Oncogenesis and cancer stem cells: current opinions and future directions

被引:8
作者
Cheng, Xiaoyu [1 ]
O'Neill, Helen C. [1 ]
机构
[1] Australian Natl Univ, Coll Sci, Sch Biochem & Mol Biol, Immunol & Stem Cell Lab, Canberra, ACT 0200, Australia
关键词
cancer stem cell; haematopoietic stem cell; acute myeloid leukaemia; oncogenesis; signalling pathways; niche; ACUTE MYELOID-LEUKEMIA; TUMOR-INITIATING CELLS; NF-KAPPA-B; SELF-RENEWAL; IN-VIVO; SIGNALING PATHWAY; BONE-MARROW; HEMATOPOIETIC-CELLS; COLORECTAL-CANCER; COLON-CANCER;
D O I
10.1111/j.1582-4934.2008.00664.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:4377 / 4384
页数:8
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