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Important role of indels in somatic mutations of human cancer genes

DOI: 10.1186/1471-2350-11-128

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Abstract:

We analyzed indels' abundance and distribution, the relative ratio between indels and somatic base substitutions and the association between those two forms of mutations in a large number of somatic mutations in the Catalogue of Somatic Mutations in Cancer database. We found a strong correlation between indels and base substitutions in cancer-related genes and showed that they tend to concentrate at the same locus in the coding sequences within the same samples. More importantly, a much higher proportion of indels were observed in somatic mutations, as compared to meiotic ones. Furthermore, our analysis demonstrated a great diversity of indels at some loci of cancer-related genes. Particularly in the genes with abundant mutations, the proportion of 3n indels in oncogenes is 7.9 times higher than that in tumor suppressor genes.There are three distinct patterns of indel distribution in somatic mutations: high proportion, great abundance and non-random distribution. Because of the great influence of indels on gene function (e.g., the effect of frameshift mutation), these patterns indicate that indels are frequently under positive selection and can often be the 'driver mutations' in oncogenesis. Such driver forces can better explain why much less frameshift mutations are in oncogenes while much more in tumor suppressor genes, because of their different function in oncogenesis. These findings contribute to our understanding of mutational patterns and the relationship between indels and cancer.Humans are increasingly exposed to food-, water- and air-borne carcinogens, as well as specific carcinogenic agents related to their occupational settings and life-style choices [1,2]. Indeed, cancer is responsible for more than one-fifth of all deaths worldwide [3] and can be characterized by such hallmarks as uncontrollable growth, immortality and metastasis, and induction of inflammatory microenvironment [4]. Accumulation of genetic changes can give rise to tumorigenesis in three

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