2011 Fiscal Year Final Research Report
Role of the FOXF2 gene in the cancer activated fibroblasts that support proliferation of colon cancer cells
Project/Area Number |
22791272
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Digestive surgery
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Research Institution | Hamamatsu University School of Medicine |
Principal Investigator |
SULTANA Nishat 浜松医科大学, 医学部, リサーチアシスタント (80529503)
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Project Period (FY) |
2010 – 2011
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Keywords | 癌付随線維芽細胞 / 大腸癌 / Foxf2遺伝子 / 増殖 / 腫瘍微小環境 |
Research Abstract |
When colon cancer cells HT29 were transplanted with intestinal embryonic fibroblasts(IEFs) from the Foxf2-/-and wild-type mice, the efficiency and tumor size were highest in cotranslantation with the wild-type IEFs, higher in that with the Foxf2-/-IEFs compared to that without fibroblasts. I isolated RNas from IEFs from the Foxf2-/-and wild-type mice and applied to DNA microarray analysis. I found 23 genes were significantly higher in the wild-type compared to the Foxf2-/-mice. I chose one gene named Wnt5a and demonstrated that the Wnt5a-expressing fibroblasts increased the efficiency and tumor size of HT29 cell transplantation.
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[Journal Article] Expression of human factors CD81, claudin-1, scavenger receptor, and occludin in mouse hepatocytes does not confer susceptibility to HCV entry2011
Author(s)
Hikosaka K, Noritake H, Kimura W, Sultana N, Skarkar MTK, Tagawa Y, Uezato T, Kobayashi Y, Wakita T, Miura N
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Journal Title
Biomed Res
Volume: 32
Pages: 143-150
Peer Reviewed
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