PRMT5 Related Tumor Models
Homozygous deletion of methylthioadenosine phosphorylase (MTAP) in cancers such as glioblastoma represents a potentially targetable vulnerability. MTAP deletions occur in approximately 10 – 15% of all human cancers. When the MTAP gene is deleted, methylthioadenosine (MTA) accumulates and selectively inhibits PRMT5. This creates a synthetic lethal dependence on PRMT5 in MTAP-deleted tumors.
As a potential treatment for MTAP-deleted cancers, compound MRTX1719 is a PRMT5 inhibitor that selectively binds to the PRMT5-MTA complex and inhibits PRMT5 activity in MTAP-deleted cells. To support the discovery and optimization of new PRMT5 inhibitors, WuXi AppTec has established an extensive panel of PRMT5 related CDX and PDX models.
PRMT5 Related Tumor Models
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