Dissecting the multiple myeloma-bone microenvironment reveals new therapeutic opportunities
G Shay1, L Hazlehurst2, C C Lynch3
1Tumor Biology Department, SRB-3, H. Lee Moffitt Cancer Center and Research Institute, 12902 Magnolia Blvd, Tampa, FL, 33612, USA.
Abstract:
Multiple myeloma is a plasma cell skeletal malignancy. While therapeutic agents such as bortezomib and lenalidomide have significantly improved overall survival, the disease is currently incurable with the emergence of drug resistance limiting the efficacy of chemotherapeutic strategies. Failure to cure the disease is in part due to the underlying genetic heterogeneity of the cancer. Myeloma progression is critically dependent on the surrounding microenvironment. Defining the interactions between myeloma cells and the more genetically stable hematopoietic and mesenchymal components of the bone microenvironment is critical for the development of new therapeutic targets. In this review, we discuss recent advances in our understanding of how microenvironmental elements contribute to myeloma progression and, therapeutically, how those elements can or are currently being targeted in a bid to eradicate the disease.
Insights
Multiple myeloma remains incurable due to drug resistance and genetic heterogeneity. Targeting the bone microenvironment offers new therapeutic strategies to eradicate this plasma cell malignancy.
Area of Science:
- Oncology
- Hematology
- Cancer Biology
Background:
- Multiple myeloma is a plasma cell malignancy with limited curative options.
- Current therapies like bortezomib and lenalidomide improve survival but face drug resistance.
- Genetic heterogeneity of myeloma contributes to treatment failure.
Purpose of the Study:
- To review recent advances in understanding the role of the bone microenvironment in myeloma progression.
- To discuss therapeutic strategies targeting microenvironmental interactions for myeloma eradication.
Main Methods:
- Literature review of current research on multiple myeloma and its microenvironment.
- Analysis of therapeutic approaches targeting myeloma-bone marrow interactions.
Main Results:
- The bone microenvironment critically influences myeloma progression.
- Interactions between myeloma cells and hematopoietic/mesenchymal cells are key.
- Targeting these microenvironmental elements shows therapeutic promise.
Conclusions:
- Understanding myeloma-microenvironment interactions is crucial for developing new therapies.
- Targeting the microenvironment offers a potential strategy to overcome drug resistance and cure multiple myeloma.
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