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            Special Issue

            Genetics and Genomics of Cancer


            Guest Editor:                     Special Issue Introduction
            David N. Cooper, PhD              Tumorigenesis is a multistep process that begins with the
            Professor of Human                transformation of a single cell which acquires one or more of the
            Molecular Genetics, Institute     ''hallmarks of cancer''. Cells acquire these characteristics through
            of Medical Genetics, School       numerous somatic mutations caused by errors of DNA replication, the
            of Medicine, Cardiff              action of exogenous mutagens or endogenous DNA damage, leading
            University, UK                    to the activation of oncogenes and the inactivation of tumour
            Email:                            suppressors.  Different tumours differ with respect to their mutational
            CooperDN@cardiff.ac.uk            spectra and these patterns of mutation are often characteristic of the
                                              tumour in question. Genetic susceptibility to cancer is also conferred by
                                              inherited variants of cancer predisposition genes. As whole
                                              exome/genome sequencing becomes commonplace in a clinical
                                              genetics/personalised genomics setting, we are gradually developing
                                              an understanding of the role of both inherited and acquired variants in
                                              tumorigenesis. We plan to publish reviews of the molecular genetics of
                                              human cancers which we hope will allow the reader to compare and
                                              contrast some of the 100+ different human cancers in terms of their
                                              underlying mutational spectra.



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