COX-2 as a potential biomarker and therapeutic target in melanoma

被引:66
|
作者
Tudor, Diana Valentina [1 ]
Baldea, Ioana [1 ]
Lupu, Mihai [1 ]
Kacso, Teodor [1 ]
Kutasi, Eniko [1 ]
Hopartean, Andreea [1 ]
Stretea, Roland [1 ]
Filip, Adriana Gabriela [1 ]
机构
[1] Univ Med & Pharm Iuliu Hatieganu, Dept Physiol, Cluj Napoca 400000, Romania
关键词
Melanoma; inflammation; COX-2; inhibitors; celecoxib; MALIGNANT-MELANOMA; CYCLOOXYGENASE-2; EXPRESSION; CHRONIC INFLAMMATION; TOPICAL CELECOXIB; UP-REGULATION; TUMOR-GROWTH; SKIN-CANCER; KAPPA-B; INHIBITION; CHEMOPREVENTION;
D O I
10.20892/j.issn.2095-3941.2019.0339
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
With a constantly increasing incidence, cutaneous melanoma has raised the need for a better understanding of its complex microenvironment that may further guide therapeutic options. Melanoma is a model tumor in immuno-oncology. Inflammation represents an important hallmark of cancer capable of inducing and sustaining tumor development. The inflammatory process also orchestrates the adaptative immunosuppression of tumor cells that helps them to evade immune destruction. Besides its role in proliferation, angiogenesis, and apoptosis, cyclooxygenase-2 (COX-2) is a well-known promoter of immune suppression in melanoma. COX-2 inhibitors are closely involved in this condition. This review attempts to answer two controversial questions: is COX-2 a valuable prognostic factor? Among all COX-2 inhibitors, is celecoxib a suitable adjuvant in melanoma therapy?
引用
收藏
页码:20 / 31
页数:12
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