使用基因组微阵列比较基因组杂交技术对石蜡包埋和福尔马林固定的前列腺肿瘤进行高分辨率分析。

High-resolution analysis of paraffin-embedded and formalin-fixed prostate tumors using comparative genomic hybridization to genomic microarrays.

作者信息

Paris Pamela L, Albertson Donna G, Alers Janneke C, Andaya Armann, Carroll Peter, Fridlyand Jane, Jain Ajay N, Kamkar Sherwin, Kowbel David, Krijtenburg Pieter-Jaap, Pinkel Daniel, Schröder Fritz H, Vissers Kees J, Watson Vivienne J E, Wildhagen Mark F, Collins Colin, Van Dekken Herman

机构信息

Comprehensive Cancer Center, University of California at San Francisco, San Francisco, California 94115, USA.

出版信息

Am J Pathol. 2003 Mar;162(3):763-70. doi: 10.1016/S0002-9440(10)63873-4.

Abstract

We have used prostate cancer, the most commonly diagnosed noncutaneous neoplasm among men, to investigate the feasibility of performing genomic array analyses of archival tissue. Prostate-specific antigen and a biopsy Gleason grade have not proven to be accurate in predicting clinical outcome, yet they remain the only accepted biomarkers for prostate cancer. It is likely that distinct spectra of genomic alterations underlie these phenotypic differences, and that once identified, may be used to differentiate between indolent and aggressive tumors. Array comparative genomic hybridization allows quantitative detection and mapping of copy number aberrations in tumors and subsequent associations to be made with clinical outcome. Archived tissues are needed to have patients with sufficient clinical follow-up. In this report, 20 formalin-fixed and paraffin-embedded prostate cancer samples originating from 1986 to 1996 were studied. We present a straightforward protocol and demonstrate the utility of archived tissue for array comparative genomic hybridization with a 2400 element BAC array that provides high-resolution detection of both deletions and amplifications.

摘要

我们利用前列腺癌(男性中最常被诊断出的非皮肤肿瘤)来研究对存档组织进行基因组阵列分析的可行性。前列腺特异性抗原和活检Gleason分级在预测临床结果方面尚未被证明是准确的,但它们仍然是前列腺癌唯一被认可的生物标志物。这些表型差异很可能是由不同的基因组改变谱所导致的,一旦被识别出来,就可以用于区分惰性肿瘤和侵袭性肿瘤。阵列比较基因组杂交能够对肿瘤中的拷贝数畸变进行定量检测和定位,并随后将其与临床结果建立关联。需要存档组织来对患者进行充分的临床随访。在本报告中,我们研究了20个来自1986年至1996年的福尔马林固定石蜡包埋前列腺癌样本。我们提出了一个简单的方案,并展示了存档组织对于使用2400元件BAC阵列进行阵列比较基因组杂交的实用性,该阵列能够对缺失和扩增进行高分辨率检测。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索