Mifamurtide在化疗引起的骨肉瘤儿童骨质疏松症中的作用

Title:The Role of Mifamurtide in Chemotherapy-induced Osteoporosis of Children with Osteosarcoma

Volume: 17 Issue: 7

关键词: 骨肉瘤相关骨丢失，吸收，破骨细胞活化，肿瘤结局，癌症相关疾病，骨肉瘤随访。

摘要: Background: Osteosarcoma is the most frequent malignant bone tumor in childhood and young adulthood. Long-term survivors of osteosarcoma patients show high prevalence of osteoporosis and fractures. The immunomodulatory mifamurtide, which modulates macrophages activity, improves disease outcome.

Objective: To evaluate the role of mifamurtide on macrophage component of bone, the osteoclasts, during chemotherapy in children with osteosarcoma.

Method: Osteoclasts, obtained from peripheral blood cells of healthy donors were harvested in the presence or not of mifamurtide. Moreover, osteoclast cultures were obtained from osteosarcoma patients, at onset and during chemotherapy, alone or with mifamurtide. Pro-osteoporotic tartrateresistant acid phosphatase (TRAP), phosphokinase-β-2 (PKCβ2), vanilloid receptor type 1 (TRPV1), and anti-osteoporotic cannabinoid receptor type 2 (CB2) biomarkers were analyzed by bio-molecular (qPCR), biochemical (Western Blotting), and morphological (TRAP assay) approaches.

Results: Osteoclasts from osteosarcoma patients show significant increase of TRAP and decrease of CB2 with respect to osteoclasts from healthy donors. This osteoclast hyperactivity is more evident in osteoclasts from osteosarcoma patients during chemotherapy. Mifamurtide reduces pro-osteoporotic TRAP, PKCβ2, TRPV1 levels and increases CB2 in osteoclasts from healthy donors. Moreover, chemotherapy-induced effects on bone resorption markers are fully reverted in osteoclasts derived from osteosarcoma patients in chemotherapy plus mifamurtide.

Conclusion: Our data suggest a new therapeutic role for mifamurtide as possible anti-resorption agent in chemotherapy-induced osteoporosis in children with osteosarcoma.

Cite this article as:

The Role of Mifamurtide in Chemotherapy-induced Osteoporosis of Children with Osteosarcoma, Current Cancer Drug Targets 2017; 17 (7) . https://dx.doi.org/10.2174/1568009616666161215163426

DOI https://dx.doi.org/10.2174/1568009616666161215163426	Print ISSN 1568-0096
Publisher Name Bentham Science Publisher	Online ISSN 1873-5576