Oncogenic virus-associated neoplasia: A role for cyclin D1 genotypes influencing the age of onset of disease?

被引:21
作者
Catarino, R. [1 ,2 ,3 ]
Pereira, D. [4 ]
Breda, E. [5 ]
Coelho, A. [1 ,2 ]
Matos, A. [1 ,2 ]
Lopes, C. [1 ,2 ,3 ]
Medeiros, R. [1 ,2 ,6 ]
机构
[1] Portuguese Inst Oncol, Mol Oncol Grp, Oporto, Portugal
[2] Portuguese Inst Oncol, Virol Lab, Oporto, Portugal
[3] ICBAS, Abel Salazar Inst Biomed Sci, Oporto, Portugal
[4] Portuguese Inst Oncol, Dept Med Oncol, Oporto, Portugal
[5] Portuguese Inst Oncol, Otorrinolaringol Dept, Oporto, Portugal
[6] Fernando Pessoa Univ, Fac Hlth Sci, Oporto, Portugal
关键词
cyclin d1; genetic polymorphism; oncogenic virus-associated neoplasia; age of onset;
D O I
10.1016/j.bbrc.2008.03.039
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Cyclin D1 (CCND1) is a key regulatory protein at the G1/S checkpoint of the cell cycle. The purpose of our study was to assess the role of CCND1 genotypes influencing the age of onset of oncogenic virus-associated neoplasia. We conducted a hospital-based case-control study of 581 individuals, including 247 controls and 334 cases (108 nasopharyngeal and 226 cervical cancer cases). The polymorphism analysis was performed in blood samples by PCR-RFLP methodology. Age-adjusted logistic regression analysis indicates that individuals carrying two G-alleles have an increased genetic susceptibility for the development of oncogenic virus-associated cancers (aOR = 2.02, 95% CI 1.30-3.14, P = 0.002). Moreover, our results indicate that the waiting time for onset of oncogenic virus-associated neoplasia in patients homozygous (GG) for CCND1 genotypes (52 years) was 12 years earlier in comparison with patients carrying AG or AA genotypes (60 years) (log-rank test: P = 0.0003). Our results may be important in contributing to a more extensive knowledge of the mechanisms involved in oncogenic virus-associated carcinogenesis, as CCND1 may be an important target for the development of new strategies for cancer treatment and prevention. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:118 / 122
页数:5
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