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首页> 外文期刊>BJU international >Influence of caspases 8 and 9 gene promoter polymorphism on prostate cancer susceptibility and early development of hormone refractory prostate cancer.
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Influence of caspases 8 and 9 gene promoter polymorphism on prostate cancer susceptibility and early development of hormone refractory prostate cancer.

机译:Caspase 8和9基因启动子多态性对前列腺癌易感性和激素难治性前列腺癌的早期发展的影响。

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OBJECTIVE: To investigate, by genotyping CASP8 (-652 6N del/ins) and CASP9 (-1263 A > G; -293 19N del/ins), whether inactivation of apoptosis by genetic polymorphism of caspases 8 and 9 play an integral role in the mechanism of cancer development. To investigate the role of these polymorphisms in susceptibility to early development of hormone refractory prostate cancer. PATIENTS AND METHODS: The study included 175 histologically confirmed cases of prostate cancer and 198 age and ethnicity matched healthy controls. CASP9-1263 A > G polymorphism was genotyped using the polymerase chain reaction-restriction fragment length polymorphism method. CASP9-293 del/ins and CASP8-652 del/ins polymorphisms were genotyped and the deletion pattern analysed by polyacrylamide gel electrophoresis. RESULTS: Our results demonstrated that presence of CASP9-1263 G allele was associated with reduced risk for prostate cancer (odds ratio 0.6, 95%CI 0.39-0.92, P= 0.02). Other variant CASP9 was not associated with prostate cancer risk. Coincidentally, the presence of CASP9-1263 G allele was associated with increased risk for progression of prostate cancer to bone metastasis (odds ratio -2.28, 95%CI 1.14-4.53, P= 0.02). CASP8-652 (+/-) genotype was associated with increased hazard for early development of hormone refractory prostate cancer (hazard ratio 2.44, 95%CI 1.2-5.85, P= 0.045). CONCLUSION: Our results support the hypothesis that variants of CASP9 may influence the susceptibility to prostate cancer and its progression to bone metastasis. CASP8 polymorphism may influence the progression of prostate cancer disease to a hormone refractory state.
机译:目的:通过对CASP8(-652 6N del / ins)和CASP9(-1263 A> G; -293 19N del / ins)进行基因分型,研究胱天蛋白酶8和9的基因多态性对细胞凋亡的失活是否在其中发挥重要作用。癌症发展的机制。调查这些多态性在激素难治性前列腺癌的早期发展易感性中的作用。患者与方法:该研究包括175例经组织学证实的前列腺癌病例,以及198例年龄和种族相匹配的健康对照者。使用聚合酶链反应-限制性片段长度多态性方法对CASP9-1263 A> G多态性进行基因分型。对CASP9-293 del / ins和CASP8-652 del / ins多态性进行基因分型,并通过聚丙烯酰胺凝胶电泳分析缺失模式。结果:我们的结果表明,CASP9-1263 G等位基因的存在与降低前列腺癌的风险有关(比值比为0.6,95%CI为0.39-0.92,P = 0.02)。其他变异CASP9与前列腺癌风险无关。巧合的是,CASP9-1263 G等位基因的存在与前列腺癌发展为骨转移的风险增加相关(几率-2.28,95%CI 1.14-4.53,P = 0.02)。 CASP8-652(+/-)基因型与激素难治性前列腺癌早期发展的危险增加相关(危险比2.44,95%CI 1.2-5.85,P = 0.045)。结论:我们的结果支持以下假设:CASP9变异体可能影响对前列腺癌的敏感性及其向骨转移的进展。 CASP8多态性可能影响前列腺癌疾病发展至激素难治性状态。

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