• 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

亲吻素(KiSS-1):抑制肿瘤转移的关键因子

Kisspeptins (KiSS-1): essential players in suppressing tumor metastasis.

作者信息

Prabhu Venugopal Vinod, Sakthivel Kunnathur Murugesan, Guruvayoorappan Chandrasekharan

机构信息

Department of Biotechnology, Karunya University, Tamil Nadu, India E-mail :

出版信息

Asian Pac J Cancer Prev. 2013;14(11):6215-20. doi: 10.7314/apjcp.2013.14.11.6215.

DOI:10.7314/apjcp.2013.14.11.6215
PMID:24377507
Abstract

Kisspeptins (KPs) encoded by the KiSS-1 gene are C-terminally amidated peptide products, including KP- 10, KP-13, KP-14 and KP-54, which are endogenous agonists for the G-protein coupled receptor-54 (GPR54). Functional analyses have demonstrated fundamental roles of KiSS-1 in whole body homeostasis including sexual differentiation of brain, action on sex steroids and metabolic regulation of fertility essential for human puberty and maintenance of adult reproduction. In addition, intensive recent investigations have provided substantial evidence suggesting roles of Kisspeptin signalling via its receptor GPR54 in the suppression of metastasis with a variety of cancers. The present review highlights the latest studies regarding the role of Kisspeptins and the KiSS-1 gene in tumor progression and also suggests targeting the KiSS-1/GPR54 system may represent a novel therapeutic approach for cancers. Further investigations are essential to elucidate the complex pathways regulated by the Kisspeptins and how these pathways might be involved in the suppression of metastasis across a range of cancers.

摘要

由KiSS-1基因编码的亲吻素(KPs)是C末端酰胺化的肽产物,包括KP-10、KP-13、KP-14和KP-54,它们是G蛋白偶联受体54(GPR54)的内源性激动剂。功能分析表明,KiSS-1在全身稳态中发挥着重要作用,包括大脑的性别分化、对性类固醇的作用以及对人类青春期和成年生殖维持至关重要的生育能力的代谢调节。此外,最近的深入研究提供了大量证据,表明亲吻素通过其受体GPR54发出的信号在多种癌症的转移抑制中发挥作用。本综述重点介绍了关于亲吻素和KiSS-1基因在肿瘤进展中的作用的最新研究,并表明靶向KiSS-1/GPR54系统可能代表一种针对癌症的新型治疗方法。进一步的研究对于阐明亲吻素调节的复杂途径以及这些途径如何参与一系列癌症的转移抑制至关重要。

相似文献

1
Kisspeptins (KiSS-1): essential players in suppressing tumor metastasis.亲吻素(KiSS-1):抑制肿瘤转移的关键因子
Asian Pac J Cancer Prev. 2013;14(11):6215-20. doi: 10.7314/apjcp.2013.14.11.6215.
2
[KISS-1/GPR54 genes and their role in reproduction].[KISS-1/GPR54基因及其在生殖中的作用]
Yi Chuan. 2008 Apr;30(4):419-25. doi: 10.3724/sp.j.1005.2008.00419.
3
Kisspeptins: a multifunctional peptide system with a role in reproduction, cancer and the cardiovascular system.亲吻素:一个在生殖、癌症和心血管系统中发挥作用的多功能肽系统。
Br J Pharmacol. 2007 Aug;151(8):1143-53. doi: 10.1038/sj.bjp.0707295. Epub 2007 May 21.
4
Molecular evolution of multiple forms of kisspeptins and GPR54 receptors in vertebrates.脊椎动物中多种形式的亲吻素和GPR54受体的分子进化
Endocrinology. 2009 Jun;150(6):2837-46. doi: 10.1210/en.2008-1679. Epub 2009 Jan 22.
5
Sex steroids and leptin regulate the "first Kiss" (KiSS 1/G-protein-coupled receptor 54 system) in human gonadotropin-releasing-hormone-secreting neuroblasts.性类固醇和瘦素调节人促性腺激素释放激素分泌神经母细胞中的“初吻”(KiSS 1/G蛋白偶联受体54系统)。
J Sex Med. 2008 May;5(5):1097-1113. doi: 10.1111/j.1743-6109.2008.00782.x. Epub 2008 Mar 4.
6
GPR54 and KiSS-1: role in the regulation of puberty and reproduction.GPR54与KiSS-1:在青春期及生殖调节中的作用
Rev Endocr Metab Disord. 2006 Dec;7(4):257-63. doi: 10.1007/s11154-006-9020-2.
7
GPR54 and kisspeptin in reproduction.生殖中的GPR54与 kisspeptin
Hum Reprod Update. 2006 Sep-Oct;12(5):631-9. doi: 10.1093/humupd/dml023. Epub 2006 May 26.
8
The roles of kisspeptins and G protein-coupled receptor-54 in pubertal development.亲吻素和G蛋白偶联受体54在青春期发育中的作用。
Curr Opin Pediatr. 2006 Aug;18(4):442-7. doi: 10.1097/01.mop.0000236396.79580.cc.
9
The kisspeptin (KiSS-1)/GPR54 system in cancer biology.癌症生物学中的亲吻素(KiSS-1)/G蛋白偶联受体54(GPR54)系统
Cancer Treat Rev. 2008 Dec;34(8):682-92. doi: 10.1016/j.ctrv.2008.05.007. Epub 2008 Jun 25.
10
The Kiss-1/Kiss-1R complex as a negative regulator of cell motility and cancer metastasis (Review). Kiss-1/Kiss-1R 复合物作为细胞迁移和癌症转移的负调节剂(综述)。
Int J Mol Med. 2013 Oct;32(4):747-54. doi: 10.3892/ijmm.2013.1472. Epub 2013 Aug 21.

引用本文的文献

1
Kisspeptin Variations in Patients with Polycystic Ovary Syndrome-A Prospective Case Control Study.多囊卵巢综合征患者 kisspeptin 变化的前瞻性病例对照研究。
Medicina (Kaunas). 2022 Jun 8;58(6):776. doi: 10.3390/medicina58060776.
2
KISS1 in breast cancer progression and autophagy.KISS1 在乳腺癌进展和自噬中的作用。
Cancer Metastasis Rev. 2019 Sep;38(3):493-506. doi: 10.1007/s10555-019-09814-4.
3
Computational study of putative functional variants in human kisspeptin.人亲吻素中假定功能变体的计算研究。
J Genet Eng Biotechnol. 2017 Dec;15(2):419-422. doi: 10.1016/j.jgeb.2017.07.007. Epub 2017 Aug 2.
4
Kisspeptin and Cancer: Molecular Interaction, Biological Functions, and Future Perspectives.亲吻素与癌症:分子相互作用、生物学功能及未来展望
Front Endocrinol (Lausanne). 2018 Mar 27;9:115. doi: 10.3389/fendo.2018.00115. eCollection 2018.
5
Conformational analysis of a synthetic fish kisspeptin 1 peptide in membrane mimicking environments.膜模拟环境中一种合成鱼吻素1肽的构象分析
PLoS One. 2017 Oct 4;12(10):e0185892. doi: 10.1371/journal.pone.0185892. eCollection 2017.
6
TGF-β-Dependent Growth Arrest and Cell Migration in Benign and Malignant Breast Epithelial Cells Are Antagonistically Controlled by Rac1 and Rac1b.转化生长因子-β 依赖性生长停滞以及良性和恶性乳腺上皮细胞中的细胞迁移受Rac1和Rac1b的拮抗调控。
Int J Mol Sci. 2017 Jul 20;18(7):1574. doi: 10.3390/ijms18071574.
7
Cancer metastasis: enactment of the script for human reproductive drama.癌症转移:人类生殖剧脚本的上演。
Cancer Cell Int. 2017 May 2;17:51. doi: 10.1186/s12935-017-0421-y. eCollection 2017.
8
Downregulation of miR-199b is associated with distant metastasis in colorectal cancer via activation of SIRT1 and inhibition of CREB/KISS1 signaling.miR-199b的下调通过激活SIRT1和抑制CREB/KISS1信号通路与结直肠癌的远处转移相关。
Oncotarget. 2016 Jun 7;7(23):35092-105. doi: 10.18632/oncotarget.9042.
9
Kisspeptin signalling and its roles in humans.亲吻素信号传导及其在人类中的作用。
Singapore Med J. 2015 Dec;56(12):649-56. doi: 10.11622/smedj.2015183.