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Immunotherapy is not one drug class. It includes: -Immune checkpoint inhibitors (PD-1, PD-L1, CTLA-4) -CAR-T therapies -Monoclonal antibodies -Cytokine therapies (IL-2, IFN-α) -Cancer vaccines -Bispecific T-cell engagersPD-1 blockade antibody therapy is one of the cornerstone approaches in modern cancer immunotherapy. Under normal physiological conditions, when PD-1 binds to its ligands (PD-L1 or PD-L2) on other cells, it functions as a "checkpoint" to reduce overly active T cell responses and prevent autoimmunity. PD-1 blockade therapies involve monoclonal antibodies that target either PD-1 or its ligand PD-L1. • By blocking the interaction between PD-1 and its ligands, these antibodies effectively release the "brakes" on T cells. • The re-activated T cells can then recognize and destroy cancer cells more efficiently.
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| Also known as BIRC4. XIAP is inhibited by DIABLO (Smac) and HTRA2 (Omi), two death-signaling proteins released into the cytoplasm by the mitochondria. High proportions of XIAP may function as a tumor marker. In developing prostate cancer, XIAP is one of four IAPs overexpressed in the prostatic epithelium. XIAP functions predominantly as a protumorigenic protein in the context of cancer. Its upregulation is commonly observed in various tumor types and is associated with poor patient outcomes and resistance to therapy due to its potent inhibition of apoptosis. |
| 1360- | Ash, | immuno, | Withaferin A Increases the Effectiveness of Immune Checkpoint Blocker for the Treatment of Non-Small Cell Lung Cancer |
| - | in-vitro, | Lung, | H1650 | - | in-vitro, | Lung, | A549 | - | in-vitro, | CRC, | HCT116 | - | in-vitro, | BC, | MDA-MB-231 | - | in-vivo, | NA, | NA |
Query results interpretion may depend on "conditions" listed in the research papers. Such Conditions may include : -low or high Dose -format for product, such as nano of lipid formations -different cell line effects -synergies with other products -if effect was for normal or cancerous cells
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