PLoS ONE · 2008 · 42 citations · 31 references
MedicineCell BiologyOncologyChemotherapyStem Cell BiologyTumor HeterogeneityCancer Stem Cell BiologyCancer Stem Cell HeterogeneityCancer Stem CellsColorectal CancerMalignant NeoplasmsStem Cell TumorigenicityCancer Stem Cell - Mediated ResistanceCancer Stem Cell ClonalityCancer Stem Cell EnrichmentCancer Stem Cell Functional HeterogeneityCancer Stem Cell Phenotypic HeterogeneityCancer Stem Cell TraitsCancer Stem Cell-mediated ResistanceTherapy-resistant Cancer Stem Cells
Background: Patients generally die of cancer after the failure of current therapies to eliminate residual disease. A subpopulation of tumor cells, termed cancer stem cells (CSC), appears uniquely able to fuel the growth of phenotypically and histologically diverse tumors. It has been proposed, therefore, that failure to effectively treat cancer may in part be due to preferential resistance of these CSC to chemotherapeutic agents. The subpopulation of human colorectal tumor cells with an ESA + CD44 + phenotype are uniquely responsible for tumorigenesis and have the capacity to generate heterogeneous tumors in a xenograft setting (i.e. CoCSC). We hypothesized that if non-tumorigenic cells are more susceptible to chemotherapeutic agents, then residual tumors might be expected to contain a higher frequency of CoCSC.
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Prospective identification of tumorigenic breast cancer cells
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