In vivo antitumor efficacy of 17-AAG loaded PMMA in a human multiple myeloma xenograft mouse model

Clinical and Experimental Medicine - Tập 23 - Trang 45-54 - 2022
Xiangjun Shi1, Yanzhe Wei2,3, Xingchen Yao3, Boran Du4, Xiaoguang Wu5, Xiangyu Kong5, Xinru Du3
1Department of Hematology, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China
2Department of Orthopedics, Shenzhen University General Hospital, Shenzhen, China
3Department of Orthopedics, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China
4Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China
5Department of Anatomy, Chengde Medical University, Hebei, China

Tóm tắt

Multiple myeloma (MM) is a monoclonal malignancy characterized by abnormal proliferation of plasma cells. The disease clinically manifests as anemia, hypercalcemia, renal insufficiencies, and osteolytic damage. Osteolytic damage goes with severe bone pain, spinal instability, and pathological fracture, symptoms that are collectively referred to as multiple myeloma bone disease (MMBD). Polymethylmethacrylate (PMMA) bone cement is widely used for bone repair after MMBD surgery, owing to its excellent biomechanical properties and fast curing. To date, however, efficacy of drug-loading PMMA in inhibition of tumor growth and angiogenesis remains unknown. Here, we report that 17-AAG-loaded PMMA bone cement inhibits MM growth in vivo and suppresses tumor diffusion to peripheral tissues. In addition, 17-AAG-loaded PMMA promotes MM apoptosis by downregulating Bax and active Caspase-3.

Tài liệu tham khảo

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