Evidence map›Paper›PMID 25070956›Full record

ArticleThe Journal of cell biology2014

Paxillin inhibits HDAC6 to regulate microtubule acetylation, Golgi structure, and polarized migration.

Nicholas O Deakin, Christopher E Turner

Abstract read
In one paragraph

Article in The Journal of cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

65 citing papers in PubMed, 98 citations in OpenAlex.

  1. Trial
  2. The histone deacetylase family in health and disease.Signal transduction and targeted therapy · 2026
    Review
  3. Review
  4. Role of HDAC6 in carcinomas.Discover oncology · 2026
    Review
  5. Article
  6. Article
  7. Review
  8. Tubulin Acetylation: A Critical Regulator of Microtubule Function.Results and problems in cell differentiation · 2025
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. HDAC6: A unique HDAC family member as a cancer target.Cellular oncology (Dordrecht, Netherlands) · 2022
    Review

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

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

2 authors at 1 institution in 1 country.

Nicholas O DeakinDepartment of Cell and Developmental Biology, State University of New York Upstate Medical University, Syracuse, NY 13210.
Christopher E TurnerDepartment of Cell and Developmental Biology, State University of New York Upstate Medical University, Syracuse, NY 13210 turnerce@upstate.edu.
SUNY Upstate Medical University · US

Funding

STRUCTURE AND FUNCTION OF PAXILLINR01GM047607 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI TURNER, CHRISTOPHER E · 1996 to 2017
$5.5M
Paxillin and Hic-5 in Coordination of Cancer Cell Invasion MechanismsR01CA163296 · NCI · UPSTATE MEDICAL UNIVERSITY · PI TURNER, CHRISTOPHER E · 2012 to 2016
$1.6M
NCI NIH HHS R01 CA163296NCI NIH HHS R01CA163296NIGMS NIH HHS R01 GM047607NIGMS NIH HHS R01GM47607
6 · The paper itself

Abstract

Polarized cell migration is essential for normal organism development and is also a critical component of cancer cell invasion and disease progression. Directional cell motility requires the coordination of dynamic cell-extracellular matrix interactions as well as repositioning of the Golgi apparatus, both of which can be controlled by the microtubule (MT) cytoskeleton. In this paper, we have identified a new and conserved role for the focal adhesion scaffold protein paxillin in regulating the posttranslational modification of the MT cytoskeleton through an inhibitory interaction with the α-tubulin deacetylase HDAC6. We also determined that through HDAC6-dependent regulation of the MT cytoskeleton, paxillin regulates both Golgi organelle integrity and polarized cell invasion and migration in both three-dimensional and two-dimensional matrix microenvironments. Importantly, these data reveal a fundamental role for paxillin in coordinating MT acetylation-dependent cell polarization and migration in both normal and transformed cells.

Indexed as

Cell MovementProtein Processing, Post-TranslationalAcetylationAnimalsCell Line, TumorCell PolarityExtracellular MatrixGolgi ApparatusHistone Deacetylase 6Histone DeacetylasesHumansMiceMicrotubulesNIH 3T3 CellsPaxillinHDAC6 protein, humanHistone Deacetylase 6Histone DeacetylasesPaxillinPXN protein, human

Identifiers

PMID25070956
PMCPMC4121979
OpenAlexW2146626507

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.