Genetic Footprints of Human Papilloma Virus in Ocular Surface Squamous Neoplasia
Journal of Ophthalmic and Optometric Sciences,
Vol. 4 No. 3 (2020),
23 June 2020
,
Page 54-69
https://doi.org/10.22037/joos.v4i3.38970
Abstract
Ocular surface squamous neoplasia (OSSN) after melanoma and lymphoma is the third most common tumor. Including a wide range of ocular malignancy from mild form of epithelial abnormality to invasive squamous cell carcinoma (SCC). Overall, the lesions are different in size but mostly occur in specific tissue called limbus due to the structure of the eye ball, that is the most common area for sunlight exposing. Beside exposure to the sunlight and the UV radiation there are other risk factors and genetic co factors related to the OSSN including immune suppression under the infection to the Human immunodeficiency virus (HIV) or Human papilloma virus (HPV) and also mutation in specific genes regulating cell cycles. However, the exact relation between many of these factors and OSSN has not been revealed and need further researches in this area.
In this review we aimed to study OSSN from different views specially risk factors and a glimpse of genetic insights specially related to human viral genome. Later, categorizing the role of them to pave the way in answering different questions related to the OSSN among types of that. On the other hand, although there is no evidence for straight relation between p53 mutations in OSSN, here we tried to mention the separated pathway’s role in p53 malfunction or disabled in different process leading to cancers namely OSSN.
- Human Immunodeficiency Virus
- Human Papilloma Virus
- ; Ocular Surface Squamous Neoplasia
- p53 Gene
- Squamous Carcinoma
How to Cite
References
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