The role of metallothionein genes in tumor-promoting effect of bone marrow-derived mesenchymal stem cells in human colon cancer
Project/Area Number |
24700979
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Tumor biology
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Research Institution | Hiroshima University |
Principal Investigator |
SHINAGAWA KEI 広島大学, 大学病院, 医科診療医 (50623609)
|
Project Period (FY) |
2012-04-01 – 2014-03-31
|
Project Status |
Completed (Fiscal Year 2013)
|
Budget Amount *help |
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2013: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
Fiscal Year 2012: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
|
Keywords | 間葉系幹細胞 / メタロチオネイン / フィブロネクチン / 大腸癌 |
Research Abstract |
To elucidate the role of bone marrow-derived mesenchymal stem cells (MSCs) on tumor growth and metastasis in human colon cancer, we performed microarray analysis of gene expression in KM12SM cells co-cultured with MSCs. Expression of metallothionein (MT) or fibronectin (FN) mRNA by KM12SM cells was increased markedly by indirect or direct co-culture with MSCs, respectively. We also examined MT and FN expression in surgical specimens of human colorectal neoplasms by immunohistochemistry. Expression of MT and FN in tumor cells was detected at the invasive edge. Furthermore, in an orthotopic nude mouse model of colon cancer, expression of FN was high in tumor nests near MSCs recruited in the tumor microenvironment, and expression of E-cadherin was decreased in tumor cells that expressed FN. These findings suggest MSCs recruited into tumor stroma may promote tumor growth and metastasis through induction of mesenchymal-epithelial transition in invasive colorectal cancers.
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Report
(3 results)
Research Products
(8 results)