Journal
FEBS LETTERS
Volume 476, Issue 3, Pages 203-207Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/S0014-5793(00)01727-0
Keywords
gut-enriched Kruppel-like factor; tumorigenesis; Min mouse; familial adenomatous polyposis; reverse transcription-polymerase chain reaction; DNA methylation
Funding
- NCI NIH HHS [R01 CA084197-02, R01 CA084197] Funding Source: Medline
- NIDDK NIH HHS [R01 DK052230-03, R01 DK052230] Funding Source: Medline
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Gut-enriched Kruppel-like factor (GKLF) is a zinc finger-containing transcription factor, the expression of which is associated with growth arrest. We compared Gklf expression in intestinal and colonic adenomas to normal mucosa in multiple intestinal neoplasia (Min) mice and familiar adenomatous polyposis (FAP) patients, respectively, using semi-quantitative RT-PCR, In Min mice, the level of Gklf transcript is highest in normal-appearing intestinal tissues and decreases as the size of the adenoma increases. In FAP patients, the level of GKLF transcript is lower in adenomas compared to paired normal-appearing mucosa from the same patient or normal colonic mucosa from control individuals without PAP, The possibility of DNA methylation as a cause for the decreased expression of Gklf in adenomas of Min mice was investigated by methylation-specific PCR, Results indicate that the Gklf gene is not methylated in either normal or tumorous tissues. The findings of our study are therefore consistent with the potential role of GKLF as a negative growth regulator of gut epithelial cells. (C) 2000 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
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