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芦荟大黄素对高转移性乳腺癌MDA-MB-231细胞侵袭和转移的影响

[Effect of Aloe emodin on invasion and metastasis of high metastatic breast cancer MDA-MB-231 cells].

作者信息

He Zhen-Hui, Huang Yue-Qun, Weng Shan-Fan, Tan Yao-Rong, He Tai-Ping, Qin Yan-Mei, Liang Nian-Ci

出版信息

Zhong Yao Cai. 2013 Sep;36(9):1481-5.

Abstract

OBJECTIVE

To investigate the effect of Aloe emodin (AE) on the invasive and metastatic abilities of human high metastatic breast cancer MDA-MB-231 cells.

METHODS

MTT assay was used to evaluate the viability of MDA-MB-231 cells after treated with AE for 6 h and 24 h. The adhesive potential of MDA-MB-231 cells to FN and LN was tested by cell-matrix adhesion assay. The effect of AE on invasion of MDA-MB-231 cells was measured by Transwell chamber assay. Scratch wound healing assay was applied to determine the effect on migration of MDA-MB-231 cells. The effect of AE on MDA-MB-231 lung metastasis was determined on an experimental metastatic model.

RESULTS

80 micromol/L AE significantly inhibited the invasion, adhesion to FN, LN of MDA-MB-231 cells in vitro, the inhibitory rates were (52.98 +/- 5.46)%, (34.99 +/- 2.63)%, (28.73 +/- 7.00)%, respectively. After 24 h treatment, AE significantly inhibited the migration of MDA-MB-231 cells. The number and volume of lung metastatic nodules formed by MDA-MB-231 cells after 80 micromol/L AE 24 h treatment were decreased compared with control group.

CONCLUSION

AE can suppress the metastasis of MDA-MB-231 cells. Their mechanisms may be related to the inhibition of the capabilities of invasion and migration of MDA-MB-231 cells.

摘要

目的

研究芦荟大黄素(AE)对人高转移性乳腺癌MDA-MB-231细胞侵袭和转移能力的影响。

方法

采用MTT法评估AE作用6小时和24小时后MDA-MB-231细胞的活力。通过细胞-基质黏附试验检测MDA-MB-231细胞对纤连蛋白(FN)和层粘连蛋白(LN)的黏附能力。采用Transwell小室试验测定AE对MDA-MB-231细胞侵袭的影响。应用划痕伤口愈合试验确定对MDA-MB-231细胞迁移的影响。在实验性转移模型上确定AE对MDA-MB-231细胞肺转移的影响。

结果

80微摩尔/升AE显著抑制MDA-MB-231细胞在体外的侵袭以及对FN、LN的黏附,抑制率分别为(52.98±5.46)%、(34.99±2.63)%、(28.73±7.00)%。处理24小时后,AE显著抑制MDA-MB-231细胞的迁移。与对照组相比,80微摩尔/升AE处理24小时后MDA-MB-231细胞形成的肺转移结节数量和体积减少。

结论

AE可抑制MDA-MB-231细胞的转移。其机制可能与抑制MDA-MB-231细胞的侵袭和迁移能力有关。

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