4.6 Review

The Role of p53 in Progression of Cutaneous Squamous Cell Carcinoma

期刊

CANCERS
卷 13, 期 18, 页码 -

出版社

MDPI
DOI: 10.3390/cancers13184507

关键词

p53; skin; cancer; squamous cell carcinoma

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资金

  1. Jane and Aatos Erkko Foundation
  2. Finnish Cancer Research Foundation
  3. Sigrid Juselius Foundation
  4. Turku University Hospital VTR grant [13336]
  5. Finnish Medical Foundation
  6. Cancer Foundation of Southwest Finland

向作者/读者索取更多资源

Skin cancers, including cutaneous squamous cell carcinoma (cSCC), are the most common types of cancer worldwide, primarily caused by long-term exposure to solar ultraviolet radiation. cSCC is the most common metastatic skin cancer associated with poor prognosis. The inactivation mutation of p53 and accumulation of additional oncogenic mutations play a critical role in the progression of cSCC.
Simple Summary Skin cancers are the most common types of cancer worldwide, and their incidence is increasing. Epidermal keratinocyte-derived cutaneous squamous cell carcinoma (cSCC) is the most common metastatic skin cancer, and it is associated with poor prognosis in the advanced stage. The most important risk factor for cSCC is long-term exposure to solar ultraviolet radiation, which induces oncogenic mutations in epidermal keratinocytes. The most common mutations are inactivating mutations in tumor suppressor p53, which result in accumulation of additional mutations. Recently, the role of p53 in the progression and invasion of cSCC has also been elucidated. In this review we will discuss the role of p53 in development of cSCC and as a potential new therapeutic target in advanced cSCC. Skin cancers are the most common types of cancer worldwide, and their incidence is increasing. Melanoma, basal cell carcinoma (BCC), and cutaneous squamous cell carcinoma (cSCC) are the three major types of skin cancer. Melanoma originates from melanocytes, whereas BCC and cSCC originate from epidermal keratinocytes and are therefore called keratinocyte carcinomas. Chronic exposure to ultraviolet radiation (UVR) is a common risk factor for skin cancers, but they differ with respect to oncogenic mutational profiles and alterations in cellular signaling pathways. cSCC is the most common metastatic skin cancer, and it is associated with poor prognosis in the advanced stage. An important early event in cSCC development is mutation of the TP53 gene and inactivation of the tumor suppressor function of the tumor protein 53 gene (TP53) in epidermal keratinocytes, which then leads to accumulation of additional oncogenic mutations. Additional genomic and proteomic alterations are required for the progression of premalignant lesion, actinic keratosis, to invasive and metastatic cSCC. Recently, the role of p53 in the invasion of cSCC has also been elucidated. In this review, the role of p53 in the progression of cSCC and as potential new therapeutic target for cSCC will be discussed.

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