• 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

CPNE3 的上调通过抑制 FAK 通路失活来抑制脑胶质瘤细胞的侵袭、迁移和增殖。

Upregulation of CPNE3 suppresses invasion, migration and proliferation of glioblastoma cells through FAK pathway inactivation.

机构信息

Department of Neurosurgery, Chongqing General Hospital, University of Chinese Academy of Science, 118 Xingguang Avenue, Liangjiang New Area, Chongqing, 400016, China.

出版信息

J Mol Histol. 2021 Jun;52(3):589-596. doi: 10.1007/s10735-021-09966-0. Epub 2021 Mar 16.

DOI:10.1007/s10735-021-09966-0
PMID:33725213
Abstract

Glioblastoma (GBM) is a deadly brain tumor with a bleak prognosis. In recent years, the copine III (CPNE3) protein was discovered to be associated to metastasis across various types of malignancies. Nevertheless, its function has not been well documented in glioma. This study characterizes CPNE3 expression in GBM along with its impact and underlying molecular mechanism with regards to cellular migration, invasion and proliferation. Immunohistochemistry was used to characterizes CPNE3 expression in the glioma tissues. Then, knockdown of CPNE3 expression was used to analyze the role of CPNE3 in GBM cell viability, migration, invasion. Western blot analysis was performed to measure the protein levels of FAK signaling pathway. We found that GBM tissues had higher CPNE3 expressions as compared to those in normal brain tissues. CPNE3 silencing in GBM cells impaired the migratory, invasive and proliferative abilities of GBM cells that can be attributed to inactivation of the FAK signaling pathway. Collectively, these findings highlight the role of CPNE3 as a new biomarker, offering deeper insights into its carcinogenic role in GBM.

摘要

胶质母细胞瘤(GBM)是一种预后不良的致命脑肿瘤。近年来,发现连蛋白 III(CPNE3)蛋白与各种类型恶性肿瘤的转移有关。然而,其在神经胶质瘤中的功能尚未得到很好的阐述。本研究描述了 CPNE3 在 GBM 中的表达及其对细胞迁移、侵袭和增殖的影响及潜在的分子机制。免疫组织化学用于描述神经胶质瘤组织中 CPNE3 的表达。然后,敲低 CPNE3 的表达,分析 CPNE3 在 GBM 细胞活力、迁移、侵袭中的作用。Western blot 分析用于测量 FAK 信号通路的蛋白水平。我们发现,与正常脑组织相比,GBM 组织中 CPNE3 的表达更高。CPNE3 在 GBM 细胞中的沉默削弱了 GBM 细胞的迁移、侵袭和增殖能力,这可归因于 FAK 信号通路的失活。总之,这些发现强调了 CPNE3 作为一个新的生物标志物的作用,为其在 GBM 中的致癌作用提供了更深入的见解。

相似文献

1
Upregulation of CPNE3 suppresses invasion, migration and proliferation of glioblastoma cells through FAK pathway inactivation.CPNE3 的上调通过抑制 FAK 通路失活来抑制脑胶质瘤细胞的侵袭、迁移和增殖。
J Mol Histol. 2021 Jun;52(3):589-596. doi: 10.1007/s10735-021-09966-0. Epub 2021 Mar 16.
2
EphB2 receptor controls proliferation/migration dichotomy of glioblastoma by interacting with focal adhesion kinase.EphB2 受体通过与粘着斑激酶相互作用控制神经胶质瘤的增殖/迁移二分法。
Oncogene. 2012 Dec 13;31(50):5132-43. doi: 10.1038/onc.2012.16. Epub 2012 Feb 6.
3
O6-Methylguanine-DNA methyltransferase is a novel negative effector of invasion in glioblastoma multiforme.O6-甲基鸟嘌呤-DNA 甲基转移酶是胶质母细胞瘤侵袭的新型负效应因子。
Mol Cancer Ther. 2012 Nov;11(11):2440-50. doi: 10.1158/1535-7163.MCT-11-0977. Epub 2012 Sep 17.
4
MOB2 suppresses GBM cell migration and invasion via regulation of FAK/Akt and cAMP/PKA signaling.MOB2 通过调节 FAK/Akt 和 cAMP/PKA 信号通路抑制 GBM 细胞迁移和侵袭。
Cell Death Dis. 2020 Apr 14;11(4):230. doi: 10.1038/s41419-020-2381-8.
5
IKIP downregulates THBS1/FAK signaling to suppress migration and invasion by glioblastoma cells.IKIP 通过下调 THBS1/FAK 信号抑制胶质母细胞瘤细胞的迁移和侵袭。
Oncol Res. 2024 Jun 20;32(7):1173-1184. doi: 10.32604/or.2024.042456. eCollection 2024.
6
Overexpression of HOXC10 promotes glioblastoma cell progression to a poor prognosis via the PI3K/AKT signalling pathway.HOXC10 的过表达通过 PI3K/AKT 信号通路促进胶质母细胞瘤细胞向不良预后进展。
J Drug Target. 2019 Jan;27(1):60-66. doi: 10.1080/1061186X.2018.1473408. Epub 2018 Aug 6.
7
Up-regulated circular RNA hsa_circ_0067934 contributes to glioblastoma progression through activating PI3K-AKT pathway.上调的环状 RNA hsa_circ_0067934 通过激活 PI3K-AKT 通路促进胶质母细胞瘤进展。
Eur Rev Med Pharmacol Sci. 2019 Apr;23(8):3447-3454. doi: 10.26355/eurrev_201904_17709.
8
S100A11 functions as novel oncogene in glioblastoma via S100A11/ANXA2/NF-κB positive feedback loop.S100A11 通过 S100A11/ANXA2/NF-κB 正反馈环在胶质母细胞瘤中作为新的癌基因发挥作用。
J Cell Mol Med. 2019 Oct;23(10):6907-6918. doi: 10.1111/jcmm.14574. Epub 2019 Aug 20.
9
PPFIBP1 induces glioma cell migration and invasion through FAK/Src/JNK signaling pathway.PPFIBP1 通过 FAK/Src/JNK 信号通路诱导神经胶质瘤细胞迁移和侵袭。
Cell Death Dis. 2021 Sep 3;12(9):827. doi: 10.1038/s41419-021-04107-7.
10
Silencing of PROS1 induces apoptosis and inhibits migration and invasion of glioblastoma multiforme cells.PROS1基因沉默可诱导多形性胶质母细胞瘤细胞凋亡,并抑制其迁移和侵袭。
Int J Oncol. 2016 Dec;49(6):2359-2366. doi: 10.3892/ijo.2016.3755. Epub 2016 Nov 3.

引用本文的文献

1
DLX4 regulates rheumatoid arthritis fibroblast-like synoviocytes invasiveness and a cancer transcriptomic signature.DLX4调节类风湿性关节炎成纤维细胞样滑膜细胞的侵袭性及一种癌症转录组特征。
Sci Rep. 2025 Jul 11;15(1):25164. doi: 10.1038/s41598-025-08960-w.
2
Copine C plays a role in adhesion and streaming in .Copine C 在黏附和流动中起作用。
Cell Adh Migr. 2024 Dec;18(1):1-19. doi: 10.1080/19336918.2024.2315629. Epub 2024 Feb 20.
3
[High expression of CPNE3 correlates with poor long-term prognosis of gastric cancer by inhibiting cell apoptosis activating PI3K/AKT signaling].

本文引用的文献

1
Targeting focal adhesion kinase in cancer cells and the tumor microenvironment.靶向肿瘤细胞和肿瘤微环境中的黏着斑激酶。
Exp Mol Med. 2020 Jun;52(6):877-886. doi: 10.1038/s12276-020-0447-4. Epub 2020 Jun 9.
2
MOB2 suppresses GBM cell migration and invasion via regulation of FAK/Akt and cAMP/PKA signaling.MOB2 通过调节 FAK/Akt 和 cAMP/PKA 信号通路抑制 GBM 细胞迁移和侵袭。
Cell Death Dis. 2020 Apr 14;11(4):230. doi: 10.1038/s41419-020-2381-8.
3
Integrin Signaling in Cancer: Mechanotransduction, Stemness, Epithelial Plasticity, and Therapeutic Resistance.
CPNE3高表达通过抑制细胞凋亡、激活PI3K/AKT信号通路与胃癌的不良长期预后相关
Nan Fang Yi Ke Da Xue Xue Bao. 2024 Jan 20;44(1):129-137. doi: 10.12122/j.issn.1673-4254.2024.01.15.
4
miRNome and Proteome Profiling of Small Extracellular Vesicles Secreted by Human Glioblastoma Cell Lines and Primary Cancer Stem Cells.人胶质母细胞瘤细胞系和原发性癌症干细胞分泌的小细胞外囊泡的微小RNA组和蛋白质组分析
Biomedicines. 2022 Aug 4;10(8):1886. doi: 10.3390/biomedicines10081886.
5
CPNE3 interaction with RACK1 protects against myocardial ischemia/reperfusion injury.CPNE3与RACK1的相互作用可预防心肌缺血/再灌注损伤。
Exp Ther Med. 2022 Feb;23(2):128. doi: 10.3892/etm.2021.11051. Epub 2021 Dec 10.
6
Copine 3 "CPNE3" is a novel regulator for insulin secretion and glucose uptake in pancreatic β-cells.Copine 3“CPNE3”是胰腺β细胞胰岛素分泌和葡萄糖摄取的新型调节因子。
Sci Rep. 2021 Oct 19;11(1):20692. doi: 10.1038/s41598-021-00255-0.
7
The CPNE Family and Their Role in Cancers.CPNE家族及其在癌症中的作用。
Front Genet. 2021 Jul 23;12:689097. doi: 10.3389/fgene.2021.689097. eCollection 2021.
整合素信号在癌症中的作用:力学转导、干性、上皮可塑性和治疗抵抗。
Cancer Cell. 2019 Mar 18;35(3):347-367. doi: 10.1016/j.ccell.2019.01.007.
4
Integrins as A New Target for Cancer Treatment.整合素作为癌症治疗的新靶点。
Anticancer Agents Med Chem. 2019;19(5):580-586. doi: 10.2174/1871520618666181119103413.
5
Every step of the way: integrins in cancer progression and metastasis.在癌症进展和转移过程中的每一步:整合素。
Nat Rev Cancer. 2018 Sep;18(9):533-548. doi: 10.1038/s41568-018-0038-z.
6
High expression of CPNE3 predicts adverse prognosis in acute myeloid leukemia.CPNE3的高表达预示急性髓系白血病的不良预后。
Cancer Sci. 2017 Sep;108(9):1850-1857. doi: 10.1111/cas.13311. Epub 2017 Aug 20.
7
European Association for Neuro-Oncology (EANO) guideline on the diagnosis and treatment of adult astrocytic and oligodendroglial gliomas.欧洲神经肿瘤学会(EANO)成人星形细胞瘤和少突胶质细胞瘤诊断和治疗指南。
Lancet Oncol. 2017 Jun;18(6):e315-e329. doi: 10.1016/S1470-2045(17)30194-8. Epub 2017 May 5.
8
Direct binding of Copine3 with Jab1 activates downstream ErbB2 signaling and motility in SKBr3 breast cancer cells.Copine3与Jab1的直接结合激活了SKBr3乳腺癌细胞中的下游ErbB2信号传导和细胞运动性。
Oncol Rep. 2016 Feb;35(2):1147-52. doi: 10.3892/or.2015.4472. Epub 2015 Dec 2.
9
Tumour exosome integrins determine organotropic metastasis.肿瘤外泌体整合素决定器官特异性转移。
Nature. 2015 Nov 19;527(7578):329-35. doi: 10.1038/nature15756. Epub 2015 Oct 28.
10
An LSC epigenetic signature is largely mutation independent and implicates the HOXA cluster in AML pathogenesis.白血病干细胞的表观遗传特征在很大程度上与突变无关,并表明HOXA基因簇参与急性髓系白血病的发病机制。
Nat Commun. 2015 Oct 7;6:8489. doi: 10.1038/ncomms9489.