PARP 抑制剂在前列腺癌中的临床应用。

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Biology Reports Pub Date : 2024-10-30 DOI:10.1007/s11033-024-10034-5
Hamidreza Saeidi, Mohsen Sarafbidabad
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引用次数: 0

摘要

尽管在治疗转移性难治性前列腺癌(mCRPC)方面取得了最新进展,但这种疾病仍然是致命的。目前已开发出一种名为聚ADP核糖聚合酶(PARP)抑制剂的新型靶向药物系列,用于治疗患有同源重组修复(HRR)基因改变的mCRPC患者。美国食品和药物管理局(FDA)最近批准了奥拉帕利(olaparib)和鲁卡帕利(rucaparib)用于治疗患有 HRR 基因改变的 mCRPC 患者。目前正在进行的试验正在研究将PARP抑制剂与放疗、化疗、免疫疗法和雄激素受体信号转导抑制剂(ARSIs)相结合的联合疗法,以提高PARP抑制剂的疗效,扩大可从治疗中获益的患者范围。本综述概述了 PARP 抑制剂在前列腺癌中的发展情况,并分析了其产生耐药性的机制。
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PARP inhibitors in prostate cancer: clinical applications.

Despite recent advancements in the treatment of metastatic castrate-resistant prostate cancer (mCRPC), this disease remains lethal. A novel family of targeted pharmaceuticals known as poly-ADP-ribose polymerase (PARP) inhibitors has been developed to treat mCRPC patients with homologous recombination repair (HRR) gene alterations. The FDA recently approved olaparib and rucaparib for treating mCRPC patients with HRR gene alterations. Ongoing trials are investigating combination therapies involving PARP inhibitors combined with radiation, chemotherapy, immunotherapy, and androgen receptor signaling inhibitors (ARSIs) to improve the effectiveness of PARP inhibitors and broaden the range of patients who can benefit from the treatment. This review provides an overview of the development of PARP inhibitors in prostate cancer and analyzes the mechanisms underlying their resistance.

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来源期刊
Molecular Biology Reports
Molecular Biology Reports 生物-生化与分子生物学
CiteScore
5.00
自引率
0.00%
发文量
1048
审稿时长
5.6 months
期刊介绍: Molecular Biology Reports publishes original research papers and review articles that demonstrate novel molecular and cellular findings in both eukaryotes (animals, plants, algae, funghi) and prokaryotes (bacteria and archaea).The journal publishes results of both fundamental and translational research as well as new techniques that advance experimental progress in the field and presents original research papers, short communications and (mini-) reviews.
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