Related Experiment Video
Updated: Feb 2, 2026

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Targeting tyrosine kinases for treatment of ocular tumors
Dong Hyun Jo1,2, Jin Hyoung Kim1,2, Jeong Hun Kim3,4,5,6
1Fight Against Angiogenesis-Related Blindness (FARB) Laboratory, Clinical Research Institute, Seoul National University Hospital, Seoul, 03080, Republic of Korea.
Abstract:
Uveal melanoma is the most common intraocular primary malignant tumor in adults, and retinoblastoma is the one in children. Current mainstay treatment options include chemotherapy using conventional drugs and enucleation, the total removal of the eyeball. Targeted therapies based on profound understanding of molecular mechanisms of ocular tumors may increase the possibility of preserving the eyeball and the vision. Tyrosine kinases, which modulate signaling pathways regarding various cellular functions including proliferation, differentiation, and attachment, are one of the attractive targets for targeted therapies against uveal melanoma and retinoblastoma. In this review, the roles of both types of tyrosine kinases, receptor tyrosine kinases and non-receptor tyrosine kinases, were summarized in relation with ocular tumors. Although the conventional treatment options for uveal melanoma and retinoblastoma are radiotherapy and chemotherapy, respectively, specific tyrosine kinase inhibitors will enhance our armamentarium against them by controlling cancer-associated signaling pathways related to tyrosine kinases. This review can be a stepping stone for widening treatment options and realizing targeted therapies against uveal melanoma and retinoblastoma.
Insights
Targeted therapies show promise for treating ocular tumors like uveal melanoma and retinoblastoma. By inhibiting tyrosine kinases, these treatments may improve outcomes and preserve vision, offering new hope beyond conventional methods.
Area of Science:
- Ophthalmology
- Oncology
- Molecular Biology
Background:
- Uveal melanoma and retinoblastoma are primary ocular malignancies in adults and children, respectively.
- Current treatments like chemotherapy and enucleation have limitations.
- Targeted therapies offer potential for improved outcomes and eyeball preservation.
Purpose of the Study:
- To review the role of tyrosine kinases in ocular tumors.
- To explore targeted therapy strategies for uveal melanoma and retinoblastoma.
- To highlight tyrosine kinase inhibitors as potential novel treatments.
Main Methods:
- Literature review focusing on tyrosine kinases in ocular oncology.
- Analysis of molecular mechanisms in uveal melanoma and retinoblastoma.
- Synthesis of current and emerging therapeutic approaches.
Main Results:
- Tyrosine kinases (receptor and non-receptor) are crucial in ocular tumor cell signaling.
- Targeting these kinases can modulate proliferation, differentiation, and attachment.
- Tyrosine kinase inhibitors represent a promising therapeutic avenue.
Conclusions:
- Targeted inhibition of tyrosine kinases offers a new strategy for ocular tumor treatment.
- This approach may enhance conventional therapies for uveal melanoma and retinoblastoma.
- Further research into tyrosine kinase inhibitors could expand treatment options and improve vision preservation.
Related Concept Videos
Receptor Tyrosine Kinases
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
Protein Kinases and Phosphatases
Protein kinases
Many proteins in the cell are regulated by phosphorylation, the addition of a phosphate group. A family of enzymes called kinases...
Protein Kinases and Phosphatases
cAMP-dependent Protein Kinase Pathways
Open Angle Glaucoma: Treatment
Drugs such as carbonic anhydrase inhibitors, α2- and...

