Evidence map›Paper›PMID 25458010›Full record

ArticleDevelopmental cell2014

DEPDC1B coordinates de-adhesion events and cell-cycle progression at mitosis.

Stefano Marchesi, Francesca Montani, Gianluca Deflorian, Rocco D'Antuono, Alessandro Cuomo, Serena Bologna, Carmela Mazzoccoli, Tiziana Bonaldi, Pier Paolo Di Fiore, Francesco Nicassio

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 14% 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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 102 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Illuminating DEPDC1B in Multi-pronged Regulation of Tumor Progression.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  20. Review

6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 1 country.

Stefano MarchesiIstituto Europeo di Oncologia (IEO), 20141 Milan, Italy; Fondazione IFOM-Istituto FIRC di Oncologia Molecolare, 20139 Milan, Italy; Center for Genomic Science of IIT@SEMM, Istituto Italiano di Tecnologia (IIT), 20139 Milan, Italy.
Francesca MontaniIstituto Europeo di Oncologia (IEO), 20141 Milan, Italy.
Gianluca DeflorianFondazione IFOM-Istituto FIRC di Oncologia Molecolare, 20139 Milan, Italy.
Rocco D'AntuonoFondazione IFOM-Istituto FIRC di Oncologia Molecolare, 20139 Milan, Italy.
Alessandro CuomoIstituto Europeo di Oncologia (IEO), 20141 Milan, Italy.
Serena BolognaFondazione IFOM-Istituto FIRC di Oncologia Molecolare, 20139 Milan, Italy.
Carmela MazzoccoliLaboratory of Preclinical and Translational Research, IRCCS, Centro di Riferimento Oncologico della Basilicata, 85028 Rionero in Vulture (PZ), Italy.
Tiziana BonaldiIstituto Europeo di Oncologia (IEO), 20141 Milan, Italy.
Pier Paolo Di FioreIstituto Europeo di Oncologia (IEO), 20141 Milan, Italy; Fondazione IFOM-Istituto FIRC di Oncologia Molecolare, 20139 Milan, Italy; Dipartimento di Scienze della Salute, Università degli Studi di Milano, 20142 Milan, Italy. Electronic address: pierpaolo.difiore@ieo.eu.
Francesco NicassioIstituto Europeo di Oncologia (IEO), 20141 Milan, Italy; Fondazione IFOM-Istituto FIRC di Oncologia Molecolare, 20139 Milan, Italy; Center for Genomic Science of IIT@SEMM, Istituto Italiano di Tecnologia (IIT), 20139 Milan, Italy. Electronic address: francesco.nicassio@iit.it.
European Institute of Oncology · ITIFOM · ITItalian Institute of Technology · ITCentro di Riferimento Oncologico della Basilicata · ITUniversity of Milan · IT

Funding

European Research Council 233033
6 · The paper itself

Abstract

Cells entering mitosis become rounded, lose attachment to the substrate, and increase their cortical rigidity. Pivotal to these events is the dismantling of focal adhesions (FAs). How mitotic reshaping is linked to commitment to divide is unclear. Here, we show that DEPDC1B, a protein that accumulates in G2, coordinates de-adhesion events and cell-cycle progression at mitosis. DEPDC1B functions as an inhibitor of a RhoA-based signaling complex, which assembles on the FA-associated protein tyrosine phosphatase, receptor type, F (PTPRF) and mediates the integrity of FAs. By competing with RhoA for the interaction with PTPRF, DEPDC1B promotes the dismantling of FAs, which is necessary for the morphological changes preceding mitosis. The circuitry is relevant in whole organisms, as shown by the control exerted by the DEPDC1B/RhoA/PTPRF axis on mitotic dynamics during zebrafish development. Our results uncover an adhesion-dependent signaling mechanism that coordinates adhesion events with the control of cell-cycle progression.

Indexed as

AnimalsCell AdhesionCell Cycle ProteinsCells, CulturedHumansMitosisPhosphorylationSignal TransductionZebrafishZebrafish ProteinsCell Cycle ProteinsDEPDC1B protein, zebrafishZebrafish Proteins

Identifiers

PMID25458010
PMCPMC4250264
OpenAlexW2128098893

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.