Evidence map›Paper›PMID 27903215›Full record

ArticleCurrent cancer drug targets2017

Identification of Novel Agents for the Treatment of Brain Metastases of Breast Cancer.

Vinay K Venishetty, Werner J Geldenhuys, Tori B Terell-Hall, Jessica I G Griffith, Gregory R Sondag, Fayez F Safadi, Paul R Lockman

Abstract read
In one paragraph

Article in Current cancer drug targets, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 100% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

7 authors at 3 institutions in 1 country.

Vinay K VenishettyDepartment of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX. United States.
Werner J GeldenhuysDepartment of Pharmaceutical Sciences, School of Pharmacy, West Virginia University, Morgantown, WV. United States.
Tori B Terell-HallDepartment of Pharmaceutical Sciences, School of Pharmacy, West Virginia University, Morgantown, WV. United States.
Jessica I G GriffithDepartment of Pharmaceutical Sciences, School of Pharmacy, West Virginia University, Morgantown, WV. United States.
Gregory R SondagDepartment of Anatomy and Neurobiology, College of Medicine, Northeast Ohio Medical University, Rootstown, OH. United States.
Fayez F SafadiDepartment of Anatomy and Neurobiology, College of Medicine, Northeast Ohio Medical University, Rootstown, OH. United States.
Paul R LockmanDepartment of Pharmaceutical Sciences, School of Pharmacy, West Virginia University, Morgantown, WV. United States.
West Virginia University · USNortheast Ohio Medical University · USTexas Tech University · US

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI JUDITH FEINBERG · 2012 to 2026
$81.0M
Prevention and treatment of brain micrometastases of breast cancerR01CA166067 · NCI · WEST VIRGINIA UNIVERSITY · PI LOCKMAN, PAUL R · 2013 to 2017
$1.5M
NCI NIH HHS R01 CA166067NIGMS NIH HHS U54 GM104942
6 · The paper itself

Abstract

backgroundBrain cancer from metastasized breast cancer has a high mortality rate in women. The treatment of lesions is hampered in large part by the blood-brain barrier (BBB), which prevents adequate distribution of anti-cancer compounds to brain metastases.

methodIn this study we used a novel screening method to identify candidate molecules that are well-suited to utilizing the BBB choline transporter for distribution into the brain parenchyma.

resultsFrom our screen we identified two compounds, Ch-1 and Ch-2 that were able to reduce the brain tumor burden in a murine mouse model of brain metastasis of breast cancer. These compounds also significantly increased the survival of mice by more than 10 days. Mechanistic studies indicated that Ch-1 is able to prevent the activation of the pro-survival mitogen-activated kinases (MAPKs) by osteoactivin (OA; Glycoprotein nonmetastatic melanoma protein B GPNMB).

conclusionThe results from this study show that nutrient transporter virtual screening is a viable novel alternative to traditional drug screening programs to identify anti-cancer compounds for the treatment of brain cancers.

Indexed as

AnimalsAntineoplastic AgentsApoptosisBrain NeoplasmsBreast NeoplasmsCell Line, TumorFemaleHumansMiceAntineoplastic AgentsADMEbrain cancerchemotherapyCNSdistributiondrug discoveryDrug resistance

Identifiers

PMID27903215
PMCPMC5438904
OpenAlexW2560048019

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.