Harnessing nucleic acid-based therapeutics for atherosclerotic cardiovascular disease: state of the art

被引:22
|
作者
Lasemi, Fatemeh Vandat [1 ]
Tehran, Maryam Mahjoubin [1 ]
Aghaee-Bakhtiari, Seyed Hamid [1 ,2 ]
Jalili, Amin [1 ]
Jaafari, Mahmoud Reza [3 ,4 ]
Sahebkar, Amirhossein [4 ,5 ,6 ]
机构
[1] Mashhad Univ Med Sci, Fac Med, Dept Med Biotechnol, Mashhad, Razavi Khorasan, Iran
[2] Mashhad Univ Med Sci, Bioinformat Res Grp, Mashhad, Razavi Khorasan, Iran
[3] Mashhad Univ Med Sci, Pharmaceut Technol Inst, Nanotechnol Res Ctr, Mashhad, Razavi Khorasan, Iran
[4] Mashhad Univ Med Sci, Pharmaceut Technol Inst, Biotechnol Res Ctr, Mashhad, Razavi Khorasan, Iran
[5] Mashhad Univ Med Sci, Neurogen Inflammat Res Ctr, Mashhad, Razavi Khorasan, Iran
[6] Mashhad Univ Med Sci, Sch Pharm, Mashhad, Razavi Khorasan, Iran
关键词
APOLIPOPROTEIN C-III; DENSITY-LIPOPROTEIN CHOLESTEROL; B SYNTHESIS INHIBITOR; IMPROVES HEPATIC STEATOSIS; VEIN GRAFT FAILURE; ANTISENSE OLIGONUCLEOTIDES; LDL-CHOLESTEROL; DOUBLE-BLIND; TARGETING APOLIPOPROTEIN(A); INSULIN SENSITIVITY;
D O I
10.1016/j.drudis.2019.04.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dyslipidemia is one of the major but modifiable risk factors for atherosclerotic cardiovascular disease (ACVD). Despite the accessibility of statins and other lipid-lowering drugs, the burden of ACVD is still high globally, highlighting the need for new therapeutic approaches. Nucleic acid-based technologies, including antisense oligonucleotides (ASOs), small interfering (si)RNAs, miRNAs, and decoys, are emerging therapeutic modalities for the treatment of ACVD. These technologies aim to degrade gene mRNA transcripts to decrease the levels of atherogenic lipoproteins. Using gene-silencing approaches, the levels of atherogenic lipoproteins can be decreased by targeting proteins that have key roles in lipoprotein metabolism. Here, we highlight preclinical and clinical findings using these approaches for the development of novel therapies against ACVD.
引用
收藏
页码:1116 / 1131
页数:16
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