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Updated: Sep 9, 2025

Measuring Bone Remodeling and Recreating the Tumor-Bone Microenvironment Using Calvaria Co-culture and Histomorphometry
Published on: March 14, 2020
Contribution of the immune bone marrow microenvironment to tumor growth and bone deconstruction: implications for
E Massy1, C B Confavreux1, M Point2
1Service de Rhumatologie Sud, Centre Expert des Métastases Osseuses (CEMOS), Institut de Cancérologie des Hospices Civils de Lyon, Pierre Bénite, France; INSERM, UMR 1033, LYOS, Lyon, France; Université Claude Bernard Lyon I, Villeurbanne, France; Centre de Recherche en Cancerologie de Lyon (CRCL) - UMR INSERM 1052 CNRS 5286, Lyon, France.
Abstract:
Bone metastases are frequent complications of many solid tumors, leading to painful skeletal morbidities and increasing mortality for patients with advanced cancer. Once in bone, cancer cells deregulate bone homeostasis, altering the functions of bone-forming (osteoblasts) and bone-resorbing (osteoclasts) cells, which results in skeletal deconstruction. Aside from bone cells, cancer cells in the bone marrow interact with other cell populations, including immune cells that also play an integral part in the regulation of bone homeostasis. In this respect, immune checkpoint inhibitors (ICIs) have become a standard of care in immunotherapy for the treatment of patients with advanced cancer. Strikingly, however, those with bone metastases have a shorter survival when treated with ICIs than ICI-treated cancer patients without bone metastases. In this Review, after presenting the immune cells involved in bone metastasis, we review preclinical and clinical findings assessing ICI efficacy both in bone and extraosseous metastases, and we discuss the clinical utility of using bone-targeted agents -including denosumab and bisphosphonates- to improve anti-tumoral efficacy of ICI treatments in patients with cancer and bone metastases.
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