COX-2 as a potential biomarker and therapeutic target in melanoma.
Diana Valentina TudorIoana BâldeaMihai LupuTeodor KacsoEniko KutasiAndreea HopârteanRoland StreteaAdriana Gabriela FilipPublished in: Cancer biology & medicine (2021)
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?
Keyphrases
- oxidative stress
- skin cancer
- prognostic factors
- stem cells
- dna methylation
- palliative care
- squamous cell carcinoma
- gene expression
- papillary thyroid
- cell death
- endoplasmic reticulum stress
- bone marrow
- transcription factor
- cell proliferation
- risk factors
- nitric oxide
- lymph node metastasis
- young adults
- replacement therapy