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1.
Genes Dis ; 9(3): 610-637, 2022 May.
Artigo em Inglês | MEDLINE | ID: mdl-35782976

RESUMO

Ocular cells like, retinal pigment epithelium (RPE) is a highly specialized pigmented monolayer of post-mitotic cells, which is located in the posterior segment of the eye between neuro sensory retina and vascular choroid. It functions as a selective barrier and nourishes retinal visual cells. As a result of high-level oxygen consumption of retinal cells, RPE cells are vulnerable to chronic oxidative stress and an increased level of reactive oxygen species (ROS) generated from mitochondria. These oxidative stress and ROS generation in retinal cells lead to RPE degeneration. Various sources including mtDNA damage could be an important factor of oxidative stress in RPE. Gene therapy and mitochondrial transfer studies are emerging fields in ocular disease research. For retinal degenerative diseases stem cell-based transplantation methods are developed from basic research to preclinical and clinical trials. Translational research contributions of gene and cell therapy would be a new strategy to prevent, treat and cure various ocular diseases. This review focuses on the effect of oxidative stress in ocular cell degeneration and recent translational researches on retinal degenerative diseases to cure blindness.

2.
Mutat Res Rev Mutat Res ; 776: 23-31, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29807575

RESUMO

Studies on monogenic diseases are considered valuable because they give insights and expand our knowledge on gene function and regulation. Despite all the current advancement in science and technology, a deep understanding and knowledge as to why only those particular genes are affected in a disease is still vague. We also lack profound illumination as to why only certain mutations are seen in a disease. Though useful from a research perspective, a majority of these diseases are lethal resulting in death of the affected individual. Unfortunately, in the fast - growing land of India, the incidence of monogenic diseases is very high with few counter-measures in place. This article encompasses a list of all monogenic diseases ever to be reported in India with special focus on five diseases which has been stated to have the highest incidence in India. Here, we discuss about the limited research carried out in India on these high incidence monogenic diseases, the other diseases related to those genes, the range of treatments available for these diseases in India in contrast to its availability around the world and the need to develop treatment strategies to reduce the mortality and morbidity due to these rare but daunting diseases.


Assuntos
Doenças Genéticas Inatas/epidemiologia , Mutação , Anemia Falciforme/epidemiologia , Anemia Falciforme/genética , Anemia Falciforme/terapia , Doenças Genéticas Inatas/genética , Doenças Genéticas Inatas/terapia , Humanos , Doença de Huntington/epidemiologia , Doença de Huntington/genética , Doença de Huntington/terapia , Incidência , Índia/epidemiologia , Distrofia Muscular de Duchenne/epidemiologia , Distrofia Muscular de Duchenne/genética , Distrofia Muscular de Duchenne/terapia , Neurofibromatose 1/epidemiologia , Neurofibromatose 1/genética , Neurofibromatose 1/terapia , Talassemia beta/epidemiologia , Talassemia beta/genética , Talassemia beta/terapia
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