Precise treatment of cystic fibrosis – current treatments and perspectives for using CRISPR
| Autor: | Victor Turcanu, Holly Joyce, Josie Colemeadow |
|---|---|
| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
Pharmacology Genetics Cas9 Lumacaftor Biology Bioinformatics medicine.disease Precision medicine Cystic fibrosis Ivacaftor 03 medical and health sciences chemistry.chemical_compound 030104 developmental biology 0302 clinical medicine 030228 respiratory system chemistry Fibrosis Drug Discovery medicine Molecular Medicine CRISPR Stem cell medicine.drug |
| Zdroj: | Expert Review of Precision Medicine and Drug Development. 1:169-180 |
| ISSN: | 2380-8993 |
| DOI: | 10.1080/23808993.2016.1146077 |
| Popis: | Cystic fibrosis (CF) affects about 70,000 individuals worldwide, whose lives are shortened mainly due to chronic pulmonary infections resulting from impaired clearance of abnormally viscous airway mucus. The development of novel drugs targeting specific CFTR gene mutations in a precision medicine framework improved treatment, so that for patients born in 2000–2003 in the UK, the median life expectancy was estimated at around 40 years. Moreover the discovery of the CRISPR (Classes of Regularly Interspaced Palindromic Repeats) and Cas9 (Crispr-ASsociated) nuclease system opened the perspective of specifically correcting the defective CFTR gene as recently demonstrated in a model of intestinal stem cell organoids from CF patients. In the present review, we shall outline the existing state-of-art treatments and the perspectives for the precision treatment of CF opened by CRISPR. |
| Databáze: | OpenAIRE |
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