Chemistry:Eprenetapopt
From HandWiki
Eprenetapopt (APR-246) is an experimental anti-cancer drug which acts by reactivating certain mutant forms of p53, a tumour-suppressing gene which is commonly mutated into inactive forms as an early step in the development of malignant cancers. It has been researched over many years for treatment of numerous forms of cancer and reached late-stage clinical trials, but has never yet been approved for medical use due to inconsistent results. Nevertheless, it continues to be studied especially as a combination treatment alongside other anti-cancer medications, or in patients whose cancers have particular mutant forms of p53 thought to be susceptible to treatment with eprenetapopt.[1][2][3][4][5]
References
- ↑ "Mutant p53 as a target for cancer treatment". European Journal of Cancer 83: 258–265. September 2017. doi:10.1016/j.ejca.2017.06.023. PMID 28756138.
- ↑ "New directions for emerging therapies in acute myeloid leukemia: the next chapter". Blood Cancer Journal 10 (10): 107. October 2020. doi:10.1038/s41408-020-00376-1. PMID 33127875.
- ↑ "Current Therapy of the Patients with MDS: Walking towards Personalized Therapy". Journal of Clinical Medicine 10 (10): 2107. May 2021. doi:10.3390/jcm10102107. PMID 34068316.
- ↑ "Eprenetapopt Plus Azacitidine After Allogeneic Hematopoietic Stem-Cell Transplantation for TP53-Mutant Acute Myeloid Leukemia and Myelodysplastic Syndromes". Journal of Clinical Oncology 40 (34): 3985–3993. December 2022. doi:10.1200/JCO.22.00181. PMID 35816664.
- ↑ "TP53-mutated acute myeloid leukemia and myelodysplastic syndrome: biology, treatment challenges, and upcoming approaches". Annals of Hematology 103 (4): 1049–1067. April 2024. doi:10.1007/s00277-023-05462-5. PMID 37770618.
