Evidence map›Paper›PMID 33095241›Full record

ReviewEssays in biochemistry2020

RecQ helicases in DNA repair and cancer targets.

Joseph A Newman, Opher Gileadi

Open access · hybridAbstract readReview
In one paragraph

Review in Essays in biochemistry, 2020. 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
1.3field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Structural Chemistry of Helicase Inhibition.Journal of medicinal chemistry · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Whole Genome Resequencing Revealed the Effect of HelicaseInternational journal of molecular sciences · 2023
    Article
  10. Inhibition ofInternational journal of molecular sciences · 2022
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. 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

2 authors at 1 institution in 1 country.

Joseph A NewmanStructural Genomics Consortium, University of Oxford, Oxford OX3 7DQ, U.K.
Opher GileadiStructural Genomics Consortium, University of Oxford, Oxford OX3 7DQ, U.K.
Genomics England · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Helicases are enzymes that use the energy derived from ATP hydrolysis to catalyze the unwinding of DNA or RNA. The RecQ family of helicases is conserved through evolution from prokaryotes to higher eukaryotes and plays important roles in various DNA repair pathways, contributing to the maintenance of genome integrity. Despite their roles as general tumor suppressors, there is now considerable interest in exploiting RecQ helicases as synthetic lethal targets for the development of new cancer therapeutics. In this review, we summarize the latest developments in the structural and mechanistic study of RecQ helicases and discuss their roles in various DNA repair pathways. Finally, we consider the potential to exploit RecQ helicases as therapeutic targets and review the recent progress towards the development of small molecules targeting RecQ helicases as cancer therapeutics.

Indexed as

DNA RepairGenomic InstabilityHumansNeoplasmsRecQ HelicasesRecQ HelicasesDNA damageDNA synthesis and repairprotein structuresynthetic lethality

Identifiers

PMID33095241
PMCPMC7588665
OpenAlexW3094369614

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.