Article
Persistence of p53 mutations and resistance of keratinocytes to apoptosis are associated with the increased susceptibility of mice lacking the XPC gene to UV carcinogenesis.
Oncogene - 2 Dec 1999
Ananthaswamy H N, Ouhtit A, Evans R L, Gorny A, Khaskina P, Sands A T, Conti C J
Abstract excerpt
Like xeroderma pigmentosum (XP) patients, transgenic mice lacking nucleotide excision repair (NER) genes such as XPA and XPC are extremely susceptible to ultraviolet (UV)-induced skin cancer. Because the p53 gene is an important target for UV carcinogenesis and because the p53 protein modulates NER, we investigated the consequences of NER deficiency on UV-induced p53 mutations in XPC-/- mouse skin tumors....
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
