Nakanishi K, Kawai T, Suzuki M, Torikata C
Department of Pathology, National Defense Medical College, Tokorozawa, Japan.
Mod Pathol. 1996 Mar;9(3):292-7.
Epidermal growth factor (EGF) and transforming growth factor-alpha (TGF-alpha) stimulate cellular proliferation, whereas epidermal growth factor receptor (EGFR) and c-erb-B-2 oncoprotein are involved in the regulation of cellular growth. Although the immunoreactivity for growth factors and oncogene products in transitional cell carcinoma (TCC) of the urinary bladder has been shown to correlate with clinicopathologic findings and prognoses, there have been no such reports on TCC of the upper urinary tract (TCC-UUT). The present study investigated the prognostic value of these growth factors (EGF and TGF-alpha) and oncogene products (EGFR and c-erb-B-2) in TCC-UUT. Formalin-fixed, paraffin-embedded tumor tissues from 133 patients with TCC-UUT were analyzed using immunohistochemical staining. Immunohistochemically, EGF was recognized as positive in 50.4% of the samples, TGF-alpha in 27.8%, EGFR in 41.3%, and c-erb-B-2 oncoprotein in 6.8%. The immunoreactivity for EGF and c-erb-B-2 oncoprotein was significantly (P < 0.05) correlated with both stage and grade, whereas TGF-alpha correlated only with stage and EGFR only with grade. The 5-year survival rate for all cases taken together was 66.7%. Univariate analysis revealed that patients with EGF- and c-erb-B-2 oncoprotein-positive tumors had a worse clinical course than patients with EGF- and c-erb-B-2 oncoprotein-negative tumors, whereas in the final models of multivariate analysis, stage was found to be the only prognostic factor. Detection of immunoreactivity for growth factors and oncogene products does not appear to be of any real value in deciding the prognosis of TCC-UUT.
表皮生长因子(EGF)和转化生长因子-α(TGF-α)可刺激细胞增殖,而表皮生长因子受体(EGFR)和c-erb-B-2癌蛋白则参与细胞生长的调节。尽管已证明膀胱移行细胞癌(TCC)中生长因子和癌基因产物的免疫反应性与临床病理结果及预后相关,但关于上尿路移行细胞癌(TCC-UUT)尚无此类报道。本研究调查了这些生长因子(EGF和TGF-α)及癌基因产物(EGFR和c-erb-B-2)在TCC-UUT中的预后价值。使用免疫组织化学染色分析了133例TCC-UUT患者福尔马林固定、石蜡包埋的肿瘤组织。免疫组织化学检测显示,50.4%的样本中EGF呈阳性,27.8%的样本中TGF-α呈阳性,41.3%的样本中EGFR呈阳性,6.8%的样本中c-erb-B-2癌蛋白呈阳性。EGF和c-erb-B-2癌蛋白的免疫反应性与分期和分级均显著相关(P<0.05),而TGF-α仅与分期相关,EGFR仅与分级相关。所有病例的5年生存率为66.7%。单因素分析显示,EGF和c-erb-B-2癌蛋白阳性肿瘤患者的临床病程比EGF和c-erb-B-2癌蛋白阴性肿瘤患者更差,而在多因素分析的最终模型中,分期是唯一的预后因素。检测生长因子和癌基因产物的免疫反应性在决定TCC-UUT的预后方面似乎没有任何实际价值。