Johansson C Christian, Egyházi Suzanne, Masucci Giuseppe, Harlin Helena, Mougiakakos Dimitrios, Poschke Isabel, Nilsson Bo, Garberg Liss, Tuominen Rainer, Linden Diana, Stolt Marianne Frostvik, Hansson Johan, Kiessling Rolf
Department of Oncology and Pathology, Cancer Center Karolinska, R8:01, Karolinska University Hospital, Karolinska Institutet, 171 76 Stockholm, Sweden.
Cancer Immunol Immunother. 2009 Jul;58(7):1085-94. doi: 10.1007/s00262-008-0631-1. Epub 2008 Nov 28.
New prognostic markers are needed for malignant melanoma. Inducible nitric oxide synthase (iNOS) and cyclooxygenase type 2 (COX-2) have been described to correlate with progression of melanoma. Moreover, activating mutations in BRAF/NRAS oncogenes are often detected in melanoma. The BRAF/NRAS mutation status and expression of COX-2 and iNOS were examined to compare their prognostic value for overall survival (OS) in stage III malignant cutaneous melanoma.
The expression of iNOS and COX-2 in metastatic lymph nodes from 21 rapidly progressing (OS from date of diagnosis of stage III disease < or =14 months) and 17 slowly progressing (OS > or =60 months) stage III cutaneous melanoma patients was examined by immunohistochemistry. The presence of BRAF/NRAS mutations was analyzed using direct DNA sequencing. Chi2 exact trend test and logistic regression analysis were used for statistical analysis.
Both iNOS (P = 0.002) and COX-2 (P = 0.048) alone significantly predicted OS. The BRAF/NRAS mutation status did not significantly differ between patient groups, although iNOS significantly (P = 0.013) correlated with BRAF mutation frequency. Furthermore, the odds ratio (OR) with respect to OS of iNOS (OR = 10.4) was higher than that of COX-2 (OR = 5.6) and was stable in the multivariate analysis of OS together with disease stage IIIB/C, ulceration, number of metastatic lymph nodes, and Breslow tumor thickness.
Our data show that iNOS is an independent and stronger prognostic factor for OS in stage III malignant cutaneous melanoma than COX-2.
恶性黑色素瘤需要新的预后标志物。已有研究表明诱导型一氧化氮合酶(iNOS)和环氧合酶-2(COX-2)与黑色素瘤的进展相关。此外,黑色素瘤中常检测到BRAF/NRAS癌基因的激活突变。本研究检测了BRAF/NRAS突变状态以及COX-2和iNOS的表达,以比较它们对III期恶性皮肤黑色素瘤总生存期(OS)的预后价值。
通过免疫组织化学检测21例进展迅速(III期疾病诊断日期起OS≤14个月)和17例进展缓慢(OS≥60个月)的III期皮肤黑色素瘤患者转移淋巴结中iNOS和COX-2的表达。采用直接DNA测序分析BRAF/NRAS突变的存在情况。采用卡方精确趋势检验和逻辑回归分析进行统计分析。
单独的iNOS(P = 0.002)和COX-2(P = 0.048)均能显著预测OS。患者组间BRAF/NRAS突变状态无显著差异,尽管iNOS与BRAF突变频率显著相关(P = 0.013)。此外,iNOS相对于OS的优势比(OR = 10.4)高于COX-2(OR = 5.6),并且在与疾病IIIB/C期、溃疡、转移淋巴结数量和Breslow肿瘤厚度一起进行的OS多变量分析中保持稳定。
我们的数据表明,在III期恶性皮肤黑色素瘤中,iNOS是比COX-2更强的独立预后因素。