CD133-positive cells are resistant to TRAIL due to up-regulation of FLIP |
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Authors: | Zobalova Renata McDermott Laura Stantic Marina Prokopova Katerina Dong Lan-Feng Neuzil Jiri |
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Affiliation: | aApoptosis Research Group, School of Medical Science, Griffith Institute of Health and Medical Research, Griffith University Gold Coast Campus, Parklands Avenue, Southport, Qld, Australia;bMolecular Therapy Group, Institute of Biotechnology, Czech Academy of Sciences, Czech Republic |
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Abstract: | ![]() Recent research shows that Cancer stem cells (CSCs) are relatively resistant to apoptosis induction. We studied the effect of the immunological apoptogen TRAIL on Jurkat cells enriched in the CD133-positive population. CD133high Jurkat cells were more resistant to apoptosis than their CD133low counterparts, and showed higher level of expression of FLIP, an inhibitor of death receptor-mediated apoptosis. Breast cancer MCF7 cells showed high level of expression CD133 in the unseparated culture, with accompanying high level of FLIP. Down-regulation of FLIP by siRNA resulted in sensitisation of the cells to TRAIL, as documented by more robust apoptosis. We conclude that high expression of FLIP is at least one of the reasons for resistance of CSCs to apoptosis induced by the death ligand TRAIL. |
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Keywords: | TRAIL CD133 FLIP Apoptosis |
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