• 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

泽布替尼部分逆转前列腺癌细胞中的 GST 甲基化,并恢复对 DNA 小沟结合物布罗他滨的敏感性。

Zebularine partially reverses GST methylation in prostate cancer cells and restores sensitivity to the DNA minor groove binder brostallicin.

机构信息

Laboratory of Molecular Pharmacology; Department of Oncology; IRCCS-Istituto di Ricerche Farmacologiche Mario Negri; Milan, Italy.

出版信息

Epigenetics. 2013 Jun;8(6):656-65. doi: 10.4161/epi.24916. Epub 2013 Jun 14.

DOI:10.4161/epi.24916
PMID:23771052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3857345/
Abstract

Brostallicin is a DNA minor groove binder that shows enhanced antitumor activity in cells with high glutathione S-transferase (GST)/glutathione content. Prostate cancer cells present, almost invariably, methylation of the GSTP1 gene promoter and, as a consequence, low levels of GST-pi expression and activity. In these cells, brostallicin shows very little activity. We tested whether pretreatment of heavily GST-methylated prostate cancer cells with demethylating agents could enhance the activity of brostallicin. Human prostate cancer cells LNCaP and DU145 were used for these studies both in vitro and in vivo. The demethylating agent zebularine was used in combination with brostallicin. Methylation specific PCR and pyrosequencing were used to determine the level of GST methylation. Pretreatment with demethylating agents enhanced the in vitro activity of brostallicin in LNCaP cells. Zebularine, in particular, induced an enhancement of activity in vivo comparable to that obtained by transfecting the human GSTP1 gene in LNCaP cells in vitro. Molecular analysis performed on tumor xenografts in mice pretreated with zebularine failed to detect re-expression of GST-pi and demethylation of GSTP1. However, we found demethylation in the GSTM1 gene, with consequent re-expression of GST-mu at the mRNA level. These results indicate that zebularine, both in vitro and in vivo, enhances the activity of brostallicin and that this enhancement correlates with re-expression of GST-pi and GST-mu. These findings highlight the potential therapeutic value of combining demethylating agents and brostallicin in tumors with GST methylation that poorly respond to brostallicin.

摘要

布罗他丁是一种 DNA 小沟结合物,在谷胱甘肽 S-转移酶 (GST)/谷胱甘肽含量高的细胞中显示出增强的抗肿瘤活性。前列腺癌细胞几乎总是存在 GSTP1 基因启动子的甲基化,因此 GST-π表达和活性水平较低。在这些细胞中,布罗他丁的活性非常低。我们测试了先用去甲基化剂预处理高度 GST 甲基化的前列腺癌细胞是否可以增强布罗他丁的活性。我们在体外和体内使用人前列腺癌细胞 LNCaP 和 DU145 进行这些研究。使用去甲基化剂 zebularine 与布罗他丁联合使用。甲基化特异性 PCR 和焦磷酸测序用于确定 GST 甲基化水平。用去甲基化剂预处理可增强 LNCaP 细胞中布罗他丁的体外活性。特别是 zebularine 诱导了体内活性的增强,与体外转染人 GSTP1 基因在 LNCaP 细胞中获得的增强相当。用 zebularine 预处理的小鼠肿瘤异种移植进行的分子分析未能检测到 GST-π的重新表达和 GSTP1 的去甲基化。然而,我们发现 GSTM1 基因的去甲基化,导致 GST-μ在 mRNA 水平上的重新表达。这些结果表明,zebularine 无论是在体外还是体内,都能增强布罗他丁的活性,这种增强与 GST-π和 GST-μ的重新表达相关。这些发现强调了在 GST 甲基化的肿瘤中联合使用去甲基化剂和布罗他丁的潜在治疗价值,这些肿瘤对布罗他丁反应不佳。

相似文献

1
Zebularine partially reverses GST methylation in prostate cancer cells and restores sensitivity to the DNA minor groove binder brostallicin.泽布替尼部分逆转前列腺癌细胞中的 GST 甲基化,并恢复对 DNA 小沟结合物布罗他滨的敏感性。
Epigenetics. 2013 Jun;8(6):656-65. doi: 10.4161/epi.24916. Epub 2013 Jun 14.
2
Brostallicin, a novel anticancer agent whose activity is enhanced upon binding to glutathione.布罗斯他利辛,一种新型抗癌剂,其活性在与谷胱甘肽结合后会增强。
Cancer Res. 2002 Apr 15;62(8):2332-6.
3
Enhancement of in vivo antitumor activity of classical anticancer agents by combination with the new, glutathione-interacting DNA minor groove-binder, brostallicin.经典抗癌药物与新型谷胱甘肽相互作用性DNA小沟结合剂溴丝菌素联合使用可增强其体内抗肿瘤活性。
Clin Cancer Res. 2003 Nov 1;9(14):5402-8.
4
Brostallicin (PNU-166196), a new minor groove DNA binder: preclinical and clinical activity.布罗他滨(PNU-166196),一种新型的小沟 DNA 结合物:临床前和临床活性。
Expert Opin Investig Drugs. 2009 Dec;18(12):1939-46. doi: 10.1517/13543780903401284.
5
Expression level and DNA methylation status of glutathione-S-transferase genes in normal murine prostate and TRAMP tumors.正常小鼠前列腺和TRAMP肿瘤中谷胱甘肽-S-转移酶基因的表达水平及DNA甲基化状态
Prostate. 2009 Sep 1;69(12):1312-24. doi: 10.1002/pros.20976.
6
Role of glutathione transferases in the mechanism of brostallicin activation.谷胱甘肽转移酶在布罗他滨激活机制中的作用。
Biochemistry. 2010 Jan 12;49(1):226-35. doi: 10.1021/bi901689s.
7
Phase I dose-escalation study of brostallicin, a minor groove binder, in combination with cisplatin in patients with advanced solid tumors.布罗他滨联合顺铂治疗晚期实体瘤患者的 I 期剂量递增研究。
Cancer Chemother Pharmacol. 2010 Jul;66(2):389-94. doi: 10.1007/s00280-009-1175-6. Epub 2009 Nov 22.
8
Brostallicin: a new concept in minor groove DNA binder development.布罗斯他利辛:小沟DNA结合剂开发的新概念。
Anticancer Drugs. 2004 Jan;15(1):1-6. doi: 10.1097/00001813-200401000-00001.
9
Reversal of GSTP1 CpG island hypermethylation and reactivation of pi-class glutathione S-transferase (GSTP1) expression in human prostate cancer cells by treatment with procainamide.通过普鲁卡因胺处理使人类前列腺癌细胞中GSTP1 CpG岛高甲基化逆转并重新激活pi类谷胱甘肽S-转移酶(GSTP1)表达
Cancer Res. 2001 Dec 15;61(24):8611-6.
10
Brostallicin versus doxorubicin as first-line chemotherapy in patients with advanced or metastatic soft tissue sarcoma: an European Organisation for Research and Treatment of Cancer Soft Tissue and Bone Sarcoma Group randomised phase II and pharmacogenetic study.布罗佐立辛与多柔比星作为晚期或转移性软组织肉瘤患者的一线化疗药物:一项欧洲癌症研究与治疗组织软组织和骨肉瘤组随机 2 期和遗传药理学研究。
Eur J Cancer. 2014 Jan;50(2):388-96. doi: 10.1016/j.ejca.2013.10.002. Epub 2013 Nov 8.

引用本文的文献

1
The paradigm of drug resistance in cancer: an epigenetic perspective.癌症耐药性的范式:表观遗传学视角。
Biosci Rep. 2022 Apr 29;42(4). doi: 10.1042/BSR20211812.
2
DNA Methylation Malleability and Dysregulation in Cancer Progression: Understanding the Role of PARP1.DNA 甲基化的可塑性和失调在癌症进展中的作用:PARP1 的作用。
Biomolecules. 2022 Mar 8;12(3):417. doi: 10.3390/biom12030417.
3
Understanding the Mechanisms by Which Epigenetic Modifiers Avert Therapy Resistance in Cancer.了解表观遗传修饰因子避免癌症治疗耐药性的机制。
Front Oncol. 2020 Jun 24;10:992. doi: 10.3389/fonc.2020.00992. eCollection 2020.
4
Pan-Cancer Analysis Reveals the Functional Importance of Protein Lysine Modification in Cancer Development.泛癌分析揭示了蛋白质赖氨酸修饰在癌症发展中的功能重要性。
Front Genet. 2018 Jul 17;9:254. doi: 10.3389/fgene.2018.00254. eCollection 2018.
5
Targeting DNA Methyltranferases in Urological Tumors.靶向泌尿肿瘤中的DNA甲基转移酶
Front Pharmacol. 2018 Apr 13;9:366. doi: 10.3389/fphar.2018.00366. eCollection 2018.
6
Incorporating DNA Methyltransferase Inhibitors (DNMTis) in the Treatment of Genitourinary Malignancies: A Systematic Review.将 DNA 甲基转移酶抑制剂 (DNMTis) 纳入泌尿生殖系统恶性肿瘤的治疗中:系统评价。
Target Oncol. 2018 Feb;13(1):49-60. doi: 10.1007/s11523-017-0546-x.
7
Epigenetic modulators as therapeutic targets in prostate cancer.表观遗传调节剂作为前列腺癌的治疗靶点
Clin Epigenetics. 2016 Sep 15;8:98. doi: 10.1186/s13148-016-0264-8. eCollection 2016.
8
Mutagen Synergy: Hypermutability Generated by Specific Pairs of Base Analogs.诱变剂协同作用:特定碱基类似物对产生的高突变性
J Bacteriol. 2016 Sep 22;198(20):2776-83. doi: 10.1128/JB.00391-16. Print 2016 Oct 15.
9
Reversing drug resistance of cisplatin by hsp90 inhibitors in human ovarian cancer cells.热休克蛋白90抑制剂逆转人卵巢癌细胞对顺铂的耐药性
Int J Clin Exp Med. 2015 May 15;8(5):6687-701. eCollection 2015.
10
Brain feminization requires active repression of masculinization via DNA methylation.大脑女性化需要通过DNA甲基化来积极抑制男性化。
Nat Neurosci. 2015 May;18(5):690-7. doi: 10.1038/nn.3988. Epub 2015 Mar 30.

本文引用的文献

1
The emerging role of histone lysine demethylases in prostate cancer.组蛋白赖氨酸去甲基酶在前列腺癌中的新兴作用。
Mol Cancer. 2012 Aug 6;11:52. doi: 10.1186/1476-4598-11-52.
2
Global methylation profiling for risk prediction of prostate cancer.全球甲基化分析预测前列腺癌风险。
Clin Cancer Res. 2012 May 15;18(10):2882-95. doi: 10.1158/1078-0432.CCR-11-2090.
3
DNA methylation of GSTP1 in human prostate tissues: pyrosequencing analysis.人前列腺组织中GSTP1的DNA甲基化:焦磷酸测序分析
Korean J Urol. 2012 Mar;53(3):200-5. doi: 10.4111/kju.2012.53.3.200. Epub 2012 Mar 19.
4
An integrated genomic and epigenomic approach predicts therapeutic response to zebularine in human liver cancer.综合基因组和表观基因组方法预测 zebularine 对人肝癌的治疗反应。
Sci Transl Med. 2010 Oct 20;2(54):54ra77. doi: 10.1126/scitranslmed.3001338.
5
Mechanistic insights on the inhibition of c5 DNA methyltransferases by zebularine.关于 zebularine 抑制 c5 DNA 甲基转移酶的机制见解。
PLoS One. 2010 Aug 24;5(8):e12388. doi: 10.1371/journal.pone.0012388.
6
Cyclopentenone prostaglandins with dienone structure promote cross-linking of the chemoresistance-inducing enzyme glutathione transferase P1-1.具有二烯酮结构的环戊烯酮前列腺素可促进化学抗性诱导酶谷胱甘肽转移酶 P1-1 的交联。
Mol Pharmacol. 2010 Oct;78(4):723-33. doi: 10.1124/mol.110.065391. Epub 2010 Jul 14.
7
Role of glutathione transferases in the mechanism of brostallicin activation.谷胱甘肽转移酶在布罗他滨激活机制中的作用。
Biochemistry. 2010 Jan 12;49(1):226-35. doi: 10.1021/bi901689s.
8
Brostallicin (PNU-166196), a new minor groove DNA binder: preclinical and clinical activity.布罗他滨(PNU-166196),一种新型的小沟 DNA 结合物:临床前和临床活性。
Expert Opin Investig Drugs. 2009 Dec;18(12):1939-46. doi: 10.1517/13543780903401284.
9
DNA-dependent protein kinase (DNA-PK)-deficient human glioblastoma cells are preferentially sensitized by Zebularine.DNA 依赖性蛋白激酶(DNA-PK)缺陷型人神经胶质瘤细胞对 zebularine 更为敏感。
Carcinogenesis. 2010 Feb;31(2):184-91. doi: 10.1093/carcin/bgp284. Epub 2009 Nov 23.
10
Effects of a novel DNA methyltransferase inhibitor zebularine on human breast cancer cells.新型 DNA 甲基转移酶抑制剂 zebularine 对人乳腺癌细胞的影响。
Breast Cancer Res Treat. 2010 Apr;120(3):581-92. doi: 10.1007/s10549-009-0420-3. Epub 2009 May 21.