Evidence map›Paper›PMID 36449542›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

High-throughput functional annotation of natural products by integrated activity profiling.

Suzie K Hight, Trevor N Clark, Kenji L Kurita, Elizabeth A McMillan, Walter Bray, Anam F Shaikh, Aswad Khadilkar, F P Jake Haeckl, Fausto Carnevale-Neto, Scott La and 8 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. MOAST: Mechanism of Action Similarity Tool.bioRxiv : the preprint server for biology · 2025
    Article
  6. Prediction of Bioactive Metabolites from AmericanJournal of natural products · 2025
    Article
  7. Article
  8. High-throughput protein crystallography to empower natural product-based drug discovery.Acta crystallographica. Section F, Structural biology communications · 2025
    Article
  9. Molecules (Basel, Switzerland) · 2025
    Article
  10. Review
  11. Discovery of Acyl-Surugamide A2 from MarineMolecules (Basel, Switzerland) · 2024
    Article
  12. Article
  13. Review
  14. Review
  15. 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

18 authors.

Suzie K HightDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Trevor N ClarkDepartment of Chemistry, Simon Fraser University, Burnaby, BC V5A 1S6, Canada.ORCID 0000-0002-8758-404X
Kenji L KuritaDepartment of Chemistry, Simon Fraser University, Burnaby, BC V5A 1S6, Canada.
Elizabeth A McMillanDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Walter BrayDepartment of Chemistry, University of California Santa Cruz, Santa Cruz, CA 95064.ORCID 0000-0002-4766-5240
Anam F ShaikhDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Aswad KhadilkarDepartment of Chemistry, University of California Santa Cruz, Santa Cruz, CA 95064.ORCID 0000-0002-0689-985X
F P Jake HaecklDepartment of Chemistry, Simon Fraser University, Burnaby, BC V5A 1S6, Canada.ORCID 0000-0002-2776-5957
Fausto Carnevale-NetoDepartment of Chemistry, Simon Fraser University, Burnaby, BC V5A 1S6, Canada.
Scott LaDepartment of Chemistry, University of California Santa Cruz, Santa Cruz, CA 95064.ORCID 0000-0002-8974-8722
Akshar LohithDepartment of Chemistry, University of California Santa Cruz, Santa Cruz, CA 95064.ORCID 0000-0001-7523-5259
Rachel M VadenDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Jeon LeeDepartment of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0002-9071-7157
Shuguang WeiDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0001-5737-2647
R Scott LokeyDepartment of Chemistry, University of California Santa Cruz, Santa Cruz, CA 95064.ORCID 0000-0001-9891-1248
Michael A WhiteDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Roger G LiningtonDepartment of Chemistry, Simon Fraser University, Burnaby, BC V5A 1S6, Canada.ORCID 0000-0003-1818-4971
John B MacMillanDepartment of Chemistry, University of California Santa Cruz, Santa Cruz, CA 95064.ORCID 0000-0003-1430-1077

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
DIVISION OF CELL &MOLECULAR BIOLOGY TRAINING PROGRAMT32GM008203 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI COBB, MELANIE H. · 1987 to 2018
$7.0M
Cancer Biology Training GrantT32CA124334 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI SHAY, JERRY WILLIAM · 2007 to 2021
$5.3M
Marine Actinomycetes as a Resource for Anticancer Natural ProductsR01CA149833 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MACMILLAN, JOHN B · 2010 to 2014
$1.6M
NCCIH NIH HHS U41 AT008718NCI NIH HHS R01 CA149833NCI NIH HHS T32 CA124334NIGMS NIH HHS T32 GM008203
6 · The paper itself

Abstract

Determining mechanism of action (MOA) is one of the biggest challenges in natural products discovery. Here, we report a comprehensive platform that uses Similarity Network Fusion (SNF) to improve MOA predictions by integrating data from the cytological profiling high-content imaging platform and the gene expression platform Functional Signature Ontology, and pairs these data with untargeted metabolomics analysis for de novo bioactive compound discovery. The predictive value of the integrative approach was assessed using a library of target-annotated small molecules as benchmarks. Using Kolmogorov-Smirnov (KS) tests to compare in-class to out-of-class similarity, we found that SNF retains the ability to identify significant in-class similarity across a diverse set of target classes, and could find target classes not detectable in either platform alone. This confirmed that integration of expression-based and image-based phenotypes can accurately report on MOA. Furthermore, we integrated untargeted metabolomics of complex natural product fractions with the SNF network to map biological signatures to specific metabolites. Three examples are presented where SNF coupled with metabolomics was used to directly functionally characterize natural products and accelerate identification of bioactive metabolites, including the discovery of the azoxy-containing biaryl compounds parkamycins A and B. Our results support SNF integration of multiple phenotypic screening approaches along with untargeted metabolomics as a powerful approach for advancing natural products drug discovery.

Indexed as

Biological ProductsGene FusionGene LibraryMetabolomicsBiological Productsmetabolomicsnatural productspharmacology

Identifiers

PMID36449542
PMCPMC9894231

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.