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1
Stimulation of autophagic activity in human glioma cells by anti-proliferative ardipusilloside I isolated from Ardisia pusilla.从矮地茶中分离得到的具有抗增殖活性的 Ardipusilloside I 可刺激人神经胶质瘤细胞自噬活性。
Life Sci. 2014 Aug 6;110(1):15-22. doi: 10.1016/j.lfs.2014.06.016. Epub 2014 Jun 28.
2
Prognostic value of erythrocyte sedimentation rate and C-reactive protein in the blood of patients with glioma.红细胞沉降率和 C 反应蛋白在脑胶质瘤患者血液中的预后价值。
Anticancer Res. 2014 Jan;34(1):339-47.
3
Tumor cells and neovasculature dual targeting delivery for glioblastoma treatment.肿瘤细胞和新生血管双重靶向递药治疗脑胶质母细胞瘤。
Biomaterials. 2014 Feb;35(7):2374-82. doi: 10.1016/j.biomaterials.2013.11.076. Epub 2013 Dec 15.
4
Ardipusilloside I induces apoptosis by regulating Bcl-2 family proteins in human mucoepidermoid carcinoma Mc3 cells.刺五加苷I通过调节人黏液表皮样癌Mc3细胞中的Bcl-2家族蛋白诱导细胞凋亡。
BMC Complement Altern Med. 2013 Nov 21;13:322. doi: 10.1186/1472-6882-13-322.
5
Modulation of peripheral immune responses by paclitaxel-ifosfamide-cisplatin chemotherapy in advanced non-small-cell lung cancer.紫杉醇-异环磷酰胺-顺铂化疗对晚期非小细胞肺癌外周免疫反应的调节。
J Cancer Res Clin Oncol. 2013 Dec;139(12):1995-2003. doi: 10.1007/s00432-013-1514-1. Epub 2013 Sep 26.
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Therapy targets in glioblastoma and cancer stem cells: lessons from haematopoietic neoplasms.胶质母细胞瘤和癌症干细胞的治疗靶点:来自造血肿瘤的启示。
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Collaborative overexpression of matrix metalloproteinase-1 and vascular endothelial growth factor-C predicts adverse prognosis in patients with gliomas.基质金属蛋白酶-1 和血管内皮生长因子-C 的协同过表达预测胶质瘤患者的不良预后。
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8
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Mediators Inflamm. 2013;2013:979748. doi: 10.1155/2013/979748. Epub 2013 Jun 24.
9
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10
p38 MAPK inhibitors attenuate pro-inflammatory cytokine production and the invasiveness of human U251 glioblastoma cells.p38 MAPK 抑制剂可减弱人 U251 神经胶质瘤细胞促炎细胞因子的产生和侵袭性。
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使用可生物降解植入物局部递送穿心莲苷I对脑肿瘤生长的疗效。

Efficacy of local delivery of ardipusilloside I using biodegradable implants against cerebral tumor growth.

作者信息

Dang Huan, Wang Ji, Cheng Jiang-Xue, Wang Peng-Yuan, Wang Ying, Cheng Li-Fei, Du Caigan, Wang Xiao-Juan

机构信息

State Key Laboratory of Military Stomatology, Department of Pharmacy, School of Stomatology, The Fourth Military Medical University Xi'an, Shaanxi 710032, China.

Department of Pharmacy, Shaanxi University of Chinese Medicine Xianyang, Shaanxi 712046, China.

出版信息

Am J Cancer Res. 2014 Dec 15;5(1):243-54. eCollection 2015.

PMID:25628934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4300708/
Abstract

Ardipusilloside I (ADS-I) is a natural compound that can be isolated from the Chinese medicinal herb Ardisiapusilla A.DC, and has been reported to inhibit the growth of glioblastoma cells in cultures. This study was designed to test its efficacy by the delivery using biodegradable implants against glioblastoma in vivo. ADS-I was incorporated into polymer microspheres, which were prepared by a mixture of poly (D, L-lactic acid) and poly (D, L-lactic-co-glycolic acid) polymers and then fabricated into wafers. The anti-glioma activities of ADS-I-loaded wafers were examined by methylthiazol tetrazolium (MTT) assay in cultured rat C6 glioma cells, and by magnetic resonance imaging (MRI) and survival monitoring in C6 glioma-bearing rats. Here, we showed that ADS-I-loaded wafers sustained ADS-I release in vitro for 36 days in Higuchi model of kinetics, and had the same cytotoxic activity as ADS-I in the solution against the growth of C6 glioma cells in cultures. In C6 glioma-bearing rats, ADS-I wafer implants inhibited tumor growth in a dose-dependent matter, and were more effective than the same dosage of ADS-I in the solution. The tumor suppression efficacies of ADS-I wafer implants were positively correlated with an increase in tumor cell apoptosis and prolonged animal survival, and were associated with a decrease in vascular endothelial growth factor, C-reactive protein, tumor necrosis factor-α and interleukin-6, and an increase in interleukin-2 expression. In conclusion, this study demonstrates significant efficacy of local delivery of ADS-I using polymer implants against glioma tumor growth in vivo, suggesting the potential of ADS-I-loaded wafers for glioma treatment.

摘要

紫金牛苷 I(ADS-I)是一种天然化合物,可从中国草药紫金牛中分离得到,据报道它能抑制培养的胶质母细胞瘤细胞的生长。本研究旨在通过使用可生物降解植入物在体内递送 ADS-I 来测试其疗效。将 ADS-I 掺入聚合物微球中,聚合物微球由聚(D,L-乳酸)和聚(D,L-乳酸-共-乙醇酸)聚合物的混合物制备,然后制成薄片。通过甲基噻唑基四氮唑(MTT)法在培养的大鼠 C6 胶质瘤细胞中检测负载 ADS-I 的薄片的抗胶质瘤活性,并通过磁共振成像(MRI)和对荷 C6 胶质瘤大鼠的生存监测来评估。在此,我们表明,在 Higuchi 动力学模型中,负载 ADS-I 的薄片在体外可持续释放 ADS-I 达 36 天,并且在溶液中与 ADS-I 对培养的 C6 胶质瘤细胞生长具有相同的细胞毒性活性。在荷 C6 胶质瘤大鼠中,负载 ADS-I 的薄片植入物以剂量依赖的方式抑制肿瘤生长,并且比相同剂量的溶液中的 ADS-I 更有效。负载 ADS-I 的薄片植入物的肿瘤抑制效果与肿瘤细胞凋亡增加和动物存活时间延长呈正相关,并且与血管内皮生长因子、C 反应蛋白、肿瘤坏死因子-α 和白细胞介素-6 的减少以及白细胞介素-2 表达的增加有关。总之,本研究证明了使用聚合物植入物局部递送 ADS-I 对体内胶质瘤肿瘤生长具有显著疗效,表明负载 ADS-I 的薄片在胶质瘤治疗方面具有潜力。