Recent Advances in Ocular Oncology

A special issue of Biomedicines (ISSN 2227-9059). This special issue belongs to the section "Cancer Biology and Oncology".

Deadline for manuscript submissions: closed (30 June 2024) | Viewed by 1067

Special Issue Editor


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Guest Editor
Chaim Sheba Medical Center Israel, Tel Aviv-Yafo, Israel
Interests: ophthalmology; ocular oncology

Special Issue Information

Dear Colleagues,

From all tumors in the human tumor eye make up to 4.3%. Eye neoplasms can affect all parts of the eye, and can be a benign tumor or a malignant tumor (cancer). In recent years, advances in the identification of new intraocular biomarkers for eye tumors, new diagnostic imaging techniques, and some new insights into treatment modalities have contributed to the development of ophthalmic oncology. Nevertheless, the local treatment of some eye tumors remains a challenging topic. The treatment of ocular tumors is generally a multi-specialty effort, requiring coordination between the ophthalmologist and other medical specialties involved in the diagnosis and treatment of ocular and orbital tumors.

On this special ocular oncology issue, updated information on different ophthalmic tumors will be provided, including  pathogenesis, counteracting strategies, diagnosis, prognosis and current options of treatment. Original research articles and review articles are invited. 

Dr. Vicktoria Vishnevskia-Dai
Guest Editor

Manuscript Submission Information

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Keywords

  • eye diseases
  • ocular oncology
  • uveal melanoma
  • retinoblastoma
  • iris and conjuctival tumors

Published Papers (2 papers)

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Research

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16 pages, 5263 KiB  
Article
The Impact of DAXX, HJURP and CENPA Expression in Uveal Melanoma Carcinogenesis and Associations with Clinicopathological Parameters
by Alexandros Pergaris, Georgia Levidou, Georgios Mandrakis, Maria-Ioanna Christodoulou, Michail V. Karamouzis, Jerzy Klijanienko and Stamatios Theocharis
Biomedicines 2024, 12(8), 1772; https://doi.org/10.3390/biomedicines12081772 - 6 Aug 2024
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Abstract
Uveal melanomas (UMs) represent rare malignant tumors associated with grim prognosis for the majority of patients. DAXX (Death Domain-Associated Protein), HJURP (Holliday Junction Recognition Protein) and CENPA (Centromere Protein A) proteins are implicated in epigenetic mechanisms, now in the spotlight of cancer research [...] Read more.
Uveal melanomas (UMs) represent rare malignant tumors associated with grim prognosis for the majority of patients. DAXX (Death Domain-Associated Protein), HJURP (Holliday Junction Recognition Protein) and CENPA (Centromere Protein A) proteins are implicated in epigenetic mechanisms, now in the spotlight of cancer research to better understand the molecular background of tumorigenesis. Herein, we investigated their expression in UM tissues using immunohistochemistry and explored possible correlations with a multitude of clinicopathological and survival parameters. The Cancer Genome Atlas Program (TCGA) was used for the investigation of their mRNA levels in UM cases. Nuclear DAXX expression correlated with an advanced T-stage (p = 0.004), while cytoplasmic expression marginally with decreased disease-free survival (DFS) (p = 0.084). HJURP nuclear positivity also correlated with advanced T-status (p = 0.054), chromosome 3 loss (p = 0.042) and increased tumor size (p = 0.03). More importantly, both nuclear and cytoplasmic HJURP immunopositivity correlated with decreased overall survival (OS) (p = 0.011 and 0.072, respectively) and worse DFS (p = 0.071 and 0.019, respectively). Lastly, nuclear CENPA overexpression was correlated with presence of irido-corneal angle involvement (p = 0.015) and loss of chromosome 3 (p = 0.041). Nuclear and cytoplasmic CENPA immunopositivity associated with decreased OS (p = 0.028) and DFS (p = 0.018), respectively. HJURP and CENPA mRNA overexpression exhibited strong association with tumor epithelioid histology and was linked to worse prognosis. Our results show the compounding role of DAXX, HJURP and CENPA in UM carcinogenesis, designating them as potential biomarkers for assessing prognosis and possible targets for novel therapeutic interventions. Full article
(This article belongs to the Special Issue Recent Advances in Ocular Oncology)
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Review

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29 pages, 5692 KiB  
Review
Uveal Melanoma: Comprehensive Review of Its Pathophysiology, Diagnosis, Treatment, and Future Perspectives
by Merve Kulbay, Emily Marcotte, Raheem Remtulla, Tsz Hin Alexander Lau, Manuel Paez-Escamilla, Kevin Y. Wu and Miguel N. Burnier, Jr.
Biomedicines 2024, 12(8), 1758; https://doi.org/10.3390/biomedicines12081758 - 5 Aug 2024
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Abstract
Uveal melanoma (UM) is the most common intraocular malignancy in adults. Recent advances highlight the role of tumor-derived extracellular vesicles (TEV) and circulating hybrid cells (CHC) in UM tumorigenesis. Bridged with liquid biopsies, a novel technology that has shown incredible performance in detecting [...] Read more.
Uveal melanoma (UM) is the most common intraocular malignancy in adults. Recent advances highlight the role of tumor-derived extracellular vesicles (TEV) and circulating hybrid cells (CHC) in UM tumorigenesis. Bridged with liquid biopsies, a novel technology that has shown incredible performance in detecting cancer cells or products derived from tumors in bodily fluids, it can significantly impact disease management and outcome. The aim of this comprehensive literature review is to provide a summary of current knowledge and ongoing advances in posterior UM pathophysiology, diagnosis, and treatment. The first section of the manuscript discusses the complex and intricate role of TEVs and CHCs. The second part of this review delves into the epidemiology, etiology and risk factors, clinical presentation, and prognosis of UM. Third, current diagnostic methods, ensued by novel diagnostic tools for the early detection of UM, such as liquid biopsies and artificial intelligence-based technologies, are of paramount importance in this review. The fundamental principles, limits, and challenges associated with these diagnostic tools, as well as their potential as a tracker for disease progression, are discussed. Finally, a summary of current treatment modalities is provided, followed by an overview of ongoing preclinical and clinical research studies to provide further insights on potential biomolecular pathway alterations and therapeutic targets for the management of UM. This review is thus an important resource for all healthcare professionals, clinicians, and researchers working in the field of ocular oncology. Full article
(This article belongs to the Special Issue Recent Advances in Ocular Oncology)
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