Ranelletti F O, Almadori G, Rocca B, Ferrandina G, Ciabattoni G, Habib A, Galli J, Maggiano N, Gessi M, Lauriola L
Institute of Histology, Università Cattolica del S. Cuore, Roma, Italy.
Int J Cancer. 2001 Nov 20;95(6):343-9. doi: 10.1002/1097-0215(20011120)95:6<343::aid-ijc1060>3.0.co;2-d.
Epidermal growth factor receptor (EGFR) overexpression is an unfavorable prognostic marker in laryngeal squamous cell carcinoma (SCC). EGFR stimulates cyclooxygenase-2 (COX-2) expression in normal human keratinocytes and squamous carcinoma cells. Based on these observations a prognostic role of COX-2 expression in laryngeal SCC can be hypothesized. Consequently, COX-2 expression was studied in laryngeal SCC (median follow-up = 47 months; range: 2-87 months) by quantitative immunohistochemistry (n = 61) and EGFR by binding assay (n = 51). Well-differentiated regions of laryngeal SCC revealed strong COX-2 immunostaining, whereas histologically normal areas neighboring tumor as well as poorly-differentiated tumors were negative. Immunohistochemical results were confirmed by Western blot analyses. Cox's regression analysis showed that the combination of low levels of COX-2 integrated density and high levels of EGFR covariates provided strong prediction, at 5-year follow-up, of both poor overall survival (chi(2) = 12.905; p = 0.0016) and relapse-free survival (chi(2) = 9.209; p = 0.01). In vitro studies on CO-K3 cell line, obtained from an EGFR positive, COX-2 negative poorly-differentiated laryngeal SCC, revealed that EGF stimulation failed to induce COX-2 expression and PGE2 production suggesting a change in EGFR signaling pathway. These findings indicate that COX-2 is overexpressed in less aggressive, low grade laryngeal SCC, whereas its expression is lost when tumors progress to a more malignant phenotype.
表皮生长因子受体(EGFR)过表达是喉鳞状细胞癌(SCC)的一个不良预后标志物。EGFR可刺激正常人角质形成细胞和鳞状癌细胞中环氧合酶-2(COX-2)的表达。基于这些观察结果,可以推测COX-2表达在喉SCC中具有预后作用。因此,通过定量免疫组织化学(n = 61)研究了喉SCC中的COX-2表达(中位随访时间 = 47个月;范围:2 - 87个月),并通过结合试验研究了EGFR(n = 51)。喉SCC的高分化区域显示出强烈的COX-2免疫染色,而肿瘤周围的组织学正常区域以及低分化肿瘤均为阴性。免疫组织化学结果通过蛋白质印迹分析得到证实。Cox回归分析表明,低水平的COX-2积分密度和高水平的EGFR协变量相结合,在5年随访时,对总生存期差(χ² = 12.905;p = 0.0016)和无复发生存期差(χ² = 9.209;p = 0.01)均具有很强的预测能力。对从EGFR阳性、COX-2阴性的低分化喉SCC中获得的CO-K3细胞系进行的体外研究表明,表皮生长因子(EGF)刺激未能诱导COX-2表达和前列腺素E2(PGE2)产生,提示EGFR信号通路发生了变化。这些发现表明,COX-2在侵袭性较小、低级别喉SCC中过表达,而当肿瘤进展为更恶性的表型时其表达消失。