellular matrix, the decreased MT stability observed in p27 null cells results in accelerated lipid raft trafficking and increased RhoA activity. Importantly, cell morphology, motility, MT network composition, and distribution of p27 null cells were rescued by the concomitant genetic ablation of Stathmin, implicating that the balanced expression of p27 and stathmin represents a crucial determinant for cytoskeletal organization and cellular behavior in 3D contexts.

Indexed as

Cell MovementCell ShapeEndocytosis3T3 CellsAnimalsCyclin-Dependent Kinase Inhibitor p27Cytoplasmic VesiclesEmbryo, MammalianExtracellular MatrixFibroblastsMembrane MicrodomainsMiceMice, KnockoutMicrotubulesrhoA GTP-Binding ProteinStathminCyclin-Dependent Kinase Inhibitor p27rhoA GTP-Binding ProteinStathmin

Identifiers

PMID20194624
PMCPMC2863592
OpenAlexW2156363172

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.