HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

p53 polymorphism at codon 72--does it constitute a risk for squamous intraepithelial lesions and invasive cancer of the cervix in Central Europeans?

AbstractBACKGROUND:
Polymorphisms of the tumour suppresser gene p53 especially at codon 72 are suspected to be associated with an increased risk for malignant transformation. In invasive cervical cancer, the arginine form of the p53 gene is estimated to be more susceptible to degradation mediated by tumour-associated human papilloma viruses (HPV) than the proline form.
METHODS:
To test the prevalence of p53 polymorphism at codon 72 in 133 healthy women, 50 patients suffering from squamous intraepithelial lesions of the cervix (SIL), and 105 patients with invasive cervical cancer, we developed a polymerase chain reaction (PCR) and microtiter plate-based hybridisation assay. Furthermore, we tested whether the two p53 isoforms increased the risk of developing cervical cancer.
RESULTS:
The proportions of individual homozygous for arginine, homozygous for proline and heterozygous for arginine and proline in the investigated patient groups did not significantly deviate from the Hardy-Weinberg equilibrium. We found no increased risk of developing cervical cancer in respect to p53 polymorphism, independent of histological diagnosis.
DISCUSSION:
In conformity with other study groups, our findings do not support the hypothesis that the p53 polymorphism at codon 72 is important in determining an increased risk of developing HPV-associated SIL or invasive cervical cancer in Central Europeans.
AuthorsE Kucera, D Tong, A Reinthaller, S Leodolter, R Zeillinger, G Sliutz
JournalWiener klinische Wochenschrift (Wien Klin Wochenschr) Vol. 112 Issue 18 Pg. 817-20 (Sep 29 2000) ISSN: 0043-5325 [Print] Austria
PMID11072671 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Codon
  • Tumor Suppressor Protein p53
Topics
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Austria
  • Cell Transformation, Neoplastic (genetics, pathology)
  • Cervix Uteri (pathology)
  • Codon
  • Female
  • Genetic Predisposition to Disease (genetics)
  • Humans
  • Middle Aged
  • Neoplasm Invasiveness
  • Papillomaviridae (genetics)
  • Papillomavirus Infections (genetics)
  • Polymorphism, Genetic (genetics)
  • Risk Factors
  • Tumor Suppressor Protein p53 (genetics)
  • Tumor Virus Infections (genetics)
  • Uterine Cervical Neoplasms (genetics, pathology)
  • Uterine Cervical Dysplasia (genetics, pathology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: