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龙葵水提物在体外和体内抑制小鼠黑色素瘤细胞转移。

Solanum nigrum Linn. water extract inhibits metastasis in mouse melanoma cells in vitro and in vivo.

机构信息

Institute of Biochemistry and Biotechnology, Chung Shan Medical University, and Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan.

出版信息

J Agric Food Chem. 2010 Nov 24;58(22):11913-23. doi: 10.1021/jf1022065. Epub 2010 Oct 28.

Abstract

Metastatic melanoma is an aggressive skin cancer notoriously resistant to current cancer therapies. Thus, new treatment strategies are urgently needed. Solanum nigrum Linn., commonly used in Oriental medicine, has showed antineoplastic activity in human cancer cell lines. The aim of this study was to evaluate the inhibitive effect of S. nigrum Linn. water extract (SNWE) on melanoma metastasis and dissect the underlying mechanisms of SNWE actions. B16-F1 cells were analyzed for migrating and invasive abilities with SNWE treatment, and several putative targets involved in metastatic melanoma were examined. In parallel, primary mouse xenograft and lung metastasis of melanoma models were established to examine the therapeutic potential of SNWE. The results indicated SNWE significantly inhibited B16-F1 cell migration and invasion. Meanwhile, decreased Akt activity and PKCα, Ras, and NF-κB protein expressions were detected in dose-dependent manners. In line with this notion, >50% reduced tumor weight and lung metastatic nodules were observed in 1% SNWE fed mice. This was associated with reduced serum MMP-9 as well as Akt activity and PKCα, Ras, and NF-κB protein expressions. Thus, this work indicates SNWE has potential application for treating metastatic melanoma.

摘要

转移性黑色素瘤是一种侵袭性皮肤癌,目前的癌症疗法对其疗效不佳。因此,迫切需要新的治疗策略。在东方医学中常用的龙葵已显示出对人类癌细胞系的抗肿瘤活性。本研究旨在评估龙葵水提取物(SNWE)对黑色素瘤转移的抑制作用,并探讨 SNWE 作用的潜在机制。用 SNWE 处理 B16-F1 细胞,分析其迁移和侵袭能力,并检测几种可能参与转移性黑色素瘤的靶标。同时,建立了原发性小鼠异种移植和黑色素瘤肺转移模型,以研究 SNWE 的治疗潜力。结果表明,SNWE 显著抑制了 B16-F1 细胞的迁移和侵袭。同时,在剂量依赖性方式下检测到 Akt 活性和 PKCα、Ras 和 NF-κB 蛋白表达降低。与此一致的是,在 1% SNWE 喂养的小鼠中,肿瘤重量和肺转移结节减少了>50%。这与血清 MMP-9 以及 Akt 活性和 PKCα、Ras 和 NF-κB 蛋白表达降低有关。因此,这项工作表明 SNWE 具有治疗转移性黑色素瘤的潜力。

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