TY - JOUR
T1 - Recent trends of NFkB decoy oligodeoxynucleotide-based nanotherapeutics in lung diseases
AU - Mehta, Meenu
AU - Paudel, Keshav Raj
AU - Shukla, Shakti Dhar
AU - Allam, Venkata Sita Rama Raju
AU - Kannaujiya, Vinod Kumar
AU - Panth, Nisha
AU - Das, Amlan
AU - Parihar, Vipan Kumar
AU - Chakraborty, Amlan
AU - Ali, Md Khadem
AU - Jha, Niraj Kumar
AU - Xenaki, Dikaia
AU - Su, Qian Peter
AU - Wich, Peter Richard
AU - Adams, Jon
AU - Hansbro, Philip Michael
AU - Chellappan, Dinesh Kumar
AU - Oliver, Brian Gregory George
AU - Dua, Kamal
N1 - Funding Information:
Authors would like to thank Graduate School of Health (GSH), University of Technology Sydney for GSH Seed grant 2021 . Meenu Mehta is supported by the International Research Training Program Scholarship (IRTP), Australia. Keshav Raj Paudel is supported by a fellowship from Prevent Cancer Foundation (PCF) and the International Association for the Study of Lung Cancer (IASLC) foundation, USA. Kamal Dua is supported by a project grant from Sydney Partnership for Health, Education, Research and Enterprise (SPHERE) for the TRIPLE I CAG Secondment/Exchange grant.
Funding Information:
Authors would like to thank Graduate School of Health (GSH), University of Technology Sydney for GSH Seed grant 2021. Meenu Mehta is supported by the International Research Training Program Scholarship (IRTP), Australia. Keshav Raj Paudel is supported by a fellowship from Prevent Cancer Foundation (PCF) and the International Association for the Study of Lung Cancer (IASLC) foundation, USA. Kamal Dua is supported by a project grant from Sydney Partnership for Health, Education, Research and Enterprise (SPHERE) for the TRIPLE I CAG Secondment/Exchange grant.
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/9/10
Y1 - 2021/9/10
N2 - Nuclear factor κB (NFκB) is a unique protein complex that plays a major role in lung inflammation and respiratory dysfunction. The NFκB signaling pathway, therefore becomes an avenue for the development of potential pharmacological interventions, especially in situations where chronic inflammation is often constitutively active and plays a key role in the pathogenesis and progression of the disease. NFκB decoy oligodeoxynucleotides (ODNs) are double-stranded and carry NFκB binding sequences. They prevent the formation of NFκB-mediated inflammatory cytokines and thus have been employed in the treatment of a variety of chronic inflammatory diseases. However, the systemic administration of naked decoy ODNs restricts their therapeutic effectiveness because of their poor pharmacokinetic profile, instability, degradation by cellular enzymes and their low cellular uptake. Both structural modification and nanotechnology have shown promising results in enhancing the pharmacokinetic profiles of potent therapeutic substances and have also shown great potential in the treatment of respiratory diseases such as asthma, chronic obstructive pulmonary disease and cystic fibrosis. In this review, we examine the contribution of NFκB activation in respiratory diseases and recent advancements in the therapeutic use of decoy ODNs. In addition, we also highlight the limitations and challenges in use of decoy ODNs as therapeutic molecules, cellular uptake of decoy ODNs, and the current need for novel delivery systems to provide efficient delivery of decoy ODNs. Furthermore, this review provides a common platform for discussion on the existence of decoy ODNs, as well as outlining perspectives on the latest generation of delivery systems that encapsulate decoy ODNs and target NFκB in respiratory diseases.
AB - Nuclear factor κB (NFκB) is a unique protein complex that plays a major role in lung inflammation and respiratory dysfunction. The NFκB signaling pathway, therefore becomes an avenue for the development of potential pharmacological interventions, especially in situations where chronic inflammation is often constitutively active and plays a key role in the pathogenesis and progression of the disease. NFκB decoy oligodeoxynucleotides (ODNs) are double-stranded and carry NFκB binding sequences. They prevent the formation of NFκB-mediated inflammatory cytokines and thus have been employed in the treatment of a variety of chronic inflammatory diseases. However, the systemic administration of naked decoy ODNs restricts their therapeutic effectiveness because of their poor pharmacokinetic profile, instability, degradation by cellular enzymes and their low cellular uptake. Both structural modification and nanotechnology have shown promising results in enhancing the pharmacokinetic profiles of potent therapeutic substances and have also shown great potential in the treatment of respiratory diseases such as asthma, chronic obstructive pulmonary disease and cystic fibrosis. In this review, we examine the contribution of NFκB activation in respiratory diseases and recent advancements in the therapeutic use of decoy ODNs. In addition, we also highlight the limitations and challenges in use of decoy ODNs as therapeutic molecules, cellular uptake of decoy ODNs, and the current need for novel delivery systems to provide efficient delivery of decoy ODNs. Furthermore, this review provides a common platform for discussion on the existence of decoy ODNs, as well as outlining perspectives on the latest generation of delivery systems that encapsulate decoy ODNs and target NFκB in respiratory diseases.
KW - Decoy oligodeoxynucleotide
KW - Novel delivery systems
KW - Nuclear factor kappa B
KW - Respiratory disorder
U2 - 10.1016/j.jconrel.2021.08.010
DO - 10.1016/j.jconrel.2021.08.010
M3 - Article
C2 - 34375688
AN - SCOPUS:85112352735
SN - 0168-3659
VL - 337
SP - 629
EP - 644
JO - Journal of Controlled Release
JF - Journal of Controlled Release
ER -