Evidence map›Paper›PMID 16651637›Full record

ArticleThe American journal of pathology2006

Expression of protein kinase CK2 in astroglial cells of normal and neovascularized retina.

Andrei A Kramerov, Mehrnoosh Saghizadeh, Hao Pan, Andrea Kabosova, Mathias Montenarh, Khalil Ahmed, John S Penn, Candy K Chan, David R Hinton, Maria B Grant and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 58 citations in OpenAlex.

  1. Protein Kinase CK2-A Putative Target for the Therapy of Diabetes Mellitus?International journal of molecular sciences · 2019
    Review
  2. Review
  3. Article
  4. Stem cell therapies in the treatment of diabetic retinopathy and keratopathy.Experimental biology and medicine (Maywood, N.J.) · 2016
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Hyperoxia therapy of pre-proliferative ischemic retinopathy in a mouse model.Investigative ophthalmology & visual science · 2011
    Article
  10. Article
  11. Article
  12. Protein kinase CK2 and new binding partners during spermatogenesis.Cellular and molecular life sciences : CMLS · 2010
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. ZBED4, a BED-type zinc-finger protein in the cones of the human retina.Investigative ophthalmology & visual science · 2009
    Article
  18. Article
  19. 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

11 authors at 8 institutions in 2 countries.

Andrei A KramerovOphthalmology Research Laboratories, Cedars-Sinai Medical Center, University of California at Los Angeles School of Medicine, 90048, USA. kramerova@cshs.org
Mehrnoosh Saghizadeh
Hao Pan
Andrea Kabosova
Mathias Montenarh
Khalil Ahmed
John S Penn
Candy K Chan
David R Hinton
Maria B Grant
Alexander V Ljubimov
Cedars-Sinai Medical Center · USUniversity of Southern California · USSaarland University · DEUniversity of California, Los Angeles · USUniversity of Florida · USUniversity of Minnesota Medical Center · USVanderbilt University · USVeterans Health Administration · US

Funding

STUDIES OF NORMAL AND NEOPLASTIC PROSTATER01CA015062 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI AHMED, KHALIL · 1985 to 2002
$578k
NCI NIH HHS R01 CA015062NEI NIH HHS 2R01 EY7709
6 · The paper itself

Abstract

We previously documented protein kinase CK2 involvement in retinal neovascularization. Here we describe retinal CK2 expression and combined effects of CK2 inhibitors with the somatostatin analog octreotide in a mouse model of oxygen-induced retinopathy (OIR). CK2 expression in human and rodent retinas with and without retinopathy and in astrocytic and endothelial cultures was examined by immunohistochemistry, Western blotting, and reverse transcriptase-polymerase chain reaction. A combination of CK2 inhibitors, emodin or 4,5,6,7-tetrabromobenzotriazole, with octreotide was injected intraperitoneally from postnatal (P) day P11 to P17 to block mouse OIR. All CK2 subunits (alpha, alpha', beta) were expressed in retina, and a novel CK2alpha splice variant was detected by reverse transcriptase-polymerase chain reaction. CK2 antibodies primarily reacted with retinal astrocytes, and staining was increased around new intraretinal vessels in mouse OIR and rat retinopathy of prematurity, whereas preretinal vessels were negative. Cultured astrocytes showed increased perinuclear CK2 staining compared to endothelial cells. In the OIR model, CK2 mRNA expression increased modestly on P13 but not on P17. Octreotide combined with emodin or 4,5,6,7-tetrabromobenzotriazole blocked mouse retinal neovascularization more efficiently than either compound alone. Based on its retinal localization, CK2 may be considered a new immunohistochemical astrocytic marker, and combination of CK2 inhibitors and octreotide may be a promising future treatment for proliferative retinopathies.

Indexed as

Angiogenesis InhibitorsAnimalsAstrocytesCasein Kinase IIDrug CombinationsEmodinEnzyme InhibitorsHumansImmunohistochemistryInfant, NewbornMiceMolecular Sequence DataRatsRetinaRetinal NeovascularizationRetinopathy of PrematurityAngiogenesis InhibitorsCasein Kinase IIDrug CombinationsEmodinEnzyme InhibitorsSomatostatin

Identifiers

PMID16651637
PMCPMC1606582
OpenAlexW2080554031

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.