Models of Congenital Adrenal Hyperplasia for Gene Therapies Testing

Author:

Glazova Olga12ORCID,Bastrich Asya1,Deviatkin Andrei12ORCID,Onyanov Nikita2ORCID,Kaziakhmedova Samira2,Shevkova Liudmila12,Sakr Nawar12ORCID,Petrova Daria1,Vorontsova Maria V.12ORCID,Volchkov Pavel12ORCID

Affiliation:

1. Gene Editing Laboratory, Endocrinology Research Centre, 117292 Moscow, Russia

2. Genome Engineering Laboratory, Moscow Institute of Physics and Technology, 141700 Dolgoprudniy, Russia

Abstract

The adrenal glands are important endocrine organs that play a major role in the stress response. Some adrenal glands abnormalities are treated with hormone replacement therapy, which does not address physiological requirements. Modern technologies make it possible to develop gene therapy drugs that can completely cure diseases caused by mutations in specific genes. Congenital adrenal hyperplasia (CAH) is an example of such a potentially treatable monogenic disease. CAH is an autosomal recessive inherited disease with an overall incidence of 1:9500–1:20,000 newborns. To date, there are several promising drugs for CAH gene therapy. At the same time, it remains unclear how new approaches can be tested, as there are no models for this disease. The present review focuses on modern models for inherited adrenal gland insufficiency and their detailed characterization. In addition, the advantages and disadvantages of various pathological models are discussed, and ways of further development are suggested.

Funder

Ministry of Science and Higher Education of the Russian Federation

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. A Humanized and Viable Animal Model for Congenital Adrenal Hyperplasia–CYP21A2-R484Q Mutant Mouse;International Journal of Molecular Sciences;2024-05-07

2. Congenital Adrenal Hyperplasia;Pediatrics in Review;2024-02-01

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