Zhou Wenya, Hao Mengze, Du Xiaoling, Chen Kexin, Wang Guowen, Yang Jilong
Department of Bone and Soft Tissue Tumor, Tianjin Medical University Cancer Hospital and Institute, Tianjin 300060, China and National Clinical Research Center for Cancer, Tianjin Medical University Cancer Hospital and Institute, Tianjin 300060, China.
Discov Med. 2014 Jun;17(96):301-7.
Osteosarcoma is an aggressive cancer in skeletal system with unknown molecular mechanisms of etiology and pathogenesis, therefore it remains a challenge for current therapeutic strategies to effectively treat osteosarcoma. The aim of this review is to give an overview of the molecular and mechanistic changes identified in recent years which might be new targets for the treatment of osteosarcoma. These molecules play important roles in different biological and pathological programs of osteosarcoma, including the altered oncogenes and tumor suppressor genes, molecules involved in tumor cell migration and invasion, angiogenesis, apoptosis and proliferation, miRNAs, and molecules involved in osteoclast function and multidrug resistance. Further research on these molecules in osteosarcoma will provide new insights into the target therapy for osteosarcoma.
骨肉瘤是骨骼系统中的一种侵袭性癌症,其病因和发病机制的分子机制尚不清楚,因此,当前的治疗策略有效治疗骨肉瘤仍然是一项挑战。本综述的目的是概述近年来发现的分子和机制变化,这些变化可能是治疗骨肉瘤的新靶点。这些分子在骨肉瘤的不同生物学和病理过程中发挥重要作用,包括癌基因和肿瘤抑制基因的改变、参与肿瘤细胞迁移和侵袭的分子、血管生成、细胞凋亡和增殖、微小RNA,以及参与破骨细胞功能和多药耐药的分子。对骨肉瘤中这些分子的进一步研究将为骨肉瘤的靶向治疗提供新的见解。