• 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

MMP-14 和 MMP-19 的共表达预示着人类脑胶质瘤患者的不良预后。

Co-expression of MMP-14 and MMP-19 predicts poor survival in human glioma.

机构信息

Department of Neurosurgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, 710038, People's Republic of China.

出版信息

Clin Transl Oncol. 2013 Feb;15(2):139-45. doi: 10.1007/s12094-012-0900-5. Epub 2012 Jul 19.

DOI:10.1007/s12094-012-0900-5
PMID:22855183
Abstract

AIM

Matrix metalloproteinase (MMP)-14 and MMP-19 have been demonstrated to play an important role in the development of human gliomas. However, their prognostic values are not clear. The aim of this study was to investigate whether co-expression of MMP-14 and MMP-19 has prognostic relevance in human gliomas.

METHODS

Immunohistochemistry and western blot were used to investigate the expression of MMP-14 and MMP-19 proteins in 128 patients with gliomas.

RESULTS

The expression levels of MMP-14 and MMP-19 proteins in glioma tissues were both significantly higher (both P < 0.001) than those in non-neoplastic brain tissues according to the immunohistochemistry analysis, which was confirmed by the western blot analysis. Additionally, the overexpression of either MMP-14 or MMP-19 was significantly associated with the advanced WHO grade (both P = 0.02), the low Karnofsky performance score (KPS) (P = 0.008 and 0.01, respectively) and the poor overall survival (both P = 0.01). Moreover, the Multivariate Cox proportional-hazards regression analysis revealed that the increased expressions of MMP-14 and MMP-19 were both independent prognostic factors for poor overall survival (both P = 0.02). Furthermore, the co-expression of MMP-14 and MMP-19 was additively and more significantly (P = 0.006) associated with adverse prognosis in patients with gliomas than respective expression of MMP-14 and MMP-19.

CONCLUSIONS

These findings indicated for the first time that the co-expression of MMP-14 and MMP-19 is significantly correlated with prognosis in glioma patients, suggesting that the co-expression of these proteins may be used as both an early diagnostic and independent prognostic marker.

摘要

目的

基质金属蛋白酶(MMP)-14 和 MMP-19 已被证明在人类脑胶质瘤的发展中发挥重要作用。然而,它们的预后价值尚不清楚。本研究旨在探讨 MMP-14 和 MMP-19 的共表达是否与人类脑胶质瘤的预后相关。

方法

免疫组织化学和 Western blot 用于检测 128 例脑胶质瘤患者中 MMP-14 和 MMP-19 蛋白的表达。

结果

根据免疫组织化学分析,胶质瘤组织中 MMP-14 和 MMP-19 蛋白的表达水平均明显高于非肿瘤性脑组织(均 P < 0.001),Western blot 分析也证实了这一点。此外,MMP-14 或 MMP-19 的过表达均与高级别 WHO 分级(均 P = 0.02)、较低的 Karnofsky 表现评分(KPS)(分别为 P = 0.008 和 0.01)和较差的总生存时间(均 P = 0.01)显著相关。此外,多变量 Cox 比例风险回归分析显示,MMP-14 和 MMP-19 的表达增加均是总生存时间不良的独立预后因素(均 P = 0.02)。此外,与 MMP-14 和 MMP-19 各自的表达相比,MMP-14 和 MMP-19 的共表达与胶质瘤患者的预后不良更显著相关(P = 0.006)。

结论

这些发现首次表明,MMP-14 和 MMP-19 的共表达与胶质瘤患者的预后显著相关,提示这些蛋白的共表达可能被用作早期诊断和独立的预后标志物。

相似文献

1
Co-expression of MMP-14 and MMP-19 predicts poor survival in human glioma.MMP-14 和 MMP-19 的共表达预示着人类脑胶质瘤患者的不良预后。
Clin Transl Oncol. 2013 Feb;15(2):139-45. doi: 10.1007/s12094-012-0900-5. Epub 2012 Jul 19.
2
Collaborative overexpression of matrix metalloproteinase-1 and vascular endothelial growth factor-C predicts adverse prognosis in patients with gliomas.基质金属蛋白酶-1 和血管内皮生长因子-C 的协同过表达预测胶质瘤患者的不良预后。
Cancer Epidemiol. 2013 Oct;37(5):697-702. doi: 10.1016/j.canep.2013.06.006. Epub 2013 Jul 17.
3
Overexpression of a disintegrin and metalloprotease 8 in human gliomas is implicated in tumor progression and prognosis.人神经胶质瘤中整联蛋白和金属蛋白酶 8 的过表达与肿瘤进展和预后相关。
Med Oncol. 2012 Sep;29(3):2032-7. doi: 10.1007/s12032-011-0084-9. Epub 2011 Oct 9.
4
Oncogenic reg IV is a novel prognostic marker for glioma patient survival.致癌基因 reg IV 是一种新的胶质母细胞瘤患者生存预后标志物。
Diagn Pathol. 2012 Jun 19;7:69. doi: 10.1186/1746-1596-7-69.
5
Co-expression of midkine and pleiotrophin predicts poor survival in human glioma.中期因子与多效生长因子的共表达预示着人类胶质瘤患者的不良生存预后。
J Clin Neurosci. 2014 Nov;21(11):1885-90. doi: 10.1016/j.jocn.2014.02.020. Epub 2014 Jul 4.
6
Down-regulation of Nedd4L is associated with the aggressive progression and worse prognosis of malignant glioma.Nedd4L 的下调与恶性脑胶质瘤的侵袭性进展和预后不良有关。
Jpn J Clin Oncol. 2012 Mar;42(3):196-201. doi: 10.1093/jjco/hyr195. Epub 2012 Jan 4.
7
Overexpression of CCL20 and its receptor CCR6 predicts poor clinical prognosis in human gliomas.CCL20 和其受体 CCR6 的过表达预示着人类脑胶质瘤的临床预后不良。
Med Oncol. 2012 Dec;29(5):3491-7. doi: 10.1007/s12032-012-0314-9. Epub 2012 Aug 28.
8
Up-regulation of microRNA-15b correlates with unfavorable prognosis and malignant progression of human glioma.微小RNA-15b的上调与人类胶质瘤的不良预后和恶性进展相关。
Int J Clin Exp Pathol. 2015 May 1;8(5):4943-52. eCollection 2015.
9
Downregulation of chromatin remodeling factor CHD5 is associated with a poor prognosis in human glioma.染色质重塑因子 CHD5 的下调与人类神经胶质瘤的不良预后相关。
J Clin Neurosci. 2013 Jul;20(7):958-63. doi: 10.1016/j.jocn.2012.07.021. Epub 2013 May 23.
10
Upregulation of matrix metalloproteinase-1 and proteinase-activated receptor-1 promotes the progression of human gliomas.基质金属蛋白酶-1 和蛋白酶激活受体-1 的上调促进了人类脑胶质瘤的进展。
Pathol Res Pract. 2011 Jan 15;207(1):24-9. doi: 10.1016/j.prp.2010.10.003. Epub 2010 Nov 18.

引用本文的文献

1
Enhancing Prognostic Signatures in Glioblastoma with Feature Selection and Regularised Cox Regression.通过特征选择和正则化Cox回归增强胶质母细胞瘤的预后特征
Genes (Basel). 2025 Apr 23;16(5):473. doi: 10.3390/genes16050473.
2
Comparison of 5-aminolevulinic acid and MMP-14 targeted peptide probes in preclinical models of GBM.5-氨基酮戊酸与MMP-14靶向肽探针在胶质母细胞瘤临床前模型中的比较
Theranostics. 2025 Feb 24;15(8):3517-3531. doi: 10.7150/thno.107210. eCollection 2025.
3
Decoding the Role of Kinesin Superfamily Proteins in Glioma Progression.

本文引用的文献

1
Matrix metalloproteinase 14 and 19 expression is associated with thoracic aortic aneurysms.基质金属蛋白酶 14 和 19 的表达与胸主动脉瘤有关。
J Thorac Cardiovasc Surg. 2012 Aug;144(2):459-66. doi: 10.1016/j.jtcvs.2011.08.043. Epub 2011 Sep 28.
2
Molecular characterization of porcine MMP19 and MMP23B genes and its association with immune traits.猪 MMP19 和 MMP23B 基因的分子特征及其与免疫特性的关联。
Int J Biol Sci. 2011;7(8):1101-13. doi: 10.7150/ijbs.7.1101. Epub 2011 Sep 14.
3
Inhibition of matrix metalloproteinase 14 (MMP-14)-mediated cancer cell migration.
解析驱动蛋白超家族蛋白在胶质瘤进展中的作用
J Mol Neurosci. 2025 Jan 23;75(1):10. doi: 10.1007/s12031-025-02308-9.
4
Molecular Determinants for Photodynamic Therapy Resistance and Improved Photosensitizer Delivery in Glioma.用于光动力疗法耐药性的分子决定因素和脑胶质瘤中光敏剂传递的改进。
Int J Mol Sci. 2024 Aug 9;25(16):8708. doi: 10.3390/ijms25168708.
5
The tumor-associated fibrotic reactions in microenvironment aggravate glioma chemoresistance.微环境中肿瘤相关的纤维化反应会加重胶质瘤的化疗耐药性。
Front Oncol. 2024 May 28;14:1388700. doi: 10.3389/fonc.2024.1388700. eCollection 2024.
6
Unravelling molecular dynamics in living cells: Fluorescent protein biosensors for cell biology.解析活细胞中的分子动力学:用于细胞生物学的荧光蛋白生物传感器
J Microsc. 2025 May;298(2):123-184. doi: 10.1111/jmi.13270. Epub 2024 Feb 15.
7
Screening MT1-MMP Activity and Inhibition in Three-Dimensional Tumor Spheroids.在三维肿瘤球体中筛选MT1-MMP活性及抑制作用
Biomedicines. 2023 Feb 15;11(2):562. doi: 10.3390/biomedicines11020562.
8
Comprehensive Analysis of Inflammatory Response-Related Genes, and Prognosis and Immune Infiltration in Patients With Low-Grade Glioma.低级别胶质瘤患者炎症反应相关基因、预后及免疫浸润的综合分析
Front Pharmacol. 2021 Oct 12;12:748993. doi: 10.3389/fphar.2021.748993. eCollection 2021.
9
Molecular and Cellular Complexity of Glioma. Focus on Tumour Microenvironment and the Use of Molecular and Imaging Biomarkers to Overcome Treatment Resistance.脑胶质瘤的分子和细胞复杂性。关注肿瘤微环境和使用分子及影像生物标志物克服治疗抵抗。
Int J Mol Sci. 2020 Aug 6;21(16):5631. doi: 10.3390/ijms21165631.
10
OSlgg: An Online Prognostic Biomarker Analysis Tool for Low-Grade Glioma.OSlgg:一种用于低级别胶质瘤的在线预后生物标志物分析工具。
Front Oncol. 2020 Jul 7;10:1097. doi: 10.3389/fonc.2020.01097. eCollection 2020.
抑制基质金属蛋白酶 14(MMP-14)介导的癌细胞迁移。
J Biol Chem. 2011 Sep 23;286(38):33167-77. doi: 10.1074/jbc.M111.256644. Epub 2011 Jul 27.
4
Single nucleotide polymorphisms and haplotypes of MMP-14 are associated with the risk and pathological development of oral cancer.单核苷酸多态性和 MMP-14 单倍型与口腔癌的风险和病理发展有关。
Ann Surg Oncol. 2012 Jul;19 Suppl 3:S319-27. doi: 10.1245/s10434-011-1736-x. Epub 2011 Apr 22.
5
MicroRNA-10b induces glioma cell invasion by modulating MMP-14 and uPAR expression via HOXD10.miR-10b 通过调节 HOXD10 诱导 MMP-14 和 uPAR 的表达促进胶质瘤细胞侵袭。
Brain Res. 2011 May 10;1389:9-18. doi: 10.1016/j.brainres.2011.03.013. Epub 2011 Mar 16.
6
New signaling pathways from cancer progression modulators to mRNA expression of matrix metalloproteinases in breast cancer cells.从癌症进展调节剂到乳腺癌细胞中基质金属蛋白酶 mRNA 表达的新信号通路。
J Cell Physiol. 2011 Dec;226(12):3378-84. doi: 10.1002/jcp.22694.
7
Role of MMP14 gene polymorphisms in susceptibility and pathological development to hepatocellular carcinoma.MMP14 基因多态性在肝癌易感性和病理发展中的作用。
Ann Surg Oncol. 2011 Aug;18(8):2348-56. doi: 10.1245/s10434-011-1574-x. Epub 2011 Feb 5.
8
Catalytic activity of Matrix metalloproteinase-19 is essential for tumor suppressor and anti-angiogenic activities in nasopharyngeal carcinoma.基质金属蛋白酶-19 的催化活性对于鼻咽癌中的肿瘤抑制和抗血管生成活性至关重要。
Int J Cancer. 2011 Oct 15;129(8):1826-37. doi: 10.1002/ijc.25855. Epub 2011 Apr 1.
9
Expressions of matrix metalloproteinase-7 and matrix metalloproteinase-14 associated with the activation of extracellular signal-regulated kinase1/2 in human brain gliomas of different pathological grades.不同病理分级人脑胶质瘤中细胞外信号调节激酶 1/2 激活相关的基质金属蛋白酶-7 和基质金属蛋白酶-14 的表达。
Med Oncol. 2011 Dec;28 Suppl 1:S433-8. doi: 10.1007/s12032-010-9660-7. Epub 2010 Aug 31.
10
Many new down- and up-regulatory signaling pathways, from known cancer progression suppressors to matrix metalloproteinases, differ widely in cells of various cancers.许多新的下调和上调信号通路,从已知的癌症进展抑制剂到基质金属蛋白酶,在不同癌症的细胞中差异很大。
J Cell Physiol. 2010 Aug;224(2):549-58. doi: 10.1002/jcp.22157.