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Differential Pain-Related Behaviors and Bone Disease in Immunocompetent Mouse Models of Myeloma
Marta Diaz-delCastillo1, Danna Kamstrup1, Rikke Brix Olsen1
1Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences University of Copenhagen Copenhagen Denmark.
Abstract:
Bone pain is a serious and debilitating symptom of multiple myeloma (MM) that impairs the quality of life of patients. The underlying mechanisms of the pain are unknown and understudied, and there is a need for immunocompetent preclinical models of myeloma-induced bone pain. The aim of this study was to provide the first in-depth behavioral characterization of an immunocompetent mouse model of MM presenting the clinical disease features: osteolytic bone disease and bone pain. We hypothesized that a widely used syngeneic model of MM, established by systemic inoculation of green fluorescent protein-tagged myeloma cells (5TGM1-GFP) in immunocompetent C57Bl/KaLwRijHsd (BKAL) mice, would present pain-related behaviors. Disease phenotype was confirmed by splenomegaly, high serum paraprotein, and tumor infiltration in the bone marrow of the hind limbs; however, myeloma-bearing mice did not present pain-related behaviors or substantial bone disease. Thus, we investigated an alternative model in which 5TGM1-GFP cells were directly inoculated into the intrafemoral medullary cavity. This localized myeloma model presented the hallmarks of the disease, including high serum paraprotein, tumor growth, and osteolytic bone lesions. Compared with control mice, myeloma-bearing mice presented myeloma-induced pain-related behaviors, a phenotype that was reversed by systemic morphine treatment. Micro-computed tomography analyses of the myeloma-inoculated femurs showed bone disease in cortical and trabecular bone. Repeated systemic bisphosphonate treatment induced an amelioration of the nociceptive phenotype, but did not completely reverse it. Furthermore, intrafemorally injected mice presented a profound denervation of the myeloma-bearing bones, a previously unknown feature of the disease. This study reports the intrafemoral inoculation of 5TGM1-GFP cells as a robust immunocompetent model of myeloma-induced bone pain, with consistent bone loss. Moreover, the data suggest that myeloma-induced bone pain is caused by a combinatorial mechanism including osteolysis and bone marrow denervation. © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research.
Insights
A new mouse model effectively mimics multiple myeloma bone pain and bone loss. This model reveals that bone pain results from osteolysis and nerve damage in the bone marrow.
Area of Science:
- Oncology
- Pain Research
- Preclinical Models
Background:
- Bone pain is a debilitating symptom of multiple myeloma (MM) significantly impacting patient quality of life.
- Current understanding of MM-induced bone pain mechanisms is limited, necessitating better preclinical models.
- Immunocompetent models are crucial for studying MM and associated pain.
Purpose of the Study:
- To characterize an immunocompetent mouse model of MM-induced bone pain.
- To investigate the underlying mechanisms of pain and bone disease in this model.
- To establish a robust preclinical tool for MM bone pain research.
Main Methods:
- Systemic inoculation of 5T22GM1-GFP myeloma cells in BKAL mice was initially tested.
- Intrafemoral (within the femur) inoculation of 5T22GM1-GFP cells was used to establish a localized MM model.
- Pain-related behaviors, bone disease (osteolysis), tumor burden, and nerve changes were assessed.
- Pharmacological interventions (morphine, bisphosphonates) and micro-computed tomography were employed.
Main Results:
- Systemic inoculation failed to induce significant pain or bone disease.
- Intrafemoral inoculation successfully established MM with osteolytic bone lesions and pain-related behaviors.
- Pain behaviors were reversed by morphine and partially ameliorated by bisphosphonates.
- Significant bone marrow denervation was observed in myeloma-affected bones.
Conclusions:
- Intrafemoral inoculation of 5T22GM1-GFP cells creates a robust immunocompetent model for MM-induced bone pain and osteolysis.
- MM-induced bone pain likely results from a combination of osteolysis and bone marrow denervation.
- This model provides a valuable platform for studying MM bone pain and testing therapeutic strategies.
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