Evidence map›Paper›PMID 21125314›Full record

ArticleMolecular and cellular biochemistry2011

Treatment of cultured human astrocytes and vascular endothelial cells with protein kinase CK2 inhibitors induces early changes in cell shape and cytoskeleton.

A A Kramerov, A G Golub, V G Bdzhola, S M Yarmoluk, K Ahmed, M Bretner, A V Ljubimov

Abstract read
In one paragraph

Article in Molecular and cellular biochemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. CSNK2B Mutation: A Rare Cause of IGHD.Clinical endocrinology · 2025
    Article
  3. Article
  4. Article
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  9. Knockdown of CK2α reducesInternational journal of medical sciences · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Targeting protein kinase CK2 suppresses prosurvival signaling pathways and growth of glioblastoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    Article
  16. Article
  17. Article
  18. 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

7 authors at 4 institutions in 3 countries.

A A KramerovOphthalmology Research Laboratories, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA. kramerova@cshs.org
A G Golub
V G Bdzhola
S M Yarmoluk
K Ahmed
M Bretner
A V Ljubimov
Institute of Molecular Biology and Genetics · UACedars-Sinai Medical Center · USInstitute of Biochemistry and Biophysics, Polish Academy of Sciences · PLUniversity of Minnesota · US

Funding

ZONA-FREE HAMSTER OVA ASSAY AS AN INDICATOR OF MALE FERTILITYM01RR000425 · NCRR · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI ANDERSON, GAIL V · 1985 to 2011
$74.2M
Mechanisms of Epithelial Alterations in Diabetic CorneaR01EY013431 · NEI · CEDARS-SINAI MEDICAL CENTER · PI Alexander V Ljubimov · 2001 to 2026
$11.3M
Studies of Normal and Neoplastic ProstateU01CA015062 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI AHMED, KHALIL · 2004 to 2008
$1.1M
Modulation of Apoptosis in Prostate CancerI01BX001731 · VA · MINNEAPOLIS VA MEDICAL CENTER · PI AHMED, KHALIL · 2012 to 2015
–
BLRD VA I01 BX001731NCI NIH HHS U01 CA015062NCI NIH HHS U01-CA15062NCRR NIH HHS M01 RR000425NCRR NIH HHS M01 RR00425NEI NIH HHS R01 EY013431NEI NIH HHS R01 EY13431
6 · The paper itself

Abstract

Ubiquitous protein kinase CK2 is a key regulator of cell migration, proliferation and tumor growth. CK2 is abundant in retinal astrocytes, and its inhibition suppresses retinal neovascularization in a mouse retinopathy model. In human astrocytes, CK2 co-distributes with GFAP-containing intermediate filaments, which implies its association with cytoskeleton. Contrary to astrocytes, CK2 is co-localized in microvascular endothelial cells (HBMVEC) with microtubules and actin stress fibers, but not with vimentin-containing intermediate filaments. Specific CK2 inhibitors (TBB, TBI, TBCA and DMAT) and nine novel CK2 inhibiting compounds (TID43, TID46, Quinolone-7, Quinolone-39, FNH28, FNH62, FNH64, FNH68 and FNH74) were tested at 10-200 μM for their ability to induce morphological alterations in cultured human astrocytes (HAST-40), and HBMVEC (For explanation of the inhibitor names, see "Methods" section). CK2 inhibitors caused dramatic changes in shape of cultured cells with effective inhibitor concentrations between 50 and 100 μM. Attached cells retracted, acquired shortened processes, and eventually rounded up and detached. CK2 inhibitor-induced morphological alterations were completely reversible and were not blocked by caspase inhibition. However, longer treatment or higher inhibitor concentration did cause apoptosis. The speed and potency of the CK2 inhibitors effects on cell shape and adhesion were inversely correlated with serum concentration. Western analyses showed that TBB and TBCA elicited a significant (about twofold) increase in the activation of p38 and ERK1/2 MAP kinases that may be involved in cytoskeleton regulation. This novel early biological cell response to CK2 inhibition may underlie the anti-angiogenic effect of CK2 suppression in the retina.

Indexed as

AnimalsAstrocytesCasein Kinase IICattleCell Line, TumorCell ShapeCulture MediaCytoskeletonEndothelial CellsEnzyme ActivationHumansMitogen-Activated Protein KinasesPhosphorylationProtein Kinase InhibitorsTriazoles4,5,6,7-tetrabromobenzotriazoleCasein Kinase IICulture MediaMitogen-Activated Protein KinasesProtein Kinase InhibitorsTriazoles

Identifiers

PMID21125314
PMCPMC3426611
OpenAlexW1980537236

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.