Evidence map›Paper›PMID 27411305›Full record

ReviewAntioxidants & redox signaling2017

NOS Expression and NO Function in Glioma and Implications for Patient Therapies.

Anh N Tran, Nathaniel H Boyd, Kiera Walker, Anita B Hjelmeland

Abstract readReview
In one paragraph

Review in Antioxidants & redox signaling, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

33 citing papers in PubMed, 62 citations in OpenAlex.

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  19. Nitric Oxide and S-Nitrosylation in Cancers: Emphasis on Breast Cancer.Breast cancer : basic and clinical research · 2020
    Review
  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

4 authors at 1 institution in 1 country.

Anh N TranDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham , Birmingham, Alabama.
Nathaniel H BoydDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham , Birmingham, Alabama.
Kiera WalkerDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham , Birmingham, Alabama.
Anita B HjelmelandDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham , Birmingham, Alabama.
University of Alabama at Birmingham · US

Funding

CONTEMPORARY THERAPEUTICS FOR ANAPLASTIC GLIOMASP20CA151129 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GILLESPIE, G. YANCEY · 2011 to 2013
$2.3M
Training Program in Brain Tumor BiologyT32NS048039 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BENVENISTE, ETTY N · 2007 to 2017
$2.0M
Biosynthetic Metabolic Pathway Regulation of Glioma GrowthR01NS104339 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HJELMELAND, ANITA BORTON · 2018 to 2022
$1.9M
A20 Promotes Glioma Stem Cell Mediated TumorigenesisR01CA151522 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HJELMELAND, ANITA BORTON · 2010 to 2014
$1.2M
Identification of Glucose Transporter 3 Inhibitors for Glioblastoma TreatmentR21NS096531 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AUGELLI-SZAFRAN, CORINNE ELIZABETH, HJELMELAND, ANITA BORTON · 2016 to 2017
$537k
Microenvironmental Regulation of Glioblastoma Angiogenesis via CHD7F31CA200085 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BOYD, NATHANIEL · 2015 to 2017
$86k
NCI NIH HHS F31 CA200085NCI NIH HHS P20 CA151129NCI NIH HHS R01 CA151522NINDS NIH HHS R01 NS104339NINDS NIH HHS R21 NS096531NINDS NIH HHS T32 NS048039
6 · The paper itself

Abstract

significanceGliomas are central nervous system tumors that primarily occur in the brain and arise from glial cells. Gliomas include the most common malignant brain tumor in adults known as grade IV astrocytoma, or glioblastoma (GBM). GBM is a deadly disease for which the most significant advances in treatment offer an improvement in survival of only ∼2 months. CRITICAL ISSUES: To develop novel treatments and improve patient outcomes, we and others have sought to determine the role of molecular signals in gliomas. Recent Advances: One signaling molecule that mediates important biologies in glioma is the free radical nitric oxide (NO). In glioma cells and the tumor microenvironment, NO is produced by three isoforms of nitric oxide synthase (NOS), NOS1, NOS2, and NOS3. NO and NOS affect glioma growth, invasion, angiogenesis, immunosuppression, differentiation state, and therapeutic resistance. FUTURE DIRECTIONS: These multifaceted effects of NO and NOS on gliomas both in vitro and in vivo suggest the potential of modulating the pathway for antiglioma patient therapies. Antioxid. Redox Signal. 26, 986-999.

Indexed as

Antineoplastic AgentsBrain NeoplasmsCell MovementGene Expression Regulation, NeoplasticGliomaHumansNeoplasm InvasivenessNitric OxideNitric Oxide SynthaseSignal TransductionTumor MicroenvironmentAntineoplastic AgentsNitric OxideNitric Oxide Synthasecancer stem cellgliomanitric oxide/NOnitric oxide synthase/NOStherapy

Identifiers

PMID27411305
PMCPMC5467121
OpenAlexW2467404533

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.