| Literature DB >> 16492679 |
Nathalie Gonin-Laurent1, Anne Gibaud, Mathilde Huygue, Sandrine H Lefèvre, Morgane Le Bras, Laurent Chauveinc, Xavier Sastre-Garau, François Doz, Livia Lumbroso, Sylvie Chevillard, Bernard Malfoy.
Abstract
The mutagenic properties of ionizing radiation are well known, but the presence of specific mutations in human radiation-induced tumours is not established. We have studied a series of 36 secondary sarcomas arising in the irradiation field of a primary tumour following radiotherapy. The allelic status and the presence of mutations of the TP53 gene were investigated. The mutation pattern was compared with data from sporadic sarcomas recorded in the IARC TP53 somatic mutations database. A high proportion (58%) of the radiation-induced sarcomas exhibited a somatic inactivating mutation for one allele of TP53, systematically associated with a loss of the other allele. The high frequency (52%) of short deletions observed in the mutation pattern of radiation-induced sarcomas may be related to the induction of DNA breaks by ionizing radiation. The lack of hyper-reactivity of CpG dinucleotides and the presence of recurrent sites of mutation at codons 135 and 237 seem also to be specific for radiation tumorigenesis.Entities:
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Year: 2006 PMID: 16492679 DOI: 10.1093/carcin/bgi356
Source DB: PubMed Journal: Carcinogenesis ISSN: 0143-3334 Impact factor: 4.944