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阳离子脂质体共载基因与化疗药物用于癌症治疗的研究进展 被引量:14

Research progress in co-delivery of gene and chemotherapy drugs with cationic liposome carrier for cancer therapy
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摘要 尽管传统癌症化疗方法已取得明显的进展,但由于化疗药物的多药耐药性及毒副作用限制其应用。为了克服多药耐药性,需要增加药物剂量及用药次数,反而导致更强的毒副作用,最终限制了化疗药物的临床使用。阳离子脂质体作为新型基因与药物传递系统,近年来备受众多研究学者的青睐。最重要的是阳离子脂质体共载基因与化疗药物进行联合治疗具有良好的协同增效作用,主要是外源基因可以沉默相关基因的表达,且提高胞内化疗药物浓度。该方法可以减少药物的使用剂量以达到相同治疗效果。从某种程度上克服了传统化疗的主要限制。因此在未来癌症治疗中,共载基因与药物联合治疗递送体系将发挥更大作用,特别有望用于多药耐药肿瘤中的临床治疗。 Despite recent advances in conventional therapeutic approaches for cancer,the efficacy of chemotherapy for cancer is limited due to the drug resistance and toxic side effects during treatment.To overcome drug resistance,higher doses of the toxic chemotherapy drugs are frequently administered,thus leading to even severe adverse side effects,which have limited their clinical application.Cationic liposome as a novel non-viral carrier for co-delivery of gene and chemotherapy drugs in cancer gene therapy has already attracted more and more attention in recent years.Most importantly,this combined strategy can generate a significant synergistic effect,which can silence the related gene expression and increase the concentration of the intracellular chemotherapy drugs.This approach allows the use of a much lower dose of the chemotherapy drugs to achieve same therapeutic effect,which may have the potential for overcoming some major limitations of the conventional chemotherapy.In conclusion,co-delivery of gene and chemotherapy drugs with cationic liposome delivery system will play a vital role in the future and especially could be a promising clinical treatment for drug-resistant tumors.
出处 《药学学报》 CAS CSCD 北大核心 2012年第8期986-992,共7页 Acta Pharmaceutica Sinica
基金 国家自然科学基金资助项目(31170939 81171471 51103049) 福建省自然科学基金资助项目(2010J05027 2011J01223)
关键词 阳离子脂质体 基因 化疗药物 共载 肿瘤治疗 cationic liposome; gene; chemotherapy drug; co-delivery; cancer therapy
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  • 1赵光,叶玲,张瑾峰,王喆.生物材料聚酰胺-胺树状大分子合成及其体外细胞相容性评价[J].中国生物医学工程学报,2005,24(6):750-754. 被引量:4
  • 2Feron O.Targeting the tumor vascular compartment to improve conventional cancer therapy[J].Trends Pharmacol Sci,2004,25:546-542.
  • 3Ran S,Downes A,Thorpe PE.Increased exposure of anionic phospholipids on the surface of tumor blood vessels[J].Cancer Res,2002,62:6132-6140.
  • 4Mounkes LC,Zhong W,Cipres-Palacin G,et al.Proteoglycans mediate cationic liposome-DNA complex-based gene delivery in vitro and in vivo[J].J Biol Chem,1998,273:26164-26170.
  • 5Augustin HG,Kozian DH,Johnson RC.Differentiation of endothelial cells:analysis of the constructive and activated endothelial cell phenotypes[J].Bioessays,1994,16:901-906.
  • 6Campbell RB,Fukumura D,Brown EB,et al.Cationic charge determines the distribution of liposomes between the vascular and extravascular compartments of tumors[J].Cancer Res,2002,62:6831-6836.
  • 7Tozera GM,Ameer-Begb SM,Bakera J,et al.Intravital imaging of tumour vascular networks using multi-photon fluorescence microscopy[J].Adv Drug Deliv Rev,2005,57:135-152.
  • 8Michaelis U,Teifel M.Cationic lipid complexes to target tumor endothelium[M] // Siemann DW.Vascular-Targeted Therapies Oncology.New York:John Wiley & Sons,2006:221-245.
  • 9Strieth S,Eichhorn ME,Sauer B,et al.Neovascular targeting chemotherapy:encapsulation of paclitaxel in cationic liposomes impairs functional tumor microvasculature[J].Int J Cancer,2004,110:117-124.
  • 10Schmitt-Sody M,Strieth S,Krasnici S,et al.Neovascular targeting therapy:paclitaxel encapsulated in cationic liposomes improves antitumoral efficacy[J].Clin Cancer Res,2003,9:2335-2341.

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