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1
Breast cancer significantly contributes to cancer morbidity and mortality, particularly through central nervous system (CNS) metastasis.
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2
LYN, a non-receptor tyrosine kinase, plays a critical role in signaling pathways that influence cell motility, invasion, and survival in breast cancer.
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3
Alterations in LYN expression and mutations may promote CNS tropism in breast cancer by affecting intravasation, survival, and blood-brain barrier (BBB) transmigration.
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4
Most LYN mutations in breast cancer are rare and heterogeneous, with uncertain oncogenicity and no established clinical actionability.
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5
Current clinical strategies for targeting LYN in breast cancer are limited, emphasizing the need for biomarker-guided approaches rather than broad-spectrum therapies.