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Aberrant expression of genes and proteins in pterygium and their implications in the pathogenesis
Qing-Yang Feng1, Zi-Xuan Hu2, Xi-Ling Song2
1Department of Ophthalmology, the First Affiliated Hospital of Jinan University, Guangzhou 510630, Guangdong Province, China.
Abstract:
Pterygium is a common ocular surface disease induced by a variety of factors. The exact pathogenesis of pterygium remains unclear. Numbers of genes and proteins are discovered in pterygium and they function differently in the occurrence and development of this disease. We searched the Web of Science and PubMed throughout history for literatures about the subject. The keywords we used contain pterygium, gene, protein, angiogenesis, fibrosis, proliferation, inflammation, pathogenesis and therapy. In this review, we summarize the aberrant expression of a range of genes and proteins in pterygium compared with normal conjunctiva or cornea, including growth factors, matrix metalloproteinases and tissue inhibitors of metalloproteinases, interleukins, tumor suppressor genes, proliferation related proteins, apoptosis related proteins, cell adhesion molecules, extracellular matrix proteins, heat shock proteins and tight junction proteins. We illustrate their possible mechanisms in the pathogenesis of pterygium as well as the related intervention based on them for pterygium therapy.
Insights
Pterygium pathogenesis involves numerous genes and proteins affecting growth, inflammation, and tissue remodeling. Understanding these molecular players offers new therapeutic avenues for this common eye condition.
Area of Science:
- Ophthalmology
- Molecular Biology
- Genetics
Background:
- Pterygium is a prevalent ocular surface disease with complex and incompletely understood pathogenesis.
- Numerous genes and proteins are implicated in pterygium development, influencing key biological processes.
Purpose of the Study:
- To review and summarize the aberrant expression of genes and proteins in pterygium.
- To elucidate their potential roles in pterygium pathogenesis and therapeutic interventions.
Main Methods:
- Comprehensive literature search of Web of Science and PubMed databases.
- Keywords included pterygium, gene, protein, angiogenesis, fibrosis, proliferation, inflammation, pathogenesis, and therapy.
- Systematic review and synthesis of findings on molecular alterations in pterygium.
Main Results:
- Aberrant expression of growth factors, matrix metalloproteinases (MMPs), tissue inhibitors of metalloproteinases (TIMPs), interleukins, tumor suppressor genes, proliferation and apoptosis-related proteins, cell adhesion molecules, extracellular matrix proteins, heat shock proteins, and tight junction proteins were identified.
- These molecular changes contribute to key pathological features such as angiogenesis, fibrosis, and inflammation.
Conclusions:
- The identified genes and proteins offer insights into pterygium pathogenesis.
- Targeting these molecular pathways presents potential therapeutic strategies for pterygium treatment.
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