• 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

生存素/黑色素瘤凋亡抑制蛋白作为恶性肿瘤治疗的潜在治疗靶点。

Livin/melanoma inhibitor of apoptosis protein as a potential therapeutic target for the treatment of malignancy.

作者信息

Chang Hong, Schimmer Aaron D

机构信息

Princess Margaret Hospital, Room 9-516, 610 University Avenue, Toronto, Ontario, Canada.

出版信息

Mol Cancer Ther. 2007 Jan;6(1):24-30. doi: 10.1158/1535-7163.MCT-06-0443.

DOI:10.1158/1535-7163.MCT-06-0443
PMID:17237263
Abstract

Livin, also called melanoma inhibitor of apoptosis protein (IAP) or kidney IAP, is a member of the IAP family of caspase inhibitors that selectively binds the endogenous IAP antagonist SMAC and caspase-3, caspase-7, and caspase-9. As such, Livin inhibits apoptosis, and its overexpression renders malignant cells resistant to chemotherapy. Therefore, inhibitors of Livin could be useful adjuncts to chemotherapy in the treatment of malignancies. This review will discuss Livin as a potential therapeutic target and strategies for its inhibition, including antisense oligonucleotides, small-molecule inhibitors, and immune-mediated approaches.

摘要

生存素,也称为黑色素瘤凋亡抑制蛋白(IAP)或肾IAP,是半胱天冬酶抑制蛋白IAP家族的成员,它能选择性地结合内源性IAP拮抗剂SMAC以及半胱天冬酶-3、半胱天冬酶-7和半胱天冬酶-9。因此,生存素可抑制细胞凋亡,其过表达使恶性细胞对化疗产生抗性。所以,生存素抑制剂可能是治疗恶性肿瘤化疗中的有用辅助药物。本综述将讨论生存素作为潜在治疗靶点及其抑制策略,包括反义寡核苷酸、小分子抑制剂和免疫介导方法。

相似文献

1
Livin/melanoma inhibitor of apoptosis protein as a potential therapeutic target for the treatment of malignancy.生存素/黑色素瘤凋亡抑制蛋白作为恶性肿瘤治疗的潜在治疗靶点。
Mol Cancer Ther. 2007 Jan;6(1):24-30. doi: 10.1158/1535-7163.MCT-06-0443.
2
Proteolytic cleavage of Livin (ML-IAP) in apoptotic melanoma cells potentially mediated by a non-canonical caspase.凋亡黑素瘤细胞中Livin(ML-IAP)的蛋白水解切割可能由一种非典型半胱天冬酶介导。
J Dermatol Sci. 2006 Sep;43(3):189-200. doi: 10.1016/j.jdermsci.2006.05.007. Epub 2006 Jun 27.
3
Livin, a novel inhibitor of apoptosis protein family member.生存素,一种新型凋亡抑制蛋白家族成员。
J Biol Chem. 2001 Feb 2;276(5):3238-46. doi: 10.1074/jbc.M003670200. Epub 2000 Oct 9.
4
Research progress on Livin protein: an inhibitor of apoptosis.凋亡抑制蛋白 Livin 的研究进展。
Mol Cell Biochem. 2011 Nov;357(1-2):39-45. doi: 10.1007/s11010-011-0873-7. Epub 2011 May 27.
5
Isoform-specific silencing of the Livin gene by RNA interference defines Livin beta as key mediator of apoptosis inhibition in HeLa cells.通过RNA干扰对Livin基因进行亚型特异性沉默确定Livinβ是HeLa细胞中凋亡抑制的关键介质。
J Mol Med (Berl). 2006 Mar;84(3):232-40. doi: 10.1007/s00109-005-0021-5. Epub 2005 Dec 31.
6
Suppression of livin gene expression by siRNA leads to growth inhibition and apoptosis induction in human bladder cancer T24 cells.小干扰RNA抑制livin基因表达可导致人膀胱癌T24细胞生长抑制和凋亡诱导。
Biosci Biotechnol Biochem. 2010;74(5):1039-44. doi: 10.1271/bbb.90934. Epub 2010 May 7.
7
Inhibitors of apoptosis: clinical implications in cancer.凋亡抑制剂:癌症中的临床意义。
Apoptosis. 2017 Dec;22(12):1487-1509. doi: 10.1007/s10495-017-1429-4.
8
Caspase-mediated cleavage converts Livin from an antiapoptotic to a proapoptotic factor: implications for drug-resistant melanoma.半胱天冬酶介导的切割将生存素从抗凋亡因子转变为促凋亡因子:对耐药性黑色素瘤的影响。
Cancer Res. 2003 Oct 1;63(19):6340-9.
9
The oncolytic activity of Newcastle disease virus NDV-HUJ on chemoresistant primary melanoma cells is dependent on the proapoptotic activity of the inhibitor of apoptosis protein Livin.新城疫病毒 NDV-HUJ 对化疗耐药性原发性黑素瘤细胞的溶瘤活性依赖于凋亡抑制蛋白 Livin 的促凋亡活性。
J Virol. 2010 Jan;84(1):639-46. doi: 10.1128/JVI.00401-09.
10
Engineering ML-IAP to produce an extraordinarily potent caspase 9 inhibitor: implications for Smac-dependent anti-apoptotic activity of ML-IAP.工程化改造ML-IAP以产生一种极其有效的半胱天冬酶9抑制剂:对ML-IAP的Smac依赖性抗凋亡活性的影响。
Biochem J. 2005 Jan 1;385(Pt 1):11-20. doi: 10.1042/BJ20041108.

引用本文的文献

1
Tazarotene-Induced Gene 3 (TIG3) Induces Apoptosis in Melanoma Cells Through the Modulation of Inhibitors of Apoptosis Proteins.他扎罗汀诱导基因3(TIG3)通过调节凋亡抑制蛋白诱导黑色素瘤细胞凋亡。
Biomedicines. 2025 Jul 17;13(7):1749. doi: 10.3390/biomedicines13071749.
2
Livin promotes Th2-type immune response in airway allergic diseases.Livin 促进气道过敏性疾病中的 Th2 型免疫应答。
Immunol Res. 2022 Oct;70(5):624-632. doi: 10.1007/s12026-022-09294-9. Epub 2022 Jun 18.
3
BIRC7 and STC2 Expression Are Associated With Tumorigenesis and Poor Outcome in Extrahepatic Cholangiocarcinoma.
BIRC7 和 STC2 的表达与肝外胆管癌的肿瘤发生和不良预后相关。
Technol Cancer Res Treat. 2020 Jan-Dec;19:1533033820971676. doi: 10.1177/1533033820971676.
4
Methylation-mediated miR-214 regulates proliferation and drug sensitivity of renal cell carcinoma cells through targeting LIVIN.甲基化介导的 miR-214 通过靶向 LIVIN 调节肾细胞癌细胞的增殖和药物敏感性。
J Cell Mol Med. 2020 Jun;24(11):6410-6425. doi: 10.1111/jcmm.15287. Epub 2020 May 12.
5
Clinical benefits of Livin peptide-loaded DCs/CIKs combined with chemotherapy in advanced non-small cell lung cancer.负载Livin肽的树突状细胞/细胞因子诱导的杀伤细胞联合化疗在晚期非小细胞肺癌中的临床益处
Am J Cancer Res. 2019 Feb 1;9(2):406-414. eCollection 2019.
6
High BIRC7 Expression Might Be an Independent Prognostic Indicator of Poor Recurrence-Free Survival in Patients With Prostate Cancer.高BIRC7表达可能是前列腺癌患者无复发生存期不佳的独立预后指标。
Technol Cancer Res Treat. 2018 Jan 1;17:1533033818809694. doi: 10.1177/1533033818809694.
7
Immune surveillance in melanoma: From immune attack to melanoma escape and even counterattack.黑色素瘤中的免疫监视:从免疫攻击到黑色素瘤逃逸,甚至反击。
Cancer Biol Ther. 2017 Jul 3;18(7):451-469. doi: 10.1080/15384047.2017.1323596. Epub 2017 May 17.
8
Molecular impact of selective NFKB1 and NFKB2 signaling on DLBCL phenotype.选择性NFKB1和NFKB2信号传导对弥漫性大B细胞淋巴瘤(DLBCL)表型的分子影响。
Oncogene. 2017 Jul 20;36(29):4224-4232. doi: 10.1038/onc.2017.90. Epub 2017 Apr 3.
9
Silencing the gene enhances the cytotoxic effects of anticancer drugs on colon cancer cells.使该基因沉默可增强抗癌药物对结肠癌细胞的细胞毒性作用。
Ann Surg Treat Res. 2016 Dec;91(6):273-277. doi: 10.4174/astr.2016.91.6.273. Epub 2016 Nov 25.
10
Overexpression of Livin promotes migration and invasion of colorectal cancer cells by induction of epithelial-mesenchymal transition via NF-κB activation.Livin的过表达通过激活NF-κB诱导上皮-间质转化,从而促进结肠癌细胞的迁移和侵袭。
Onco Targets Ther. 2016 Feb 29;9:1011-21. doi: 10.2147/OTT.S93738. eCollection 2016.