NRP2表达抑制对结肠癌细胞LoVo移植瘤淋巴管生成和转移的影响  被引量:6

Influence of inhibition neuropilins-2 expression on lymphangiogenesis and metastasis in colorectal carcinoma

在线阅读下载全文

作  者:周琪[1] 梁后杰[2] 阎晓初[3] 彭秋平[2] 周进明[2] 吴峰[3] 高俊勇[1] 刘以淑[1] 

机构地区:[1]重庆市涪陵中心医院肿瘤科,408000 [2]第三军医大学西南医院肿瘤科,重庆400038 [3]第三军医大学西南医院病理研究所,400038

出  处:《临床肿瘤学杂志》2009年第6期481-486,共6页Chinese Clinical Oncology

基  金:国家自然科学基金资助项目(30572159)

摘  要:目的:探讨抑制Neuropilins-2(NRP2)基因表达对结肠癌淋巴管生成和转移的影响。方法:采用RNA干扰(RNAi)下调结肠癌LoVo细胞株NRP2表达,接种NRP2 RNAi的LoVo细胞株于裸鼠,建立裸鼠结肠癌结肠原位移植瘤模型,分别观察移植后4、6、8和12周裸鼠结肠原位移植瘤淋巴管生成以及转移的情况。结果:成功建立结肠癌裸鼠原位移植瘤动物模型。下调结肠癌LoVo细胞株NRP2表达能显著降低裸鼠结肠原位移植瘤的淋巴管密度以及远处转移。结论:抑制NRP2表达可以抑制结肠癌的淋巴管生成和转移,它将是一个潜在的肿瘤治疗靶点。Objective:To explore the role and imquence of inhibition neuropilins-2 (NRP2) expression on lymphangiogenesis and metastasis in colorectal carcinoma. Methods:To downregulate NRP2 expression by RNA interference. To transfection NRP2 RNAi vector into LoVo cells and transplanted into nude mouses. After havesting the xenotransplant neoplasm respectively 4,6,8,12 weeks, the expression of NRP2 and proliferation, and the lymphantic density, lymphonode metastasis and distance organ metastasis in the xenotransplant tumor were dectected and compared with the control group. Results : An orthotopic transplantation model of human primary colorectal cancer was successfully established in nude mice, which could completely repeat the natural clinicopathologic course of human primary colorectal cancer, and metastasis pattern of the model was similar to that of clinical patients. It significantly decreased the lymphantic density, lymphonode metastasis and distance organ metastasis in the xenotransplant tumor of LoVo cells, which downregulated NRP2 expression. Conclusion:To inhibite lymphangiogenesis and the metastasis in colorectal carcinoma by downregulating NRP2 expression, it may be a potential target of therapy for tumors.

关 键 词:NRP2 RNA干扰 移植瘤 淋巴管生成 转移 

分 类 号:R735.3[医药卫生—肿瘤]

 

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