钙黏蛋白表达与表皮生长因子受体分子靶向治疗敏感/耐药的相关性  被引量:1

Correlation of E-cadherin Expression and the Sensitivity to EGFR-TKI Molecular Targeted Therapy

在线阅读下载全文

作  者:邢荣春[1,2] 郑军[1,2] 刘伟[1,2] 姚汝铖[1,2] 

机构地区:[1]三峡大学第一临床医学院 [2]湖北省宜昌市中心人民医院普通外科,宜昌443003

出  处:《医药导报》2014年第5期582-585,共4页Herald of Medicine

摘  要:目的探讨钙黏蛋白表达与表皮生长因子受体(EGFR)分子靶向治疗敏感或耐药的相关性。方法乳腺癌细胞(MCF-7和MDA-MB-231)、膀胱癌细胞株(T24)、子宫颈鳞癌细胞(SiHa)、大细胞肺癌细胞株(H460)、肝癌细胞株(SK-HEP-1和MHCC97-H)以及单核细胞白血病(THP-1)等8种细胞分别用表皮生长因子受体酪胺酸激酶抑制药(EGFR-TKI)PD153035和吉非替尼处理48 h,采用噻唑蓝(MTT)法检测其敏感或耐药性,计算各细胞的半数抑制浓度(IC50),并与各细胞钙黏蛋白水平比较,观察相关性。结果随着PD153035和吉非替尼浓度的升高,MCF-7、MDA-MB-231、T24及SiHa细胞生存率明显下降,表现为敏感,钙黏蛋白表达阳性;H460、SK-HEP-1、MHCC97-H及THP-1细胞生存率未见明显下降,表现为耐药,钙黏蛋白表达阴性。结论 EGFR-TKI对上皮性肿瘤细胞的生存率与钙黏蛋白的表达水平存在相关性;钙黏蛋白可能在调节EGFR分子靶向治疗的敏感性方面起重要作用;钙黏蛋白作为标志物为临床筛选合适的患者进行EGFR-TKI分子靶向治疗提供了重要线索。Objective To explore the correlation of E-cadherin expression and the sensitivity to EGFR-TKI molecular targeted therapy. Methods Eight kinds of cells,MCF-7,MDA-MB-231,T24,SiHa,H460,SK-HEP-1,MHCC97-H and THP-1 were treated with EGFR-TKI PD153035 and gefitinib,respectively,for 48 hours. The drug-sensitivity was detected by MTT,and the IC50 of cells were calculated. The E-cadherin protein were detected and compared. Results Followed with PD153035 and gefitinib treatment,the survival rates of MCF-7,MDA-MB-231,T24 and SiHa significantly reduced,and more E-cadherin protein expressed. However, the survival rates of the H460, SK-HEP-1, MHCC97-H, and THP-1 cells showed opposite results. Conclusion The sensitivity of epithelial cancer cells to EGFR-TKI is correlated with E-cadherin expression. E-cadherin may play a significant role on regulateing the sensitivity to EGFR-TKI molecular targeted therapy. E-cadherin is a key biomarker for recruiting appropriate patients for EGFR-TKI molecular targeted therapy.

关 键 词:钙黏蛋白 表皮生长因子受体酪胺酸激酶抑制药 耐药 靶向治疗 

分 类 号:R979.1[医药卫生—药品] R965.1[医药卫生—药学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象