纳米载体
小干扰RNA
卵巢癌
基因沉默
基因敲除
遗传增强
RNA干扰
癌症研究
体内
癌症
医学
生物信息学
药理学
生物
核糖核酸
基因
生物技术
内科学
药品
生物化学
作者
Eshrat Gharaei Fathabadi,Andrew N. Shelling,Raida Al‐Kassas
标识
DOI:10.1517/17425247.2012.683173
摘要
INTRODUCTION: Novel therapeutic strategies have been investigated for ovarian cancer to reduce toxicity and to improve outcomes for patients. Short interfering RNA (siRNA), which directs the sequence-specific degradation of target mRNA and provides specificity of gene knockdown, represents a unique class of potential therapeutics for ovarian cancer. However, siRNA molecules are rapidly degraded in plasma and are unable to passively diffuse through cellular membranes. Nanocarriers can efficiently protect siRNA from in vivo degradation and are able to deliver these active macromolecules to tumor cells even after intravenous administration. AREAS COVERED: Strategies of gene therapy and the role of siRNA in ovarian cancer treatment are introduced, followed by an overview of nanocarriers for siRNA delivery, the advantages of the systems and the types of targeting to tumor cells. Classes of nanocarriers for delivery of siRNA, their functionalities and modalities are discussed with emphasis on the promising vehicles. EXPERT OPINION: Gene silencing therapy based on siRNA represents a possible opportunity for treatment of ovarian cancer patients. However, this approach requires selection of suitable nanocarriers that can safely and effectively deliver siRNA to the target site to induce its effect. Very little work has been done in this field; therefore, it is a good direction for future development.
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