Evidence map›Paper›PMID 29323792›Full record

ArticleThe FEBS journal2018

The retinamide VNLG-152 inhibits f-AR/AR-V7 and MNK-eIF4E signaling pathways to suppress EMT and castration-resistant prostate cancer xenograft growth.

Vidya P Ramamurthy, Senthilmurugan Ramalingam, Lalji K Gediya, Vincent C O Njar

Open access · bronzeAbstract read
In one paragraph

Article in The FEBS journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
4.6field-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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

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  18. Deeping in the Role of the MAP-Kinases Interacting Kinases (MNKs) in Cancer.International journal of molecular sciences · 2020
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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

4 authors at 2 institutions in 1 country.

Vidya P RamamurthyDepartment of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA.
Senthilmurugan RamalingamDepartment of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA.
Lalji K GediyaDepartment of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA.
Vincent C O NjarDepartment of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA.
University of Maryland, Baltimore · USUniversity of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center

Funding

Targeting Pancreatic Cancer with Novel Mnk-eIF4E and AR Modulating AgentsR21CA195694 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI NJAR, VINCENT COLLINS OFUKA · 2015 to 2016
$395k
Retinoids, RAMBAs, and Histone Deacetylase InhibitorsR21CA117991 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI NJAR, VINCENT COLLINS OFUKA · 2005 to 2006
$347k
NCI NIH HHS R21 CA117991NCI NIH HHS R21 CA195694
6 · The paper itself

Abstract

VNLG-152 is a novel retinamide (NR) shown to suppress growth and progression of genetically diverse prostate cancer cells via inhibition of androgen receptor signaling and eukaryotic initiation factor 4E (eIF4E) translational machinery. Herein, we report therapeutic effects of VNLG-152 on castration-resistant prostate cancer (CRPC) growth and metastatic phenotype in a CRPC tumor xenograft model. Administration of VNLG-152 significantly and dose-dependently suppressed the growth of aggressive CWR22Rv1 tumors by 63.4% and 76.3% at 10 and 20 mg·kg

Indexed as

Xenograft Model Antitumor AssaysAlternative SplicingAnimalsAntineoplastic AgentsCell Line, TumorEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsMaleMiceProstatic Neoplasms, Castration-ResistantProtein IsoformsProtein Serine-Threonine KinasesReceptors, AndrogenRNA InterferenceAntineoplastic AgentsIntracellular Signaling Peptides and ProteinsMKNK1 protein, humanMKNK2 protein, humanProtein IsoformsProtein Serine-Threonine KinasesReceptors, AndrogenretinamideTretinoinCRPC/mCRPCf-AR/AR-V7Mnk-eIF4EVNLG-152

Identifiers

PMID29323792
PMCPMC7367498
OpenAlexW2783025387

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.