Influence of down-regulation of RAGE receptor on HMGB1 expression and the volume of transplanted tumor
10.3969/j.issn.1006-5725.2017.14.011
- VernacularTitle:高级糖基化终末产物受体下调对高迁移率族蛋白B1表达及移植瘤体积的影响
- Author:
Xinjun WANG
;
Zhuo YANG
;
Ruyi YANG
;
Shaolong ZHOU
- Keywords:
receptor for advanced glycation end products;
high mobility group protein B1;
glioma;
apoptosis
- From:
The Journal of Practical Medicine
2017;33(14):2295-2298
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the down-regulation of advanced receptor for advanced glycation end products(RAGE)on expression of high mobility group protein B1(HMGB1)in glioma cells line and the volume change of transplanted tumor in nude mice. Methods HMGB1 expression in glioma LN229 cells line (divided into a control group and a study group) was observed by immunohistochemical assay and Western blot. The control group received normal saline,whereas the study group received RAGE receptor blocking agent FPS-ZM1. Expression of HMGB1 protein was detected by the same methods. The difference of the expression was examined by independent sample t test. 30 Nu/Nu nude mice were randomly divided into two groups;the above two kinds cell lines were injected into the same area of the left back of nude mice. Six weeks after injection ,the volume size was measured six times ,and the variance of repeated measurement data was used to analyze the difference of the volume change. Results HMGB1 protein was mainly expressed in the cytoplasm and nucleus. As compared with the control group,HMGB1 protein expression levels were decreased in the study group(P < 0.05),the growth rate of transplanted tumor in nude mice was significantly faster in the control group than in the study group ,the difference was statistically significant(P < 0.05). Conclusions The growth and invasion of HMGB1 protein may be involved in glioma by RAGE receptor. RAGE receptor blocker FPS-ZM1 can significantly reduce the expression of HMGB1 protein and inhibit the growth of transplanted tumor volume. It is expected to be used for the research on glioma cell apoptosis.
