Oligonucleotide-Based Therapies for Renal Diseases

被引:15
作者
Carton-Garcia, Fernando [1 ,2 ]
Saande, Cassondra Jeanette [2 ]
Meraviglia-Crivelli, Daniel [1 ]
Aldabe, Rafael [2 ,3 ]
Pastor, Fernando [1 ,3 ]
机构
[1] Univ Navarra, CIMA, Ctr Appl Med Res, Mol Therapeut Program, Pamplona 31008, Spain
[2] Univ Navarra, Ctr Appl Med Res, CIMA, Gene Therapy & Regulat Gene Express Program, Pamplona 31008, Spain
[3] Recinto Complejo Hosp Navarra, Inst Invest Sanitaria Navarra IDISNA, Pamplona 31008, Spain
关键词
chronic kidney disease; kidney; oligonucleotide therapeutics; kidney delivery; nanocarrier; nanoparticle; aptamer; POLYCYSTIC KIDNEY-DISEASE; IN-VITRO SELECTION; ANTISENSE OLIGONUCLEOTIDES; CHITOSAN/SIRNA NANOPARTICLES; TARGETED MUTATION; DOWN-REGULATION; GENE-TRANSFER; NUCLEIC-ACID; SIRNA; RNA;
D O I
10.3390/biomedicines9030303
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The global burden of chronic kidney disease (CKD) is increasing every year and represents a great cost for public healthcare systems, as the majority of these diseases are progressive. Therefore, there is an urgent need to develop new therapies. Oligonucleotide-based drugs are emerging as novel and promising alternatives to traditional drugs. Their expansion corresponds with new knowledge regarding the molecular basis underlying CKD, and they are already showing encouraging preclinical results, with two candidates being evaluated in clinical trials. However, despite recent technological advances, efficient kidney delivery remains challenging, and the presence of off-targets and side-effects precludes development and translation to the clinic. In this review, we provide an overview of the various oligotherapeutic strategies used preclinically, emphasizing the most recent findings in the field, together with the different strategies employed to achieve proper kidney delivery. The use of different nanotechnological platforms, including nanocarriers, nanoparticles, viral vectors or aptamers, and their potential for the development of more specific and effective treatments is also outlined.
引用
收藏
页数:24
相关论文
共 144 条
[1]   Aptamers: A Review of Their Chemical Properties and Modifications for Therapeutic Application [J].
Adachi, Tatsuo ;
Nakamura, Yoshikazu .
MOLECULES, 2019, 24 (23)
[2]   PHARMACOKINETICS OF ANTISENSE OLIGONUCLEOTIDES [J].
AGRAWAL, S ;
TEMSAMANI, J ;
GALBRAITH, W ;
TANG, JY .
CLINICAL PHARMACOKINETICS, 1995, 28 (01) :7-16
[3]   Targeted fibrillar nanocarbon RNAi treatment of acute kidney injury [J].
Alidori, Simone ;
Akhavein, Nima ;
Thorek, Daniel L. J. ;
Behling, Katja ;
Romin, Yevgeniy ;
Queen, Dawn ;
Beattie, Bradley J. ;
Manova-Todorova, Katia ;
Bergkvist, Magnus ;
Scheinberg, David A. ;
McDevitt, Michael R. .
SCIENCE TRANSLATIONAL MEDICINE, 2016, 8 (331)
[4]  
Anderson Emily, 2008, V442, P45, DOI 10.1007/978-1-59745-191-8_4
[5]   Genome editing with CRISPR-Cas nucleases, base editors, transposases and prime editors [J].
Anzalone, Andrew V. ;
Koblan, Luke W. ;
Liu, David R. .
NATURE BIOTECHNOLOGY, 2020, 38 (07) :824-844
[6]   Nephron segment-specific gene expression using AAV vectors [J].
Asico, Laureano D. ;
Cuevas, Santiago ;
Ma, Xiaobo ;
Jose, Pedro A. ;
Armando, Ines ;
Konkalmatt, Prasad R. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2018, 497 (01) :19-24
[7]   Kidney transplant: New opportunities and challenges [J].
Augustine, Joshua .
CLEVELAND CLINIC JOURNAL OF MEDICINE, 2018, 85 (02) :138-144
[8]   RNA-Based Therapeutics: From Antisense Oligonucleotides to miRNAs [J].
Bajan, Sarah ;
Hutvagner, Gyorgy .
CELLS, 2020, 9 (01)
[9]   SELEX methods on the road to protein targeting with nucleic acid aptamers [J].
Bayat, Payam ;
Nosrati, Rahim ;
Alibolandi, Mona ;
Rafatpanah, Houshang ;
Abnous, Khalil ;
Khedri, Mostafa ;
Ramezani, Mohammad .
BIOCHIMIE, 2018, 154 :132-155
[10]   Bioconjugated Oligonucleotides: Recent Developments and Therapeutic Applications [J].
Benizri, Sebastien ;
Gissot, Arnaud ;
Martin, Andrew ;
Vialet, Brune ;
Grinstaff, Mark W. ;
Barthelemy, Philippe .
BIOCONJUGATE CHEMISTRY, 2019, 30 (02) :366-383