Evidence map›Paper›PMID 25444911›Full record

ArticleCancer letters2015

UNC45A localizes to centrosomes and regulates cancer cell proliferation through ChK1 activation.

Yasmeen Jilani, Su Lu, Huang Lei, Larry M Karnitz, Ahmed Chadli

Open access · greenAbstract read
In one paragraph

Article in Cancer letters, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Metazoan evolution of the armadillo repeat superfamily.Cellular and molecular life sciences : CMLS · 2017
    Article
  11. Centrosomes in the DNA damage response--the hub outside the centre.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2016
    Review
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

5 authors at 2 institutions in 2 countries.

Yasmeen JilaniMolecular Oncology and Biomarkers Program, GRU Cancer Center, Georgia Regents University, 1410 Laney Walker Blvd, CN-3151, Augusta, GA 30912, USA.
Su LuMolecular Oncology and Biomarkers Program, GRU Cancer Center, Georgia Regents University, 1410 Laney Walker Blvd, CN-3151, Augusta, GA 30912, USA.
Huang LeiCancer Immunology, Inflammation, and Tolerance Program, Georgia Regents University Cancer Center, Medical College of Georgia, Georgia Regents University, Augusta, GA 30912.
Larry M KarnitzDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
Ahmed ChadliMolecular Oncology and Biomarkers Program, GRU Cancer Center, Georgia Regents University, 1410 Laney Walker Blvd, CN-3151, Augusta, GA 30912, USA. Electronic address: achadli@gru.edu.
Augusta University · USMayo Clinic · US

Funding

Predoctoral Training Program in Molecular PharmacologyT32GM072474 · NIGMS · MAYO CLINIC ROCHESTER · PI KARNITZ, LARRY M · 2005 to 2020
$2.4M
Targeting the core components of the Hsp90 chaperoning machineR01GM102443 · NIGMS · AUGUSTA UNIVERSITY · PI CHADLI, AHMED · 2012 to 2014
$743k
NIGMS NIH HHS R01 GM102443NIGMS NIH HHS R01 GM102443-01NIGMS NIH HHS T32 GM072474
6 · The paper itself

Abstract

The UCS family of proteins regulates cellular functions through their interactions with myosin. Here we show that one member of this family, UNC45A, is also a novel centrosomal protein. UNC45A is required for cellular proliferation of cancer cell in vitro and for tumor growth in vivo through its ability to bind and regulate ChK1 nuclear-cytoplasmic localization in an Hsp90-independent manner. Immunocytochemical and biochemical fractionation studies revealed that UNC45A and ChK1 co-localize to the centrosome. Inhibition of UNC45A expression reduced ChK1 activation and its tethering to the centrosome, events required for proper centrosome function. Lack of UNC45A caused the accumulation of multi-nucleated cells, consistent with a defect in Chk1 regulation of centrosomes. These findings identify a novel centrosomal function for UNC45A and its role in cell proliferation and tumorigenesis.

Indexed as

CarcinogenesisCell ProliferationCentrosomeCheckpoint Kinase 1Gene Knockdown TechniquesHeLa CellsHumansIntracellular Signaling Peptides and ProteinsMolecular ChaperonesProtein KinasesRNA, Small InterferingTransfectionCheckpoint Kinase 1CHEK1 protein, humanIntracellular Signaling Peptides and ProteinsMolecular ChaperonesProtein KinasesRNA, Small InterferingUNC45A protein, humanCentrosomeChaperoneChK1Hsp90TumorigenesisUNC45A

Identifiers

PMID25444911
PMCPMC4277927
OpenAlexW2074834552

What OpenQuestion holds

Textmetadata
LicenceTDM
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.