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首页> 外文期刊>International Journal of Basic & Clinical Pharmacology >Rucaparib: a PARP inhibitor for the treatment of advanced ovarian cancer
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Rucaparib: a PARP inhibitor for the treatment of advanced ovarian cancer

机译:鲁卡帕利布(rucaparib):一种用于治疗晚期卵巢癌的PARP抑制剂

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Ovarian cancers arise from the uncontrolled growth and replication of epithelial cells of the surface of ovary which constitutes 90% of cases. PARP (poly ADP-ribose polymerase) inhibitors are a novel type of therapy that prevents cancer cells from repairing their DNA which have been damaged by other chemotherapeutic agents. Rucaparib is a novel drug that was approved by the US FDA in 2016 for the treatment of patients with deleterious BRCA mutation associated advanced ovarian cancer. Inhibition of the PARP enzymes leads to the increased formation of PARP-DNA complexes which results in DNA damage, apoptosis and cell death. Nausea, fatigue including asthenia, vomiting, anemia, abdominal pain, constipation, decreased appetite, diarrhea, thrombocytopenia and dyspnea were the common adverse effects seen among rucaparib users. Even though, the drug may cause myleodysplastic syndrome/ acute myeloid leukemia (MDS/AML) it remains as novel therapeutic target for the treatment of advanced ovarian cancer involving BRCA mutation.
机译:卵巢癌是由卵巢表面上皮细胞的不受控制的生长和复制引起的,占90%的病例。 PARP(聚ADP-核糖聚合酶)抑制剂是一种新型治疗方法,可防止癌细胞修复已被其他化学治疗剂破坏的DNA。 Rucaparib是一种新型药物,已于2016年获得美国FDA的批准,用于治疗与有害BRCA突变相关的晚期卵巢癌患者。 PARP酶的抑制导致PARP-DNA复合物形成的增加,这导致DNA损伤,细胞凋亡和细胞死亡。恶心,乏力包括乏力,呕吐,贫血,腹痛,便秘,食欲下降,腹泻,血小板减少和呼吸困难是rucaparib使用者常见的不良反应。即使该药物可能引起骨髓增生异常综合症/急性髓细胞性白血病(MDS / AML),它仍然是治疗涉及BRCA突变的晚期卵巢癌的新型治疗靶标。

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