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Growth plate and bone radioprotection and radiorecovery
Our laboratory has been funded continuously by the NIH since 2000 for our work evaluating the mechanisms of damaging effects of irradiation on bone growth. Most recently, the focus has been on selective stimulation of radiorecovery pathways. This work involves in vitro and in vivo work with histomorphometric, 免疫组织化学, and molecular evaluation at the RNA and protein level. This area of research is relevant to children being treated for bone and soft-tissue sarcomas.
骨肉瘤
Utilizing both in vitro and in vivo work including an orthotopic intraosseous osteosarcoma injection model, differential expression of genes and pathways related to metastatic potential are being evaluated.
化疗相关性骨质疏松
Our laboratory has established the high prevalence of premature low bone mineral density in young adults following chemotherapy for pediatric malignancies, 包括骨和软组织肉瘤. However, the specific mechanisms of this adverse outcome have not been elucidated. 此外, the precise role of specific novel agents in the simultaneous treatment of osteosarcoma and low bone mineral density has yet to be explored, leaving room for exploration and development of new treatments.
辐射相关骨折
Building upon our extensive experience exploring the damaging effects of irradiation treatments on growth plate function in pediatric patients with malignant bone and soft-tissue tumors, an in vivo nude mouse model has been established to evaluate the more common problem of fracture following bone irradiation. 这个问题涉及许多专业, 包括妇科肿瘤学, where pelvic irradiation frequently leads to pelvic stress fractures, 还有小儿肿瘤学, 成人肿瘤, 放射肿瘤学, 和矫形手术.
选择引用 (完整列表请参考PubMed链接)
Arrington S, Damron TA, Mann KA, Allen MJ. Concurrent administration of zoledronic zcid and irradiation leads to improved bone density, microarchitecture and biomechanical strength in a mouse model of tumor-induced osteolysis. 已接受在 J外科肿瘤科2007年11月.
Arrington SA, Schoonmaker JE, Damron TA, Mann KA, Allen MJ. Temporal changes in bone mass and mechanical properties in a murine model of tumor osteolysis. 骨 2006年3月,38 (3):359 - 67. 二五年十一月五日
Damron TA, Horton J, Naqvi A, Loomis RM, Margulies BS, Strauss JA, CE Farnum, Spadaro JA. Combination radioprotectants maintain chondrocyte proliferation better than single agents by decreasing early parathyroid hormone related protein changes after growth plate irradiation. 辐射的研究 2006年3月,265 (3):350 - 8.
达姆龙TA，沃德WG，斯图尔特A. 骨肉瘤, chondrosarcoma, and Ewings sarcoma: National Cancer Database Report. 临床骨科相关研究 [2007年3月22日出版]459:40-47,2007.
Horton JA, Bariteau JT, Loomis RM, Strauss JA, Damron TA. 幼年大鼠骨骼成熟的个体发育. 阿娜特列克.2008年3月,291 (3):283 - 92.
Horton JA, Margulies BS, Strauss JA, Bariteau JT, Damron TA, Spadaro JA, Farnum CE. Restoration of growth plate function following radiotherapy is driven by increased proliferative and synthetic activity of expansions of chondrocytic clones. J骨科 [Epub ahead of print 2006 Aug 17] 2006 Oct;24(10):1945-56.
马格利斯，霍顿JA，王勇，Damron TA, Allen MJ. Effects of radiation therapy on chondrocytes in vitro. 钙化组织. 2006年5月,78(5):302 - 13所示. 2006年5月9日.
Spadaro JA, Damron TA, Horton JA, Margulies BS, Murray GM, Clemente DA, Strauss JA. Density and structural changes in the bone of growing rats after weekly alendronate administration with and without a methotrexate challenge. J骨科. 2006年5月,24 (5):936 - 44.
Spadaro JA, Horton JA, Margulies BS, Strauss JA, Farnum CE, Damron TA. Radioprotectant combinations spare radiation-induced damage to the physis more than fractionation alone. 国际放射生物学杂志科学通报，2005;81(10):759-65.
Wang Y, Zhang M, Middleton FA, Horton JA, Pritchard M, Spadaro JA, Farnum CE, Damron TA. Connective tissue growth factor and insulin-like growth factor 2 show upregulation in early growth plate radiorecovery response following irradiation. 细胞组织器官. 2007;186(3):192-203. Epub 2007年7月12日.
Zhang M, Wang Y, Middleton FA, Horton JA, Farnum CE, Damron TA. Growth plate zonal microarray analysis shows upregulation of extracellular matrix genes and down-regulation of metalloproteinsaes and cathepsins following irradiation. 国际结缔组织 [2007年6月5日印刷版].