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Antisense Oligonucleotide: A Potential Therapeutic Intervention for Chronic Kidney Disease
被引:4
|作者:
Li, Yalin
[1
]
Tan, Yuqin
[2
]
Zhang, Rui
[2
]
Wang, Tao
[3
]
Na, Ning
[2
]
Zheng, Tong
[2
]
Veedu, Rakesh N.
[4
,5
]
Chen, Suxiang
[4
]
机构:
[1] Henan Univ Anim Husb & Econ, Sch Food & Biol Engn, Zhengzhou 450018, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Kidney Transplantat, Guangzhou 510635, Peoples R China
[3] Univ Western Australia, Telethon Kids Inst, Perth 6009, Australia
[4] Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth 6150, Australia
[5] Perron Inst Neurol & Translat Sci, Perth 6001, Australia
来源:
KIDNEY AND DIALYSIS
|
2022年
/
2卷
/
01期
关键词:
chronic kidney disease;
antisense oligonucleotide;
therapeutics;
GROWTH-FACTOR-BETA;
RENIN-ANGIOTENSIN SYSTEM;
LOCKED NUCLEIC-ACID;
APOL1 RISK VARIANTS;
TGF-BETA;
HIGH GLUCOSE;
CHEMICAL-MODIFICATION;
MESANGIAL CELLS;
TRANSFORMING GROWTH-FACTOR-BETA-1;
STIMULATED PROLIFERATION;
D O I:
10.3390/kidneydial2010004
中图分类号:
R5 [内科学];
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号:
1002 ;
100201 ;
摘要:
Chronic kidney disease (CKD) is a global public health issue that places an increasing burden on the healthcare systems of both the developed and developing countries. CKD is a progressive and irreversible condition, affecting approximately 10% of the population worldwide. Patients that have progressed to end-stage renal disease (ESRD) require expensive renal replacement therapy, i.e., dialysis or kidney transplantation. Current CKD therapy largely relies on the use of angiotensin-converting enzyme inhibitors (ACEis) and angiotensin receptor blockers (ARBs). However, these treatments by no means halt the progression of CKD to ESRD. Therefore, the development of new therapies is urgently needed. Antisense oligonucleotide (ASO) has recently attracted considerable interest as a drug development platform. Thus far, eight ASO-based drugs have been granted approval by the US Food and Drug Administration for the treatment of various diseases. Herein, we review the ASOs developed for the identification of CKD-relevant genes and/or the simultaneous development of the ASOs as potential therapeutics towards treating CKD.
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页码:16 / 37
页数:22
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