Evidence map›Paper›PMID 28645367›Full record

ArticleMethods in enzymology2017

Base Excision Repair Variants in Cancer.

Carolyn G Marsden, Julie A Dragon, Susan S Wallace, Joann B Sweasy

Open access · greenAbstract read
In one paragraph

Article in Methods in enzymology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Activated STAT3 Is a Novel Regulator of theInternational journal of molecular sciences · 2021
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Enhanced Expression ofFrontiers in genetics · 2021
    Article
  14. Review
  15. Article
  16. Prognostic Value of SLC4A4 and its Correlation with Immune Infiltration in Colon Adenocarcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  17. Review
  18. Article
  19. Isoforms of Base Excision Repair Enzymes Produced by Alternative Splicing.International journal of molecular sciences · 2019
    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

4 authors at 1 institution in 1 country.

Carolyn G MarsdenThe Markey Center for Molecular Genetics, University of Vermont, Burlington, VT, United States.
Julie A DragonThe Markey Center for Molecular Genetics, University of Vermont, Burlington, VT, United States.
Susan S WallaceThe Markey Center for Molecular Genetics, University of Vermont, Burlington, VT, United States.
Joann B SweasyThe Markey Center for Molecular Genetics, University of Vermont, Burlington, VT, United States; Yale University School of Medicine, New Haven, CT, United States. Electronic address: joann.sweasy@yale.edu.
University of Vermont · US

Funding

SUBSTRATE SPECIFICITY OF THE BER OXIDATIVE DNA GLYCOSYLASESP01CA098993 · NCI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI LEE, ANDREA J · 2004 to 2021
$25.9M
NCI NIH HHS P01 CA098993
6 · The paper itself

Abstract

Base excision repair (BER) is a key genome maintenance pathway that removes endogenously damaged DNA bases that arise in cells at very high levels on a daily basis. Failure to remove these damaged DNA bases leads to increased levels of mutagenesis and chromosomal instability, which have the potential to drive carcinogenesis. Next-generation sequencing of the germline and tumor genomes of thousands of individuals has uncovered many rare mutations in BER genes. Given that BER is critical for genome maintenance, it is important to determine whether BER genomic variants have functional phenotypes. In this chapter, we present our in silico methods for the identification and prioritization of BER variants for further study. We also provide detailed instructions and commentary on the initial cellular assays we employ to dissect potentially important phenotypes of human BER variants and highlight the strengths and weaknesses of our approaches. BER variants possessing interesting functional phenotypes can then be studied in more detail to provide important mechanistic insights regarding the role of aberrant BER in carcinogenesis.

Indexed as

DNA RepairBreast NeoplasmsCell Line, TumorCell Transformation, NeoplasticComputer SimulationGenomic InstabilityHumansMutagenesisPolymerase Chain ReactionBase excision repairCancerCellular transformationDNA glycosylaseDNA polymeraseGenomic instabilityMutagenesisReplication stress

Identifiers

PMID28645367
PMCPMC5859333
OpenAlexW2610579157

What OpenQuestion holds

Textmetadata
LicenceTDM
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.