Biological activity of galectin-4 and its roles in colorectal cancer and normal tissue.
Project/Area Number |
26860213
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Pathological medical chemistry
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Research Institution | Kagawa University |
Principal Investigator |
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Project Period (FY) |
2014-04-01 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
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Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
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Keywords | ガレクチン / 大腸がん / 消化管 / レクチン / 腸 / ツメガエル / CRISPR |
Outline of Final Research Achievements |
Galectin-4 is a major galectin isoform existed in the digestive tract, and it may contribute to the differentiation of epithelial cell. Recently, many immunohistochemical studies have shown that the galectin-4 is highly expressed in normal tissues, but decreased in the adenoma and the invasion front of colonic cancers. These facts suggest that the galectin-4 has specific activity, which might be involved in tumor suppression. However, the direct correlation between disappearance of galectin-4 and its molecular mechanism of tumor inhibition remain to be understood. To investigate the role of galectin-4 in tumor growth, we prepared the stable transfectants of galectin-4 in human colonic cancer cells (CRCs). Then, we found that overexpression of the galectin-4 suppresses growth of CRCs. Furthermore, knockdown of galectin-4 resulted in an increased CRCs proliferation. These results suggest that galectin-4 contributes to the suppression of colorectal cancer.
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Report
(3 results)
Research Products
(7 results)
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[Journal Article] Cooperative interactions of oligosaccharide and peptide moieties of a glycopeptide derived from IgE with galectin-92016
Author(s)
Nakakita, S.-I., Itoh, A., Nakakita, Y., Nonaka, Y., Ogawa, T., Nakamura, T., Nishi, N.
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Journal Title
J. Biol. Chem.
Volume: 291
Issue: 2
Pages: 968-979
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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