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Stoyanova R , Clapper ML , Bellacosa A , Henske EP , Testa JR , Ross EA , Yeung AT , Nicolas E , Tsichlis N , Li YS , Linehan WM , Howard S , Campbell KS , Godwin AK , Boman BM , Crowell JA , Kopelovich L , Knudson AG
Altered gene expression in phenotypically normal renal cells from carriers of tumor suppressor gene mutations
Cancer Biol Ther. 2004 Dec;3(12) :1313-21
AbstractBACKGROUND: The inherently complex signaling networks of tumors result from genetic and epigenetic alterations that occur during cancer initiation and progression. METHODS: In an attempt to identify early molecular changes associated with dominantly inherited predisposition to "two-hit" renal tumors, the expression profiles of primary cultures of phenotypically normal renal epithelial cells from individuals bearing a germline mutation in either the von Hippel-Lindau (VHL) or the tuberous sclerosis complex (TSC) gene were compared to that of renal epithelial cells from control nonmutation carriers by microarray analysis. RESULTS: Reliability of the microarray data from pooled samples was confirmed by real-time RT-PCR. Principal Component Analysis revealed substantial differences in the gene expression profiles of the renal epithelial cells from VHL and TSC mutation carriers. In several instances, the microarray data confirm our present knowledge of the cellular pathways affected by biallelic VHL and TSC mutations. CONCLUSIONS: These findings demonstrate that heterozygosity for a mutant tumor suppressor gene may alter the expression profiles of phenotypically normal epithelial cells in a gene-specific manner. Detectable effects of "one-hit" represent early molecular changes in tumorigenesis that may serve as targets for chemopreventive intervention.
NotesStoyanova, Radka Clapper, Margie L Bellacosa, Alfonso Henske, Elizabeth P Testa, Joseph R Ross, Eric A Yeung, Anthony T Nicolas, Emmanuelle Tsichlis, Nicolaos Li, Yue-Sheng Linehan, W Marston Howard, Sharon Campbell, Kerry S Godwin, Andrew K Boman, Bruce M Crowell, James A Kopelovich, Levy Knudson, Alfred G CA-06927/CA/NCI NIH HHS/United States N01 CN-95037/CN/NCI NIH HHS/United States Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. United States Cancer biology & therapy Cancer Biol Ther. 2004 Dec;3(12):1313-21. Epub 2004 Dec 9.