• 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

三磷酸腺苷门控 P2X7 受体作为前列腺癌的一个潜在靶点。

ATP-gated P2X7 receptor as a potential target for prostate cancer.

机构信息

School of Laboratory Medicine, Weifang Medical University, Weifang, 261053, Shandong, China.

出版信息

Hum Cell. 2022 Sep;35(5):1346-1354. doi: 10.1007/s13577-022-00729-x. Epub 2022 Jun 3.

DOI:10.1007/s13577-022-00729-x
PMID:35657562
Abstract

Prostate cancer is the most common malignancy of the male genitourinary system and is one of the leading causes of male cancer death. The P2X7 receptor is an important member of purine receptor family. It is a gated ion channel with adenosine triphosphate (ATP) as the ligand, which exists in a variety of immune tissues and cells and can be involved in tumorigenesis and tumor progression. Studies have shown that the P2X7 receptor is abnormally expressed in prostate cancer, and is related to the level of prostate-specific antigen, P2X7 receptor may be an early biomarker of prostate cancer. The P2X7 receptor is essential in the occurrence and development of prostate cancer. The P2X7 receptor mainly affects the invasion and metastasis of prostate cancer cells through epithelial mesenchymal transition/invasion-related genes and the PI3K/AKT and ERK1/2 signaling pathways. The P2X7 receptor could be a promising therapeutic target for prostate cancer.

摘要

前列腺癌是男性泌尿生殖系统最常见的恶性肿瘤,也是男性癌症死亡的主要原因之一。P2X7 受体是嘌呤受体家族的重要成员。它是一种由三磷酸腺苷(ATP)作为配体的门控离子通道,存在于多种免疫组织和细胞中,可参与肿瘤的发生和发展。研究表明,P2X7 受体在前列腺癌中异常表达,与前列腺特异性抗原水平有关,P2X7 受体可能是前列腺癌的早期生物标志物。P2X7 受体在前列腺癌的发生发展中起关键作用。P2X7 受体主要通过上皮间质转化/侵袭相关基因以及 PI3K/AKT 和 ERK1/2 信号通路影响前列腺癌细胞的侵袭和转移。P2X7 受体可能成为前列腺癌有前途的治疗靶点。

相似文献

1
ATP-gated P2X7 receptor as a potential target for prostate cancer.三磷酸腺苷门控 P2X7 受体作为前列腺癌的一个潜在靶点。
Hum Cell. 2022 Sep;35(5):1346-1354. doi: 10.1007/s13577-022-00729-x. Epub 2022 Jun 3.
2
P2X7 mediates ATP-driven invasiveness in prostate cancer cells.P2X7介导前列腺癌细胞中由三磷酸腺苷驱动的侵袭性。
PLoS One. 2014 Dec 8;9(12):e114371. doi: 10.1371/journal.pone.0114371. eCollection 2014.
3
P2X7 receptor promotes migration and invasion of non-small cell lung cancer A549 cells through the PI3K/Akt pathways.P2X7 受体通过 PI3K/Akt 通路促进非小细胞肺癌 A549 细胞的迁移和侵袭。
Purinergic Signal. 2023 Dec;19(4):685-697. doi: 10.1007/s11302-023-09928-z. Epub 2023 Mar 1.
4
Highly-expressed P2X7 receptor promotes growth and metastasis of human HOS/MNNG osteosarcoma cells via PI3K/Akt/GSK3β/β-catenin and mTOR/HIF1α/VEGF signaling.高表达的 P2X7 受体通过 PI3K/Akt/GSK3β/β-catenin 和 mTOR/HIF1α/VEGF 信号通路促进人 HOS/MNNG 骨肉瘤细胞的生长和转移。
Int J Cancer. 2019 Aug 15;145(4):1068-1082. doi: 10.1002/ijc.32207. Epub 2019 Mar 18.
5
Research progress on the P2X7 receptor in liver injury and hepatocellular carcinoma.P2X7 受体在肝损伤和肝癌中的研究进展。
Chem Biol Drug Des. 2023 Mar;101(3):794-808. doi: 10.1111/cbdd.14182. Epub 2022 Nov 29.
6
Purinergic P2X7R as a potential target for pancreatic cancer.嘌呤能 P2X7R 作为胰腺癌的潜在靶点。
Clin Transl Oncol. 2023 Aug;25(8):2297-2305. doi: 10.1007/s12094-023-03123-7. Epub 2023 Mar 1.
7
P2X7 integrates PI3K/AKT and AMPK-PRAS40-mTOR signaling pathways to mediate tumor cell death.P2X7 整合 PI3K/AKT 和 AMPK-PRAS40-mTOR 信号通路来介导肿瘤细胞死亡。
PLoS One. 2013;8(4):e60184. doi: 10.1371/journal.pone.0060184. Epub 2013 Apr 2.
8
Atorvastatin prevents ATP-driven invasiveness via P2X7 and EHBP1 signaling in PTEN-expressing prostate cancer cells.阿托伐他汀通过 PTEN 表达的前列腺癌细胞中的 P2X7 和 EHBP1 信号通路抑制 ATP 驱动的侵袭。
Carcinogenesis. 2014 Jul;35(7):1547-55. doi: 10.1093/carcin/bgu019. Epub 2014 Jan 22.
9
P2X7 receptor stimulates breast cancer cell invasion and migration via the AKT pathway.P2X7受体通过AKT信号通路刺激乳腺癌细胞的侵袭和迁移。
Oncol Rep. 2015 Jul;34(1):103-10. doi: 10.3892/or.2015.3979. Epub 2015 May 13.
10
P2X7 receptor: a critical regulator and potential target for breast cancer.P2X7 受体:乳腺癌的关键调节因子和潜在治疗靶点。
J Mol Med (Berl). 2021 Mar;99(3):349-358. doi: 10.1007/s00109-021-02041-x. Epub 2021 Jan 23.

引用本文的文献

1
P2 purinergic receptor expression and function in tumor-related immune cells.P2嘌呤能受体在肿瘤相关免疫细胞中的表达与功能
Purinergic Signal. 2024 Oct 10. doi: 10.1007/s11302-024-10054-7.
2
Role of the P2X7 receptor in breast cancer progression.P2X7受体在乳腺癌进展中的作用。
Purinergic Signal. 2024 Jul 23. doi: 10.1007/s11302-024-10039-6.
3
P2 purinergic receptors regulate the progression of colorectal cancer.P2嘌呤能受体调节结直肠癌的进展。

本文引用的文献

1
An introduction to the special issue "The contribution of pannexin-1, connexins and CALHM ATP-release channels to purinergic signalling".特刊“泛连接蛋白-1、连接蛋白和CALHM ATP释放通道对嘌呤能信号传导的贡献”引言
Purinergic Signal. 2021 Dec;17(4):519. doi: 10.1007/s11302-021-09825-3.
2
P2X7 Variants in Oncogenesis.P2X7变体在肿瘤发生中的作用
Cells. 2021 Jan 19;10(1):189. doi: 10.3390/cells10010189.
3
Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications.雄激素受体信号通路在前列腺癌中的作用:从遗传学到临床应用。
Purinergic Signal. 2023 Dec 28. doi: 10.1007/s11302-023-09983-6.
Cells. 2020 Dec 10;9(12):2653. doi: 10.3390/cells9122653.
4
P2X receptors in cancer growth and progression.P2X受体在癌症生长和进展中的作用
Biochem Pharmacol. 2021 May;187:114350. doi: 10.1016/j.bcp.2020.114350. Epub 2020 Nov 28.
5
Update of P2X receptor properties and their pharmacology: IUPHAR Review 30.P2X 受体特性及其药理学更新:国际药理学联合会评论 30.
Br J Pharmacol. 2021 Feb;178(3):489-514. doi: 10.1111/bph.15299. Epub 2020 Dec 21.
6
The P2X7 purinergic receptor: a potential therapeutic target for lung cancer.P2X7 嘌呤能受体:肺癌的潜在治疗靶点。
J Cancer Res Clin Oncol. 2020 Nov;146(11):2731-2741. doi: 10.1007/s00432-020-03379-4. Epub 2020 Sep 5.
7
Effect of P2X7 receptor on tumorigenesis and its pharmacological properties.P2X7 受体对肿瘤发生的影响及其药理学特性。
Biomed Pharmacother. 2020 May;125:109844. doi: 10.1016/j.biopha.2020.109844. Epub 2020 Jan 28.
8
Absence of VEGFR-1/Flt-1 signaling pathway in mice results in insensitivity to discogenic low back pain in an established disc injury mouse model.在已建立的椎间盘损伤小鼠模型中,VEGFR-1/Flt-1 信号通路缺失的小鼠对椎间盘源性腰痛不敏感。
J Cell Physiol. 2020 Jun;235(6):5305-5317. doi: 10.1002/jcp.29416. Epub 2019 Dec 25.
9
Structure, function and techniques of investigation of the P2X7 receptor (P2X7R) in mammalian cells.哺乳动物细胞中P2X7受体(P2X7R)的结构、功能及研究技术
Methods Enzymol. 2019;629:115-150. doi: 10.1016/bs.mie.2019.07.043. Epub 2019 Sep 3.
10
Full-Length P2X Structures Reveal How Palmitoylation Prevents Channel Desensitization.全长 P2X 结构揭示了棕榈酰化如何防止通道脱敏。
Cell. 2019 Oct 17;179(3):659-670.e13. doi: 10.1016/j.cell.2019.09.017. Epub 2019 Oct 3.