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红景天苷对MCF-7乳腺癌细胞的抑制作用。

Inhibitory effects of salidroside on MCF-7 breast cancer cells .

作者信息

Sun An-Qi, Ju Xiu-Lian

机构信息

Key Laboratory for Green Chemical Process of Ministry of Education, School of Chemical Engineering & Pharmacy, 34756Wuhan Institute of Technology, Wuhan, People's Republic of China.

The College of Post and Telecommunication, 34756Wuhan Institute of Technology, Wuhan, People's Republic of China.

出版信息

J Int Med Res. 2020 Nov;48(11):300060520968353. doi: 10.1177/0300060520968353.

DOI:10.1177/0300060520968353
PMID:33238796
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7705297/
Abstract

OBJECTIVE

We investigated the antitumor effects of salidroside and preliminarily examined its underlying mechanisms by establishing a nude mouse model bearing MCF-7 breast cancer cell xenografts.

METHODS

The mice were grouped and intraperitoneally injected with salidroside, paclitaxel, or physiological saline. Tumor samples were weighed, and immunohistochemical staining with hematoxylin and eosin and anti-CD34 antibody was performed. Tumor cell apoptosis was observed using the terminal deoxynucleotidyl transferase deoxyuridine dUTP nick end labeling assay. Bcl-1, p53, Bax, and caspase 3 expression in tumor tissues was determined via western blotting.

RESULTS

The tumor inhibition rate of high-dose salidroside was 75.16%, which was significantly higher than the rates for paclitaxel and saline. A tumor tissue pathology analysis revealed that high-dose salidroside inhibited tumor cell proliferation and promoted tumor cell apoptosis. Western blotting revealed that Bcl-2 and p53 expression were significantly lower in the salidroside group than in the other groups, whereas Bax and caspase 3 (17 kDa) expression were increased.

CONCLUSIONS

Salidroside was more effective than paclitaxel in inhibiting tumor growth in MCF-7 breast cancer cell-bearing nude mice. The mechanism of action may involve Bcl-2 and p53 downregulation and Bax and caspase 3 upregulation, thereby increasing proapoptotic factor expression and inducing tumor cell apoptosis.

摘要

目的

通过建立荷MCF-7乳腺癌细胞异种移植瘤的裸鼠模型,研究红景天苷的抗肿瘤作用并初步探讨其潜在机制。

方法

将小鼠分组,分别腹腔注射红景天苷、紫杉醇或生理盐水。称取肿瘤样本重量,并进行苏木精-伊红染色及抗CD34抗体免疫组化染色。采用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记法观察肿瘤细胞凋亡情况。通过蛋白质免疫印迹法检测肿瘤组织中Bcl-1、p53、Bax和半胱天冬酶3的表达。

结果

高剂量红景天苷的肿瘤抑制率为75.16%,显著高于紫杉醇组和生理盐水组。肿瘤组织病理学分析显示,高剂量红景天苷可抑制肿瘤细胞增殖并促进肿瘤细胞凋亡。蛋白质免疫印迹法显示,红景天苷组中Bcl-2和p53的表达显著低于其他组,而Bax和半胱天冬酶3(17 kDa)的表达增加。

结论

在荷MCF-7乳腺癌细胞的裸鼠中,红景天苷在抑制肿瘤生长方面比紫杉醇更有效。其作用机制可能涉及下调Bcl-2和p53以及上调Bax和半胱天冬酶3,从而增加促凋亡因子表达并诱导肿瘤细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c099/7705297/188d4a9dabaf/10.1177_0300060520968353-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c099/7705297/9283b438d0aa/10.1177_0300060520968353-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c099/7705297/ab5036eaea13/10.1177_0300060520968353-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c099/7705297/81ed37ae9ec2/10.1177_0300060520968353-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c099/7705297/f5f243aab4fa/10.1177_0300060520968353-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c099/7705297/188d4a9dabaf/10.1177_0300060520968353-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c099/7705297/9283b438d0aa/10.1177_0300060520968353-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c099/7705297/ab5036eaea13/10.1177_0300060520968353-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c099/7705297/81ed37ae9ec2/10.1177_0300060520968353-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c099/7705297/f5f243aab4fa/10.1177_0300060520968353-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c099/7705297/188d4a9dabaf/10.1177_0300060520968353-fig5.jpg

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