TY - JOUR
T1 - Non-Coding RNAs in the Therapeutic Landscape of Pathological Cardiac Hypertrophy
AU - Silva, Joana
AU - da Costa Martins, Paula A
N1 - Funding Information:
Funding: J.S. was supported by the European Union’s Horizon 2020 research and innovation programme under Marie Skłodowska–Curie grant agreement no. 813716. P.A.d.C.M. was supported by a Dutch Heart Foundation grant (NHS2015T066) and Project Twinning “RESETageing” (952266).
Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/5/31
Y1 - 2022/5/31
N2 - Cardiovascular diseases are a major health problem, and long-term survival for people diagnosed with heart failure is, still, unrealistic. Pathological cardiac hypertrophy largely contributes to morbidity and mortality, as effective therapeutic approaches are lacking. Non-coding RNAs (ncRNAs) arise as active regulators of the signaling pathways and mechanisms that govern this pathology, and their therapeutic potential has received great attention in the last decades. Preclinical studies in large animal models have been successful in ameliorating cardiac hypertrophy, and an antisense drug for the treatment of heart failure has, already, entered clinical trials. In this review, we provide an overview of the molecular mechanisms underlying cardiac hypertrophy, the involvement of ncRNAs, and the current therapeutic landscape of oligonucleotides targeting these regulators. Strategies to improve the delivery of such therapeutics and overcome the actual challenges are, also, defined and discussed. With the fast advance in the improvement of oligonucleotide drug delivery, the inclusion of ncRNAs-targeting therapies for cardiac hypertrophy seems, increasingly, a closer reality.
AB - Cardiovascular diseases are a major health problem, and long-term survival for people diagnosed with heart failure is, still, unrealistic. Pathological cardiac hypertrophy largely contributes to morbidity and mortality, as effective therapeutic approaches are lacking. Non-coding RNAs (ncRNAs) arise as active regulators of the signaling pathways and mechanisms that govern this pathology, and their therapeutic potential has received great attention in the last decades. Preclinical studies in large animal models have been successful in ameliorating cardiac hypertrophy, and an antisense drug for the treatment of heart failure has, already, entered clinical trials. In this review, we provide an overview of the molecular mechanisms underlying cardiac hypertrophy, the involvement of ncRNAs, and the current therapeutic landscape of oligonucleotides targeting these regulators. Strategies to improve the delivery of such therapeutics and overcome the actual challenges are, also, defined and discussed. With the fast advance in the improvement of oligonucleotide drug delivery, the inclusion of ncRNAs-targeting therapies for cardiac hypertrophy seems, increasingly, a closer reality.
KW - non-coding RNAs
KW - cardiac hypertrophy
KW - cardiac pathological remodeling
KW - antisense oligonucleotide-based therapeutics
KW - drug delivery
KW - HEART-FAILURE
KW - IN-VIVO
KW - MYOCARDIAL HYPERTROPHY
KW - SIGNALING PATHWAYS
KW - FAILING HEART
KW - GENE-TRANSFER
KW - PRESSURE
KW - DYSFUNCTION
KW - OVERLOAD
KW - EXPRESSION
U2 - 10.3390/cells11111805
DO - 10.3390/cells11111805
M3 - (Systematic) Review article
C2 - 35681500
SN - 2073-4409
VL - 11
JO - Cells
JF - Cells
IS - 11
M1 - 1805
ER -