Le Bao T, Raguraman Prithi, Kosbar Tamer R, Fletcher Susan, Wilton Steve D, Veedu Rakesh N
Centre for Comparative Genomics, Murdoch University, Murdoch, WA 6150, Australia; Perron Institute for Neurological and Translational Science, Nedlands, WA 6009, Australia.
Perron Institute for Neurological and Translational Science, Nedlands, WA 6009, Australia.
Mol Ther Nucleic Acids. 2019 Mar 1;14:142-157. doi: 10.1016/j.omtn.2018.11.007. Epub 2018 Nov 20.
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.
癌症是全球主要死因之一,而传统的癌症治疗方法,如手术、化疗和放疗,并未针对潜在的分子病理学问题,导致治疗不充分和肿瘤复发。血管生成因子,如表皮生长因子(EGF)、血小板衍生生长因子(PDGF)、碱性成纤维细胞生长因子(bFGF)、转化生长因子-β(TGF-β)、转化生长因子-α(TGF-α)、血管内皮生长因子(VEGF)、内皮糖蛋白和血管生成素,在调节肿瘤发展和转移中发挥重要作用,它们是开发癌症治疗药物的潜在靶点。在过去二十年中,基于核酸的治疗策略受到了广泛关注,反义寡核苷酸介导的干预是一种用于靶向操纵基因表达的重要治疗方法。反义寡核苷酸的临床益处已得到美国食品药品监督管理局的认可,Vitravene、Kynamro、Exondys51和Spinraza已获得完全或有条件批准。在此,我们综述了针对血管生成因子以治疗实体癌的反义寡核苷酸的研究范围。