AI Article Synopsis

  • Skin cancer includes various types, with non-melanoma skin cancers (NMSCs) being the most prevalent globally, primarily caused by skin exposure to ultraviolet (UV) light.
  • UV light causes genetic changes in skin cells that can promote cancer, especially when combined with a changed environment and immune suppression.
  • Recent research has led to new treatments targeting specific pathways in advanced NMSC cases, but challenges like drug resistance and side effects remain, prompting ongoing studies for better therapies.

Article Abstract

Skin cancer encompasses a range of cutaneous malignancies, with non-melanoma skin cancers (NMSCs) being the most common neoplasm worldwide. Skin exposure is the leading risk factor for initiating NMSC. Ultraviolet (UV) light induces various genomic aberrations in both tumor-promoting and tumor-suppressing genes in epidermal cells. In conjunction with interactions with a changed stromal microenvironment and local immune suppression, these aberrations contribute to the occurrence and expansion of cancerous lesions. Surgical excision is still the most common treatment for these lesions; however, locally advanced or metastatic disease significantly increases the chances of morbidity or death. In recent years, numerous pharmacological targets were found through extensive research on the pathogenic mechanisms of NMSCs, leading to the development of novel treatments including Hedgehog pathway inhibitors for advanced and metastatic basal cell carcinoma (BCC) and PD-1/PD-L1 inhibitors for locally advanced cutaneous squamous cell carcinoma (cSCC) and Merkel cell carcinoma (MCC). Despite the efficacy of these new drugs, drug resistance and tolerability issues often arise with long-term treatment. Ongoing studies aim to identify alternative strategies with reduced adverse effects and increased tolerability. This review summarizes the current and emerging therapies used to treat NMSC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11241167PMC
http://dx.doi.org/10.3390/ijms25137056DOI Listing

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