Antisense Therapy for Cardiovascular Diseases

被引:9
|
作者
Phillips, M. Ian [1 ]
Costales, Jessica [1 ]
Lee, Robert J. [1 ]
Oliveira, Edilamar [2 ]
Burns, Andrew B. [1 ]
机构
[1] Keck Grad Inst, Claremont, CA 91711 USA
[2] Univ Sao Paulo, Sch Phys Educ & Sport, Lab Biochem & Mol Biol Exercise, BR-05508 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Antisense oligonucleotides; metabolic syndrome; hypertension; hyperlipidemia; Kynamro (TM); Eteplirsen (TM); exon skipping; RECEPTOR MESSENGER-RNA; VIRAL VECTOR DELIVERY; HIGH BLOOD-PRESSURE; MOLECULAR-MECHANISMS; PROLONGED REDUCTION; GENE-THERAPY; HYPERTENSION; INHIBITION; OLIGONUCLEOTIDES; MICE;
D O I
10.2174/1381612821666150803150402
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Antisense oligonucleotide therapy is a growing field in cardiac, metabolic, and muscular diseases. This precision therapy allows for treatment of diseases due to specific genetic defects. Antisense has few side effects and is relatively long lasting. Some major targets for antisense therapy include hyperglycemia, hyperlipidemia, and hypercholesterolemia. ISIS Pharmaceuticals recently commercialized antisense therapy with Kynamro (TM) (Mipomersen) for homozygous familial hypercholesterolemia, opening the door for other antisense oligonucleotides for lowering proteins. Antisense can also be used to increase proteins that are inhibited by mutant exons. Sarepta is testing exon 51 skipping in the mutated dystrophin gene, which if successful will help affected individuals walk, and may help restore some cardiac function. These antisense techniques also could be applied as antisense therapies to overcome gene defects in hypertension, heart disease, muscular defects and metabolic syndrome.
引用
收藏
页码:4417 / 4426
页数:10
相关论文
共 50 条
  • [1] Antisense oligonucleotides as a powerful molecular strategy for gene therapy in cardiovascular diseases
    Tomita, N
    Morishita, R
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2004, 10 (07) : 797 - 803
  • [2] Antisense Therapy for Infectious Diseases
    Buthelezi, Lwanda Abonga
    Pillay, Shandre
    Ntuli, Noxolo Nokukhanya
    Gcanga, Lorna
    Guler, Reto
    [J]. CELLS, 2023, 12 (16)
  • [3] Antisense Based Therapy for Rare Neurological Diseases
    Bennett, C. Frank
    [J]. ANNALS OF NEUROLOGY, 2023, 94 : S272 - S273
  • [4] Antisense RNA therapy in inherited metabolic diseases
    Perez, B.
    Rincon, A.
    Aguado, C.
    Vega, A.
    Perez-Cerda, C.
    Merinero, B.
    Rodriguez-Pascau, L.
    Coll, M. J.
    Vilageliu, L.
    Grinberg, D.
    Desviat, L. R.
    Ugarte, M.
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2008, 31 : 152 - 152
  • [5] HDL therapy for cardiovascular diseases
    Franceschini, G.
    [J]. ATHEROSCLEROSIS SUPPLEMENTS, 2006, 7 (03) : 301 - 301
  • [6] Gene therapy for cardiovascular diseases
    Brugada, R
    Roberts, R
    [J]. EXPERT OPINION ON THERAPEUTIC PATENTS, 2000, 10 (09) : 1385 - 1393
  • [7] Testosterone therapy and cardiovascular diseases
    Cittadini, Antonio
    Isidori, Andrea M.
    Salzano, Andrea
    [J]. CARDIOVASCULAR RESEARCH, 2022, 118 (09) : 2039 - 2057
  • [8] Gene therapy for cardiovascular diseases
    Elizabeth G. Nabel
    [J]. Journal of Nuclear Cardiology, 1999, 6 : 69 - 75
  • [9] The potential role of antisense oligodeoxynucleotide therapy for cardiovascular disease
    Phillips, MI
    Galli, SM
    Mehta, JL
    [J]. DRUGS, 2000, 60 (02) : 239 - 248
  • [10] Gene therapy for cardiovascular diseases
    YlaHerttuala, S
    [J]. ANNALS OF MEDICINE, 1996, 28 (02) : 89 - 93