PI3K/Akt signaling in osteosarcoma

被引:269
|
作者
Zhang, Jian [1 ]
Yu, Xiao-Hua [2 ]
Yan, Yi-Guo [1 ]
Wang, Cheng [1 ]
Wang, Wen-Jun [1 ]
机构
[1] Univ South China, Affiliated Hosp 1, Dept Spine Surg, Hengyang 421001, Hunan, Peoples R China
[2] Univ South China, Life Sci Res Ctr, Hengyang 421001, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
OS; PI3K; Akt; PTEN; mTOR; APOPTOTIC CELL-DEATH; STEM-LIKE CELLS; DOWN-REGULATION; TUMOR-GROWTH; MATRIX METALLOPROTEINASE-2/-9; CLINICAL-SIGNIFICANCE; PATHWAY ALTERATIONS; MOUSE OSTEOSARCOMA; MAMMALIAN TARGET; TRANSGENIC MICE;
D O I
10.1016/j.cca.2014.12.041
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Osteosarcoma (OS) is the most common nonhematologic bone malignancy in children and adolescents. Despite the advances of adjuvant chemotherapy and significant improvement of survival, the prognosis remains generally poor. As such, the search for more effective anti-OS agents is urgent. The phosphatidylinositol 3-kinase (PI3K)/Akt pathway is thought to be one of the most important oncogenic pathways in human cancer. An increasing body of evidence has shown that this pathway is frequently hyperactivated in OS and contributes to disease initiation and development, including tumorigenesis, proliferation, invasion, cell cycle progression, inhibition of apoptosis, angiogenesis, metastasis and chemoresistance. Inhibition of this pathway through small molecule compounds represents an attractive potential therapeutic approach for OS. The aim of this review is to summarize the roles of the PI3K/Akt pathway in the development and progression of OS, and to highlight the therapeutic potential of targeting this signaling pathway. Knowledge obtained from the application of these compounds will help in further understanding the pathogenesis of OS and designing subsequent treatment strategies. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:182 / 192
页数:11
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