Evidence map›Paper›PMID 26407994›Full record

ReviewMolecular & cellular proteomics : MCP2016

Emerging Proteomic Technologies Provide Enormous and Underutilized Potential for Brain Cancer Research.

Qiang Tian, Vineet Sangar, Nathan D Price

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular & cellular proteomics : MCP, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

3 authors at 1 institution in 1 country.

Qiang TianFrom the ‡Institute for Systems Biology, Seattle, WA 98109.
Vineet SangarFrom the ‡Institute for Systems Biology, Seattle, WA 98109.
Nathan D PriceFrom the ‡Institute for Systems Biology, Seattle, WA 98109 nprice@systemsbiology.org.
Institute for Systems Biology · US

Funding

(PQB-4) Single cell analysis strategy for monitoring drug responses of tumorsR01CA190122 · NCI · INSTITUTE FOR SYSTEMS BIOLOGY · PI TIAN, QIANG · 2014 to 2017
$2.4M
NCI NIH HHS R01 CA190122
6 · The paper itself

Abstract

High-throughput technologies present immense opportunities to characterize brain cancer biology at a systems level. However, proteomic studies of brain cancers are still relatively scarce. Here we discuss the latest proteomic technologies, their application to profiling and quantitation of brain proteomes and how we expect these technologies will be applied to study brain cancer proteomes in the future. Mass spectrometry based proteomics with increased specificity, coverage and throughput will be pervasive in proteomics investigations of brain. Generated data needs to be captured by the curation of databases, and application of creative data analysis strategies is needed to provide meaningful insights into brain functions and associated pathologies. Overall, proteomics applications to brain cancers are in the earliest stages and the expanded use of these technologies holds enormous potential to improve our understanding of brain functions and pathologies.

Indexed as

Brain NeoplasmsDatabases, ProteinGene Expression Regulation, NeoplasticHumansMass SpectrometryNeoplasm ProteinsProteomicsNeoplasm Proteins

Identifiers

PMID26407994
PMCPMC4739660
OpenAlexW2257347166

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.