Departments of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Japan.
BJU Int. 2012 Oct;110(7):1070-5. doi: 10.1111/j.1464-410X.2012.11143.x. Epub 2012 Apr 23.
What's known on the subject? and What does the study add? Ras association domain family 1A (RASSF1A) is a tumour suppressor and regulates cell cycle, apoptosis and microtubule stability. This is the first study to identify associations between RASSF1A polymorphisms and clinicopathological parameters and survival in patients with clear cell renal cell carcinoma (CCRCC). RASSF1A genotyping may be useful for predicting the prognosis of the clinical course of CCRCC, and this finding might provide a better understanding of the mechanism underlying the development and progression of CCRCC. However, functional and prospective studies with a larger number of patients are needed to confirm the results.
To compare Ras association domain family 1A (RASSF1A) genotypes or haplotypes with clinicopathological characteristics and survival rates of patients with clear cell renal cell carcinoma (CCRCC).
The study cohort comprised 224 Japanese patients who underwent radical nephrectomy and had CCRCC confirmed by histopathological analysis. • Three common polymorphisms in the RASSF1A gene, 133Ala/Ser (G/T), -710C/T and -392C/T, were genotyped using TaqMan assays and haplotypes were analysed using appropriate software.
Patients with CCRCC with RASSF1A -710TT genotype exhibited a significantly higher tumour stage and higher stage grouping than those with -710CC or -710CT (P = 0.005 and P = 0.032, respectively). • There was no significant association between 133Ala/Ser or -392C/T genotype and clinicopathological characteristics. • RASSF1A 133Ala-710T-392T haplotype and -710TT genotype were significantly associated with poorer recurrence-free survival rates (P = 0.038 and P = 0.007, respectively).
This is the first study to identify associations between RASSF1A polymorphisms and clinicopathological parameters and survival in patients with CCRCC. • RASSF1A genotyping may be useful in predicting the prognosis of the clinical course of CCRCC, and this finding might provide a better understanding of the mechanism underlying the development and progression of CCRCC. • Functional and prospective studies with a larger number of patients are needed to confirm the results.
比较 Ras 相关结构域家族 1A(RASSF1A)基因型或单倍型与透明细胞肾细胞癌(ccRCC)患者的临床病理特征和生存率。
本研究队列包括 224 名日本患者,这些患者接受了根治性肾切除术,并通过组织病理学分析证实患有 ccRCC。使用 TaqMan 检测法对 RASSF1A 基因中的 3 个常见多态性(133Ala/Ser[G/T]、-710C/T 和-392C/T)进行基因分型,并使用适当的软件分析单倍型。
ccRCC 患者中 RASSF1A-710TT 基因型的肿瘤分期明显高于-710CC 或-710CT 基因型(P=0.005 和 P=0.032)。133Ala/Ser 或-392C/T 基因型与临床病理特征之间无显著相关性。RASSF1A133Ala-710T-392T 单倍型和-710TT 基因型与无复发生存率显著相关(P=0.038 和 P=0.007)。
这是第一项确定 RASSF1A 多态性与 ccRCC 患者临床病理参数和生存率之间关联的研究。RASSF1A 基因分型可能有助于预测 ccRCC 临床病程的预后,这一发现可能有助于更好地理解 ccRCC 发生和发展的机制。需要更多患者的功能和前瞻性研究来证实这些结果。