학술논문

Somatic Mutations within Myocilin due to Aging May Be a Potential Risk Factor for Glaucoma.
Document Type
article
Source
Genes. 15(2)
Subject
aging
glaucoma
somatic mutation
Humans
Cytoskeletal Proteins
Eye Proteins
Glaucoma
Glaucoma
Open-Angle
Glycoproteins
Mutation
Language
Abstract
Glaucoma is a chronic optic neuropathy that leads to irreversible vision loss. Aging and family history are the two most important risk factors of glaucoma. One of the most studied genes involved in the onset of open-angle glaucoma is myocilin (MYOC). About 105 germline mutations within MYOC are known to be associated with glaucoma and result in endoplasmic reticulum (ER) stress, which leads to trabecular meshwork (TM) cell death and subsequent intraocular pressure (IOP) elevation. However, only about 4% of the population carry these mutations. An analysis of MYOC somatic cancer-associated mutations revealed a notable overlap with pathogenic glaucoma variants. Because TM cells have the potential to accumulate somatic mutations at a rapid rate due to ultraviolet (UV) light exposure, we propose that an accumulation of somatic mutations within MYOC is an important contributor to the onset of glaucoma.