2型糖尿病
胰岛素抵抗
疾病
医学
寡核苷酸
下调和上调
糖尿病
药品
药理学
生物信息学
食品药品监督管理局
2型糖尿病
基因
生物
计算生物学
内分泌学
内科学
遗传学
作者
Suxiang Chen,Nabayet Sbuh,Rakesh N. Veedu
出处
期刊:Nucleic Acid Therapeutics
[Mary Ann Liebert]
日期:2020-10-07
卷期号:31 (1): 39-57
被引量:22
标识
DOI:10.1089/nat.2020.0891
摘要
Type 2 diabetes (T2D) is a chronic metabolic disorder characterized by persistent hyperglycemia resulting from inefficient signaling and insufficient production of insulin. Conventional management of T2D has largely relied on small molecule-based oral hypoglycemic medicines, which do not halt the progression of the disease due to limited efficacy and induce adverse effects as well. To this end, antisense oligonucleotide has attracted immense attention in developing antidiabetic agents because of their ability to downregulate the expression of disease-causing genes at the RNA and protein level. To date, seven antisense agents have been approved by the United States Food and Drug Administration for therapies of a variety of human maladies, including genetic disorders. Herein, we provide a comprehensive review of antisense molecules developed for suppressing the causative genes believed to be responsible for insulin resistance and hyperglycemia toward preventing and treating T2D.
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