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一种具有内在抗肿瘤活性的新型阳离子脂质,以促进TRAIL DNA的基因治疗。

A novel cationic lipid with intrinsic antitumor activity to facilitate gene therapy of TRAIL DNA.

作者信息

Luo Cong, Miao Lei, Zhao Yi, Musetti Sara, Wang Yuhua, Shi Kai, Huang Leaf

机构信息

Division of Molecular Pharmaceutics and Center for Nanotechnology in Drug Delivery, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA; Department of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.

Division of Molecular Pharmaceutics and Center for Nanotechnology in Drug Delivery, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.

出版信息

Biomaterials. 2016 Sep;102:239-48. doi: 10.1016/j.biomaterials.2016.06.030. Epub 2016 Jun 16.

Abstract

Metformin (dimethylbiguanide) has been found to be effective for the treatment of a wide range of cancer. Herein, a novel lipid (1,2-di-(9Z-octadecenoyl)-3-biguanide-propane (DOBP)) was elaborately designed by utilizing biguanide as the cationic head group. This novel cationic lipid was intended to act as a gene carrier with intrinsic antitumor activity. When compared with 1,2-di-(9Z-octadecenoyl)-3-trimethylammonium-propane (DOTAP), a commercially available cationic lipid with a similar structure, the blank liposomes consisting of DOBP showed much more potent antitumor effects than DOTAP in human lung tumor xenografts, following an antitumor mechanism similar to metformin. Given its cationic head group, biguanide, DOBP could encapsulate TNF-related apoptosis-inducing ligand (TRAIL) plasmids into Lipid-Protamine-DNA (LPD) nanoparticles (NPs) for systemic gene delivery. DOBP-LPD-TRAIL NPs demonstrated distinct superiority in delaying tumor progression over DOTAP-LPD-TRAIL NPs, due to the intrinsic antitumor activity combined with TRAIL-induced apoptosis in the tumor. These results indicate that DOBP could be used as a versatile and promising cationic lipid for improving the therapeutic index of gene therapy in cancer treatment.

摘要

二甲双胍(二甲基双胍)已被发现对多种癌症的治疗有效。在此,通过利用双胍作为阳离子头部基团,精心设计了一种新型脂质(1,2 - 二 -(9Z - 十八碳烯酰基)- 3 - 双胍丙烷(DOBP))。这种新型阳离子脂质旨在作为一种具有内在抗肿瘤活性的基因载体。与结构相似的市售阳离子脂质1,2 - 二 -(9Z - 十八碳烯酰基)- 3 - 三甲基铵丙烷(DOTAP)相比,由DOBP组成的空白脂质体在人肺肿瘤异种移植模型中显示出比DOTAP更强的抗肿瘤作用,其抗肿瘤机制与二甲双胍相似。鉴于其阳离子头部基团双胍,DOBP可以将肿瘤坏死因子相关凋亡诱导配体(TRAIL)质粒封装到脂质 - 鱼精蛋白 - DNA(LPD)纳米颗粒(NPs)中用于全身基因递送。由于内在抗肿瘤活性与TRAIL诱导的肿瘤细胞凋亡相结合,DOBP - LPD - TRAIL NPs在延缓肿瘤进展方面表现出比DOTAP - LPD - TRAIL NPs明显的优势。这些结果表明,DOBP可作为一种通用且有前景的阳离子脂质,用于提高癌症治疗中基因治疗的治疗指数。

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