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家蝇蜂毒素对人肝癌 BEL-7402 细胞黏附和迁移的影响。

Effects of Musca domestica cecropin on the adhesion and migration of human hepatocellular carcinoma BEL-7402 cells.

机构信息

School of Basic Courses, Guangdong Pharmaceutical University, Guangzhou, China.

出版信息

Biol Pharm Bull. 2013;36(6):938-43. doi: 10.1248/bpb.b12-00935. Epub 2013 Mar 18.

Abstract

This study was designed to explore the effects of Musca domestica antimicrobial peptides cecropin on the adhesion and migration of human hepatocellular carcinoma BEL-7402 cells. The adhesive and migratory capacities were determined by adhesion assay and transwell assay, respectively. The changes in microvilli of tumor cells were determined by scanning electron microscopy (SEM). Western blotting and quantitative polymerase chain reaction (qPCR) were carried out to determine the expression levels of proteins related to adhesion and migration, such as matrix metalloproteinase-2 (MMP2), tissue inhibitors of metalloproteinase-2 (TIMP2), and epithelial cadherin (E-cadherin). We found that Musca domestica cecropin inhibited the adhesion and migration of BEL-7402 cells, which also displayed curling microvilli, increased ball structures on cell surface, gradually broken connections between tumor cells, and even disappeared microvilli on some cells. The expression of MMP2 was significantly reduced after cecropin treatment, while the levels of TIMP2 and E-cadherin were significantly increased. These results suggest that Musca domestica cecropin inhibits the adhesion and migration of human hepatocellular carcinoma BEL-7402 cells by destroying the microvilli of tumor cells and changing the expression of MMP2, TIMP2 and E-cadherin.

摘要

本研究旨在探讨家蝇抗菌肽 Cecropin 对人肝癌 BEL-7402 细胞黏附和迁移的影响。通过黏附实验和 Transwell 实验分别测定黏附和迁移能力。扫描电子显微镜(SEM)观察肿瘤细胞微绒毛的变化。采用 Western blot 和定量聚合酶链反应(qPCR)检测与黏附和迁移相关的蛋白表达水平,如基质金属蛋白酶-2(MMP2)、金属蛋白酶组织抑制剂-2(TIMP2)和上皮钙黏蛋白(E-cadherin)。结果发现,家蝇 Cecropin 抑制 BEL-7402 细胞的黏附和迁移,同时肿瘤细胞的微绒毛卷曲,表面出现球状物,肿瘤细胞间连接逐渐断裂,甚至部分细胞微绒毛消失。 Cecropin 处理后 MMP2 的表达明显降低,而 TIMP2 和 E-cadherin 的水平明显升高。这些结果表明,家蝇 Cecropin 通过破坏肿瘤细胞的微绒毛和改变 MMP2、TIMP2 和 E-cadherin 的表达来抑制人肝癌 BEL-7402 细胞的黏附和迁移。

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