Therapeutic siRNAs: small molecules with bigger function
In the realm of molecular medicine, therapeutic small-interfering RNA (siRNA) is a promising class of molecules with exciting new opportunities in healthcare. An essential component of RNA interference (RNAi) is siRNA. In clinical setup, siRNA may be engineered to specifically target genes linked to...
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Format: | Article |
Language: | English |
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Manipal College of Medical Sciences, Pokhara
2024-01-01
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Series: | Asian Journal of Medical Sciences |
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Online Access: | https://www.nepjol.info/index.php/AJMS/article/view/59983 |
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author | Ruby Dhar Arun Kumar Subhradip Karmakar |
author_facet | Ruby Dhar Arun Kumar Subhradip Karmakar |
author_sort | Ruby Dhar |
collection | DOAJ |
description | In the realm of molecular medicine, therapeutic small-interfering RNA (siRNA) is a promising class of molecules with exciting new opportunities in healthcare. An essential component of RNA interference (RNAi) is siRNA. In clinical setup, siRNA may be engineered to specifically target genes linked to certain diseases, providing a focused and accurate method of modulating gene expression. Many important factors characterize the use of therapeutic siRNA. Target gene expression is selectively silenced by therapeutic siRNA through the use of the RNAi pathway. Guided by corresponding messenger RNA (mRNA) sequences, the double-stranded siRNA molecule is integrated into the RNA-induced silencing complex (RISC). This mechanism causes translational repression or mRNA cleavage, which in turn causes the relevant protein to be downregulated. Therapeutic siRNA is a promising avenue in several areas. siRNA can be used in oncology to target oncogenes or other important regulators, inhibiting cancer cell proliferation. Furthermore, by modifying the expression of genes linked to disease, siRNA may be used to treat viral infections, neurological conditions, and other rare and hereditary diseases. The selectivity of therapeutic siRNA is one of its main advantages. siRNA sequences can be engineered and customized to target specific genes linked to different diseases like cancer or genetic disorders. This focused strategy improves the accuracy of the therapeutic intervention and reduces off-target effects. In a recent article by Nissen et al., siRNA targeting LP(a) in a trial with 48 participants without cardiovascular disease and with lipoprotein(a) concentrations of 75 nmol/L or greater (or ≥30 mg/dL), was used to evaluate its tolerability and efficacy to reduce LP(a). Results showed that Lepodisiran was found to be well tolerated and resulted in dose-dependent, long-lasting reduction in serum lipoprotein(a) concentrations in phase 1 trial with elevated lipoprotein(a) levels. Therapeutic siRNA-based diagnosis is rapidly advancing, and several siRNA-based medications are now entering clinical trials. These trials aim to assess the pharmacokinetics, safety, and effectiveness of siRNA therapeutics in human subjects, offering crucial new information about their potential as a treatment option. Despite the therapeutic potential of siRNA, clinical translation of siRNA faces a challenge in its effective delivery. Naked siRNA molecules are more likely to degrade with a poor half-life and poor cellular uptake. Therefore, to increase the stability and delivery of therapeutic siRNA to target cells, a variety of delivery systems, such as lipid nanoparticles, viral vectors, and polymer-based carriers, are being investigated. |
first_indexed | 2024-03-08T18:00:58Z |
format | Article |
id | doaj.art-20b95fc98561469fbc6ff558e6466c38 |
institution | Directory Open Access Journal |
issn | 2467-9100 2091-0576 |
language | English |
last_indexed | 2024-03-08T18:00:58Z |
publishDate | 2024-01-01 |
publisher | Manipal College of Medical Sciences, Pokhara |
record_format | Article |
series | Asian Journal of Medical Sciences |
spelling | doaj.art-20b95fc98561469fbc6ff558e6466c382024-01-02T01:16:55ZengManipal College of Medical Sciences, PokharaAsian Journal of Medical Sciences2467-91002091-05762024-01-0115112https://doi.org/10.3126/ajms.v15i1.59983Therapeutic siRNAs: small molecules with bigger functionRuby Dhar 0https://orcid.org/0000-0003-3600-6554Arun Kumar 1https://orcid.org/0000-0002-8800-0296Subhradip Karmakar 2https://orcid.org/0000-0002-4757-8729Scientist, Room 3020, Department of Biochemistry, All India Institute of Medical Sciences, New Delhi Professor, Department of Biochemistry, Narayan Medical College, Gopal Narayan Singh University, Sasaram, Bihar, India Additional Professor, Department of Biochemistry, All India Institute of Medical Sciences, New Delhi, India In the realm of molecular medicine, therapeutic small-interfering RNA (siRNA) is a promising class of molecules with exciting new opportunities in healthcare. An essential component of RNA interference (RNAi) is siRNA. In clinical setup, siRNA may be engineered to specifically target genes linked to certain diseases, providing a focused and accurate method of modulating gene expression. Many important factors characterize the use of therapeutic siRNA. Target gene expression is selectively silenced by therapeutic siRNA through the use of the RNAi pathway. Guided by corresponding messenger RNA (mRNA) sequences, the double-stranded siRNA molecule is integrated into the RNA-induced silencing complex (RISC). This mechanism causes translational repression or mRNA cleavage, which in turn causes the relevant protein to be downregulated. Therapeutic siRNA is a promising avenue in several areas. siRNA can be used in oncology to target oncogenes or other important regulators, inhibiting cancer cell proliferation. Furthermore, by modifying the expression of genes linked to disease, siRNA may be used to treat viral infections, neurological conditions, and other rare and hereditary diseases. The selectivity of therapeutic siRNA is one of its main advantages. siRNA sequences can be engineered and customized to target specific genes linked to different diseases like cancer or genetic disorders. This focused strategy improves the accuracy of the therapeutic intervention and reduces off-target effects. In a recent article by Nissen et al., siRNA targeting LP(a) in a trial with 48 participants without cardiovascular disease and with lipoprotein(a) concentrations of 75 nmol/L or greater (or ≥30 mg/dL), was used to evaluate its tolerability and efficacy to reduce LP(a). Results showed that Lepodisiran was found to be well tolerated and resulted in dose-dependent, long-lasting reduction in serum lipoprotein(a) concentrations in phase 1 trial with elevated lipoprotein(a) levels. Therapeutic siRNA-based diagnosis is rapidly advancing, and several siRNA-based medications are now entering clinical trials. These trials aim to assess the pharmacokinetics, safety, and effectiveness of siRNA therapeutics in human subjects, offering crucial new information about their potential as a treatment option. Despite the therapeutic potential of siRNA, clinical translation of siRNA faces a challenge in its effective delivery. Naked siRNA molecules are more likely to degrade with a poor half-life and poor cellular uptake. Therefore, to increase the stability and delivery of therapeutic siRNA to target cells, a variety of delivery systems, such as lipid nanoparticles, viral vectors, and polymer-based carriers, are being investigated.https://www.nepjol.info/index.php/AJMS/article/view/59983sirnaclinical uselp(a)selectivitysirna delivery |
spellingShingle | Ruby Dhar Arun Kumar Subhradip Karmakar Therapeutic siRNAs: small molecules with bigger function Asian Journal of Medical Sciences sirna clinical use lp(a) selectivity sirna delivery |
title | Therapeutic siRNAs: small molecules with bigger function |
title_full | Therapeutic siRNAs: small molecules with bigger function |
title_fullStr | Therapeutic siRNAs: small molecules with bigger function |
title_full_unstemmed | Therapeutic siRNAs: small molecules with bigger function |
title_short | Therapeutic siRNAs: small molecules with bigger function |
title_sort | therapeutic sirnas small molecules with bigger function |
topic | sirna clinical use lp(a) selectivity sirna delivery |
url | https://www.nepjol.info/index.php/AJMS/article/view/59983 |
work_keys_str_mv | AT rubydhar therapeuticsirnassmallmoleculeswithbiggerfunction AT arunkumar therapeuticsirnassmallmoleculeswithbiggerfunction AT subhradipkarmakar therapeuticsirnassmallmoleculeswithbiggerfunction |