2012 Fiscal Year Final Research Report
Treatment strategy of pancreatic cancer by regulating FGFR2IIIc isoform
| Project/Area Number |
22591531
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Digestive surgery
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| Research Institution | Nippon Medical School |
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Principal Investigator |
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| Co-Investigator(Renkei-kenkyūsha) |
NAITO Zenya 日本医科大学, 大学院・医学研究科, 教授 (20237184)
MATSUDA Yoko 日本医科大学, 医学部, 講師 (20363187)
YAMAMOTO Tetsushi 日本医科大学, 医学部, 助教 (20453920)
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| Project Period (FY) |
2010 – 2012
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| Keywords | FGFR-2 IIIc / ESRP1 / siRNA / 癌幹細胞 / 選択的スプライシング / 線維芽細胞増殖 / 因子受容体 |
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| Research Abstract |
Fibroblast Growth Factor Receptor 2 IIIc (FGFR-2 IIIc) was abundant in 70% of pancreatic cancer cases, which correlated with the decreased duration of the development of liver metastasis after surgery. FGFR-2 IIIc transfected cells exhibited increased proliferation in vitro and formed larger subcutaneous and orthotopic tumors. Suppression of FGFR-2 IIIc expression inhibited the proliferation of pancreatic cancer cells, whereas an anti-FGFR-2 IIIc antibody inhibited the proliferation and migration of the cells (Ishiwata et al., Am J Pathol, 2012). Epithelial Splicing Regulatory Protein1 (ESRP1) binds the FGFR2 in the intron between exon IIIb and IIIc, and primarily promotes FGFR-2 IIIb expression. ESRP1 transfected pancreatic cancer cells formed significantly fewer liver metastases as compared to control cells. Thus, high FGFR-2 IIIc levels in pancreatic cancer contribute to disease aggressiveness, and FGFR-2 IIIc may be a noveland important therapeutic target in pancreatic cancer.
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[Journal Article] Overexpressed fibroblast growth factor receptor 2 in the invasive front of colorectal cancer as a potential therapeutic target of colorectal cancer.2011
Author(s)
Mastuda Y, Ishiwata T, Yamahatsu K, Kawahara K, Hagio M, Peng W-X, Yamamoto T, Nakazawa N, Seya T, Ohaki Y, Naito Z
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Journal Title
Cancer Letters
Volume: 309(2)
Pages: 209-19
Peer Reviewed
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