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人类前列腺癌中Y染色体特异性基因的缺失

Deletion of Y-chromosome specific genes in human prostate cancer.

作者信息

Perinchery G, Sasaki M, Angan A, Kumar V, Carroll P, Dahiya R

机构信息

Department of Urology, Veterans Affairs Medical Center, and University of California San Francisco, 94121, USA.

出版信息

J Urol. 2000 Apr;163(4):1339-42.

Abstract

PURPOSE

The present study is based on the hypothesis that deletion of Y-chromosome-specific genes is associated with prostate cancer. To test this hypothesis, we analyzed the deletion of six Y-chromosome-specific genes in prostate cancer samples.

MATERIALS AND METHODS

Fifty human prostate cancer specimens were processed for microdissection of pure epithelial cells. DNA was extracted from these cells and amplified using PCR and analyzed for loss of six different Y-chromosome-specific genes (SRY, ZFY, BPY1, SMCY, RBM1 and BPY2). We used D8S262 primer (chromosome 8p23) for internal control to assess the quality and loading of DNA for each sample.

RESULTS

Deletion was observed in most of the prostate cancer specimens with at least one Y-chromosome-specific gene. The loss of SRY gene (Yp11.32) was shown in 38% of cases whereas the other genes show 18% loss in ZFY (Yp11.31), 14% in BPY1 (Yq11.2), 52% in SMCY (Yq11.22), 32% in RBM1 (Yq11.23) and 42% in BPY2 (Yq12.1). The loss of most genes analyzed is seen more frequent in advanced stages and grades of prostate cancer.

CONCLUSION

There was a significant loss of Y-chromosome-specific genes in prostate cancer. The loss of SRY and BPY2 genes was more frequent in higher stages and grades of prostate cancer. This is the first report to demonstrate that the loss of Y-chromosome-specific genes is associated with prostate cancer, suggesting their role in pathogenesis of this disease.

摘要

目的

本研究基于Y染色体特异性基因缺失与前列腺癌相关的假说。为验证该假说,我们分析了前列腺癌样本中六个Y染色体特异性基因的缺失情况。

材料与方法

对50例人类前列腺癌标本进行处理,以显微切割出纯上皮细胞。从这些细胞中提取DNA,通过聚合酶链反应(PCR)进行扩增,并分析六个不同Y染色体特异性基因(SRY、ZFY、BPY1、SMCY、RBM1和BPY2)的缺失情况。我们使用D8S262引物(8号染色体p23)作为内部对照,以评估每个样本DNA的质量和上样量。

结果

在大多数前列腺癌标本中观察到至少一个Y染色体特异性基因的缺失。38%的病例出现SRY基因(Yp11.32)缺失,而其他基因的缺失情况为:ZFY(Yp11.31)为18%,BPY1(Yq11.2)为14%,SMCY(Yq11.22)为52%,RBM1(Yq11.23)为32%,BPY2(Yq12.1)为42%。在前列腺癌的晚期和高分级阶段,所分析的大多数基因缺失更为常见。

结论

前列腺癌中存在Y染色体特异性基因的显著缺失。SRY和BPY2基因在前列腺癌的较高分期和分级中缺失更为频繁。这是首次报道证明Y染色体特异性基因缺失与前列腺癌相关,提示它们在该疾病发病机制中的作用。

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