Prognostic significance of cyclooxygenase-2 in laryngeal squamous cell carcinoma

被引:5
|
作者
Ranelletti, FO
Almadori, G
Rocca, B
Ferrandina, G
Ciabattoni, G
Habib, A
Galli, J
Maggiano, N
Gessi, M
Lauriola, L
机构
[1] Univ Cattolica Sacro Cuore, Inst Histol, I-00168 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Inst Otolaryngol, I-00168 Rome, Italy
[3] Univ Cattolica Sacro Cuore, Inst Internal Med, I-00168 Rome, Italy
[4] Univ Cattolica Sacro Cuore, Inst Gynecol, I-00168 Rome, Italy
[5] Univ G DAnnunzio, Dept Sci Farmaco, Chieti, Italy
[6] Hop Lariboisiere, INSERM U348, F-75475 Paris, France
[7] Univ Cattolica Sacro Cuore, Inst Pathol, Rome, Italy
关键词
cyclooxygenase-2; epidermal growth factor receptor; laryngeal squamous cell carcinoma; prognostic markers;
D O I
10.1002/1097-0215(20011120)95:6<343::AID-IJC1060>3.0.CO;2-D
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 an 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. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:343 / 349
页数:7
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