Evidence map›Paper›PMID 31622553›Full record

ArticleACS chemical biology2019

Dual Inhibitors of 8-Oxoguanine Surveillance by OGG1 and NUDT1.

Yu-Ki Tahara, Anna M Kietrys, Marian Hebenbrock, Yujeong Lee, David L Wilson, Eric T Kool

Abstract read
In one paragraph

Article in ACS chemical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. 8-Oxoguanine: A Lesion, an Epigenetic Mark, or a Molecular Signal?International journal of molecular sciences · 2025
    Review
  3. Article
  4. Genetic predisposition to polyposis syndromes.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  5. Article
  6. Review
  7. Structural and Functional Insights into UDGs.Protein and peptide letters · 2025
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Selective Inhibition of DNA Polymerase β by a Covalent Inhibitor.Journal of the American Chemical Society · 2021
    Article
  14. Article
  15. Review
  16. Review
  17. Inhibitors of DNA Glycosylases as Prospective Drugs.International journal of molecular sciences · 2020
    Review
  18. 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

6 authors.

Yu-Ki TaharaDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.
Anna M KietrysDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.ORCID 0000-0002-8725-9079
Marian HebenbrockDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.ORCID 0000-0002-9339-5165
Yujeong LeeDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.
David L WilsonDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.ORCID 0000-0002-1922-427X
Eric T KoolDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.ORCID 0000-0002-7310-2935

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Vittorio Sebastiano · 2007 to 2026
$71.4M
Measuring and Modulating Oxidative DNA Damage Surveillance PathwaysR01CA217809 · NCI · STANFORD UNIVERSITY · PI KOOL, ERIC T. · 2017 to 2024
$3.7M
POLYFLUOROPHORES ASSEMBLED ON A DNA SCAFFOLDR01GM067201 · NIGMS · STANFORD UNIVERSITY · PI KOOL, ERIC T. · 2003 to 2011
$2.2M
Highly Reactive Hydrazone Chemistry: Orthogonal Modification in Cellular ContextsR01GM110050 · NIGMS · STANFORD UNIVERSITY · PI KOOL, ERIC T. · 2015 to 2018
$1.2M
NCI NIH HHS P30 CA124435NCI NIH HHS R01 CA217809NIGMS NIH HHS R01 GM067201NIGMS NIH HHS R01 GM110050
6 · The paper itself

Abstract

Oxidative damage in DNA is one of the primary sources of mutations in the cell. The activities of repair enzymes 8-oxoguanine DNA glycosylase (OGG1) and human MutT Homologue 1 (NUDT1 or MTH1), which work together to ameliorate this damage, are closely linked to mutagenesis, genotoxicity, cancer, and inflammation. Here we have undertaken the development of small-molecule dual inhibitors of the two enzymes as tools to test the relationships between these pathways and disease. The compounds preserve key structural elements of known inhibitors of the two enzymes, and they were synthesized and assayed with recently developed luminescence assays of the enzymes. Further structural refinement of initial lead molecules yielded compound

Indexed as

AnimalsCell Line, TumorDNA GlycosylasesDNA Repair EnzymesEnzyme InhibitorsGuanineHumansPhosphoric Monoester Hydrolases8-hydroxyguanine8-oxodGTPaseDNA GlycosylasesDNA Repair EnzymesEnzyme InhibitorsGuanineoxoguanine glycosylase 1, humanPhosphoric Monoester Hydrolases

Identifiers

PMID31622553
PMCPMC7061906

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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.