Friess H, Fukuda A, Tang W H, Eichenberger A, Furlan N, Zimmermann A, Korc M, Büchler M W
Department of Visceral and Transplantation Surgery, University of Bern, Inselspital, CH-3010 Bern, Switzerland.
World J Surg. 1999 Oct;23(10):1010-8. doi: 10.1007/s002689900616.
The epidermal growth factor receptor family consists of four closely related transmembrane receptors: epidermal growth factor receptor (EGF-R), c-erbB-2, c-erbB-3, and c-erbB-4. Overexpression of each receptor may lead to cell transformation and contributes to tumor progression in various malignancies. Although these factors have been analyzed in many cancers separately, little is known about their concomitant expression in esophageal cancer. Based on the finding that EGF-R and c-erbB-2 form highly active transmembranous heterodimers that enhance cell growth and proliferation, we used Northern blot analysis and immunohistochemistry to analyze the concomitant expression of EGF-R, c-erbB-2, and c-erbB-3 in tissue samples obtained from 39 patients undergoing esophagectomy for esophageal cancer. Northern blot analysis revealed a fourfold increase (p < 0.01) in EGF-R mRNA levels in the esophageal cancer samples in comparison with normal tissue samples. The c-erbB-2 receptor was only 1.25-fold elevated in the esophageal cancers, which failed to be statistically significant (p = 0.31). In contrast, c-erbB-3 mRNA levels were 3.5-fold lower (p < 0.01) in the esophageal cancers than in the normal tissues. Immunohistochemical analysis showed weak EGF-R, c-erbB-2, and c-erbB-3 immunostaining in the normal esophageal tissue. In esophageal cancer samples, immunoreactivity for EGF-R, c-erbB-2, and c-erbB-3 was mainly located in the cancer cells. Strong EGF-R, c-erbB-2, and c-erbB-3 immunoreactivity was present in 59%, 64%, and 64% of the esophageal cancer samples, respectively. In consecutive tissue sections, identical cancer cell clusters often exhibited these three closely related receptors simultaneously. However, correlation of the immunohistochemical findings with the clinicopathologic patient parameters revealed that the presence of EGF-R, c-erbB-2, or c-erbB-3 had no influence on patient survival (p > 0.05). In addition, the simultaneous presence of these receptors did not influence survival. Our findings indicate that in esophageal cancer the presence of EGF-R, c-erbB-2, and c-erbB-3 alone or in combination seems to have no major influence on patient prognosis and does not alter tumor growth behavior significantly.
表皮生长因子受体(EGF-R)、c-erbB-2、c-erbB-3和c-erbB-4。每个受体的过表达都可能导致细胞转化,并在各种恶性肿瘤中促进肿瘤进展。尽管这些因子已在许多癌症中分别进行了分析,但它们在食管癌中的共表达情况却知之甚少。基于EGF-R和c-erbB-2形成高活性跨膜异二聚体并增强细胞生长和增殖这一发现,我们使用Northern印迹分析和免疫组织化学方法,对39例因食管癌接受食管切除术患者的组织样本中EGF-R、c-erbB-2和c-erbB-3的共表达情况进行了分析。Northern印迹分析显示,与正常组织样本相比,食管癌样本中EGF-R mRNA水平增加了四倍(p < 0.01)。c-erbB-2受体在食管癌中仅升高了1.25倍,差异无统计学意义(p = 0.31)。相反,食管癌中c-erbB-3 mRNA水平比正常组织低3.5倍(p < 0.01)。免疫组织化学分析显示,正常食管组织中EGF-R、c-erbB-2和c-erbB-3免疫染色较弱。在食管癌样本中,EGF-R、c-erbB-2和c-erbB-3的免疫反应性主要位于癌细胞中。EGF-R、c-erbB-2和c-erbB-3免疫反应性强的情况分别出现在59%、64%和64%的食管癌样本中。在连续的组织切片中,相同的癌细胞簇常常同时显示这三种密切相关的受体。然而,免疫组织化学结果与患者临床病理参数的相关性显示,EGF-R、c-erbB-2或c-erbB-3的存在对患者生存率没有影响(p > 0.05)。此外,这些受体的同时存在也不影响生存率。我们的研究结果表明,在食管癌中,单独或联合存在EGF-R、c-erbB-2和c-erbB-3似乎对患者预后没有重大影响,也不会显著改变肿瘤生长行为。