| Literature DB >> 34127435 |
Anna Han1, Zachary T Schug2, Andrew E Aplin3.
Abstract
Melanoma is derived from melanocytes located in multiple regions of the body. Cutaneous melanoma (CM) represents the major subgroup, but less-common subtypes including uveal melanoma (UM), mucosal melanoma (MM), and acral melanoma (AM) arise that have distinct genetic profiles. Treatments effective for CM are ineffective in UM, AM, and MM, and patient survival remains poor. As reprogrammed cancer metabolism is associated with tumorigenesis, the underlying mechanisms are well studied and provide therapeutic opportunities in many cancers; however, metabolism is less well studied in rarer melanoma subtypes. We summarize current knowledge of the metabolic alterations in rare melanoma and potential applications of targeting cancer metabolism to improve the therapeutic options available to UM, AM, and MM patients.Entities:
Keywords: acral; melanoma; metabolism; mucosal; uveal
Mesh:
Year: 2021 PMID: 34127435 PMCID: PMC8295200 DOI: 10.1016/j.trecan.2021.05.005
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025