Ren Ye, Guo Fengjing, Chen Anmin, Deng Rui, Wang Jiang
Department of Orthopedics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
J Huazhong Univ Sci Technolog Med Sci. 2012 Feb;32(1):82-86. doi: 10.1007/s11596-012-0014-x. Epub 2012 Jan 27.
Matrix metalloproteinase-2 (MMP-2) level and the ERK1/2 signal pathway are dependent factors for the growth and metastasis of cancer. However, the impact of MMP-2 in combination with ERK1/2 in tumor patients with drug resistance is unknown. To determine the relationship between MMP-2 and the ERK1/2 signal pathway, we established an adriamycin (ADM)-induced MG-63 (ADM-MG-63) cell line. With the increase of the ERK1/2 pathway blocker PD98059, we detected the expression levels of MMP-2 and p-ERK1/2 by Western blot in ADM-MG-63 cells. In ADM-MG-63 cells transfected with MMP-2-siRNA, the expression of ERK1/2 was detected for understanding the function of the ERK1/2 signal pathway. Three siRNAs for MMP-2 (MMP-2-siRNA) were designed, and the optimal one was selected and tested at different time points of 24, 48 and 72 h. Under an ADM-induced condition, ADM-MG-63 cells were finally stable living in the medium of ADM (200 ng/mL). PD98059 could effectively suppress the expression levels of p-ERK1/2 and MMP-2. When the MMP-2 was silenced by using MMP-2-siRNA, the expression of p-ERK1/2 was enhanced. It is concluded that MMP-2 may be involved in ADM resistance dependent on ERK1/2 signal pathway, suggesting interference in ERK1/2 may be a new method of targeted therapy for tumor resistance.
基质金属蛋白酶-2(MMP-2)水平和ERK1/2信号通路是癌症生长和转移的相关因素。然而,MMP-2与ERK1/2联合对耐药肿瘤患者的影响尚不清楚。为了确定MMP-2与ERK1/2信号通路之间的关系,我们建立了阿霉素(ADM)诱导的MG-63(ADM-MG-63)细胞系。随着ERK1/2通路阻滞剂PD98059浓度的增加,我们通过蛋白质免疫印迹法检测了ADM-MG-63细胞中MMP-2和p-ERK1/2的表达水平。在转染了MMP-2-siRNA的ADM-MG-63细胞中,检测ERK1/2的表达以了解ERK1/2信号通路的功能。设计了三种针对MMP-2的小干扰RNA(MMP-2-siRNA),并选择了最佳的一种在24、48和72小时的不同时间点进行检测。在ADM诱导的条件下,ADM-MG-63细胞最终在含200 ng/mL ADM的培养基中稳定存活。PD98059可有效抑制p-ERK1/2和MMP-2的表达水平。当使用MMP-2-siRNA使MMP-2沉默时,p-ERK1/2的表达增强。结论是MMP-2可能通过ERK1/2信号通路参与阿霉素耐药,提示干扰ERK1/2可能是肿瘤耐药靶向治疗的一种新方法。