首页> 美国卫生研究院文献>Molecular Therapy. Nucleic Acids >Antisense Oligonucleotides Targeting Angiogenic Factors as Potential Cancer Therapeutics
【2h】

Antisense Oligonucleotides Targeting Angiogenic Factors as Potential Cancer Therapeutics

机译:靶向血管生成因子的反义寡核苷酸作为潜在的癌症治疗药物

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Cancer is one of the leading causes of death worldwide, and conventional cancer therapies such as surgery, chemotherapy, and radiotherapy do not address the underlying molecular pathologies, leading to inadequate treatment and tumor recurrence. Angiogenic factors, such as EGF, PDGF, bFGF, TGF-β, TGF-α, VEGF, endoglin, and angiopoietins, play important roles in regulating tumor development and metastasis, and they serve as potential targets for developing cancer therapeutics. Nucleic acid-based therapeutic strategies have received significant attention in the last two decades, and antisense oligonucleotide-mediated intervention is a prominent therapeutic approach for targeted manipulation of gene expression. Clinical benefits of antisense oligonucleotides have been recognized by the U.S. Food and Drug Administration, with full or conditional approval of Vitravene, Kynamro, Exondys51, and Spinraza. Herein we review the scope of antisense oligonucleotides that target angiogenic factors toward tackling solid cancers.
机译:癌症是世界范围内主要的死亡原因之一,常规的癌症疗法(例如手术,化学疗法和放射疗法)无法解决潜在的分子病理学问题,从而导致治疗不足和肿瘤复发。 EGF,PDGF,bFGF,TGF-β,TGF-α,VEGF,内皮糖蛋白和血管生成素等血管生成因子在调节肿瘤的发展和转移中起着重要的作用,它们是开发癌症治疗剂的潜在靶标。在过去的二十年中,基于核酸的治疗策略受到了广泛的关注,而反义寡核苷酸介导的干预是靶向治疗基因表达的重要治疗方法。在Vitravene,Kynamro,Exondys51和Spinraza的全部或有条件的批准下,反义寡核苷酸的临床益处已被美国食品和药物管理局认可。在本文中,我们综述了靶向血管生成因子以应对实体癌的反义寡核苷酸的范围。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号