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Investigation of MicroRNA Expression in Anterior Lens Capsules of Senile Cataract Patients and MicroRNA Differences According to the Cataract Type

PURPOSE: We investigated the microRNAs (miRNAs) expression in the anterior lens capsules of patients with senile cataract and compared it to that in the anterior lens capsules of healthy controls. Moreover, we compared the differences in miRNAs expression according to the types of cataracts. METHODS...

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Autores principales: Kim, Yu Jeong, Lee, Won June, Ko, Byoung-Woo, Lim, Han Woong, Yeon, Yeji, Ahn, Seong Joon, Lee, Byung Ro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7888284/
https://www.ncbi.nlm.nih.gov/pubmed/34003899
http://dx.doi.org/10.1167/tvst.10.2.14
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author Kim, Yu Jeong
Lee, Won June
Ko, Byoung-Woo
Lim, Han Woong
Yeon, Yeji
Ahn, Seong Joon
Lee, Byung Ro
author_facet Kim, Yu Jeong
Lee, Won June
Ko, Byoung-Woo
Lim, Han Woong
Yeon, Yeji
Ahn, Seong Joon
Lee, Byung Ro
author_sort Kim, Yu Jeong
collection PubMed
description PURPOSE: We investigated the microRNAs (miRNAs) expression in the anterior lens capsules of patients with senile cataract and compared it to that in the anterior lens capsules of healthy controls. Moreover, we compared the differences in miRNAs expression according to the types of cataracts. METHODS: Individual lens epithelium samples were collected from 33 senile patients and 10 controls. The cataract patients were classified into cortical, nuclear, posterior and anterior subcapsular and mixed. The expression of 12 different miRNAs in lens epithelium was measured using real-time polymerase chain reaction and compared between the senile cataract patients and controls. The differences of miRNA levels according to cataract type were analyzed. RESULTS: The expression levels of let-7g-5p, miR-23a-3p, miR-23b-3p, and miR-125a-5p were significantly upregulated in patients with senile cataract when compared with those in the control group (P < 0.05). The expressions of let-7a-5p, let-7d-5p, miR-16-5p and miR-22-3p were significantly downregulated in the senile cataracts (P < 0.05). Let-7a-5p, let-7d-5p, let-7g-5p and mir-23b-3p had significant difference in expression between nuclear and anterior subcapsular cataracts. CONCLUSIONS: The eight differentially expressed miRNAs may be involved in the pathogenesis of senile cataract, in particular, related to oxidative stress and autophagy. TRANSLATIONAL RELEVANCE: We infer that several miRNAs in lens epithelial cells are promising candidate biomarkers of senile cataracts.
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spelling pubmed-78882842021-02-22 Investigation of MicroRNA Expression in Anterior Lens Capsules of Senile Cataract Patients and MicroRNA Differences According to the Cataract Type Kim, Yu Jeong Lee, Won June Ko, Byoung-Woo Lim, Han Woong Yeon, Yeji Ahn, Seong Joon Lee, Byung Ro Transl Vis Sci Technol Article PURPOSE: We investigated the microRNAs (miRNAs) expression in the anterior lens capsules of patients with senile cataract and compared it to that in the anterior lens capsules of healthy controls. Moreover, we compared the differences in miRNAs expression according to the types of cataracts. METHODS: Individual lens epithelium samples were collected from 33 senile patients and 10 controls. The cataract patients were classified into cortical, nuclear, posterior and anterior subcapsular and mixed. The expression of 12 different miRNAs in lens epithelium was measured using real-time polymerase chain reaction and compared between the senile cataract patients and controls. The differences of miRNA levels according to cataract type were analyzed. RESULTS: The expression levels of let-7g-5p, miR-23a-3p, miR-23b-3p, and miR-125a-5p were significantly upregulated in patients with senile cataract when compared with those in the control group (P < 0.05). The expressions of let-7a-5p, let-7d-5p, miR-16-5p and miR-22-3p were significantly downregulated in the senile cataracts (P < 0.05). Let-7a-5p, let-7d-5p, let-7g-5p and mir-23b-3p had significant difference in expression between nuclear and anterior subcapsular cataracts. CONCLUSIONS: The eight differentially expressed miRNAs may be involved in the pathogenesis of senile cataract, in particular, related to oxidative stress and autophagy. TRANSLATIONAL RELEVANCE: We infer that several miRNAs in lens epithelial cells are promising candidate biomarkers of senile cataracts. The Association for Research in Vision and Ophthalmology 2021-02-11 /pmc/articles/PMC7888284/ /pubmed/34003899 http://dx.doi.org/10.1167/tvst.10.2.14 Text en Copyright 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Article
Kim, Yu Jeong
Lee, Won June
Ko, Byoung-Woo
Lim, Han Woong
Yeon, Yeji
Ahn, Seong Joon
Lee, Byung Ro
Investigation of MicroRNA Expression in Anterior Lens Capsules of Senile Cataract Patients and MicroRNA Differences According to the Cataract Type
title Investigation of MicroRNA Expression in Anterior Lens Capsules of Senile Cataract Patients and MicroRNA Differences According to the Cataract Type
title_full Investigation of MicroRNA Expression in Anterior Lens Capsules of Senile Cataract Patients and MicroRNA Differences According to the Cataract Type
title_fullStr Investigation of MicroRNA Expression in Anterior Lens Capsules of Senile Cataract Patients and MicroRNA Differences According to the Cataract Type
title_full_unstemmed Investigation of MicroRNA Expression in Anterior Lens Capsules of Senile Cataract Patients and MicroRNA Differences According to the Cataract Type
title_short Investigation of MicroRNA Expression in Anterior Lens Capsules of Senile Cataract Patients and MicroRNA Differences According to the Cataract Type
title_sort investigation of microrna expression in anterior lens capsules of senile cataract patients and microrna differences according to the cataract type
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7888284/
https://www.ncbi.nlm.nih.gov/pubmed/34003899
http://dx.doi.org/10.1167/tvst.10.2.14
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