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Introduction <p>Without histological analysis, the diagnosis and grading of ocular surface squamous neoplasia (OSSN) are challenging in clinical differentiation between malignant and premalignant lesions. This study examined EZH2 expression in corneal and conjunctival epithelial benign hyperplasia, intraepithelial neoplasia (CIN) and squamous cell carcinoma (SCC), and evaluated its relationship with clinicopathological features for diagnostic value.</p> Methods <p>Immunohistochemistry was used to detect EZH2 protein expression in 13 cases of benign corneal and conjunctival epithelial benign&#xa0;hyperplasia, 66 CIN cases, and 26 SCC cases. Statistical analysis was performed to assess the relationship between EZH2 expression and clinicopathological features including age, gender, laterality, tumor diameter and histopathological differentiation.</p> Results <p>The mean age of all patients was 58.4 ± 16.56&#xa0;years, with a predominance of males. A positive EZH2 expression rate as high as 96.2% (101/105) was observed. The EZH2 intensity, ranging from negative (−) to strong (+ + +), showed significant statistical differences among the groups (<i>p</i> = 0.000) and was notably elevated in SCC compared to the other four groups (<i>p</i> &lt; 0.05). Mean immunoreactive scores were 2.15 ± 1.21 for epithelial benign hyperplasia, 2.60 ± 1.95 for CINI, 3.76 ± 3.56 for CINII, 4.47 ± 3.33 for CINIII (including carcinoma in situ), 7.62 ± 2.80 for SCC, respectively. High EZH2 immunoexpression showed no association with age, gender or laterality but correlated significantly with tumor diameter and histopathological differentiation (<i>p</i> = 0.010, <i>p</i> = 0.000).</p> Conclusion <p>EZH2 expression increases with CIN grade and is highest in SCC, indicating its involvement in tumor development and invasion. These findings support its potential as a diagnostic and prognostic indicator, as well as a therapeutic target.</p>

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EZH2 expression in corneal and conjunctival intraepithelial neoplasia and squamous cell carcinoma: a potential marker for diagnosis

  • 期刊论文

  • 发表日期：

    2025年6月1日

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  • Huanhuan Gao,
  • Lijuan Tang,
  • Zhuangling Lin,
  • Shuxia Chen,
  • Wenxin Zhang,
  • Jianxian Lin,
  • Ping Zhang

摘要

Introduction

Without histological analysis, the diagnosis and grading of ocular surface squamous neoplasia (OSSN) are challenging in clinical differentiation between malignant and premalignant lesions. This study examined EZH2 expression in corneal and conjunctival epithelial benign hyperplasia, intraepithelial neoplasia (CIN) and squamous cell carcinoma (SCC), and evaluated its relationship with clinicopathological features for diagnostic value.

Methods

Immunohistochemistry was used to detect EZH2 protein expression in 13 cases of benign corneal and conjunctival epithelial benign hyperplasia, 66 CIN cases, and 26 SCC cases. Statistical analysis was performed to assess the relationship between EZH2 expression and clinicopathological features including age, gender, laterality, tumor diameter and histopathological differentiation.

Results

The mean age of all patients was 58.4 ± 16.56 years, with a predominance of males. A positive EZH2 expression rate as high as 96.2% (101/105) was observed. The EZH2 intensity, ranging from negative (−) to strong (+ + +), showed significant statistical differences among the groups (p = 0.000) and was notably elevated in SCC compared to the other four groups (p < 0.05). Mean immunoreactive scores were 2.15 ± 1.21 for epithelial benign hyperplasia, 2.60 ± 1.95 for CINI, 3.76 ± 3.56 for CINII, 4.47 ± 3.33 for CINIII (including carcinoma in situ), 7.62 ± 2.80 for SCC, respectively. High EZH2 immunoexpression showed no association with age, gender or laterality but correlated significantly with tumor diameter and histopathological differentiation (p = 0.010, p = 0.000).

Conclusion

EZH2 expression increases with CIN grade and is highest in SCC, indicating its involvement in tumor development and invasion. These findings support its potential as a diagnostic and prognostic indicator, as well as a therapeutic target.