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Summary of the 2014 MD Anderson International Meeting in Gynecologic Oncology: Emerging therapies in gynecologic cancer

机译:2014年MD安德森国际妇科肿瘤学国际会议摘要:妇科癌症的新兴疗法

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The 2014 MD Anderson International Meeting in Gynecologic Oncology: Emerging Therapies in Gynecologic Cancer, held in Madrid, Spain (February 19-21,2014), brought together over 500 attendees from 26 countries. This conference report summarizes the key presentations on clinical and translational research from this meeting. RNA interference strategies in future therapeutics of ovarian cancer Since the discovery of RNA interference (RNAi), there has been a huge expansion of the basic understanding of RNAi biology as well as the development of novel technologies for therapeutic applications. Conventional approaches such as small molecule inhibitors cannot be used against many targets due to a variety of factors. Also, most small molecule inhibitors lack specificity and can be associated with intolerable side effects. The use of siRNA is preferable to other approaches such as antisense oligomers due to a longer duration of target inhibition and reduced toxicity. One of the major challenges related to the use of RNAi therapeutics pertains to achieving highly efficient systemic delivery without off-target effects. We have developed biocompatible nanoparti-cle delivery systems (e.g., l,2-dioleoyl-sn-glycero-3-phosphatidylcho-line (DOPC)) that are safe and effective. EPHARNA is an EphA2-targeted siRNA packaged into DOPC nanoliposomes, which is nearing phase I clinical testing. Additional delivery platforms such as chitosan and rHDL nanoparticles have been developed to allow unique applications for siRNA delivery such as targeting stromal genes as well as enhanced hepatic delivery.
机译:2014年2月19日至21日在西班牙马德里举行的2014年MD安德森国际妇科肿瘤学国际会议:妇科癌症的新兴疗法聚集了26个国家的500多名与会者。该会议报告总结了这次会议上有关临床和转化研究的主要演讲。卵巢癌未来治疗中的RNA干扰策略自从发现RNA干扰(RNAi)以来,人们对RNAi生物学的基本理解以及用于治疗应用的新技术的发展已大大扩展。由于多种因素,诸如小分子抑制剂之类的常规方法不能用于许多目标。而且,大多数小分子抑制剂缺乏特异性,并且可能与不可忍受的副作用有关。 siRNA的使用优于其他方法,例如反义寡聚物,因为靶标抑制作用的持续时间更长且毒性降低。与RNAi治疗剂的使用有关的主要挑战之一涉及在没有脱靶效应的情况下实现高效的全身递送。我们已经开发出了安全有效的生物相容性纳米颗粒递送系统(例如1,2-二油酰基-sn-甘油-3-磷脂酰胆碱(DOPC))。 EPHARNA是包装在DOPC纳米脂质体中的,靶向EphA2的siRNA,已接近I期临床测试。已经开发了诸如壳聚糖和rHDL纳米粒子的其他传递平台,以实现siRNA传递的独特应用,例如靶向基质基因以及增强的肝传递。

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