Evidence map›Paper›PMID 31525021›Full record

ArticleACS chemical biology2019

Small-Molecule Inhibition of UBE2T/FANCL-Mediated Ubiquitylation in the Fanconi Anemia Pathway.

Matthew J Cornwell, Graeme J Thomson, Julia Coates, Rimma Belotserkovskaya, Ian D Waddell, Stephen P Jackson, Yaron Galanty

Open access · hybridAbstract 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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Ubiquitin-conjugating Enzymes in Cancer.International journal of biological sciences · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
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  11. Article
  12. Review
  13. Article
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  15. Review
  16. TheAnnals of translational medicine · 2020
    Article
  17. Article
  18. Cracking the Monoubiquitin Code of Genetic Diseases.International journal of molecular sciences · 2020
    Review
  19. Review
  20. 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

7 authors at 2 institutions in 1 country.

Matthew J CornwellThe Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Biochemistry , University of Cambridge , Cambridge CB2 1QN , United Kingdom.
Graeme J ThomsonDrug Discovery Unit, Cancer Research UK Manchester Institute , University of Manchester , Wilmslow Road , Manchester M20 4BX , United Kingdom.
Julia CoatesThe Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Biochemistry , University of Cambridge , Cambridge CB2 1QN , United Kingdom.
Rimma BelotserkovskayaThe Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Biochemistry , University of Cambridge , Cambridge CB2 1QN , United Kingdom.
Ian D WaddellDrug Discovery Unit, Cancer Research UK Manchester Institute , University of Manchester , Wilmslow Road , Manchester M20 4BX , United Kingdom.
Stephen P JacksonThe Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Biochemistry , University of Cambridge , Cambridge CB2 1QN , United Kingdom.
Yaron GalantyThe Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Biochemistry , University of Cambridge , Cambridge CB2 1QN , United Kingdom.ORCID 0000-0001-7167-9004
University of Cambridge · GBUniversity of Manchester · GB

Funding

Cancer Research UK 17098Cancer Research UK 18796Cancer Research UK C309/A8274Cancer Research UK C480/A1141Cancer Research UK C6946/A24843Cancer Research UK C6/A18796Wellcome Trust 203144Wellcome Trust 206388/Z/17/Z
6 · The paper itself

Abstract

The Fanconi anemia pathway orchestrates the repair of DNA interstrand cross-links and stalled replication forks. A key step in this pathway is UBE2T and FANCL-dependent monoubiquitylation of the FANCD2-FANCI complex. The Fanconi anemia pathway represents an attractive therapeutic target, because activation of this pathway has been linked to chemotherapy resistance in several cancers. However, to date, very few selective inhibitors of ubiquitin conjugation pathways are known. By using a high-throughput screen-compatible assay, we have identified a small-molecule inhibitor of UBE2T/FANCL-mediated FANCD2 monoubiquitylation that sensitizes cells to the DNA cross-linking agent, carboplatin.

Indexed as

Cell Line, TumorFanconi AnemiaFanconi Anemia Complementation Group L ProteinHigh-Throughput Screening AssaysHumansSmall Molecule LibrariesUbiquitinationUbiquitin-Conjugating EnzymesFANCL protein, humanFanconi Anemia Complementation Group L ProteinSmall Molecule LibrariesUBE2T protein, humanUbiquitin-Conjugating Enzymes

Identifiers

PMID31525021
PMCPMC6804243
OpenAlexW2974277108

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.