| Literature DB >> 29380860 |
Sarah Craig1, Charles H Earnshaw2, Amaya Virós1.
Abstract
Melanoma is a clinically heterogeneous disease, and current strategies for treatment of the primary tumour are based on pathological criteria alone. In the recent past, several DNA-sequencing and RNA-sequencing studies of primary and advanced melanoma samples have identified unique relationships between somatic mutations, genomic aberrations, and the genetic fingerprint of ultraviolet radiation (UVR). The recurrent patterns of genomic alterations reveal different disease pathways, drug targets and mechanisms limiting drug response. Here, we examine the known associations between the molecular categories of melanoma and the multidimensional UVR damage.Entities:
Keywords: acute inflammation; epidermis; skin
Mesh:
Substances:
Year: 2018 PMID: 29380860 DOI: 10.1002/path.5039
Source DB: PubMed Journal: J Pathol ISSN: 0022-3417 Impact factor: 7.996