Molecular mechanism of solid tumor growth inhibition by a new differentiation inducer and rapamycin
Project/Area Number |
21591686
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
General surgery
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Research Institution | Research Institute for Clinical Oncology, Saitama Cancer Center |
Principal Investigator |
KASUKABE Takashi 埼玉県立がんセンター, 臨床腫瘍研究所, 主幹 (50152658)
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Project Period (FY) |
2009 – 2011
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Project Status |
Completed (Fiscal Year 2011)
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Budget Amount *help |
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2011: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2010: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2009: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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Keywords | Cotylenin A / Rapamycin / 分化誘導剤 / 乳癌細胞 / 増殖抑制 / 併用効果 / Aktリン酸化 / mTOR / 三酸化ヒ素 / アポトーシス / 卵巣癌細胞 / セルシグナリング / Akt |
Research Abstract |
We have examined whether a new differentiation inducer of leukemic cells can suppress the proliferation of solid tumor cells. We recently found that cotylenin A and rapamycin synergistically inhibited the growth of human mammary cancer cells in vitro and in vivo. In this study we found that the abrogation by cotylenin of the rapamycin-induced feedback activation of Akt signaling contributed, at least in part, to the synergistic growth inhibition of mammary cancer cells induced by treatment with cotylenin A and rapamycin.
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Report
(4 results)
Research Products
(18 results)
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[Journal Article] Ellagic acid, a natural polyphenolic compound, induces apoptosis and potentiates retinoic acid-induced differentiation of human leukemia HL-60 cells2010
Author(s)
Hagiwara, Y., Kasukabe, T., Kaneko, Y., Niitsu, N., Okabe-Kado, J.
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Journal Title
J. Hematol
Volume: 92
Pages: 136-143
NAID
Related Report
Peer Reviewed
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[Journal Article]2009
Author(s)
Okabe-Kado, J., Kasukabe, T., Honma, Y., Kobayashi, H., Maseki, N., Kaneko, Y
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Journal Title
Int. J. Hematol
Volume: 90
Pages: 143-152
Related Report
Peer Reviewed
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