Evidence map›Paper›PMID 28294973›Full record

ArticleMarine drugs2017

FUSION-Guided Hypothesis Development Leads to the Identification of N⁶,N⁶-Dimethyladenosine, a Marine-Derived AKT Pathway Inhibitor.

Rachel M Vaden, Nathaniel W Oswald, Malia B Potts, John B MacMillan, Michael A White

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Microbiology spectrum · 2023
    Article
  2. Article
  3. High-throughput functional annotation of natural products by integrated activity profiling.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  4. Review
  5. Article
  6. Review
  7. Improving natural product research translation: From source to clinical trial.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  8. Article
  9. Chromomycin AThe Journal of general physiology · 2018
    Article
  10. Review
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

5 authors at 2 institutions in 1 country.

Rachel M VadenDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75235, USA. Rachel.Vaden2@UTSouthwestern.edu.
Nathaniel W OswaldDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75235, USA. Nathaniel.Oswald@UTSouthwestern.edu.
Malia B PottsDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75235, USA. Malia.Potts@StJude.org.
John B MacMillanDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75235, USA. John.MacMillan@UTSouthwestern.edu.
Michael A WhiteDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75235, USA. Michael.White@UTSouthwestern.edu.
The University of Texas Southwestern Medical Center · USSt. Jude Children's Research Hospital · US

Funding

Urgent Covid-19 Revision to the Center for High-Throughput Functional Annotation of Natural ProductsU41AT008718 · NCCIH · UT SOUTHWESTERN MEDICAL CENTER · PI CECH, NADJA B, LININGTON, ROGER G · 2015 to 2024
$10.1M
Lung cancer oncogenotype-selective drug target discoveryU01CA176284 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MACMILLAN, JOHN B, MINNA, JOHN D. · 2013 to 2016
$2.8M
Marine Actinomycetes as a Resource for Anticancer Natural ProductsR01CA149833 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MACMILLAN, JOHN B · 2010 to 2014
$1.6M
Targeting Mechanistic Subtypes of Neoplastic DiseaseR35CA197717 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI WHITE, MICHAEL A. · 2015 to 2015
$725k
NCCIH NIH HHS U41 AT008718NCI NIH HHS R01 CA149833NCI NIH HHS R35 CA197717NCI NIH HHS U01 CA176284
6 · The paper itself

Abstract

Chemicals found in nature have evolved over geological time scales to productively interact with biological molecules, and thus represent an effective resource for pharmaceutical development. Marine-derived bacteria are rich sources of chemically diverse, bioactive secondary metabolites, but harnessing this diversity for biomedical benefit is limited by challenges associated with natural product purification and determination of biochemical mechanism. Using Functional Signature Ontology (FUSION), we report the parallel isolation and characterization of a marine-derived natural product,

Indexed as

Aquatic OrganismsBacteriaBiological OntologiesBiological ProductsCarcinoma, Non-Small-Cell LungCell Line, TumorHumansLung NeoplasmsProto-Oncogene Proteins c-aktSignal TransductionBiological ProductsProto-Oncogene Proteins c-aktAKTdimethyladenosinefunctional signature ontology

Identifiers

PMID28294973
PMCPMC5367032
OpenAlexW2596445652

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.