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RASSF1A启动子甲基化在癌前和非癌性微切割前列腺上皮组织中均经常被检测到。

RASSF1A promoter methylation is frequently detected in both pre-malignant and non-malignant microdissected prostatic epithelial tissues.

作者信息

Aitchison Alan, Warren Anne, Neal David, Rabbitts Pamela

机构信息

Department of Oncology, University of Cambridge, Hills Road, Cambridge, United Kingdom.

出版信息

Prostate. 2007 May 1;67(6):638-44. doi: 10.1002/pros.20475.

Abstract

BACKGROUND

The RASSF1A gene is a tumor suppressor gene inactivated by hypermethylation in a very wide variety of malignant tumors including prostate cancer.

METHODS

In this study we have used laser capture microdissection to provide pure cell populations to investigate the methylation status of 16 CpG sites in the promoter region of this gene in prostatic intra-epithelial neoplasia, in histologically normal epithelial cells associated with these lesions and in epithelial cells from benign prostatic hyperplasia.

RESULTS

Unexpectedly, frequent methylation, detected by sequence analysis following bisulphite treatment, was observed in benign epithelium as well as in the lesions associated with prostatic intra-epithelial neoplasia and at high risk of cancer formation. Fifty percent or more CpG sites were methylated in 7/14 prostatic intra-epithelial neoplasms, 8/11 histologically normal epithelial cells and 8/12 specimens of benign prostatic tissue.

CONCLUSION

These observations suggest that methylation of the RASSF1A gene is present in both pre-malignant and benign epithelia and suggests quantitation is required for it to be an effective marker of early prostate cancer.

摘要

背景

RASSF1A基因是一种抑癌基因,在包括前列腺癌在内的多种恶性肿瘤中因高甲基化而失活。

方法

在本研究中,我们使用激光捕获显微切割技术提供纯细胞群体,以研究该基因启动子区域16个CpG位点在前列腺上皮内瘤变、与这些病变相关的组织学正常上皮细胞以及良性前列腺增生上皮细胞中的甲基化状态。

结果

出乎意料的是,在亚硫酸氢盐处理后的序列分析中,在良性上皮以及与前列腺上皮内瘤变相关且有高癌变风险的病变中均观察到频繁的甲基化。在14例前列腺上皮内瘤变中的7例、11例组织学正常上皮细胞中的8例以及12例良性前列腺组织标本中的8例中,50%或更多的CpG位点发生了甲基化。

结论

这些观察结果表明,RASSF1A基因的甲基化存在于癌前上皮和良性上皮中,并且表明需要进行定量分析才能使其成为早期前列腺癌的有效标志物。

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