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纸质出版:2013
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陈懿,王晓波,张俊勇,连峥嵘,龚建平.超声微泡携MAGL-shRNA靶向释放对大鼠肝细胞肝癌转移作用的实验研究[J].陆军军医大学学报(原第三军医大学学报),2013,35(16):1708-1712.
Chen Yi,Wang Xiaobo,Zhang Junyong,Lian Zhengrong,Gong Jianping.Effect of ultrasound microbubble carrying MAGL-shRNA on metastasis of hepatocellular carcinoma in rats[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(16):1708-1712.
陈懿,王晓波,张俊勇,连峥嵘,龚建平.超声微泡携MAGL-shRNA靶向释放对大鼠肝细胞肝癌转移作用的实验研究[J].陆军军医大学学报(原第三军医大学学报),2013,35(16):1708-1712. DOI:
Chen Yi,Wang Xiaobo,Zhang Junyong,Lian Zhengrong,Gong Jianping.Effect of ultrasound microbubble carrying MAGL-shRNA on metastasis of hepatocellular carcinoma in rats[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(16):1708-1712. DOI:
目的 观察超声微泡携单酰基甘油脂肪酶沉默基因(monoacylglycerol lipase short hairpin RNA
MAGL-shRNA)在大鼠肝细胞肝癌(hepatocellular carcinoma
HCC)组织中转染及对HCC转移的作用。 方法 建立大鼠肝细胞肝癌模型,病理解剖和二维超声验证肝脏成瘤情况。40只SD大鼠完全随机分成4组,分别为PBS液组、MAGL-shRNA质粒微泡组(MAGL-shRNA+microbubble
MB)、空白质粒微泡+超声辐照组(microbubbles+ultrasound
MB+US)、MAGL-shRNA质粒微泡+超声辐照组(MAGL-shRNA+MB+US)。每只注射1 mL,对MB+US组和MAGL-shRNA+MB+US组大鼠肝区同时给予超声辐照,辐照条件为300 kHz,2 W/cm
2
,辐照10 s,间隔10 s,共20 min。Western blot检测大鼠HCC组织MAGL蛋白的表达,免疫组化检测MAGL和基质金属蛋白酶2(matrixmetalloproteinase-2
MMP-2)的表达。比较各组动物的肿瘤转移情况。 结果 MAGL在HCC组织中表达明显高于正常肝组织(P0.05); 微泡携MAGL-shRNA可以在HCC组织被超声辐照击破后靶向释放,在各组HCC组织中均有MAGL蛋白的表达,其中MAGL-shRNA+MB+US组表达量明显低于其他组(
P
0.01); 免疫组化检测MAGL-shRNA+MB+US组MMP-2表达均低于其他组(
P
0.01); 各组动物均见肿瘤转移,但MAGL-shRNA+MB+US组转移率最低(
P
0.05)。 结论 超声辐照可破坏携MAGL-shRNA的微泡使之靶向释放并增强了MAGL-shRNA的转染效率,MAGL-MMP-2通路可能与HCC的转移相关。
Objective To determine the effect of silencing monoacylglycerol lipase by short hairpin RNA (shRNA) on the metastasis of hepatocellular carcinoma in rats by using ultrasound-targeted microbubble destruction.
Methods Liver tumor models of rats were established by intragastrically injection of 0.2% DEN in 5 times per week for 14 weeks. The successful establishment of tumor model was testified by pathologic biopsy and two-dimensional ultrasongraphy. Totally 40 rats with liver tumor were randomly divided into 4 groups
phosphate-buffered solution (PBS) group
lipid microbubbles loaded MAGL-shRNA (MAGL-shRNA+microbubble group)
pure lipid microbubbles+ultrasound (MB+US group)
and lipid microbubbles loaded MAGL-shRNA+ultrasound (MAGL-shRNA+MB+US group). The microbubbles of 1 mL containing MAGL-shRNA plasmid or not were injected through tail vein. Ultrasound radiation was applied on the rats of MB+US and MAGL-shRNA+MB+US groups after the injection of target gene
with the radiation frequency of 1 kHz
sound intensity of 2 W/cm
2
with the pulse irradiation of 10 s and interval time of 10 s for totally 20 min. The expression of MAGL protein was detected in the tumor mass by Western blotting. Protein expression of MAGL and matrix metalloproteinase-2 (MMP-2) was detected by immunohistochemistry (IHC). Tumor metastasis were observed and compared among different groups. Results The protein expression of MAGL was significantly higher in HCC tissue than in normal tissue (
P
0.05). Microbubbles containing MAGL-shRNA were injected precisely into the tumor tissue and then released to the target
and the expression of MAGL protein was found in all HCC tissue. Its expression in MAGL-shRNA+MB+US group was significantly lower than the other groups (
P
0.01). The MMP-2 expression detected by IHC in MAGL-shRNA+MB+US group was significantly lower than others (
P
0.01). Tumor metastasis was found in all groups
but the metastasis rate in MAGL-shRNA+MB+US group was the lowest (
P
0.05). Conclusion Ultrasound targeted microbubble destruction can effectively transfect MAGL-shRNA into the target tissues
and play a inhibitory effect on the metastasis in liver cancer through MAGL-MM
P-2 signal pathway.
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