Hepatocellular carcinoma (HCC) often arises in chronic viral hepatitis, MAFLD, and cirrhosis, engaging TERT promoter, TP53, CTNNB1/AXIN1, and angiogenic programs. We provide AFP/GPC3 biomarker antibodies and multi-kinase / mTOR / PI3K probes for TME, resistance, and combinations.
Focus areas: clonal evolution in cirrhosis, angiogenesis & immunotherapy, bile acid–immune axis, portal vein tumor thrombus models
Commonly used for mechanistic studies; follow your lab SOP, compound datasheets, and ethics approvals.
| Compound | Targets / pathways | Experimental notes |
|---|---|---|
| Sorafenib | Multi-kinase (VEGFR/RAF, etc.) | Classic systemic probe; log HFSR/hypertension. |
| Lenvatinib | VEGFR1–3 / FGFR / PDGFR, etc. | First-line alternative mapping; TFTs/proteinuria. |
| Regorafenib | Multi-kinase | Second-line resistance models; combo toxicity matrices. |
| Cabozantinib | MET/VEGFR/AXL, etc. | Invasion/TME remodeling readouts. |
| Everolimus | mTORC1 | mTOR-dependency validation; mind immunosuppression. |
| Apatinib | VEGFR2 (research contexts) | Alternative VEGFR2 small-molecule; verify animal PK. |
| MK-2206 | AKT1/2/3 | PI3K/AKT validation; sequential readouts with sorafenib. |