Technical Articles
Targeted therapy
FGFR4: Why Hepatocellular Carcinoma Targeting Focuses on This Selective Receptor
Among the four FGFR family members, FGFR4 alone resides in the liver and binds the KLB co-receptor. From an industry perspective, this article dissects the FGF19 axis, its association with hepatocellular carcinoma and the design logic of selective in
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- Signaling Pathway
- FGFR4
- Hepatocellular carcinoma
- FGF19
- Selective inhibitor
- Targeted therapy
- UA011375
Challenges in Targeting KRAS G12D Mutation and Novel PROTAC Technology Strategies
The KRAS gene is one of the most frequently mutated proto-oncogenes in human cancers. Among the RAS gene family (KRAS, NRAS, HRAS), KRAS mutations account for approximately 85%, and its encoded protein serves as a critical molecular switch.
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- Cancer
- KRAS[G12D]/CRBN PROTAC Kit
- Targeted therapy
- Pancreatic cancer
KRAS-Targeted Therapies: Breakthroughs and Future Prospects
Mutations in the KRAS gene represent a significant challenge in cancer treatment, particularly in pancreatic cancer, colorectal cancer, and non-small cell lung cancer (NSCLC). These mutations result in the constitutive activation of the KRAS protein, leading to hyperactivation of downstream signaling pathways and promoting tumor cell growth. However, the lack of binding pockets on the KRAS protein surface has made it difficult for traditional small-molecule drugs to directly target KRAS, rendering it once deemed an "undruggable" target.
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- Cancer
- KRAS
- Targeted therapy
- cancer treatment
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