Skip to main content
. 2020 Sep 3;8:850. doi: 10.3389/fcell.2020.00850

TABLE 1.

Verified circRNAs involved in various ocular diseases.

Ocular diseases circRNAs Expression Functions Related networks References
DR circ_0005015 Upregulated in the plasma, vitreous samples, and FVMs of DR patients. Promote the angiogenic function of HRVECs in vitro. miR-519d-3p-MMP-2/STAT3/XIAP Zhang S.-J. et al., 2017
circHIPK3 Upregulated in HRVECs under HG conditions, DR models, the plasma, vitreous samples, and FVMs of DR patients. Promote the angiogenic function of HRVECs under HG conditions in vitro. Aggravate the DM-induced retinal vascular dysfunction in vivo. c-myb, miR-30a-3p/VEGFC/FZD4/WNT2 Shan et al., 2017
circZNF609 Upregulated in HUVECs under HG conditions, DR models, the plasma, and FVMs of DR patients. Promote the angiogenic function of HUVECs under HG conditions in vitro. Aggravate the DM-induced retinal vascular dysfunction in vivo. miR-615-5p-MEF2A Liu C. et al., 2017
circDMNT3B Downregulated in HRMECs under HG conditions and the FVMs of DR patients. Suppress the angiogenic function of HRMECs under HG conditions in vitro. Ameliorate DM-induced retinal vascular dysfunction and visual damage in vivo. miR-20b-5p-BAMBI Zhu et al., 2019
circPWWP2A Upregulated in retinal pericytes under DM related stresses instead of HRVECs, DR models, and the FVMs of DR patients. Promote the viability, proliferation, antiapoptosis, recruitment toward HRVECs of pericytes under DM-related stresses in vitro but affect HRVECs indirectly via exosomes. Ameliorate DM-induced retinal vascular dysfunction and pericyte dysfunction in vivo. miR-579-angiopoietin1/occludin/SIRT1 Liu et al., 2019
circZNF532 Upregulated in retinal pericytes following DM-related stresses, DR models, and the vitreous samples of DR patients. Promote the viability, proliferation, antiapoptosis, recruitment toward HRVECs of pericytes under DM-related stresses in vitro. Ameliorate DM-induced retinal vascular dysfunction and pericyte dysfunction in vivo. SP1, miR-29a-3p-CSPG4/LOXL2/CDK2 Jiang et al., 2020
ROP circZNF609 Upregulated at the neovascularization stage of OIR models. Aggravate the oxygen-induced retinal vascular dysfunction in vivo. miR-615-5p-MEF2A Liu C. et al., 2017
Exudative AMD circZBTB44 Upregulated in chorioretinal ECs under hypoxic conditions, CNV models, the aqueous humor of nAMD patients. Promote the angiogenic function of chorioretinal vascular ECs under hypoxic conditions in vitro. Aggravate the CNV development in vivo. miR-578-VEGFA/VCAM1 Zhou et al., 2020
Atrophic AMD circNR3C1 Downregulated in RPE cells under oxidative stress and the blood serum of AMD patients. Maintain the RPE phenotypes and functions in vitro and in vivo to prevent AMD progression. miR-382-5p-PTEN-AKT/mTOR Chen X. et al., 2020
Glaucoma circZRANB1 Upregulated in glaucoma model and the aqueous humor of glaucoma patients. Promote the viability, proliferation, and activation of Müller cells directly, but indirectly inhibit RGC function in vitro. Promote the retinal reactive gliosis and glia cell activation (glaucomatous retinal neuropathy) in vivo. miR-217-RUNX2 Wang et al., 2018b
circZNF609 Upregulated in glaucoma model and the aqueous humor of glaucoma patients. Promote the viability, proliferation, and activation of Müller cells directly, but indirectly inhibit RGC function in vitro. Promote the retinal reactive gliosis and glia cell activation (glaucomatous retinal neuropathy), but inhibit RGC survival in vivo. miR-615-METRN Wang et al., 2018a
ARC circHIPK3 Downregulated in lens capsules of patients with various types of ARC. Promote the viability, proliferation, EMT and antiapoptosis upon oxidative stress of HLECs in vitro. miR-193a-3p-CRYAA Liu et al., 2018, 3
Corneal neovascularization circZNF609 Upregulated in the corneal epithelium of corneal neovascularization models. Promote the angiogenic function of HCEKs in vivo. Aggravate the corneal angiogenesis in vivo. miR-184-AKT/β-catenin/VEGF Wu et al., 2020
circKIFAP3 Downregulated in alkali burn-induced neovascularization corneal models and patients’ vascularized corneas. Suppress the angiogenic function of HUVECs in vitro. Zhou Y.-F. et al., 2019
Pterygium circ_0085020 Upregulated in pterygium tissues Promote the viability, proliferation, migration, and antiapoptosis under UV exposure of pterygium fibroblasts and epithelial cells in vitro. Li X.-M. et al., 2018
PVR circ_0043144 Upregulated in serum ERMs of PVR patient. Promote the proliferation, migration, and secretion ability of RPE cells in vitro. Yao et al., 2019
Retinoblastoma circ_0001649 Downregulated in RB cell lines and RB tissues of patients. Suppress the proliferation and antiapoptosis of RB cells in vitro. Suppress the xenograft tumor growth of RB in vivo. AKT/mTOR Xing et al., 2018
circ−0075804 Upregulated in RB cell lines and RB tissues of patients. Promote the proliferation and antiapoptosis of RB cells in vitro. Promote the xenograft tumor growth of RB in vivo. E2F3, HNRNPK Zhao et al., 2020
Conjunctival melanoma circMTUS1 Upregulated in CM tissues. Promote the proliferation of CM cell lines in vitro. Promote the xenograft tumor growth of CM in vivo. Shang et al., 2019

DR, Diabetic retinopathy; FVM, fibrovascular membrane; HRVECs, human retinal vascular ECs; MMP-2, matrix metallopeptidase 2; STAT3, signal transducer and activator of transcription 3; XIAP, x-linked inhibitor Of apoptosis; HIPK3, homeodomain interacting protein kinase 3; HG, high glucose; DM, diabetes mellitus; VEGF, vascular endothelial growth factor; FZD4, frizzled-4; WNT2, Wnt family member 2; ZNF, zinc finger protein; HUVECs, human umbilical vein endothelial cells; MEF2A, myocyte-specific enhancer factor 2A; DMNT3B, DNA (cytosine-5-)-methyltransferase 3 beta; ECs, endothelial cells; HRMECs, human retinal microvascular ECs; BAMBI, BMP and activin membrane bound inhibitor; PWWP2A, PWWP domain containing 2A; SIRT1, sirtuin 1; SP1, specificity protein 1; CSPG4, chondroitin sulfate proteoglycan 4; LOXL2, lysyl oxidase homolog 2; CDK2, cyclin-dependent kinase 2; ROP, Retinopathy of prematurity; OIR, oxygen?induced retinopathy; AMD, Age-related macular degeneration; ZBTB44, zinc finger and BTB domain containing 44; VCAM1, vascular cell adhesion protein 1; nAMD, neovascular AMD; CNV, choroidal neovascularization; NR3C1, nuclear receptor subfamily 3 group C member 1; RPE, retinal pigment epithelium; PTEN, phosphatase and tensin homolog on chromosome ten; mTOR, mammalian target of rapamycin; ZRANB1, zinc finger RAN-binding domain containing 1; RGCs, retinal ganglion cells; RUNX2, runt-related transcription factor 2; METRN, meteorin; ARC, age-related cataracts; EMT, epithelial-mesenchymal transition; HLECs, human lens epithelial cells; CRYAA, crystallin alpha A; HCEKs, corneal epithelial keratinocytes; KIFAP3, kinesin-associated protein 3; UV, ultraviolet radiation; PVR, proliferative vitreoretinopathy; ERMs, epiretinal membranes; RB, retinoblastoma; E2F3, E2F transcription factor 3; HNRNPK, heterogeneous nuclear ribonucleoprotein K; MTUS1, microtubule-associated scaffold protein 1; CM, conjunctival melanoma.