Evidence map›Paper›PMID 24392019›Full record

ArticlePloS one2013

Association between PARP-1 V762A polymorphism and breast cancer susceptibility in Saudi population.

Mohammad Alanazi, Akbar Ali Khan Pathan, Zainularifeen Abduljaleel, Zainul Arifeen, Jilani P Shaik, Huda A Alabdulkarim, Abdelhabib Semlali, Mohammad D Bazzi, Narasimha Reddy Parine

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 47 citations in OpenAlex.

  1. A Population-Specific PARP1 Gene Variation Modulates PARP Trapping.bioRxiv : the preprint server for biology · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Journal of Cancer · 2019
    Article
  9. Review
  10. Observational
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Imaging the DNA damage response with PET and SPECT.European journal of nuclear medicine and molecular imaging · 2017
    Review
  18. Article
  19. Association betweenOncoTargets and therapy · 2017
    Article
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
    Arifeen, Zainul [corrected to Abduljaleel, Zainularifeen]
5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Mohammad AlanaziGenome research chair, Department of Biochemistry, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Akbar Ali Khan PathanGenome research chair, Department of Biochemistry, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Zainularifeen Abduljaleel
Zainul ArifeenGenome research chair, Department of Biochemistry, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia ; Medical Genetics Department, Science and Technology Unit. Umm Al Qura University. Mecca, Saudi Arabia.
Jilani P ShaikGenome research chair, Department of Biochemistry, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Huda A AlabdulkarimThe Comprehensive Cancer Center at King Fahad Medical City, Riyadh, Saudi Arabia.
Abdelhabib SemlaliGenome research chair, Department of Biochemistry, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Mohammad D BazziGenome research chair, Department of Biochemistry, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Narasimha Reddy ParineGenome research chair, Department of Biochemistry, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.
King Saud University · SAKing Fahd Medical City · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic aberrations of DNA repair enzymes are known to be common events and to be associated with different cancer entities. Aim of the following study was to analyze the genetic association of rs1136410 (Val762Ala) in PARP1 gene with the risk of breast cancer using genotypic assays and insilico structural predictions. Genotypic analysis of individual locus showed statistically significant association of Val762Ala with increased susceptibility to breast cancer. Protein structural analysis was performed with Val762Ala variant allele and compared with the predicted native protein structure. Protein prediction analysis showed that this nsSNP may cause changes in the protein structure and it is associated with the disease. In addition to the native and mutant 3D structures of PARP1 were also analyzed using solvent accessibility models for further protein stability confirmation. Taken together, this the first study that confirmed Val762Ala variant has functional effect and structural impact on the PARP1 and may play an important role in breast cancer progression in Saudi population.

Indexed as

Polymorphism, Single NucleotideAmino Acid SubstitutionAsian PeopleBreast NeoplasmsComputer SimulationEnzyme StabilityFemaleGene Expression Regulation, NeoplasticGene FrequencyGenetic Predisposition to DiseaseHumansMolecular Dynamics SimulationMutationNeoplasm StagingPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) Polymerases

Identifiers

PMID24392019
PMCPMC3877358
OpenAlexW2009584660

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.