Evidence map›Paper›PMID 27435858›Full record

ArticleMolecular and cellular biochemistry2016

Examination of CK2α and NF-κB p65 expression in human benign prostatic hyperplasia and prostate cancer tissues.

Fatima Qaiser, Janeen H Trembley, Sarah Sadiq, Iqbal Muhammad, Rubina Younis, Shoaib Naiyar Hashmi, Badar Murtaza, Thomas S Rector, Abdul Khaliq Naveed, Khalil Ahmed

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biochemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Nutraceutical Effects ofNutrients · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Protein Kinase CK2, a Potential Therapeutic Target in Carcinoma ManagementAsian Pacific journal of cancer prevention : APJCP · 2019
    Review
  9. Article
  10. Review
  11. Review
  12. 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

10 authors at 6 institutions in 2 countries.

Fatima QaiserDepartment of Biochemistry and Molecular Biology, Army Medical College, National University of Sciences and Technology, Islamabad, Pakistan.
Janeen H TrembleyDepartment of Veterans Affairs, Cellular and Molecular Biochemistry Research Laboratory (151) Research Service, Minneapolis VA Health Care System, One Veterans Drive, Minneapolis, MN, 55417, USA.
Sarah SadiqDepartment of Biochemistry and Molecular Biology, Army Medical College, National University of Sciences and Technology, Islamabad, Pakistan.
Iqbal MuhammadDepartment of Histopathology, Army Medical College, Rawalpindi, Pakistan.
Rubina YounisDepartment of Histopathology, Army Medical College, Rawalpindi, Pakistan.
Shoaib Naiyar HashmiDepartment of Histopathology, Armed Forces Institute of Pathology, Combined Military Hospital, Rawalpindi, Pakistan.
Badar MurtazaArmed Forces Institute of Urology, Combined Military Hospital, Rawalpindi, Pakistan.
Thomas S RectorDepartment of Veterans Affairs, Cellular and Molecular Biochemistry Research Laboratory (151) Research Service, Minneapolis VA Health Care System, One Veterans Drive, Minneapolis, MN, 55417, USA.
Abdul Khaliq NaveedDepartment of Biochemistry and Molecular Biology, Army Medical College, National University of Sciences and Technology, Islamabad, Pakistan.
Khalil AhmedDepartment of Veterans Affairs, Cellular and Molecular Biochemistry Research Laboratory (151) Research Service, Minneapolis VA Health Care System, One Veterans Drive, Minneapolis, MN, 55417, USA. ahmedk@umn.edu.ORCID http://orcid.org/0000-0003-4531-6837
Army Medical College · PKUniversity of Minnesota · USArmed Forces Institute of Pathology · PKCombined Military Hospital · PKMinneapolis VA Health Care System · USRiphah International University · PK

Funding

A Novel Therapeutic Approach for Primary and Metastatic Prostate CancerR01CA150182 · NCI · UNIVERSITY OF MINNESOTA · PI AHMED, KHALIL · 2011 to 2015
$1.4M
BLRD VA I01 BX001731BLRD VA I01 BX003282NCI NIH HHS R01 CA150182
6 · The paper itself

Abstract

Protein kinase CK2 plays a critical role in cell growth, proliferation, and suppression of cell death. CK2 is overexpressed, especially in the nuclear compartment, in the majority of cancers, including prostate cancer (PCa). CK2-mediated activation of transcription factor nuclear factor kappa B (NF-κB) p65 is a key step in cellular proliferation, resulting in translocation of NF-κB p65 from the cytoplasm to the nucleus. As CK2 expression and activity are also elevated in benign prostatic hyperplasia (BPH), we sought to increase the knowledge of CK2 function in benign and malignant prostate by examination of the relationships between nuclear CK2 and nuclear NF-κB p65 protein expression. The expression level and localization of CK2α and NF-κB p65 proteins in PCa and BPH tissue specimens was determined. Nuclear CK2α and NF-κB p65 protein levels are significantly higher in PCa compared with BPH, and these proteins are positively correlated with each other in both diseases. Nuclear NF-κB p65 levels correlated with Ki-67 or with cytoplasmic NF-κB p65 expression in BPH, but not in PCa. The findings provide information that combined analysis of CK2α and NF-κB p65 expression in prostate specimens relates to the disease status. Increased nuclear NF-κB p65 expression levels in PCa specifically related to nuclear CK2α levels, indicating a possible CK2-dependent relationship in malignancy. In contrast, nuclear NF-κB p65 protein levels related to both Ki-67 and cytoplasmic NF-κB p65 levels exclusively in BPH, suggesting a potential separate impact for NF-κB p65 function in proliferation for benign disease as opposed to malignant disease.

Indexed as

Gene Expression Regulation, NeoplasticCasein Kinase IICell NucleusHumansKi-67 AntigenMaleNeoplasm ProteinsProstatic HyperplasiaProstatic NeoplasmsTranscription Factor RelACasein Kinase IIKi-67 AntigenNeoplasm ProteinsRELA protein, humanTranscription Factor RelABiomarkerBPHCK2Ki-67Nuclear factor kappa BProstate cancerRELA

Identifiers

PMID27435858
PMCPMC6668611
OpenAlexW2501289048

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.