Title:Advancements in CRISPR-Based Therapies for Genetic Modulation in Neurodegenerative Disorders
Volume: 25
Issue: 1
Author(s): Bharat Bhushan, Kuldeep Singh*, Shivendra Kumar and Anjali Bhardwaj
Affiliation:
- Department of Pharmacology, Rajiv Academy for Pharmacy, Mathura, Uttar Pradesh, India
Keywords:
CRISPR, gene editing, neurodegeneration, genetic modulation, therapeutic development, neurodegenerative disorders.
Abstract: Neurodegenerative disorders pose significant challenges in the realm of healthcare, as
these conditions manifest in complex, multifaceted ways, often attributed to genetic anomalies.
With the emergence of CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)
technology, a new frontier has been unveiled in the quest for targeted, precise genetic manipulation.
This abstract explores the recent advancements and potential applications of CRISPR-based
therapies in addressing genetic components contributing to various neurodegenerative disorders.
The review delves into the foundational principles of CRISPR technology, highlighting its unparalleled
ability to edit genetic sequences with unprecedented precision. In addition, it talks about the
latest progress in using CRISPR to target specific genetic mutations linked to neurodegenerative
diseases like Huntington's disease, Alzheimer's disease, amyotrophic lateral sclerosis (ALS), and
Parkinson's disease. It talks about the most important studies and trials that show how well and
safely CRISPR-based therapies work. This shows how this technology can change genetic
variants that cause diseases. Notably, the discussion emphasizes the challenges and ethical considerations
associated with the implementation of CRISPR in clinical settings, including off-target effects,
delivery methods, and long-term implications. Furthermore, the article explores the
prospects and potential hurdles in the widespread application of CRISPR technology for treating
neurodegenerative disorders. It touches upon the need for continued research, improved delivery
mechanisms, and ethical frameworks to ensure responsible and equitable access to these groundbreaking
therapies.