Introduction Stem cells and haematopoiesis The cancer stem cell hypothesis Evidence form leukaemias and solid tumours Cellular origin and the role of the niche Molecular basis of self-renewal and differentiation Concluding remarks: cancer stem cells as a target for new cancer therapy There is increasing evidence to show that only a subset of cancer cells drives the growth and progression of a tumour. These cells share similar properties with normal stem cells and are termed 'cancer stem cells'. Cancer stem cells have been identified in acute myeloid leukaemia and in some solid tumours by their distinct expression of cell surface antigens. Their long-term, self-renewing capacity is thought to be a determining factor in the maintenance and regrowth of the tumour. Studies on haematopoietic cancers show that important signalling pathways and genes for normal haematopoiesis, such as Wnt, NF-kappa B, Notch, hedgehog (Hh) and Bmi1, are oncogenic, thereby potentially involved in cancer stem cell regulation. Elimination of cancer stem cells in tumours could result in the degeneration of downstream cells, which makes them potential targets for new cancer therapies.
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Univ Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Cell Biol, Ann Arbor, MI 48109 USAUniv Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Quintana, Elsa
Shackleton, Mark
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Univ Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Cell Biol, Ann Arbor, MI 48109 USAUniv Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Shackleton, Mark
Sabel, Michael S.
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Univ Michigan, Dept Surg, Ann Arbor, MI 48109 USAUniv Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Sabel, Michael S.
Fullen, Douglas R.
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Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USAUniv Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Fullen, Douglas R.
Johnson, Timothy M.
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Univ Michigan, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
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Univ Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Cell Biol, Ann Arbor, MI 48109 USAUniv Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Quintana, Elsa
Shackleton, Mark
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机构:
Univ Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Cell Biol, Ann Arbor, MI 48109 USAUniv Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Shackleton, Mark
Sabel, Michael S.
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Univ Michigan, Dept Surg, Ann Arbor, MI 48109 USAUniv Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Sabel, Michael S.
Fullen, Douglas R.
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Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USAUniv Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA
Fullen, Douglas R.
Johnson, Timothy M.
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Univ Michigan, Dept Dermatol, Ann Arbor, MI 48109 USAUniv Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med, Ann Arbor, MI 48109 USA