» Articles » PMID: 29259894

Suppression of Corneal Neovascularization by Curcumin Inhibition of Wnt/β-catenin Pathway Activation

Overview
Specialty Ophthalmology
Date 2017 Dec 21
PMID 29259894
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Aim: To investigate whether curcumin suppressed corneal neovascularization (CNV) formation inhibiting activation of Wnt/β-catenin pathway.

Methods: Suture-induced CNV was established on Sprague-Dawley (SD) rats. Curcumin were daily administrated by subconjunctival injection. Phosphorylation of low-density lipoprotein receptor-related protein 6 (LRP6) and nuclear accumulation of β-catenin, two indicators of activated Wnt/β-catenin pathway, were determined by Western-blot analysis in subconfluent/proliferating human microvascular endothelial cells (HMEC) and neovascularized corneas. Wnt3a conditioned medium (WCM) were harvested from Wnt3a expressing cells. WCM-induced cell proliferation and endothelial tubular formation capacity was measured by MTT assay and Matrigel assay, respectively.

Results: Phosphorylation of LRP6 and nuclear accumulation of β-catenin was significantly increased in subconfluent/proliferating endothelial cells. Activation of Wnt/β-catenin pathway by WCM markedly promotes HMEC proliferation and tubular formation. Curcumin inhibited LRP6 phosphorylation and nuclear accumulation of β-catenin. In addition, curcumin attenuated WCM-induced HMEC proliferation and disrupted tubular structure of endothelial cells on Matrigel. Meanwhile curcumin suppressed suture-induced CNV and inhibited LRP6 phosphorylation as well as β-catenin accumulation in SD rats.

Conclusion: Taken together, activation of Wnt/β-catenin pathway could be involved in endothelial proliferation during suture-induced CNV formation and curcumin attenuated CNV formation inhibition of Wnt/β-catenin pathway activation.

Citing Articles

The evolving roles of Wnt signaling in stem cell proliferation and differentiation, the development of human diseases, and therapeutic opportunities.

Yu M, Qin K, Fan J, Zhao G, Zhao P, Zeng W Genes Dis. 2024; 11(3):101026.

PMID: 38292186 PMC: 10825312. DOI: 10.1016/j.gendis.2023.04.042.


The Pathomechanism, Antioxidant Biomarkers, and Treatment of Oxidative Stress-Related Eye Diseases.

Hsueh Y, Chen Y, Tsao Y, Cheng C, Wu W, Chen H Int J Mol Sci. 2022; 23(3).

PMID: 35163178 PMC: 8835903. DOI: 10.3390/ijms23031255.


Small Molecule Wnt Pathway Modulators from Natural Sources: History, State of the Art and Perspectives.

Blagodatski A, Klimenko A, Jia L, Katanaev V Cells. 2020; 9(3).

PMID: 32131438 PMC: 7140537. DOI: 10.3390/cells9030589.


Wnt Signaling in vascular eye diseases.

Wang Z, Liu C, Huang S, Chen J Prog Retin Eye Res. 2018; 70:110-133.

PMID: 30513356 PMC: 6545170. DOI: 10.1016/j.preteyeres.2018.11.008.

References
1.
Kim J, Choi J, Chung S . The effect of curcumin on corneal neovascularization in rabbit eyes. Curr Eye Res. 2010; 35(4):274-80. DOI: 10.3109/02713680903528345. View

2.
Lee K, Hu Y, Ding L, Chen Y, Takahashi Y, Mott R . Therapeutic potential of a monoclonal antibody blocking the Wnt pathway in diabetic retinopathy. Diabetes. 2012; 61(11):2948-57. PMC: 3478529. DOI: 10.2337/db11-0300. View

3.
Sundram V, Chauhan S, Ebeling M, Jaggi M . Curcumin attenuates β-catenin signaling in prostate cancer cells through activation of protein kinase D1. PLoS One. 2012; 7(4):e35368. PMC: 3327669. DOI: 10.1371/journal.pone.0035368. View

4.
Vasireddy V, Chavali V, Joseph V, Kadam R, Lin J, Jamison J . Rescue of photoreceptor degeneration by curcumin in transgenic rats with P23H rhodopsin mutation. PLoS One. 2011; 6(6):e21193. PMC: 3126808. DOI: 10.1371/journal.pone.0021193. View

5.
Ryu M, Cho M, Song J, Yun Y, Choi I, Kim D . Natural derivatives of curcumin attenuate the Wnt/beta-catenin pathway through down-regulation of the transcriptional coactivator p300. Biochem Biophys Res Commun. 2008; 377(4):1304-8. DOI: 10.1016/j.bbrc.2008.10.171. View