Evidence map›Paper›PMID 32866775›Full record

ReviewDNA repair2020

The SNM1A DNA repair nuclease.

Hannah T Baddock, Yuliana Yosaatmadja, Joseph A Newman, Christopher J Schofield, Opher Gileadi, Peter J McHugh

Open access · hybridAbstract readReview
In one paragraph

Review in DNA repair, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. DNA Damage Responses, the Trump Card of Stem Cells in the Survival Game.Advances in experimental medicine and biology · 2024
    Review
  9. Article
  10. Article
  11. Structure and Function of SNM1 Family Nucleases.Advances in experimental medicine and biology · 2023
    Review
  12. Article
  13. Review
  14. Predictive value of DNA repair gene expression for response to neoadjuvant chemotherapy in breast cancer.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2022
    Article
  15. DNA damage responses that enhance resilience to replication stress.Cellular and molecular life sciences : CMLS · 2021
    Review
  16. Article
  17. Article
  18. Review
  19. 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 at 3 institutions in 1 country.

Hannah T BaddockDepartment of Oncology, MRC Weatherall Institute of Molecular Medicine, University of Oxford, OX3 9DS, UK.
Yuliana YosaatmadjaStructural Genomics Consortium, University of Oxford, OX3 7DQ, UK.
Joseph A NewmanChemistry Research Laboratory, University of Oxford, 12 Mansfield Road, OX1 3TA, UK.
Christopher J SchofieldChemistry Research Laboratory, University of Oxford, 12 Mansfield Road, OX1 3TA, UK.
Opher GileadiStructural Genomics Consortium, University of Oxford, OX3 7DQ, UK.
Peter J McHughDepartment of Oncology, MRC Weatherall Institute of Molecular Medicine, University of Oxford, OX3 9DS, UK. Electronic address: peter.mchugh@imm.ox.ac.uk.
University of Oxford · GBOxford Research Group · GBGenomics (United Kingdom) · GB

Funding

Cancer Research UK 24759Cancer Research UK A24759Medical Research Council MR/L007665/1Wellcome Trust
6 · The paper itself

Abstract

Unrepaired, or misrepaired, DNA damage can contribute to the pathogenesis of a number of conditions, or disease states; thus, DNA damage repair pathways, and the proteins within them, are required for the safeguarding of the genome. Human SNM1A is a 5'-to-3' exonuclease that plays a role in multiple DNA damage repair processes. To date, most data suggest a role of SNM1A in primarily ICL repair: SNM1A deficient cells exhibit hypersensitivity to ICL-inducing agents (e.g. mitomycin C and cisplatin); and both in vivo and in vitro experiments demonstrate SNM1A and XPF-ERCC1 can function together in the 'unhooking' step of ICL repair. SNM1A further interacts with a number of other proteins that contribute to genome integrity outside canonical ICL repair (e.g. PCNA and CSB), and these may play a role in regulating SNM1As function, subcellular localisation, and post-translational modification state. These data also provide further insight into other DNA repair pathways to which SNM1A may contribute. This review aims to discuss all aspects of the exonuclease, SNM1A, and its contribution to DNA damage tolerance.

Indexed as

DNA RepairAnimalsCell Cycle ProteinsDNADNA AdductsDNA Repair EnzymesExodeoxyribonucleasesHumansProtein ConformationCell Cycle ProteinsDCLRE1A protein, humanDNADNA AdductsDNA Repair EnzymesExodeoxyribonucleasesDCLRE1AInterstrand crosslink repairNucleasePso2SNM1A

Identifiers

PMID32866775
PMCPMC7607226
OpenAlexW3046866955

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.