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膳食草本 的乙醇提取物在人乳腺癌细胞中表现出抗癌潜力。

Ethanol Extracts of Dietary Herb, , Exhibit Anticancer Potential in Human Breast Cancer Cells.

机构信息

1 Graduate Institute of Natural Products, College of Pharmacy, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.

2 Chi Mei Medical Center, Liouying, Tainan 73657, Taiwan.

出版信息

Integr Cancer Ther. 2019 Jan-Dec;18:1534735419866924. doi: 10.1177/1534735419866924.

Abstract

Recent advances in mammography screening, chemotherapy, and adjuvant treatment modalities have improved the survival rate of women with breast cancer. Nevertheless, the breast tumor with metastatic progression is still life-threatening. Indeed, combination therapy with Ras-ERK and PI3K inhibitors is clinically effective in malignant breast cancer treatment. Constituents from genus plants have been implicated as potent anticancer agents in terms of their efficacy of inhibiting tumor cell metastasis. In this study, we tested the effects of ethanol extracts of (rhizome, stem, and leaf extracts) in cultured human breast cancer cells and particularly focused on the Ras-ERK and PI3K/AKT pathways. We found that the rhizome and leaf extracts from inhibited cell migration, invasion, and sphere formation in MCF-7 and MDA-MB-231 cells. The potency was extended with the inhibition of serum-induced PI3K/AKT and Ras-ERK activation and epidermal growth factor (EGF)-mediated EGFR activation in MDA-MB-231 cells. These results indicate that extracts of could inhibit signal transduction at least involved in EGFR as well as the PI3K/AKT and Ras-ERK pathways, which are crucial players of tumor cell migration and invasion. Our study strongly supports that the extracts of could be a novel botanical drug lead for the development of an antimetastatic agent for the treatment of human malignant breast cancer.

摘要

近年来,乳腺癌的乳腺摄影筛查、化学疗法和辅助治疗方式取得了进展,提高了乳腺癌患者的生存率。然而,转移性进展的乳腺肿瘤仍然危及生命。事实上,Ras-ERK 和 PI3K 抑制剂的联合治疗在恶性乳腺癌治疗中具有临床疗效。属植物的成分被认为是有效的抗癌剂,因为它们具有抑制肿瘤细胞转移的功效。在这项研究中,我们测试了 (根茎、茎和叶提取物)的乙醇提取物在培养的人乳腺癌细胞中的作用,特别关注 Ras-ERK 和 PI3K/AKT 通路。我们发现,来自 的根茎和叶提取物抑制 MCF-7 和 MDA-MB-231 细胞的迁移、侵袭和球体形成。这种效力通过抑制血清诱导的 PI3K/AKT 和 Ras-ERK 激活以及 MDA-MB-231 细胞中的表皮生长因子(EGF)介导的 EGFR 激活得到了扩展。这些结果表明, 的提取物可以至少抑制信号转导,这些信号转导涉及 EGFR 以及 PI3K/AKT 和 Ras-ERK 通路,这些通路是肿瘤细胞迁移和侵袭的关键参与者。我们的研究强烈支持, 的提取物可以作为一种新型植物药物先导,用于开发治疗人类恶性乳腺癌的抗转移剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61db/6696839/bc4bdcb4a950/10.1177_1534735419866924-fig1.jpg

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