Engineering Closed-Loop, Autoregulatory Gene Circuits for Osteoarthritis Cell-Based Therapies.
Rhima M ColemanPublished in: Current rheumatology reports (2022)
Several gene circuits have been developed that reprogram cells to autonomously target inflammation, and their efficacy has been demonstrated in chondrocytes and stem cells. Gene circuits developed for metabolic disorders, such as those targeting insulin resistance and obesity, also have the potential to mitigate the impact of these conditions on OA onset and/or progression. Despite the strides made in characterizing the inflammatory environment of the OA joint, our incomplete understanding of how the multiple regulators interact to control signal transduction, gene transcription, and translation to protein limits the development of targeted disease-modifying therapeutics. Continuous advances in targeted genome editing, combined with online toolkits that simplify the design and production of gene circuits, have the potential to accelerate the discovery and clinical application of multi-target gene circuits with disease-modifying properties for the treatment of OA.
Keyphrases
- copy number
- stem cells
- genome wide
- insulin resistance
- genome editing
- genome wide identification
- crispr cas
- type diabetes
- oxidative stress
- metabolic syndrome
- small molecule
- knee osteoarthritis
- cancer therapy
- adipose tissue
- cell death
- social media
- gene expression
- mesenchymal stem cells
- health information
- combination therapy
- weight gain
- signaling pathway
- binding protein
- glycemic control
- cell cycle arrest
- amino acid