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Novel genetic and epigenetic alterations in ... - Ous-research.no

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tumors it is hard to establish which of the mutated genes are play<strong>in</strong>g a part <strong>in</strong> tumorigenesis.A scheme of divid<strong>in</strong>g the genes <strong>in</strong>to driver <strong>and</strong> by-st<strong>and</strong>er genes based on mutationfrequency has been suggested, <strong>and</strong> genes with mutation frequencies below 12% areconsidered to have <strong>no</strong> functional consequence on tumor development <strong>and</strong> be termed byst<strong>and</strong>ergenes.[8]CRC is one of the most common cancer types <strong>and</strong> has a relatively poor 5-year survival of~60% (SEER Cancer Statistics Review, 1975-2005 * ). The most important factor for survivalis tumor stage at the time of diag<strong>no</strong>sis, i.e. depth of tumor <strong>in</strong>filtration <strong>in</strong> the bowel wall,spread to lymphatic <strong>no</strong>des <strong>and</strong> distant spread. It has been shown that MSI tumors have abetter prog<strong>no</strong>sis than microsatellite stable (MSS) tumors.[9] Still, a subset of patients withMSI-tumors have unfavorable prog<strong>no</strong>sis, <strong>and</strong> identification of these patients might give theoption of improved treatment.In order to identify markers with prog<strong>no</strong>stic value we have analyzed 41 genes, selected froma literature survey,[10] <strong>in</strong> two different colorectal tumor series (<strong>in</strong> total 202 samples).MATERIAL AND METHODSHypothesis generat<strong>in</strong>g test series94 sporadic, fresh frozen, colorectal carc<strong>in</strong>omas from Sc<strong>and</strong><strong>in</strong>avian hospitals had previouslybeen selected, be<strong>in</strong>g classified as MSI. The Norwegian series of 42 samples was from an* http://seer.cancer.gov/statfacts/html/colorect.html4

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