| Project/Area Number |
24890222
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| Research Category |
Grant-in-Aid for Research Activity Start-up
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| Allocation Type | Single-year Grants |
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| Research Field |
Applied pharmacology
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| Research Institution | Takasaki University of Health and Welfare |
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Principal Investigator |
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| Project Period (FY) |
2012-08-31 – 2014-03-31
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| Project Status |
Completed (Fiscal Year 2013)
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| Budget Amount *help |
¥2,990,000 (Direct Cost: ¥2,300,000、Indirect Cost: ¥690,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
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| Keywords | バイオマーカー / がん / 診断 / 検査 / 血中循環がん遺伝子 / メチル化 / 遺伝子 / メチル化遺伝子 / 血中循環がん細胞 |
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| Research Abstract |
We have developed a high-performance DNA methylation assay for circulating tumor genomes, and it was validated as cancer monitoring system with higher sensitivity than that of conventional tumor markers for early stages of breast cancer. In this study, to develop a monitoring system for aggressive cancers in early stage of breast cancer patients, we screened methylated genes in epithelial-mesenchymal transition (EMT)-induced breast cancer cells.
EMT-induced breast cancer cell lines were prepared by transcription factor Snail over-expression, and comprehensive DNA methylation assay was performed for methylated cellular genes screening. As results, 370 methylation and un-methylation sites of 248 annotated genes were screened, and 11 methylation marker candidates were verified by quantitative RT-PCR. In conclusion, new methylated genes were selected as a biomarker for EMT-induced breast cancer cells, which could be candidate markers for early stage of aggressive breast cancer patients.
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