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细胞周期蛋白D1基因内的多态性与浅表性膀胱癌患者原位癌风险增加相关。

Polymorphism within the cyclin D1 gene is associated with an increased risk of carcinoma in situ in patients with superficial bladder cancer.

作者信息

Ito Masaaki, Habuchi Tomonori, Watanabe Jun, Higashi Shin, Nishiyama Hiroyuki, Wang Lizhong, Tsuchiya Norihiko, Kamoto Toshiyuki, Ogawa Osamu

机构信息

Department of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.

出版信息

Urology. 2004 Jul;64(1):74-8. doi: 10.1016/j.urology.2004.03.001.

Abstract

OBJECTIVES

To evaluate the prognostic value of CCND1 polymorphism in superficial and invasive transitional cell cancer of the bladder.

METHODS

CCND1 polymorphism of blood DNA from patients with transitional cell cancer of the bladder was evaluated using the polymerase chain reaction-restriction fragment length polymorphism method.

RESULTS

No statistically significant difference was found in the recurrence-free survival of patients with superficial (pTa-T1) transitional cell cancer after transurethral resection among different genotype groups (AA versus GG, P = 0.746; GA versus GG, P = 0.979). In patients with superficial bladder cancer, the occurrence of primary carcinoma in situ was significantly greater in patients with the AA genotype compared with those with the GA or GG genotypes (P = 0.006, chi-square test). No statistically significant difference was found in disease-specific survival after radical cystectomy among the different genotype subgroups (AA versus GG, P = 0.245; GA versus GG, P = 0.649).

CONCLUSIONS

Although CCND1 polymorphism is not able to serve as a prognostic marker for bladder cancer, the CCND1 variant A allele may recessively increase the risk of carcinoma in situ incidence in patients with superficial bladder cancer.

摘要

目的

评估CCND1基因多态性在浅表性和浸润性膀胱移行细胞癌中的预后价值。

方法

采用聚合酶链反应-限制性片段长度多态性方法评估膀胱移行细胞癌患者血液DNA中的CCND1基因多态性。

结果

经尿道切除术后,不同基因型组(AA与GG,P = 0.746;GA与GG,P = 0.979)的浅表性(pTa-T1)膀胱移行细胞癌患者无复发生存率无统计学显著差异。在浅表性膀胱癌患者中,AA基因型患者原位癌的发生率显著高于GA或GG基因型患者(P = 0.006,卡方检验)。不同基因型亚组在根治性膀胱切除术后的疾病特异性生存率无统计学显著差异(AA与GG,P = 0.245;GA与GG,P = 0.649)。

结论

虽然CCND1基因多态性不能作为膀胱癌的预后标志物,但CCND1变异A等位基因可能隐性增加浅表性膀胱癌患者原位癌的发病风险。

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