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Cancer Cell ; 25(6): 778-93, 2014 Jun 16.
Article in English | MEDLINE | ID: mdl-24937459

ABSTRACT

Residence of cancer-propagating cells (CPCs) within preferential microenvironmental niches has a major part in evading therapy. However, the nature of niches involved and the mechanisms protecting CPCs remain largely unknown. We addressed these issues in mouse transplantation models of acute lymphoblastic leukemia (ALL). When the engrafted leukemic cells substantially damaged adjacent microenvironment in the bone marrow (BM), after chemotherapy small foci of CPCs were retained, surrounded by sheaths of supporting cells that comprise a protective niche. We investigated patients' BM biopsies and found evidence of a similar process in patients receiving induction therapy. The efficacy of chemotherapy was enhanced by interfering with the niche formation or function. We therefore identified a therapy-induced niche that protects CPCs.


Subject(s)
Neoplastic Stem Cells/drug effects , Neoplastic Stem Cells/pathology , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology , Stem Cell Niche/drug effects , Animals , Antineoplastic Combined Chemotherapy Protocols/pharmacology , Biopsy , Bone Marrow Cells/drug effects , Bone Marrow Cells/pathology , Cytarabine/administration & dosage , Cytarabine/pharmacology , Daunorubicin/administration & dosage , Daunorubicin/pharmacology , Disease Models, Animal , Humans , Mice , Mice, Inbred NOD , Mice, SCID , Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics , Precursor Cell Lymphoblastic Leukemia-Lymphoma/metabolism , Tumor Microenvironment/drug effects , Xenograft Model Antitumor Assays
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