• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

聚(腺苷二磷酸核糖)聚合酶(PARP)抑制剂在癌症治疗中的应用策略。

Strategies for the Use of Poly(adenosine diphosphate ribose) Polymerase (PARP) Inhibitors in Cancer Therapy.

机构信息

Science for Life Laboratory, Division of Translational Medicine and Chemical Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, S-171 21 Stockholm, Sweden.

出版信息

Biomolecules. 2012 Dec 14;2(4):635-49. doi: 10.3390/biom2040635.

DOI:10.3390/biom2040635
PMID:24970153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4030856/
Abstract

Treatments with Poly(adenosine diphosphate ribose) polymerase (PARP) inhibitors have offered patients carrying cancers with mutated BRCA1 or BRCA2 genes a new and in many cases effective option for disease control. There is potentially a large patient population that may also benefit from PARP inhibitor treatment, either in monotherapy or in combination with chemotherapy. Here, we describe the multifaceted role of PARP inhibitors and discuss which treatment options could potentially be useful to gain disease control without potentiating side effects.

摘要

聚(腺苷二磷酸核糖)聚合酶(PARP)抑制剂的治疗为携带突变 BRCA1 或 BRCA2 基因的癌症患者提供了一种新的、在许多情况下有效的疾病控制选择。可能有大量的患者群体也可以从 PARP 抑制剂治疗中受益,无论是单独使用还是与化疗联合使用。在这里,我们描述了 PARP 抑制剂的多方面作用,并讨论了哪些治疗选择可能有助于在不增加副作用的情况下获得疾病控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d9/4030856/f81c862fc52b/biomolecules-02-00635-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d9/4030856/1d6421bce0a1/biomolecules-02-00635-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d9/4030856/f81c862fc52b/biomolecules-02-00635-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d9/4030856/1d6421bce0a1/biomolecules-02-00635-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d9/4030856/f81c862fc52b/biomolecules-02-00635-g002.jpg

相似文献

1
Strategies for the Use of Poly(adenosine diphosphate ribose) Polymerase (PARP) Inhibitors in Cancer Therapy.聚(腺苷二磷酸核糖)聚合酶(PARP)抑制剂在癌症治疗中的应用策略。
Biomolecules. 2012 Dec 14;2(4):635-49. doi: 10.3390/biom2040635.
2
The role of poly adenosine diphosphate ribose polymerase inhibitors in breast and ovarian cancer: current status and future directions.聚腺苷二磷酸核糖聚合酶抑制剂在乳腺癌和卵巢癌中的作用:现状与未来方向
Asia Pac J Clin Oncol. 2011 Sep;7(3):197-211. doi: 10.1111/j.1743-7563.2011.01430.x.
3
An update on current and emerging therapies for epithelial ovarian cancer: Focus on poly(adenosine diphosphate-ribose) polymerase inhibition and antiangiogenesis.上皮性卵巢癌的当前及新出现疗法的最新进展:聚焦于聚(二磷酸腺苷 - 核糖)聚合酶抑制和抗血管生成。
J Oncol Pharm Pract. 2017 Sep;23(6):454-469. doi: 10.1177/1078155216657165. Epub 2016 Jun 29.
4
Role of Poly Adenosine Diphosphate Ribose Polymerase Inhibitors in Advanced Stage Ovarian Cancer.聚腺苷二磷酸核糖聚合酶抑制剂在晚期卵巢癌中的作用
Cureus. 2018 May 24;10(5):e2685. doi: 10.7759/cureus.2685.
5
PARP inhibitors in breast cancer: Bringing synthetic lethality to the bedside.PARP 抑制剂在乳腺癌中的应用:将合成致死性带入临床实践。
Cancer. 2018 Jun 15;124(12):2498-2506. doi: 10.1002/cncr.31307. Epub 2018 Apr 16.
6
Clinical Application of Poly(ADP-Ribose) Polymerase Inhibitors in High-Grade Serous Ovarian Cancer.聚(ADP - 核糖)聚合酶抑制剂在高级别浆液性卵巢癌中的临床应用
Oncologist. 2016 May;21(5):586-93. doi: 10.1634/theoncologist.2015-0438. Epub 2016 Mar 28.
7
The status of poly(adenosine diphosphate-ribose) polymerase (PARP) inhibitors in ovarian cancer, part 2: extending the scope beyond olaparib and BRCA1/2 mutations.聚(腺苷二磷酸核糖)聚合酶(PARP)抑制剂在卵巢癌中的地位,第2部分:扩展奥拉帕利和BRCA1/2突变之外的范围
Clin Adv Hematol Oncol. 2016 Sep;14(9):704-11.
8
When and How to Use PARP Inhibitors in Prostate Cancer: A Systematic Review of the Literature with an Update on On-Going Trials.何时以及如何在前列腺癌中使用 PARP 抑制剂:文献系统评价及正在进行的试验更新。
Eur Urol Oncol. 2020 Oct;3(5):594-611. doi: 10.1016/j.euo.2020.07.005. Epub 2020 Aug 17.
9
The role of novel poly (ADP-ribose) inhibitors in the treatment of locally advanced and metastatic Her-2/neu negative breast cancer with inherited germline BRCA1/2 mutations. A review of the literature.新型聚(ADP - 核糖)抑制剂在治疗具有遗传性种系BRCA1/2突变的局部晚期和转移性Her-2/neu阴性乳腺癌中的作用。文献综述
J Med Life. 2021 Jan-Mar;14(1):17-20. doi: 10.25122/jml-2020-0132.
10
[From poly(ADP-ribose) discovery to PARP inhibitors in cancer therapy].[从聚(ADP - 核糖)的发现到PARP抑制剂在癌症治疗中的应用]
Bull Cancer. 2015 Oct;102(10):863-73. doi: 10.1016/j.bulcan.2015.07.012. Epub 2015 Sep 15.

引用本文的文献

1
Thioparib inhibits homologous recombination repair, activates the type I IFN response, and overcomes olaparib resistance.硫代帕比司他抑制同源重组修复,激活 I 型干扰素反应,并克服奥拉帕利耐药性。
EMBO Mol Med. 2023 Mar 8;15(3):e16235. doi: 10.15252/emmm.202216235. Epub 2023 Jan 18.
2
Neuroprotective Effects of Nicotinamide (Vitamin B) on Neurodegeneration in Diabetic Rat Retinas.烟酰胺(维生素 B)对糖尿病大鼠视网膜神经退行性变的神经保护作用。
Nutrients. 2022 Mar 10;14(6):1162. doi: 10.3390/nu14061162.
3
ATR prevents Ca overload-induced necrotic cell death through phosphorylation-mediated inactivation of PARP1 without DNA damage signaling.

本文引用的文献

1
Loss of function germline mutations in RAD51D in women with ovarian carcinoma.RAD51D 胚系失活突变与卵巢癌女性患者相关。
Gynecol Oncol. 2012 Dec;127(3):552-5. doi: 10.1016/j.ygyno.2012.09.009. Epub 2012 Sep 14.
2
Proteomic profiling identifies dysregulated pathways in small cell lung cancer and novel therapeutic targets including PARP1.蛋白质组学分析鉴定出小细胞肺癌中失调的通路和新的治疗靶点,包括 PARP1。
Cancer Discov. 2012 Sep;2(9):798-811. doi: 10.1158/2159-8290.CD-12-0112. Epub 2012 Sep 6.
3
PI3K inhibition impairs BRCA1/2 expression and sensitizes BRCA-proficient triple-negative breast cancer to PARP inhibition.
ATR 通过磷酸化介导的 PARP1 失活来防止 Ca 超载诱导的坏死性细胞死亡,而不触发 DNA 损伤信号。
FASEB J. 2021 May;35(5):e21373. doi: 10.1096/fj.202001636RRR.
4
Orthosiphon stamineus Extracts Inhibits Proliferation and Induces Apoptosis in Uterine Fibroid Cells.猫须草提取物抑制子宫肌瘤细胞增殖并诱导其凋亡。
Asian Pac J Cancer Prev. 2018 Oct 26;19(10):2737-2744. doi: 10.22034/APJCP.2018.19.10.2737.
5
coding variants are associated with a high risk of hepatocellular carcinoma occurrence in patients with HCV- or HBV-related liver disease.编码变异与丙型肝炎病毒(HCV)或乙型肝炎病毒(HBV)相关肝病患者发生肝细胞癌的高风险相关。
Oncotarget. 2016 Aug 17;8(38):62842-62857. doi: 10.18632/oncotarget.11327. eCollection 2017 Sep 8.
6
A phase I followed by a randomized phase II trial of two cycles carboplatin-olaparib followed by olaparib monotherapy versus capecitabine in BRCA1- or BRCA2-mutated HER2-negative advanced breast cancer as first line treatment (REVIVAL): study protocol for a randomized controlled trial.一项针对BRCA1或BRCA2突变的HER2阴性晚期乳腺癌一线治疗的I期试验,随后进行两个周期卡铂-奥拉帕利联合治疗,然后奥拉帕利单药治疗与卡培他滨对比的随机II期试验(REVIVAL):一项随机对照试验的研究方案。
Trials. 2016 Jun 21;17(1):293. doi: 10.1186/s13063-016-1423-0.
7
A fine-scale dissection of the DNA double-strand break repair machinery and its implications for breast cancer therapy.DNA双链断裂修复机制的精细剖析及其对乳腺癌治疗的意义。
Nucleic Acids Res. 2014 Jun;42(10):6106-27. doi: 10.1093/nar/gku284. Epub 2014 May 3.
PI3K 抑制会损害 BRCA1/2 的表达,并使 BRCA 功能正常的三阴性乳腺癌对 PARP 抑制敏感。
Cancer Discov. 2012 Nov;2(11):1036-47. doi: 10.1158/2159-8290.CD-11-0348. Epub 2012 Aug 22.
4
Combining a PI3K inhibitor with a PARP inhibitor provides an effective therapy for BRCA1-related breast cancer.联合使用 PI3K 抑制剂和 PARP 抑制剂可为 BRCA1 相关乳腺癌提供有效的治疗方法。
Cancer Discov. 2012 Nov;2(11):1048-63. doi: 10.1158/2159-8290.CD-11-0336. Epub 2012 Aug 22.
5
DNA-PK, ATM and ATR collaboratively regulate p53-RPA interaction to facilitate homologous recombination DNA repair.DNA-PK、ATM 和 ATR 协同调节 p53-RPA 相互作用以促进同源重组 DNA 修复。
Oncogene. 2013 May 9;32(19):2452-62. doi: 10.1038/onc.2012.257. Epub 2012 Jul 16.
6
Histone ADP-ribosylation facilitates gene transcription by directly remodeling nucleosomes.组蛋白 ADP-核糖基化通过直接重塑核小体促进基因转录。
Mol Cell Biol. 2012 Jul;32(13):2490-502. doi: 10.1128/MCB.06667-11. Epub 2012 Apr 30.
7
PARP-1 protein expression in glioblastoma multiforme.多形性胶质母细胞瘤中的 PARP-1 蛋白表达。
Eur J Histochem. 2012 Feb 27;56(1):e9. doi: 10.4081/ejh.2012.e9.
8
Mre11-dependent degradation of stalled DNA replication forks is prevented by BRCA2 and PARP1.Mre11 依赖性的停滞 DNA 复制叉降解被 BRCA2 和 PARP1 所阻止。
Cancer Res. 2012 Jun 1;72(11):2814-21. doi: 10.1158/0008-5472.CAN-11-3417. Epub 2012 Mar 23.
9
Synthetic lethality of cohesins with PARPs and replication fork mediators.着丝粒与 PARPs 和复制叉介体的合成致死性。
PLoS Genet. 2012;8(3):e1002574. doi: 10.1371/journal.pgen.1002574. Epub 2012 Mar 8.
10
Co-targeting of the PI3K pathway improves the response of BRCA1 deficient breast cancer cells to PARP1 inhibition.同时靶向抑制 PI3K 通路可提高 BRCA1 缺陷型乳腺癌细胞对 PARP1 抑制剂的反应。
Cancer Lett. 2012 Jun 28;319(2):232-241. doi: 10.1016/j.canlet.2012.01.015. Epub 2012 Jan 20.