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Gal和PEI修饰磁性纳米颗粒载体介导的c-Met siRNA构建及其抗肝癌细胞效应观察.
- Source :
-
Shandong Medical Journal . 6/15/2021, Vol. 61 Issue 17, p1-4. 4p. - Publication Year :
- 2021
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Abstract
- Objective To construct the galactose(Gal) and polyethyleneimine(PEI)-modified magnetic nanocarriers(Gal-PEI-SPIO)-mediated c-Met siRNA and to observe its antihepatocarcinoma effect. Methods Gal-PEI-SPIO nanocarriers were prepared and characterized. Agarose gel electrophoresis was used to detect the combination of carriers and siRNA. The cytotoxicity of the nanocarriers was determined by CCK-8. At the same time, q-PCR and Western blotting were used to detect the silencing efficiency of carriers carrying c-Met siRNA in cells. The effects of Gal-PEI-SPIO/c-Met siRNA nanocomposites on the migration and invasion of liver cancer MHCC-97H cells were detected by Transwell chamber method. Result Agarose gel electrophoresis showed that Gal-PEI-SPIO nanocarriers and siRNA could be closely combined when the SPIO: siRNA mass ratio was 4:1 or more. Simultaneously, when the ratio was more than 4:1,the cell activity decreased rapidly. The qPCR results showed that Gal-PEI-SPIO/siRNA nanocomposites effectively reduced the level of mRNA in MHCC-97H cells, and Western blotting showed that the Gal-PEI-SPIO/c-Met siRNA nanocomposites effectively reduced c-Met mRNA and protein levels (all P<0. 01). In cell invasion and migration experiments, GalPEI-SPIO/c-Met siRNA nanocomposites significantly reduced the invasion and migration abilities of MHCC-97H cells. Conclusion Gal-PEI-SPIO nanocarriers can bind tightly to siRNA, and can carry c-Met siRNA into hepatocellular carcinoma cells to silence c-Met, thereby inhibiting the invasion and migration of MHCC-97H cells. [ABSTRACT FROM AUTHOR]
Details
- Language :
- Chinese
- ISSN :
- 1002266X
- Volume :
- 61
- Issue :
- 17
- Database :
- Academic Search Index
- Journal :
- Shandong Medical Journal
- Publication Type :
- Academic Journal
- Accession number :
- 150915419
- Full Text :
- https://doi.org/10.3969/j.issn.1002-266X.2021.17.001