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积雪草酸通过抑制 PI3K/AKT 信号通路抑制 WAVE3 的激活来干扰乳腺癌细胞的侵袭和增殖。

Asiatic Acid Interferes with Invasion and Proliferation of Breast Cancer Cells by Inhibiting WAVE3 Activation through PI3K/AKT Signaling Pathway.

机构信息

Baoshan District Hospital of Integrated Traditional Chinese and Western Medicine of Shanghai, Shanghai 201999, China.

School of Pharmacy, Shaanxi University of Traditional Chinese Medicine, Xianyang, Shaanxi 712046, China.

出版信息

Biomed Res Int. 2020 Feb 10;2020:1874387. doi: 10.1155/2020/1874387. eCollection 2020.

Abstract

OBJECTIVE

To explore the ability of asiatic acid to interfere with the invasion and proliferation of breast cancer cells by inhibiting WAVE3 expression and activation through the PI3K/AKT signaling pathway.

METHODS

The MDA-MB-231 cells with strong invasiveness were screened by transwell assay, and plasmids with high expression of WAVE3 were constructed for transfection. The transfection effect and protein expression level of plasmids were verified by PCR and WB. The effects of asiatic acid on cell proliferation and invasion were investigated by flow cytometry. The xenografted tumor models in nude mice were established to study the antitumor activity of asiatic acid.

RESULTS

Asiatic acid significantly inhibited the activity of MDA-MB-231 cells, and the expression level of WAVE3 increased significantly in the tissue of ductal carcinoma in situ and was lower than that in the metastasis group. After plasmid transfection, the mRNA and protein expression of WAVE3 increased significantly in the cells. Asiatic acid at different concentrations had an impact on cell apoptosis and invasion and could significantly inhibit the expression of WAVE3, P53, p-PI3K, p-AKT, and other proteins. The T/C(%) of asiatic acid (50 mg/kg) for MDA-MB-231(F10) xenografted tumor in nude mice was 46.33%, with a tumor inhibition rate of 59.55%. Asiatic acid could significantly inhibit the growth of MDA-MB-231 (F10) xenografted tumors in nude mice ( < 0.05).

CONCLUSIONS

Asiatic acid interferes with the ability of breast cancer cells to invade and proliferate by inhibiting WAVE3 expression and activation and the mechanism of action may be related to the PI3K/AKT signaling pathway.

摘要

目的

通过抑制 WAVE3 表达和激活,研究齐墩果酸通过 PI3K/AKT 信号通路干扰乳腺癌细胞侵袭和增殖的能力。

方法

通过 Transwell 实验筛选侵袭性强的 MDA-MB-231 细胞,构建高表达 WAVE3 的质粒进行转染。通过 PCR 和 WB 验证质粒的转染效果和蛋白表达水平。通过流式细胞术研究齐墩果酸对细胞增殖和侵袭的影响。建立裸鼠异种移植肿瘤模型研究齐墩果酸的抗肿瘤活性。

结果

齐墩果酸显著抑制 MDA-MB-231 细胞活性,原位导管癌组织中 WAVE3 表达水平明显升高,低于转移组。质粒转染后,细胞中 WAVE3 的 mRNA 和蛋白表达明显增加。不同浓度的齐墩果酸对细胞凋亡和侵袭有影响,并能显著抑制 WAVE3、P53、p-PI3K、p-AKT 等蛋白的表达。齐墩果酸(50mg/kg)对裸鼠 MDA-MB-231(F10)异种移植肿瘤的 T/C(%)为 46.33%,肿瘤抑制率为 59.55%。齐墩果酸能显著抑制裸鼠 MDA-MB-231(F10)异种移植瘤的生长(<0.05)。

结论

齐墩果酸通过抑制 WAVE3 的表达和激活,干扰乳腺癌细胞的侵袭和增殖能力,其作用机制可能与 PI3K/AKT 信号通路有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c383/7035546/dd8f41e689d7/BMRI2020-1874387.001.jpg

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