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佩兰通过抑制MMP-9活性和VEGF生成降低恶性肿瘤的转移和血管生成能力。

Reduction of metastatic and angiogenic potency of malignant cancer by Eupatorium fortunei via suppression of MMP-9 activity and VEGF production.

作者信息

Kim Aeyung, Im Minju, Yim Nam-Hui, Ma Jin Yeul

机构信息

Korean Medicine (KM)-Based Herbal Drug Development Group, Korea Institute of Oriental Medicine (KIOM), 483 Expo-ro, Yuseong-gu, Daejeon 305-811, Republic of Korea.

出版信息

Sci Rep. 2014 Nov 11;4:6994. doi: 10.1038/srep06994.

Abstract

Eupatorium fortunei has long been used to treat nausea and poor appetite, and has been prescribed as a diuretic and detoxifying drug in Chinese medicine. Recent studies have demonstrated that E. fortunei possesses anti-bacterial, anti-oxidant, and anti-diabetic activities, as well as cytotoxicity to human leukemia cells. However, at non-toxic concentrations, the effects of an aqueous extract of E. fortunei (WEF) on the metastatic and angiogenic potential of malignant tumor cells have not been reported. In this study, we found that WEF suppressed the metastatic properties, including anchorage-independent colony formation, migration, and invasion, by downregulating the proteolytic activity of MMP-9. NF-κB activation and the phosphorylation of p38 and JNK were reduced significantly by WEF. Additionally, WEF inhibited tumor-induced angiogenesis markedly, affecting HUVEC migration, tube formation by HUVECs, and microvessel sprouting from rat aortic rings via a reduction in VEGF in tumors. In a pulmonary metastasis model, daily administration of WEF at 50 mg/kg markedly decreased metastatic colonies of intravenously injected B16F10 cells on the lung surface in C57BL/6J mice. Further, none of the WEF-administered mice exhibited systemic toxicity. Taken together, our results indicate that WEF is a potential therapeutic herbal product that may be useful for controlling malignant metastatic cancer.

摘要

佩兰长期以来被用于治疗恶心和食欲不振,在中医中被用作利尿剂和解毒剂。最近的研究表明,佩兰具有抗菌、抗氧化和抗糖尿病活性,以及对人白血病细胞的细胞毒性。然而,在无毒浓度下,佩兰水提取物(WEF)对恶性肿瘤细胞的转移和血管生成潜力的影响尚未见报道。在本研究中,我们发现WEF通过下调MMP-9的蛋白水解活性来抑制转移特性,包括非锚定依赖性集落形成、迁移和侵袭。WEF显著降低了NF-κB的激活以及p38和JNK的磷酸化。此外,WEF显著抑制肿瘤诱导的血管生成,通过降低肿瘤中的VEGF来影响HUVEC迁移、HUVECs的管形成以及大鼠主动脉环的微血管芽生。在肺转移模型中,以50mg/kg的剂量每日给予WEF可显著减少C57BL/6J小鼠肺表面静脉注射的B16F10细胞的转移集落。此外,给予WEF的小鼠均未表现出全身毒性。综上所述,我们的结果表明,WEF是一种潜在的治疗性草药产品,可能对控制恶性转移性癌症有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d014/4227014/dd852480a74a/srep06994-f1.jpg

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