Skip to main navigation Skip to search Skip to main content

Discovery of proangiogenic CD44+mesenchymal cancer stem cells in an acute myeloid leukemia patient's bone marrow

Research output: Contribution to journal › Letter › peer-review

Abstract

Here, we report a unique acute myeloid leukemia (AML) bone marrow-derived mesenchymal stem cell (MSC) with both mesenchymal and endothelial potential, which we have named Mesenchymal Cancer Stem Cells (MCSCs). These MCSCs are CD90-CD13-CD44+ and differ from MSCs in isolation, expansion, differentiation, immunophenotype, and cytokine release profile. Furthermore, blocking CD44 inhibited the proliferation and cluster formation of early MCSCs with lower ICAM-1 protein levels. Similar CD90-CD44+ cancer stem cells have been reported in both gastric and breast cancers, which grew in floating spheres in vitro and exhibited mesenchymal features and high metastatic/tumorigenic capabilities in vivo. Our novel discovery provides the first evidence that certain AMLs may be comprised of both hematopoietic and stromal malignant cells. Targeting MCSCs and their cytokine release has potential as a novel therapeutic approach in AML.

Original languageEnglish
Article number63
Pages (from-to)63
JournalJournal of Hematology and Oncology
Volume13
Issue number1
DOIs
StatePublished - Jun 3 2020

ASJC Scopus Subject Areas

  • Hematology
  • Molecular Biology
  • Oncology
  • Cancer Research

Keywords

  • Acute myeloid leukemia
  • Angiogenesis
  • CD44
  • Mesenchymal cancer stem cells
  • Mesenchymal stem cells
  • Microenvironment
  • Bone Marrow/pathology
  • Hyaluronan Receptors/analysis
  • Mesenchymal Stem Cells/chemistry
  • Cell Separation
  • Humans
  • Intercellular Signaling Peptides and Proteins/metabolism
  • Cell Adhesion
  • Leukemia, Myelomonocytic, Acute/metabolism
  • Angiogenic Proteins/metabolism
  • Antigens, Neoplasm/analysis
  • Neoplastic Stem Cells/chemistry
  • Female
  • Tumor Cells, Cultured
  • Cytokines/metabolism
  • Neoplasm Proteins/metabolism

Cite this