Abstract
Pterygium is one of the most common ocular surface diseases, and characterized by inflammatory infiltrates, proliferation, fibrosis, angiogenesis, and extracellular matrix breakdown. We investigated the association of polymorphisms in the RHO genes RHOA, RHOB, RHOC, RHOD, and RND3 (RHOE). The results of this study demonstrate for the first time the association of RHO genes with the pterygium. We displayed that the RHO gene polymorphisms were significantly associated with pterygium in the Turkish population.
1. Introduction
Pterygium, one of the most common eye disorders, is the growth of subepithelial fibrovascular tissue starting from the bulbar conjunctiva onto the cornea [1]. It is characterized by an altered basal epithelial cell proliferation, vascularization, and invasion of the adjacent corneal epithelium. Independent risk factors include age, male sex, rural life, and exposure to sun or ultraviolet (UV) light [2]. The pathogenesis of this disease remains unclear, but evidences suggest that UV light is a major contributor in the formation of pterygia [3]. Genetic and environmental factors are important in the etiology of pterygium. Genetic factors are thought to have a role in the development of pterygium, but the most of the molecular mechanisms leading to pterygium are still unknown. Pterygium formation impairs vision, limits eye movements, and can cause eye irritation, foreign body sensation, and dryness. Currently, surgery is the only effective treatment for pterygium, but recurrences are common [4]. Rho proteins are members of the Ras superfamily of small GTPases that play critical roles in many cellular processes including actin dynamics, vesicular trafficking, gene transcription, cytoskeletal reorganization, cell-cycle progression, differentiation, adhesion, and migration [5]. These proteins also contribute to pathological processes such as cancer cell migration, invasion, metastasis, fibrosis, inflammation, angiogenesis, and wound repair. Rho proteins consist of a family of 20 intracellular signaling molecules including RhoA, RhoB, RhoC, RhoD, and RhoE [6]. Involvement of the genetic variants of RHO genes in pterygium development has not been examined yet. Therefore, the purpose of the present study was to investigate possible associations between RHO gene polymorphisms and pterygium in a Turkish population.
2. Experimental Procedure
A total of 379 patients, diagnosed as pterygium at the Ophthalmology Clinic of the Gaziantep University Hospital and 324 unrelated healthy controls, were included to this study. Routine ophthalmologic evaluations were performed on all subjects. A control group of age- and sex-matched individuals was chosen randomly from a sample of patients admitted to the ophthalmology outpatient department for routine ophthalmic examinations, refractive errors, blepharitis, conjunctivitis, burning, itching, presbyopia, or senile cataracts. This study was approved by the local Ethics Committee. Peripheral venous blood samples (5 mL) were obtained and collected in sterile siliconized vacutainer tubes with 2 mg/mL disodium ethylenediaminetetraacetic acid. Genomic DNA was extracted from whole peripheral blood samples with salting-out method and stored at −20 °C until analysis [7]. Genomic DNAs were analyzed in all patients and controls using the dynamic array system (Fluidigm, South San Francisco, CA, USA) as previously described [8]. A 96.96 dynamic array on the BioMark HD system (Fluidigm, South San Francisco, CA, USA) was used for detection of polymorphism. The Digital PCR Analysis software (Fluidigm, South San Francisco, CA, USA) was used to process the data after the reaction. In the present study, 15 single nucleotide polymorphisms (SNP) were assayed. For calculation of the significance of differences in allele frequencies, the Chi-square test (with Yate’s correction) or Fisher’s exact test was used. A statistical comparison of two groups was performed with unpaired Student t-test. The original significance level was set at a p value of 0.05. Bonferroni correction for multiple testing was used for polymorphism studies, and a P value of <0.0033 (0.05/15) was considered statistically significant.
3. Results
The mean age and gender of the patients (50.9 ± 12.4 years, 51.5% female) and control (52.1 ± 14.7 years, 51.9% female) groups were similar (p > 0.05). Table 1 shows the distributions of genotypes and alleles between the case and control groups. There were marked associations for the genotype frequencies of the RHOA gene rs6784820 polymorphism between the patients and the control group. Both genotype and allele frequencies of RHOB gene rs2602160, rs62121967, rs11541350 SNPs, RHOC gene rs2306937 and rs11102522 SNPs, RHOD gene rs61891303 and rs7112925 SNPs, and RND3 (RHOE) gene rs13418763 and rs1441982 SNPs were significantly associated with pterygium. There were no marked associations with the other 5 RHO polymorphisms (RhoA gene rs2177268, rs2878298 SNPs, RhoC gene rs2999156 SNP, RhoD gene rs3923203 SNP, RhoE gene rs1528428 SNP) studied (Table 1, p > 0.0033).
Table 1.
Genotype and allele distributions of RHO gene polymorphisms in pterygium patients and control groups.
4. Discussion
This is the first study to examine the association of the RHO gene polymorphisms with the risk of developing pterygium. In this case-control study, we showed that the RHO gene polymorphisms were significantly associated with pterygium in the Turkish population. Therefore, RHO gene variants could be a risk factor for developing pterygium, and may increase susceptibility to pterygium in Turkish patients.
Acknowledgments
This study is supported by a project (SBAG 114S562) from the TUBITAK, Ankara, Turkey.
Conflicts of Interest
The authors declare no conflict of interest.
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