The investigation of function of repressor Bach1 in microenvironment of the tumor and the application to a mouse model for cancer stem cell transplantation.
Project/Area Number |
22700869
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Tumor biology
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Research Institution | Tohoku University |
Principal Investigator |
MATSUMOTO Mitsuyo 東北大学, 東北メディカル・メガバンク機構, 助教 (80400448)
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Project Period (FY) |
2010 – 2012
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Project Status |
Completed (Fiscal Year 2012)
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Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2012: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2011: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2010: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
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Keywords | BACH1 / がん微小環 / Bach1 / がん微小環境 |
Research Abstract |
We planned the construction of a Bach1^<-/-> immune-deficient mouse as a good recipient mouse model for engraftment and metastatic of human transplantable tumor cells. Therefore, we aimed to investigate the mechanism and role of Bach1 in fibroblast cell. To identify novel target genes of Bach1 in fibroblast cell, we performed ChIP-seq, DNA microarray, qPCR and western blotting analysis. These results suggest that Bach1 acts as a repressor of Pparγgene transcription in immortalized MEF (iMEF). Bach1^<-/-> iMEF more easily differentiated to adipocytes when treated with insuline, IBMX, dexamethasone and Pparγ ligand in vitro. Bach1 might play a role in adipose differentiation of fibroblast cell by modulating the actions of Pparγ.
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Report
(4 results)
Research Products
(7 results)
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[Journal Article] Individual Transcriptional Activity of Estrogen Receptors in Primary Breast Cancer and Its Clinical Significance2012
Author(s)
Gohno T, Seino Y, Hanamura T, Niwa T, Matsumoto M, Yaegashi N, Oba H, Kurosumi M, Takei H, Yamaguchi Y, Hayashi S
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Journal Title
Cancer Medicine
Volume: 1
Pages: 328-337
Related Report
Peer Reviewed
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