Pauletti G, Godolphin W, Press M F, Slamon D J
Department of Medicine, University of California, Los Angeles, School of Medicine, Los Angeles, California 90095, USA.
Oncogene. 1996 Jul 4;13(1):63-72.
Amplification and overexpression of the HER-2/neu gene occurs in 25-30% of human breast cancers. This genetic alteration is associated with a poor clinical prognosis in women with either node negative or node positive breast cancers. The initial studies testing this association were somewhat controversial and this controversy was due in large part to significant heterogeneity in both the methods and/or reagents used in testing archival material for the presence of the alteration. These methods included a number of solid matrix blotting techniques for DNA, RNA and protein as well as immunohistochemistry. Fluorescence in situ hybridization (FISH) represents the newest methodologic approach for testing for this genetic alteration. In this study, FISH is compared to Southern, Northern and Western blot analyses as well as immunohistochemistry in a large cohort of archival human breast cancer specimens. FISH was found to be superior to all other methodologies tested in assessing formalin fixed, paraffin embedded material for HER-2/neu amplification. The results from this study also confirm that overexpression of HER-2/neu rarely occurs in the absence of gene amplification in breast cancer (approximately 3% of cases). This method of analysis is rapid, reproducible and extremely reliable in detecting presence of HER-2/neu gene amplification and should have clinical utility.
HER-2/neu基因的扩增和过表达在25%至30%的人类乳腺癌中出现。这种基因改变与淋巴结阴性或阳性乳腺癌女性患者较差的临床预后相关。最初检测这种关联的研究存在一定争议,而这种争议很大程度上是由于在检测存档材料中是否存在该改变时,所使用的方法和/或试剂存在显著异质性。这些方法包括多种用于DNA、RNA和蛋白质的固相印迹技术以及免疫组织化学。荧光原位杂交(FISH)是检测这种基因改变的最新方法学手段。在本研究中,在一大组存档人类乳腺癌标本中,将FISH与Southern印迹、Northern印迹、Western印迹分析以及免疫组织化学进行了比较。结果发现,在评估福尔马林固定、石蜡包埋材料中的HER-2/neu扩增时,FISH优于所有其他测试方法。本研究结果还证实,在乳腺癌中,HER-2/neu过表达在无基因扩增的情况下很少发生(约3%的病例)。这种分析方法在检测HER-2/neu基因扩增的存在方面快速、可重复且极其可靠,应具有临床应用价值。