Evidence map›Paper›PMID 25756516›Full record

ArticleCancer biology & therapy2015

Calcium calmodulin dependent kinase kinase 2 - a novel therapeutic target for gastric adenocarcinoma.

Yashwanth Subbannayya, Nazia Syed, Mustafa A Barbhuiya, Remya Raja, Arivusudar Marimuthu, Nandini Sahasrabuddhe, Sneha M Pinto, Srikanth Srinivas Manda, Santosh Renuse, H C Manju and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.6field-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

43 citing papers in PubMed, 67 citations in OpenAlex.

  1. Trial
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  7. The role of CaMKK2 in Golgi-associated vesicle trafficking.Biochemical Society transactions · 2023
    Review
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  9. Article
  10. Review
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  12. CaMKK2 Promotes the Progression of Ovarian Carcinoma through the PI3K/PDK1/Akt Axis.Computational and mathematical methods in medicine · 2022
    Article
  13. Review
  14. Article
  15. Article
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  18. Phosphoproteomic analysis identifies CLK1 as a novel therapeutic target in gastric cancer.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2020
    Article
  19. Article
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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

23 authors at 8 institutions in 4 countries.

Yashwanth Subbannayyaa Institute of Bioinformatics ; International Technology Park ; Bangalore , India.
Nazia Syed
Mustafa A Barbhuiya
Remya Raja
Arivusudar Marimuthu
Nandini Sahasrabuddhe
Sneha M Pinto
Srikanth Srinivas Manda
Santosh Renuse
H C Manju
Mohammed Abdul Lateef Zameer
Jyoti Sharma
Mariana Brait
Kotteazeth Srikumar
Juan Carlos Roa
M Vijaya Kumar
K V Veerendra Kumar
T S Keshava Prasad
Girija Ramaswamy
Rekha Vijay Kumar
Akhilesh Pandey
Harsha Gowda
Aditi Chatterjee
Science & Technology Park (Czechia) · CZKidwai Memorial Institute of Oncology · INInstitute of Bioinformatics · INUniversity of Baltimore · USJohns Hopkins Medicine · USManipal Academy of Higher Education · INPondicherry University · INPontificia Universidad Católica de Chile · CL

Funding

Proteome Characterization Center: A Genoproteomics Pipeline for Cance ResearchU24CA160036 · NCI · JOHNS HOPKINS UNIVERSITY · PI CHAN, DANIEL WANYUI, ZHANG, HUI · 2011 to 2016
$10.7M
Networks, Pathways and Dynamics of Lysine ModificationU54GM103520 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI BADER, JOEL S. · 2012 to 2013
$7.0M
NCI NIH HHS U24CA160036NIGMS NIH HHS U54GM103520PHS HHS HHSN268201000032C
6 · The paper itself

Abstract

Gastric cancer is one of the most common gastrointestinal malignancies and is associated with poor prognosis. Exploring alterations in the proteomic landscape of gastric cancer is likely to provide potential biomarkers for early detection and molecules for targeted therapeutic intervention. Using iTRAQ-based quantitative proteomic analysis, we identified 22 proteins that were overexpressed and 17 proteins that were downregulated in gastric tumor tissues as compared to the adjacent normal tissue. Calcium/calmodulin-dependent protein kinase kinase 2 (CAMKK2) was found to be 7-fold overexpressed in gastric tumor tissues. Immunohistochemical labeling of tumor tissue microarrays for validation of CAMKK2 overexpression revealed that it was indeed overexpressed in 94% (92 of 98) of gastric cancer cases. Silencing of CAMKK2 using siRNA significantly reduced cell proliferation, colony formation and invasion of gastric cancer cells. Our results demonstrate that CAMKK2 signals in gastric cancer through AMPK activation and suggest that CAMKK2 could be a novel therapeutic target in gastric cancer.

Indexed as

AdenocarcinomaAMP-Activated Protein KinasesAntineoplastic AgentsCalcium-Calmodulin-Dependent Protein Kinase KinaseCell Line, TumorCell ProliferationEnzyme ActivationGene ExpressionGene SilencingHumansImmunohistochemistryMolecular Targeted TherapyProtein Kinase InhibitorsProteomeProteomicsReproducibility of ResultsAMP-Activated Protein KinasesAntineoplastic AgentsCalcium-Calmodulin-Dependent Protein Kinase KinaseProtein Kinase InhibitorsProteomeinvasionin vitro labelingiTRAQ, Isobaric tags for relative and absolute quantitationLC-MS/MS, Liquid chromatography-tandem mass spectrometrymass spectrometryproliferationPSM, Peptide spectrum matchSCX, Strong cation exchange chromatographysiRNA, short interfering RNAtargeted therapy

Identifiers

PMID25756516
PMCPMC4622549
OpenAlexW2052655719

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.