Ross J S, Sheehan C, Hayner-Buchan A M, Ambros R A, Kallakury B V, Kaufman R, Fisher H A, Muraca P J
Department of Pathology and Laboratory Medicine, Albany Medical College, NY 12208, USA.
Hum Pathol. 1997 Jul;28(7):827-33. doi: 10.1016/s0046-8177(97)90157-x.
HER-2/neu expression has been established as a prognostic factor in breast and other cancers. In prostate cancer (PC), a similar predictive role has been hindered by variable immunohistochemical (IHC) results. The authors studied DNA amplification of the HER-2/neu gene on 4-microm sections obtained from 62 formalin-fixed, paraffin-embedded PCs by fluorescence in situ hybridization (FISH). The results were compared with HER-2/neu protein expression as determined by IHC and correlated by logistic regression analysis with Gleason tumor grade, DNA ploidy, serum prostate specific antigen (PSA), and pathological stage. The HER-2/neu gene was localized using the Oncor (Gaithersburg, MD) digoxigenin-labeled unique sequence probe. Amplified PCs had at least 20 malignant cells, with 5 or more copies of the sequence. Amplification of HER-2/neu correlated with Gleason score (P = .0001). The mean Gleason score of unamplified tumors was 5.7 and that of amplified tumors was 7.5. Nondiploid tumors had a significantly greater rate of HER-2/neu amplification compared with diploid tumors (P = .0003). Of the 62 cases evaluated by IHC and FISH, 18 cases (29%) were overexpressed by IHC, and 27 cases (44%) were amplified by FISH. A trend for similar HER-2/neu status in each PC by the two methods did not reach statistical significance (P = .23). HER-2/neu amplification by FISH was associated with advanced pathological stage; however, this relationship reached only near-statistical significance (P = .06). There was no correlation of HER-2/neu amplification by FISH with patient age or preoperative serum PSA levels. The authors conclude that HER-2/neu gene amplification status can be determined by FISH on archival prostate cancer specimens, significantly correlates with high tumor grade and nondiploid DNA content, and is more frequently encountered in tumors with advanced pathological stage. Also, FISH is more sensitive than IHC for detection of abnormalities in the HER-2/neu gene, and further studies should be undertaken to determine whether a FISH-based HER-2/neu detection method may prove of importance in the prediction of prognosis and planning of therapy in prostate cancer patients.
HER-2/neu表达已被确立为乳腺癌及其他癌症的一个预后因素。在前列腺癌(PC)中,类似的预测作用因免疫组化(IHC)结果的多变而受到阻碍。作者通过荧光原位杂交(FISH)研究了从62例福尔马林固定、石蜡包埋的前列腺癌标本获取的4微米切片上HER-2/neu基因的DNA扩增情况。将结果与通过免疫组化测定的HER-2/neu蛋白表达进行比较,并通过逻辑回归分析与Gleason肿瘤分级、DNA倍体、血清前列腺特异性抗原(PSA)及病理分期相关联。使用Oncor(马里兰州盖瑟斯堡)地高辛标记的独特序列探针定位HER-2/neu基因。扩增的前列腺癌细胞至少有20个恶性细胞,且该序列有5个或更多拷贝。HER-2/neu的扩增与Gleason评分相关(P = .0001)。未扩增肿瘤的平均Gleason评分为5.7,扩增肿瘤的平均Gleason评分为7.5。与二倍体肿瘤相比,非二倍体肿瘤的HER-2/neu扩增率显著更高(P = .0003)。在通过免疫组化和FISH评估的62例病例中,18例(29%)免疫组化呈过表达,27例(44%)FISH检测呈扩增。两种方法在各前列腺癌病例中HER-2/neu状态相似的趋势未达到统计学显著性(P = .23)。FISH检测到的HER-2/neu扩增与晚期病理分期相关;然而,这种关系仅接近统计学显著性(P = .06)。FISH检测到的HER-2/neu扩增与患者年龄或术前血清PSA水平无关。作者得出结论,HER-2/neu基因扩增状态可通过FISH在存档的前列腺癌标本上确定,与高肿瘤分级和非二倍体DNA含量显著相关,且在病理分期较晚的肿瘤中更常见。此外,FISH在检测HER-2/neu基因异常方面比免疫组化更敏感,应进一步开展研究以确定基于FISH的HER-2/neu检测方法在预测前列腺癌患者预后及治疗规划中是否具有重要意义。