Gene Therapy and Gene Editing for Cancer Therapeutics

Shubhjeet Mandal, P. Tiwari
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Abstract

Over the past two decades, developments in human genomics have shown that cancer in the host genome is caused by somatic aberration. This discovery has inspired interest among cancer researchers; many are now using genetic engineering therapeutic methods to improve the cancer regression and seeking a possible cure for the disease. The large gene therapy sector offers a variety of therapies which are likely to become effective in preventing cancer deaths. The latest clinical trials of third generation vaccines for a wide variety of cancers have produced promising results. Cancer virotherapy, which uses viral particles replicating within the cancer cell, is an emerging method of treatment which shows great promise. The latest developments in gene editing techniques, such as CRISPR, Cas9, TALENs, and ZFNs, are being used to help to make cancer a manageable condition. Gene therapy is expected to play a significant role in potential cancer therapy as a part of a multi-modality procedure.
癌症治疗的基因治疗和基因编辑
在过去的二十年中,人类基因组学的发展表明,宿主基因组中的癌症是由体细胞畸变引起的。这一发现激发了癌症研究人员的兴趣;许多人现在正在使用基因工程治疗方法来改善癌症的消退,并寻求治疗这种疾病的可能方法。庞大的基因治疗部门提供了多种可能有效预防癌症死亡的疗法。针对多种癌症的第三代疫苗的最新临床试验产生了令人鼓舞的结果。癌症病毒疗法是一种新兴的治疗方法,它利用病毒颗粒在癌细胞内复制,显示出巨大的前景。基因编辑技术的最新发展,如CRISPR、Cas9、TALENs和ZFNs,正被用于帮助使癌症成为一种可控的疾病。基因治疗作为多模式治疗的一部分,有望在潜在的癌症治疗中发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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