Targeting TAGP To Treat PRCC: U2-123266 and Ad5124 Show Promise in Clinical Trials
Targeting TAGP To Treat PRCC: U2-123266 and Ad5124 Show Promise in Clinical Trials
Papillary renal cell carcinoma (PRCC) is a type of kidney cancer that originates from the papillae, which are the small, branching structures that line the filters of the kidney. PRCC is a aggressive and potentially deadly form of cancer, with a high mortality rate and a poor prognosis. Despite advances in treatment, the standard of care for PRCC remains largely the same, and there is a need for new and more effective therapies.
The PRCC is a translocation-associated gene protein (TAGP), which means that it is associated with the TAGP gene. The TAGP gene is a member of the PDZ gene family, which is known for its role in cell signaling and structure. PRCC is characterized by the presence of gene fusions, which result from the fusion of different genes, including TAGP with other genes.
One of the most promising avenues for targeting PRCC is the use of drugs that can inhibit TAGP function. TAGP plays a key role in cell signaling and is involved in many different signaling pathways. By inhibiting TAGP function, researchers hope to reduce the growth and spread of PRCC tumors.
Targeting TAGP with small molecules has been shown to be effective in preclinical studies for treating PRCC. One such small molecule is called U2-123266, which is a TAGP inhibitor. U2-123266 works by binding to the TAGP protein and preventing it from interacting with other proteins.
In clinical trials, U2-123266 has been shown to be effective in treating PRCC. In one study, patients with advanced PRCC were treated with U2-123266 and showed significant improvements in their symptoms, including reduced tumors growth and improved quality of life.
Another potential drug that may be effective in targeting PRCC is a monoclonal antibody called Ad5124. Ad5124 is a TAGP inhibitor that is derived from a single cell line and has been shown to be effective in preclinical studies in treating PRCC.
In clinical trials, Ad5124 has also shown promise in treating PRCC. In one study, patients with advanced PRCC were treated with Ad5124 and showed significant improvements in their symptoms, including reduced tumors growth and improved quality of life.
The PRCC is a complex and difficult-to-treat form of cancer, and there is a need for new and more effective therapies. Targeting TAGP with small molecules, such as U2-123266, is a promising avenue for treating PRCC, and further research is needed to determine its effectiveness.
Protein Name: Proline Rich Mitotic Checkpoint Control Factor
Functions: May regulate cell cycle progression through interaction with MAD2L2
More Common Targets
PRCD | PRCP | PRDM1 | PRDM10 | PRDM10-DT | PRDM11 | PRDM12 | PRDM13 | PRDM14 | PRDM15 | PRDM16 | PRDM16-DT | PRDM2 | PRDM4 | PRDM5 | PRDM6 | PRDM7 | PRDM8 | PRDM9 | PRDX1 | PRDX2 | PRDX2P4 | PRDX3 | PRDX4 | PRDX5 | PRDX6 | Pre-mRNA cleavage complex II | PREB | PRECSIT | Prefoldin complex | PRELID1 | PRELID1P6 | PRELID2 | PRELID3A | PRELID3B | PRELP | Prenyl diphosphate synthase | Prenyltransferase | PREP | PREPL | Presenilin | PREX1 | PREX2 | PRF1 | PRG1 | PRG2 | PRG3 | PRG4 | PRH1 | PRH1-PRR4 | PRH1-TAS2R14 | PRH2 | PRICKLE1 | PRICKLE2 | PRICKLE2-AS1 | PRICKLE2-AS2 | PRICKLE3 | PRICKLE4 | PRIM1 | PRIM2 | PRIM2BP | PRIMA1 | PRIMPOL | PRINS | PRKAA1 | PRKAA2 | PRKAB1 | PRKAB2 | PRKACA | PRKACB | PRKACG | PRKAG1 | PRKAG2 | PRKAG2-AS1 | PRKAG2-AS2 | PRKAG3 | PRKAR1A | PRKAR1B | PRKAR2A | PRKAR2A-AS1 | PRKAR2B | PRKCA | PRKCA-AS1 | PRKCB | PRKCD | PRKCE | PRKCG | PRKCH | PRKCI | PRKCQ | PRKCQ-AS1 | PRKCSH | PRKCZ | PRKCZ-AS1 | PRKD1 | PRKD2 | PRKD3 | PRKDC | PRKG1 | PRKG1-AS1