Jinling Hospital, Department of Orthopedics, Nanjing University, School of Medicine, Nanjing 210002, Peoples R China.
Front Biosci (Landmark Ed). 2013 Jun 1;18(4):1384-91. doi: 10.2741/4187.
The canonical Wnt-beta -catenin signaling pathway is a key component of normal skeletal development and disease. Alterations within this signaling pathway have been described in human and canine osteosarcoma (OS); however, debate exists as to whether or not alterations in this pathway contribute to OS development in humans. In metastatic OS, the Wnt-β-catenin pathway promotes the invasion and migration of OS cells and β-catenin acts as a biological marker of OS with the potential to metastasize to the lung. The participation of the Wnt-β-catenin pathway in OS development and metastasis is regulated by several factors, including hormones and alkaline phosphatase (ALP). This pathway is also involved in the resistance of OS to chemotherapy, especially in resistance to all three drugs used in standard chemotherapy, i.e. doxorubicin, cisplatin and methotrexate (MTX). In this review, we will summarize recent findings regarding the Wnt-β-catenin pathway in OS development and chemotherapy.
经典的 Wnt-β-连环蛋白信号通路是骨骼正常发育和疾病的关键组成部分。在人类和犬骨肉瘤 (OS) 中已经描述了该信号通路的改变;然而,关于该通路的改变是否有助于人类 OS 的发展仍存在争议。在转移性 OS 中,Wnt-β-连环蛋白通路促进 OS 细胞的侵袭和迁移,β-连环蛋白是 OS 的生物标志物,具有转移到肺部的潜力。Wnt-β-连环蛋白通路在 OS 发展和转移中的参与受到多种因素的调节,包括激素和碱性磷酸酶 (ALP)。该通路还参与 OS 对化疗的耐药性,特别是对标准化疗中使用的三种药物(即阿霉素、顺铂和甲氨蝶呤 (MTX))的耐药性。在这篇综述中,我们将总结关于 Wnt-β-连环蛋白通路在 OS 发展和化疗中的最新发现。