Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2146959 | Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis | 2009 | 8 Pages |
Abstract
Aneuploidy levels increased incrementally during histological progression; were significantly elevated at very early stages of neoplastic progression and could well be linked to cancer development and used to assess cancer risk. Reactive oxygen species (ROS) induced in early gastric cancer are presumably responsible for the stepwise accumulation of this particular mutation, i.e. aneuploidy. Hence, aneuploidy measured by fluorescent in situ hybridisation (FISH) coupled to brush cytology, would be worthy of consideration as a predictive marker in gastric cancer and could be clinically useful in pre-malignant disease to stratify patients by their cancer risk.
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Authors
L. Williams, A. Somasekar, D.J. Davies, J. Cronin, S.H. Doak, R. Alcolado, J.G. Williams, A.P. Griffiths, J.N. Baxter, G.J.S. Jenkins,