Runx3 expression in gastrointestinal tract epithelium: resolving the controversy

被引:24
作者
Ito, K. [1 ,2 ]
Inoue, K-i [1 ]
Bae, S-C [3 ,4 ]
Ito, Y. [1 ,2 ]
机构
[1] Inst Mol & Cell Biol, Singapore 138673, Singapore
[2] Natl Univ Singapore, Oncol Res Inst, Singapore 117548, Singapore
[3] Chungbuk Natl Univ, Sch Med, Dept Biochem, Cheongju, South Korea
[4] Chungbuk Natl Univ, Inst Tumor Res, Cheongju, South Korea
关键词
detection of Runx3; immunohistochemistry; gastrointestinal epithelial cells; monoclonal antibody; ROOT GANGLION NEURONS; GASTRIC-CANCER; GROWTH-FACTOR; TUMOR-SUPPRESSOR; REGULATES DEVELOPMENT; CELLS; GENE; ADENOCARCINOMA; METASTASIS; RUNX1/AML1;
D O I
10.1038/onc.2008.496
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We reported earlier that RUNX3 is expressed in human and mouse gastrointestinal tract (GIT) epithelium and that it functions as a tumor suppressor in gastric and colorectal tissues. However, there have been conflicting reports describing the absence of Runx3 in GIT epithelial cells. A part of the controversy may be derived from the use of a specific antibody by other groups ( referred to as G-poly). Here, we show further evidence to support our earlier observations and provide a possible explanation for this apparent controversy. We generated multiple anti-RUNX3 monoclonal antibodies and found that RUNX3 antibodies recognizing the RUNX3 N-terminal region (residues 1-234) react with RUNX3 in gastric epithelial cells, whereas those recognizing the C-terminal region (beyond residue 234) did not. G-poly primarily recognizes the region beyond 234 and hence, is unable to detect Runx3 in this tissue.
引用
收藏
页码:1379 / 1384
页数:6
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