• 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

κ 阿片受体可能通过调节乳腺癌中的血管生成而成为一种潜在的肿瘤抑制因子。

The kappa opioid receptor may be a potential tumor suppressor by regulating angiogenesis in breast cancer.

机构信息

Department of Anesthesiology, Renji Hospital, Shanghai Jiaotong University, School of Medicine, Shanghai 200127, China.

Department of Anesthesiology, Renji Hospital, Shanghai Jiaotong University, School of Medicine, Shanghai 200127, China.

出版信息

Med Hypotheses. 2021 May;150:110568. doi: 10.1016/j.mehy.2021.110568. Epub 2021 Mar 23.

DOI:10.1016/j.mehy.2021.110568
PMID:33780776
Abstract

Our hypothesis proposes that activating κ-opioid receptors (KORs) may inhibit the progression of breast cancer and improve patient prognosis. Consequently, KORs may become a promising therapeutic target for breast cancer. Activating KORs induces not only analgesic efficacy comparable to μ-opioid receptors but also shows a promising antitumor effect and with fewer opioid-induced adverse effects. Based on present studies and our bioinformatics analysis of KORs, we propose that KORs can function as a tumor suppressor by inhibiting angiogenesis in human breast cancer; therefore, analgesics that mainly activate KORs would be more suitable for breast cancer patients.

摘要

我们的假设提出,激活 κ 阿片受体(KOR)可能会抑制乳腺癌的进展并改善患者的预后。因此,KOR 可能成为治疗乳腺癌的有前途的靶点。激活 KOR 不仅会产生与 μ 阿片受体相当的镇痛效果,而且还显示出有前途的抗肿瘤作用,并且阿片类药物引起的不良反应较少。基于目前的研究和我们对 KOR 的生物信息学分析,我们提出 KOR 可以通过抑制人乳腺癌中的血管生成来发挥肿瘤抑制作用;因此,主要激活 KOR 的镇痛药将更适合乳腺癌患者。

相似文献

1
The kappa opioid receptor may be a potential tumor suppressor by regulating angiogenesis in breast cancer.κ 阿片受体可能通过调节乳腺癌中的血管生成而成为一种潜在的肿瘤抑制因子。
Med Hypotheses. 2021 May;150:110568. doi: 10.1016/j.mehy.2021.110568. Epub 2021 Mar 23.
2
Analysis of the Immunoexpression of Opioid Receptors and their Correlation with Markers of Angiogenesis, Cell Proliferation and Apoptosis in Breast Cancer.乳腺癌中阿片受体的免疫表达分析及其与血管生成、细胞增殖和凋亡标志物的相关性
Asian Pac J Cancer Prev. 2021 Feb 1;22(2):633-640. doi: 10.31557/APJCP.2021.22.2.633.
3
Pharmacological Characterization of Dezocine, a Potent Analgesic Acting as a κ Partial Agonist and μ Partial Agonist.地佐辛的药理学特征:一种强效的阿片类镇痛药,作为 κ 部分激动剂和 μ 部分激动剂。
Sci Rep. 2018 Sep 20;8(1):14087. doi: 10.1038/s41598-018-32568-y.
4
Delta and kappa opioid receptors as suitable drug targets for pain.德尔塔和卡帕阿片受体作为治疗疼痛的合适药物靶点。
Clin J Pain. 2010 Jan;26 Suppl 10:S10-5. doi: 10.1097/AJP.0b013e3181c49e3a.
5
The contribution of activated peripheral kappa opioid receptors (kORs) in the inflamed knee joint to anti-nociception.炎症膝关节中活化的外周κ阿片受体(kORs)对镇痛的作用。
Brain Res. 2016 Oct 1;1648(Pt A):11-18. doi: 10.1016/j.brainres.2016.06.048. Epub 2016 Jul 1.
6
MGM-9 [(E)-methyl 2-(3-ethyl-7a,12a-(epoxyethanoxy)-9-fluoro-1,2,3,4,6,7,12,12b-octahydro-8-methoxyindolo[2,3-a]quinolizin-2-yl)-3-methoxyacrylate], a derivative of the indole alkaloid mitragynine: a novel dual-acting mu- and kappa-opioid agonist with potent antinociceptive and weak rewarding effects in mice.MGM-9 [(E)-2-(3-乙基-7a,12a-(环氧乙氧基)-9-氟-1,2,3,4,6,7,12,12b-八氢-8-甲氧基吲哚并[2,3-a]喹嗪-2-基)-3-甲氧基丙烯酸甲酯],一种吲哚生物碱米托蒽醌的衍生物:一种新型的μ和κ阿片类双效激动剂,在小鼠中具有强效的抗伤害感受作用和微弱的奖赏效应。
Neuropharmacology. 2008 Aug;55(2):154-65. doi: 10.1016/j.neuropharm.2008.05.003. Epub 2008 May 9.
7
Morphine can produce analgesia via spinal kappa opioid receptors in the absence of mu opioid receptors.在没有μ阿片受体的情况下,吗啡可通过脊髓κ阿片受体产生镇痛作用。
Brain Res. 2006 Apr 14;1083(1):61-9. doi: 10.1016/j.brainres.2006.01.095. Epub 2006 Mar 10.
8
The Quest for More Effective Analgesics with Reduced Abuse Liability and Fewer Adverse Effects: Promises, Pitfalls, and Future Perspectives of Biased Agonists at Opioid Receptors.追求具有更低滥用倾向和更少不良反应的更有效的镇痛药:阿片受体偏激动剂的前景、挑战和未来。
Methods Mol Biol. 2021;2201:181-192. doi: 10.1007/978-1-0716-0884-5_16.
9
Antinociceptive profiles of mu and kappa opioid agonists in a rat tooth pulp stimulation procedure.μ和κ阿片类激动剂在大鼠牙髓刺激实验中的抗伤害感受特性
J Pharmacol Exp Ther. 1986 Jan;236(1):111-7.
10
Functional interaction between alpha2-adrenoceptors, mu- and kappa-opioid receptors in the guinea pig myenteric plexus: effect of chronic desipramine treatment.豚鼠肠肌丛中α2 -肾上腺素能受体、μ -阿片受体和κ -阿片受体之间的功能相互作用:慢性地昔帕明治疗的影响
Eur J Pharmacol. 2006 Dec 28;553(1-3):269-79. doi: 10.1016/j.ejphar.2006.09.025. Epub 2006 Sep 23.

引用本文的文献

1
Cancer and neurotransmitter receptors.癌症与神经递质受体
Chin Med J (Engl). 2025 Jul 5;138(13):1540-1558. doi: 10.1097/CM9.0000000000003656. Epub 2025 May 30.
2
Impact of opioids and mu-opioid receptors on oncologic metastasis.阿片类药物和μ-阿片受体对肿瘤转移的影响。
Am J Cancer Res. 2024 Sep 15;14(9):4236-4247. doi: 10.62347/SCLS3277. eCollection 2024.
3
Synthesis and Antiproliferative Activity against Cancer Cells of Indole-Aryl-Amide Derivatives.吲哚-芳基酰胺衍生物的合成及对癌细胞的抗增殖活性。
Molecules. 2022 Dec 28;28(1):265. doi: 10.3390/molecules28010265.
4
Opioids in cancer: The κ‑opioid receptor (Review).阿片类药物在癌症中的作用:κ 阿片受体(综述)。
Mol Med Rep. 2022 Feb;25(2). doi: 10.3892/mmr.2021.12560. Epub 2021 Dec 8.