Yk Wang, Cf Gao, T Yun, Z Chen, Xw Zhang, Xx Lv, Nl Meng, Wz Zhao
Department of Pathology, The 150 Centre Hospital of Chinese PLA, Medical Center of Jinan Military Region, Luoyang 471031, China.
Mol Cytogenet. 2011 Jun 20;4(1):14. doi: 10.1186/1755-8166-4-14.
The goal of this study was to investigate ERBB2(HER2) and EGFR gene amplification and protein expression in gastric cancer. Fluorescence in situ hybridization (FISH) and immunohistochemistry were used to analyze ERBB2 and EGFR gene amplification and protein expression in 69 cases of gastric cancer.
FISH analysis revealed that 20.3% of the cases exhibited ERBB2 gene amplification. Increases in ERBB2 copy number and gene amplification were present in 52.2% of the samples. Expression of the ERBB2 protein was observed in 42.0% of cases. FISH analysis detected EGFR gene amplification in 29.0% of samples. Increases in EGFR copy number and gene amplification occurred in 57.9% of samples, and EGFR protein expression was present in 52.2% of samples. Both ERBB2 and EGFR gene amplification were 3 cases (4.3%), but abnormalities in both ERBB2 and EGFR gene copy number were present 36.2% of samples. ERBB2 and EGFR gene amplification were significantly associated with the depth of tumor invasion (P < 0.05) and lymph node metastasis (P < 0.05), but not with sex, age, or histological type (P > 0.05).
Our data indicated that ERBB2 and EGFR genetic abnormalities were associated with the prognosis of gastric cancer. Clinical assessment of ERBB2 and EGFR amplification may represent an important factor for the development of personalized treatment programs for gastic cancer.
本研究的目的是调查胃癌中ERBB2(HER2)和EGFR基因扩增及蛋白表达情况。采用荧光原位杂交(FISH)和免疫组织化学方法分析69例胃癌中ERBB2和EGFR基因扩增及蛋白表达。
FISH分析显示,20.3%的病例存在ERBB2基因扩增。52.2%的样本中ERBB2拷贝数增加和基因扩增。42.0%的病例观察到ERBB2蛋白表达。FISH分析在29.0%的样本中检测到EGFR基因扩增。57.9%的样本中EGFR拷贝数增加和基因扩增,52.2%的样本中存在EGFR蛋白表达。ERBB2和EGFR基因扩增均为3例(4.3%),但ERBB2和EGFR基因拷贝数均异常的样本占36.2%。ERBB2和EGFR基因扩增与肿瘤浸润深度(P < 0.05)和淋巴结转移(P < 0.05)显著相关,但与性别、年龄或组织学类型无关(P > 0.05)。
我们的数据表明,ERBB2和EGFR基因异常与胃癌预后相关。对ERBB2和EGFR扩增进行临床评估可能是制定胃癌个性化治疗方案的重要因素。