2018
DOI: 10.18240/ijo.2018.02.04
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miR-211 promotes lens epithelial cells apoptosis by targeting silent mating-type information regulation 2 homolog 1 in age-related cataracts

Abstract: miR-211 is highly expressed in the anterior lens capsules of patients with age-related cataracts. By negatively regulating the expression of SIRT1, miR-211 promotes lens epithelial cell apoptosis and inhibits lens epithelial cell proliferation.

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Cited by 5 publications
(2 citation statements)
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“…MiRNAs, a group of small non-coding regulatory RNAs of 21-23 nucleotides in length, can regulate gene expression through base-pairing with 3' untranslated regions (3’UTR) of their target mRNAs [ 57 ]. Involved in the intracellular processes of cataracts, including apoptosis, proliferation, activity, and oxidative damage [ 50 ], several miRNAs, like miR-34a-5p [ 47 , 48 ], miR-15a [ 49 ], miR-23b-3p [ 51 ], and miR-211-5p [ 58 , 59 ], could be specifically up-expressed in the lens and regulate the apoptosis or oxidative stress of LECs in the formation of ARC in experimental studies. Naturally, we selected circRNAs which were capable of binding these miRNAs based on databases (TargetScan, miRanda, and StarBase).…”
Section: Discussionmentioning
confidence: 99%
“…MiRNAs, a group of small non-coding regulatory RNAs of 21-23 nucleotides in length, can regulate gene expression through base-pairing with 3' untranslated regions (3’UTR) of their target mRNAs [ 57 ]. Involved in the intracellular processes of cataracts, including apoptosis, proliferation, activity, and oxidative damage [ 50 ], several miRNAs, like miR-34a-5p [ 47 , 48 ], miR-15a [ 49 ], miR-23b-3p [ 51 ], and miR-211-5p [ 58 , 59 ], could be specifically up-expressed in the lens and regulate the apoptosis or oxidative stress of LECs in the formation of ARC in experimental studies. Naturally, we selected circRNAs which were capable of binding these miRNAs based on databases (TargetScan, miRanda, and StarBase).…”
Section: Discussionmentioning
confidence: 99%
“…SRA01/04 cells were seeded in a 24-well cell culture plate for 24 h. When 80-85% confluence was reached, Lipofectamine 3000 Transfection Reagent (Invitrogen, CA) was used according to the manufacturer's instructions to transfect the cells with pEGFP-SUMO-1, pEGFP-CBX4, and pFlag-SENP1 individually and pEGFP-C1 was used as control. The subsequent experiments were performed 72 h after the completion of transfection [26].…”
Section: Methodsmentioning
confidence: 99%