Evidence map›Paper›PMID 20200430›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2010

TP53, MDM2, NQO1, and susceptibility to cervical cancer.

Xiaoxia Hu, Zhengyan Zhang, Duanduan Ma, Phyllis C Huettner, L Stewart Massad, Loan Nguyen, Ingrid Borecki, Janet S Rader

Open access · bronzeAbstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 3 pooled it
2.0field-weighted citation impact, top 14% 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

34 citing papers in PubMed, 3 syntheses or guidelines pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Genetic variants of NQO1 gene increase bladder cancer risk in Indian population and meta-analysis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Pooled it
  3. MDM2 SNP309 variation increases cervical cancer risk among Asians.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Pooled it
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Observational
  14. Article
  15. Article
  16. Article
  17. Article
  18. Polymorphism Located in the Upstream Region of theJournal of cancer prevention · 2018
    Article
  19. Oncology letters · 2018
    Article
  20. 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

8 authors at 2 institutions in 1 country.

Xiaoxia HuDepartment of Obstetrics and Gynecology, Washington University School of Medicine, St. Louis, Missouri, USA.
Zhengyan Zhang
Duanduan Ma
Phyllis C Huettner
L Stewart Massad
Loan Nguyen
Ingrid Borecki
Janet S Rader
Washington University in St. Louis · USMedical College of Wisconsin · US

Funding

Genetic Susceptibility to Cervical CancerR01CA095713 · NCI · WASHINGTON UNIVERSITY · PI RADER, JANET S. · 2003 to 2009
$1.8M
NCI NIH HHS R01 CA095713
6 · The paper itself

Abstract

Host genetic variability modifies the risk of cervical cancer in women infected with oncogenic human papillomavirus (HPV). Studies have reported an association of the TP53 codon 72 arginine and cervical cancer, but the results are inconsistent. We examined the association of this single nucleotide polymorphism (SNP) in women with cervical cancer and cervical intraepithelial neoplasia grade 3, using a family-based association test. We further explored SNPs in two genes that regulate p53 stability: MDM2 (SNP309) and NQO1 (SNP609, SNP465). We also examined the relationship between host genotype and tumor HPV type. We genotyped 577 patients and their biological parents and/or siblings, using PCR-RFLP or Taqman assays. HPVs were typed by sequence-based methods. The transmission/disequilibrium test was used to detect disease-susceptibility alleles. The arginine peptide of TP53 codon 72 was overtransmitted in Caucasian families (P = 0.043), and the significance of this finding was enhanced in a subgroup of women infected with HPV16- and/or HPV18-related HPVs (P = 0.026). Allele C of NQO1 SNP609 was also overtransmitted in all cases (P = 0.026). We found no association between MDM2 SNP309 or NQO1 SNP465 and cervical cancer. Our results indicate that functional polymorphisms in TP53 codon 72 and NQO1 SNP609 associate with the risk of cervical cancer especially in women infected with type 16- and/or type 18-related HPVs.

Indexed as

Genetic Predisposition to DiseaseAdultFemaleGenes, p53Genome-Wide Association StudyGenotypeHuman papillomavirus 16Human papillomavirus 18HumansNAD(P)H Dehydrogenase (Quinone)Neoplasm StagingPapillomavirus InfectionsPolymerase Chain ReactionPolymorphism, Restriction Fragment LengthPolymorphism, Single NucleotideProto-Oncogene Proteins c-mdm2MDM2 protein, humanNAD(P)H Dehydrogenase (Quinone)NQO1 protein, humanProto-Oncogene Proteins c-mdm2

Identifiers

PMID20200430
PMCPMC2837516
OpenAlexW1990141012

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.