B cell acute lymphoblastic leukemia cells mediate RANK-RANKL–dependent bone destruction

Author:

Rajakumar Sujeetha A.12ORCID,Papp Eniko23,Lee Kathy K.45ORCID,Grandal Ildiko3,Merico Daniele6ORCID,Liu Careesa C.47,Allo Bedilu4ORCID,Zhang Lucia45ORCID,Grynpas Marc D.47,Minden Mark D.28ORCID,Hitzler Johann K.39ORCID,Guidos Cynthia J.310ORCID,Danska Jayne S.1210ORCID

Affiliation:

1. Program in Genetics and Genome Biology, Hospital for Sick Children, Toronto, Ontario M5G 0A4, Canada.

2. Department of Medical Biophysics, University of Toronto, Toronto, Ontario M5S 1A8, Canada.

3. Program in Developmental and Stem Cell Biology, Hospital for Sick Children, Toronto, Ontario M5G 0A4, Canada.

4. Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario M5T 3H7, Canada.

5. Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario M5S 1A8, Canada.

6. Center for Applied Genomics, Hospital for Sick Children, Toronto, Ontario M5G 0A4, Canada.

7. Institute of Biomaterials and Biomedical Engineering, University of Toronto, Toronto, Ontario M5S 1A8, Canada.

8. Princess Margaret Cancer Center, University Health Network, Toronto, Ontario M5G 2M9, Canada.

9. Department of Pediatrics, Division of Hematology and Oncology, Hospital for Sick Children, Toronto, Ontario M5G 1X8, Canada.

10. Department of Immunology, University of Toronto, Toronto, Ontario M5S 1A8, Canada.

Abstract

Primary B-ALL cells cause RANKL-mediated trabecular bone and growth plate destruction in patient-derived xenograft models.

Funder

Leukemia and Lymphoma Society of Canada

Ontario Institute for Cancer Research

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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