诱饵
炎症
背景(考古学)
慢性阻塞性肺病
转录因子
医学
哮喘
免疫学
生物信息学
计算生物学
生物
内科学
受体
遗传学
古生物学
基因
作者
Jessica Katrine Datsyuk,Keshav Raj Paudel,Rashi Rajput,Sofia Kokkinis,Tammam El Sherkawi,Sachin Kumar Singh,Gaurav Gupta,Dinesh Kumar Chellappan,Stewart Yeung,Philip M. Hansbro,Brian G. Oliver,Hélder A. Santos,Kamal Dua,Gabriele De Rubis
标识
DOI:10.1016/j.cbi.2023.110737
摘要
Chronic respiratory diseases like asthma and Chronic Obstructive Pulmonary Disease (COPD) have been a burden to society for an extended period. Currently, there are only preventative treatments in the form of mono- or multiple-drug therapy available to patients who need to utilize it daily. Hence, throughout the years there has been a substantial amount of research in understanding what causes inflammation in the context of these diseases. For example, the transcription factor NFκB has a pivotal role in causing chronic inflammation. Subsequent research has been exploring ways to block the activation of NFκB as a potential therapeutic strategy for many inflammatory diseases. One of the possible ways through which this is probable is the utilisation of decoy oligodeoxynucleotides, which are synthetic, short, single-stranded DNA fragments that mimic the consensus binding site of a targeted transcription factor, thereby functionally inactivating it. However, limitations to the implementation of decoy oligodeoxynucleotides include their rapid degradation by intracellular nucleases and the lack of targeted tissue specificity. An advantageous approach to overcome these limitations involves using nanoparticles as a vessel for drug delivery. In this review, all of those key elements will be explored as to how they come together as an application to treat chronic inflammation in respiratory diseases.
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