1. Decreased frequency, but normal functional integrity of mesenchymal stromal cells derived from untreated and Imatinib-treated chronic myeloid leukemia patients
- Author
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N. Delgado, P.K. Estrada-González, Eugenia Flores-Figueroa, L. Gómez-Ceja, Antonieta Chávez-González, L. Meillón, E. Sánchez-Nava, Hector Mayani, and Juan José Montesinos
- Subjects
Cancer Research ,medicine.medical_specialty ,Fusion Proteins, bcr-abl ,Antineoplastic Agents ,Piperazines ,Immunophenotyping ,In vivo ,Leukemia, Myelogenous, Chronic, BCR-ABL Positive ,hemic and lymphatic diseases ,Internal medicine ,Humans ,Medicine ,neoplasms ,business.industry ,Mesenchymal stem cell ,Myeloid leukemia ,Cell Differentiation ,Mesenchymal Stem Cells ,Imatinib ,Hematology ,In vitro ,Haematopoiesis ,Phenotype ,Pyrimidines ,Endocrinology ,Oncology ,Adipogenesis ,Benzamides ,Imatinib Mesylate ,Cancer research ,business ,medicine.drug - Abstract
In vitro, Imatinib inhibits the proliferation and stimulates the osteogenic and adipogenic differentiation of mesenchymal stromal cells (MSC). However, it is unknown whether Imatinib affects the biology of MSC in vivo. We asked whether MSC from long-term Imatinib-treated CML patients were affected by the in vivo treatment. MSC from untreated and Imatinib-treated patients displayed normal functional properties (i.e. proliferation, immunophenotype, differentiation and hematopoietic supportive capacity) - but a decreased frequency. In vitro, Imatinib lost its effect when discontinued; which suggest that it has a reversible effect on MSC. Therefore it might lose its effect on MSC after discontinuation in vivo.
- Published
- 2014