| Literature DB >> 26056002 |
Kyoko Fujimoto1, Gen Fujii2, Kenichi Taguchi3, Kaori Yasuda4, Yuta Matsuo5, Airi Hashiyama6, Michihiro Mutoh7, Hiromitsu Tanaka8, Morimasa Wada9.
Abstract
It is assumed that tumor size may be associated with malignant tumor conversion. However, the molecules responsible for determination of tumor size are not well understood. We counted the number of intestinal tumors in 8, 12 and 30-week-old Apc(Min/+) mice and measured tumor sizes, respectively. Genes involved in determining tumor size were examined using microarray analysis. Cultured cells were then, transfected with a mammalian expression vector containing a candidate gene to examine the functional role of the gene. The effect of forced expression of candidate gene on cell growth was evaluated by measuring the doubling time of the cultured cells and the growth of grafted cells in nude mice. Unexpectedly, microarray analysis identified trefoil factor family 2 (Tff2) rather than growth related genes and/or oncogenes as a most variable gene. Overexpressing Tff2 in cultured cells reduced doubling time in vitro and rapidly increased xenograft tumor size in vivo. We found Tff2 as a novel important factor that to be able to enlarge an intestinal tumor size.Entities:
Keywords: Apc(Min/+) mice; Microarray; Proliferation; Trefoil factor family 2; Tumor size
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Year: 2015 PMID: 26056002 DOI: 10.1016/j.bbrc.2015.06.025
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575