AI Article Synopsis

  • * Despite advancements in treatment, about 50% of UM patients will develop undetected metastases upon diagnosis, leading to poor survival rates.
  • * Recent studies have identified key mutations and genetic markers in UM, improving the understanding of its metastasis and highlighting the need for better genetic analysis to predict patient outcomes.

Article Abstract

Background/objectives: Although it comprises only 5% of all melanomas, uveal melanoma (UM) is the most commonly observed primary intraocular cancer.

Methods: Poor patient survival persists in spite of innovative systemic therapies. In fact, approximately fifty percent of UM patients develop metastases from micro-metastases that remain undetected at the exact time of diagnosis.

Results: The molecular understanding of UM is significantly enhanced by the recent identification of several mutations that are responsible for the metastasis, growth, and survival of UM. The crucial point is a more accurate genetic analysis for patient follow-up and metastatic risk prediction.

Conclusions: This review provides a brief summary of the molecular features of UM that are recently discovered, as well as cytogenetic markers and biochemical pathways that are associated with the development of UM metastases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11593461PMC
http://dx.doi.org/10.3390/genes15111356DOI Listing

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