2007 Fiscal Year Final Research Report Summary
Identification of apoptosis sensitivity regulating molecules in gastrointestinal cancer cells
Project/Area Number |
18590747
|
Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Gastroenterology
|
Research Institution | Keio University |
Principal Investigator |
TAKAISHI Hiromasa Keio University, School of Medicine, Instructor (80286468)
|
Co-Investigator(Kenkyū-buntansha) |
HIGUCHI Hajime Keio University, School of Medicine, Instructor (20306682)
|
Project Period (FY) |
2006 – 2007
|
Keywords | siRNA / Mcl-1 / side population |
Research Abstract |
Mcl-1(Myeloid cell leukemia-1) is an anti-apoptotic protein that regulates apoptosis sensitivity particularly in hematological and gastrointestinal malignancies. Here, we formulated the hypothesis that suppression of Mcl-1 would be an attractive strategy to overcome apoptosis resistance in Mcl-1 overexspressing gastric cancer. The AIMs was ; i) to examine Mcl-1 expression profiling among gastric cancer cell lines, and ii) to evaluate if Mcl-1 depletion sensitizes apoptosis by anti-cancer drugs. METHOD : 7 gastric cancer cell lines were used. Expression of Mcl-1 was assessed by Western blot analysis. Cells were exposed to anti-cancer drugs such as 5-fluorouracil and cisplatin. Apoptosis was quantitated by a morphological observation and caspase activity measurement. Adenovirus-mediated RNA interference (RNAi) technology was used to knock down the expression of Mcl-1. Releasing cytochrome C was evaluated by subcellular fractionation and immunoblot analysis. To evaluate if Mcl-l expressio
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n levels in cancer stem cells and non-stem cancer cells, side population (SP) cells, a cancer stem cell-enriched fraction, were identified and isolated by Hoechst 33342 staining and flowcytometry. RESULTS : 6 of 7 gastric cancer cell lines overexpressed Mcl-1 protein. There was correlation between Mcl-1 protein level and chemotherapy resistance. Depletion of Mcl-1 protein by RNAi technology effectively sensitizes the Mcl-1 expressing cells to anti-cancer drug-induced apoptosis. Mcl-1 knockdowned apoptosis was associated with mitochondrial depolarization, cytochrome c release from mitochondria and caspase activation. In addition, vast amounts of Mcl-1 mRNA were expressed in SP cells, implying that Mcl-1 mediates chemotherapy resistance in cancer stem cells. IN CONCLUSION : These results suggest that Mcl-1 mediates the resistance of apoptosis in gastric cancer cells by blocking the mitochondrial pathway of cell death. Mcl-1 depletion appears to be an attractive strategy to overcome chemotherapy resistance in gastric cancer cells. Less
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Research Products
(4 results)
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[Presentation] Transforming growth factor(TGF)-bate induces pancreatic cancer cell invasion and epithelial to mesenchymal(EMT)in side-population(SP)cells but not in non SP cells2007
Author(s)
Kabashima A, Higuchi H, Matsuzaki Y, Hasegawa G, Kuriyama N, Takaishi H, Izumiya M, Iizuka H, Sakai G, and Hibi T.
Organizer
2007 AACR Annual Meeting
Place of Presentation
Los Angeles,CA
Year and Date
20070415-18
Description
「研究成果報告書概要(和文)」より
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[Presentation] Mcl-1 depletion sensitizes the apoptosis of gastrointestinal cancer cells mediated by anti-cancer drugs2007
Author(s)
Iizuka H, Higuchi H, Sumimoto H, Kabashima A, Kuriyama N, Sakai G, Izumiya M, Ymagishi Y, Takaishi H, Kawakami Y, Mizoguchi H, and Hibi T.
Organizer
2007 AACR Annual Meeting
Place of Presentation
Los Angeles,CA
Year and Date
20070415-18
Description
「研究成果報告書概要(和文)」より
-
[Presentation] Transforming growth factor (TGF)-bate induces pancreatic cancer cell invasion and epithelial to mesenchymal (EMT) in side-population (SP) cells but not in non SP cells.2007
Author(s)
Kabashima, A., Higuchi, H., Matsuzaki, Y., Hasegawa, G., Kuriyama, N., Takaishi, H., Izumiya, M., Iizuka, H., Sakai, G., Hibi, T
Organizer
2007 AACR Annual Meeting
Place of Presentation
Los Angeles, CA
Year and Date
20070415-18
Description
「研究成果報告書概要(欧文)」より
-
[Presentation] Mcl-1 depletion sensitizes the apoptosis of gastrointestinal cancer cells mediated by anti-cancer drugs.2007
Author(s)
Iizuka, H., Higuchi, H., Sumimoto, H., Kabashima, A., Kuriyama, N., Sakai, G., Izumiya, M., Ymagishi, Y., Takaishi, H., Kawakami, Y., Mizoguchi, H., Hibi, T
Organizer
2007 AACR Annual Meeting
Place of Presentation
Los Angeles, CA
Year and Date
20070415-18
Description
「研究成果報告書概要(欧文)」より