K-ras mutations and RASSF1A promoter methylation in colorectal cancer

M. van Engeland, G.M.J.M. Roemen, M. Brink, M.M.M. Pachen, M.P. Weijenberg, A.P. de Bruine, J.W. Arends, P.A. van den Brandt, A.F.P.M. de Goeij, J. Herman

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Abstract

Human cancer is characterized by genetic and epigenetic alterations. In this study we provide evidence for the interruption of Ras signaling in sporadic colorectal cancer (CRC) by either genetic activation of the K-ras oncogene or epigenetic silencing of the putative tumor suppressor gene RASSF1A. Paraffin embedded tumor tissue samples from 222 sporadic CRC patients were analysed for K-ras codon 12 and codon 13 activating mutations and RASSF1A promoter hypermethylation. Overall, K-ras mutations were observed in 87 of 222 (39%) and RASSF1A methylation was observed in 45 of 222 (20%) of CRCs. Mutation of K-ras alone was detected in 76 of 222 (34%) CRCs. RASSF1A promoter methylation with wild-type K-ras was observed in 34 of 222 (15%) CRCs. In 101 of 222 (46%) CRCs neither K-ras mutations nor RASSF1A methylation was observed and 11 of 222 (5%) CRCs showed both K-ras mutations and RASSF1A methylation. These data show that the majority of the studied CRCs with K-ras mutations lack RASSF1A promoter methylation, an event which occurs predominantly in K-ras wild-type CRCs (P=0.023, Chi-square test).
Original languageEnglish
Pages (from-to)3792-3795
Number of pages4
JournalOncogene
Volume21
Issue number23
DOIs
Publication statusPublished - 1 Jan 2002

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