Suppr超能文献

肿瘤诱导型一氧化氮合酶和环氧化酶-2在III期恶性皮肤黑色素瘤中的预后意义

Prognostic significance of tumor iNOS and COX-2 in stage III malignant cutaneous melanoma.

作者信息

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

机构信息

Department of Oncology and Pathology, Cancer Center Karolinska, R8:01, Karolinska University Hospital, Karolinska Institutet, 171 76 Stockholm, Sweden.

出版信息

Cancer Immunol Immunother. 2009 Jul;58(7):1085-94. doi: 10.1007/s00262-008-0631-1. Epub 2008 Nov 28.

Abstract

PURPOSE

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.

EXPERIMENTAL DESIGN

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.

RESULTS

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.

CONCLUSION

Our data show that iNOS is an independent and stronger prognostic factor for OS in stage III malignant cutaneous melanoma than COX-2.

摘要

目的

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。

实验设计

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。

结果

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。

结论

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。

相似文献

1
Prognostic significance of tumor iNOS and COX-2 in stage III malignant cutaneous melanoma.
Cancer Immunol Immunother. 2009 Jul;58(7):1085-94. doi: 10.1007/s00262-008-0631-1. Epub 2008 Nov 28.
2
Prognostic value of BRAF(V⁶⁰⁰) mutations in melanoma patients after resection of metastatic lymph nodes.
Ann Surg Oncol. 2012 Dec;19(13):4314-21. doi: 10.1245/s10434-012-2457-5. Epub 2012 Jul 7.
4
The role of CCND1 alterations during the progression of cutaneous malignant melanoma.
Tumour Biol. 2012 Dec;33(6):2189-99. doi: 10.1007/s13277-012-0480-6. Epub 2012 Sep 23.
5
Prognostic significance of BRAF and NRAS mutations in melanoma: a German study from routine care.
BMC Cancer. 2017 Aug 10;17(1):536. doi: 10.1186/s12885-017-3529-5.
8
NRAS mutation status is an independent prognostic factor in metastatic melanoma.
Cancer. 2012 Aug 15;118(16):4014-23. doi: 10.1002/cncr.26724. Epub 2011 Dec 16.

引用本文的文献

1
Redox-Related Proteins in Melanoma Progression.
Antioxidants (Basel). 2022 Feb 22;11(3):438. doi: 10.3390/antiox11030438.
2
High expression of ID1 in monocytes is strongly associated with phenotypic and functional MDSC markers in advanced melanoma.
Cancer Immunol Immunother. 2020 Apr;69(4):513-522. doi: 10.1007/s00262-019-02476-9. Epub 2020 Jan 17.
4
Neutrophil-lymphocyte ratio is prognostic in early stage resected small-cell lung cancer.
PeerJ. 2019 Jul 29;7:e7232. doi: 10.7717/peerj.7232. eCollection 2019.
5
Impact of l-Arginine Metabolism on Immune Response and Anticancer Immunotherapy.
Front Oncol. 2018 Mar 16;8:67. doi: 10.3389/fonc.2018.00067. eCollection 2018.
6
Overcoming resistance to BRAF inhibitors.
Ann Transl Med. 2017 Oct;5(19):387. doi: 10.21037/atm.2017.06.09.
7
The role of nitric oxide in melanoma.
Biochim Biophys Acta Rev Cancer. 2017 Dec;1868(2):500-509. doi: 10.1016/j.bbcan.2017.09.005. Epub 2017 Sep 27.
10
The Complexity of the ERK/MAP-Kinase Pathway and the Treatment of Melanoma Skin Cancer.
Front Cell Dev Biol. 2016 Apr 27;4:33. doi: 10.3389/fcell.2016.00033. eCollection 2016.

本文引用的文献

2
Expression of cyclo-oxygenase-2 in macrophages associated with cutaneous melanoma at different stages of progression.
Prostaglandins Other Lipid Mediat. 2007 Jun;83(4):320-8. doi: 10.1016/j.prostaglandins.2007.03.003. Epub 2007 Mar 13.
3
Tumor iNOS predicts poor survival for stage III melanoma patients.
Int J Cancer. 2006 Aug 15;119(4):861-6. doi: 10.1002/ijc.21767.
4
Regulation of iNOS by the p44/42 mitogen-activated protein kinase pathway in human melanoma.
Oncogene. 2006 Jun 29;25(28):3956-62. doi: 10.1038/sj.onc.1209419. Epub 2006 Feb 13.
5
Mutually exclusive NRASQ61R and BRAFV600E mutations at the single-cell level in the same human melanoma.
Oncogene. 2006 Jun 8;25(24):3357-64. doi: 10.1038/sj.onc.1209379. Epub 2006 Feb 6.
6
Distinct sets of genetic alterations in melanoma.
N Engl J Med. 2005 Nov 17;353(20):2135-47. doi: 10.1056/NEJMoa050092.
7
Prostaglandins and cancer.
Gut. 2006 Jan;55(1):115-22. doi: 10.1136/gut.2004.047100. Epub 2005 Aug 23.
9
BRAFE600-associated senescence-like cell cycle arrest of human naevi.
Nature. 2005 Aug 4;436(7051):720-4. doi: 10.1038/nature03890.
10
Use of human tissue to assess the oncogenic activity of melanoma-associated mutations.
Nat Genet. 2005 Jul;37(7):745-9. doi: 10.1038/ng1586. Epub 2005 Jun 12.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验