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Pathologisches Institut [S. R., E. H., U. O., A. H., C. K., T. B., T. K., A. J.] and Medizinische Klinik I [W. M. B.] der Friedrich-Alexander-Universität Erlangen-Nürnberg, D-91054 Erlangen; Institut für Pathologie, Klinikum Kassel, 34125 Kassel [K. B., J. R.]; and Pathologisches Institut der Universität Regensburg, 93053 Regensburg [W. D.], Germany
Colorectal carcinomas with microsatellite instability accumulate errors in short repetitive DNA repeats, especially mono and dinucleotide repeats. One such error-prone A9 monorepeat is found in exon 17 of the TCF-4 gene. TCF-4 and ß-catenin form a transcription complex, which is important for both maintenance of normal epithelium and development of colorectal tumors. To elucidate the relevance of frameshift mutations in the TCF-4 in colorectal carcinogenesis, a variety of investigations in human tumors and cell lines was performed. It was found that mutations in the TCF-4 A9 repeat do not contribute to tumorigenesis and seem to be passenger mutations.
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E. Hiendlmeyer, S. Regus, S. Wassermann, F. Hlubek, A. Haynl, A. Dimmler, C. Koch, C. Knoll, M. van Beest, U. Reuning, et al. {beta}-Catenin Up-Regulates the Expression of the Urokinase Plasminogen Activator in Human Colorectal Tumors Cancer Res., February 15, 2004; 64(4): 1209 - 1214. [Abstract] [Full Text] [PDF] |
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M. G. Daidone, A. Costa, M. Frattini, D. Balestra, L. Bertario, M. A. Pierotti, B. M. Boman, T. Zhang, and J. Z. Fields Correspondence re: T. Zhang et al., Evidence That APC Regulates Survivin Expression: A Possible Mechanism Contributing to the Stem Cell Origin of Colon Cancer. Cancer Res., 61: 8664-8667, 2001. Cancer Res., January 15, 2004; 64(2): 776 - 779. [Full Text] [PDF] |
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