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本文引用的文献

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Roles of E-cadherin and Noncoding RNAs in the Epithelial-mesenchymal Transition and Progression in Gastric Cancer.E-钙黏蛋白和非编码 RNA 在胃癌上皮-间质转化及进展中的作用。
Int J Mol Sci. 2019 Jun 12;20(12):2870. doi: 10.3390/ijms20122870.
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A pan-cancer perspective of matrix metalloproteases (MMP) gene expression profile and their diagnostic/prognostic potential.基质金属蛋白酶(MMP)基因表达谱的泛癌分析及其诊断/预后潜力。
BMC Cancer. 2019 Jun 14;19(1):581. doi: 10.1186/s12885-019-5768-0.
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[Association between the expression of MMP1 gene and prognosis in head and neck squamous cell carcinoma].[基质金属蛋白酶1基因表达与头颈部鳞状细胞癌预后的关系]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2018 Feb;32(4):287-291. doi: 10.13201/j.issn.1001-1781.2018.04.011.
4
Gastric cancer in India: epidemiology and standard of treatment.印度的胃癌:流行病学与治疗标准
Updates Surg. 2018 Jun;70(2):233-239. doi: 10.1007/s13304-018-0527-3. Epub 2018 Apr 2.
5
Gastric cancer: epidemiology, prevention, classification, and treatment.胃癌:流行病学、预防、分类及治疗
Cancer Manag Res. 2018 Feb 7;10:239-248. doi: 10.2147/CMAR.S149619. eCollection 2018.
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E-cadherin: Its dysregulation in carcinogenesis and clinical implications.E-钙黏蛋白:在肿瘤发生中的失调及其临床意义。
Crit Rev Oncol Hematol. 2018 Jan;121:11-22. doi: 10.1016/j.critrevonc.2017.11.010. Epub 2017 Nov 20.
7
E-cadherin in gastric carcinomas: Relations with histological parameters and its prognostic value.E-钙黏蛋白在胃癌中的表达:与组织学参数的关系及其预后价值
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8
Relationships of MMP-9, E-cadherin, and VEGF expression with clinicopathological features and response to chemosensitivity in gastric cancer.基质金属蛋白酶-9、E-钙黏蛋白和血管内皮生长因子的表达与胃癌临床病理特征及化疗敏感性反应的关系
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胃癌中E-钙黏蛋白、血管内皮生长因子和基质金属蛋白酶的mRNA表达分析:一项初步研究

mRNA Expression Analysis of E-Cadherin, VEGF, and MMPs in Gastric Cancer: a Pilot Study.

作者信息

Kumar Puneet, Sebastian Arun, Verma Khushi, Dixit Ruhi, Kumari Soni, Singh Juhi, Tiwary Satyendra Kumar, Narayan Gopeshwar

机构信息

Department of Surgery, Institute of Medical Sciences, Banaras Hindu University, Varanasi, 221005 India.

Department of Molecular and Human Genetics, Institute of Science, Banaras Hindu University, Varanasi, 221005 India.

出版信息

Indian J Surg Oncol. 2021 Apr;12(Suppl 1):85-92. doi: 10.1007/s13193-020-01096-5. Epub 2020 May 22.

DOI:10.1007/s13193-020-01096-5
PMID:33994733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8119595/
Abstract

Gastric cancer (GC) is a serious fatal cancer on a global scale because of its presentation at advanced stage. The expressions of vascular endothelial growth factor (VEGF), E-cadherin, and matrix metalloproteinases (MMPs) in other cancers have been reported. However, its expression and underlying mechanisms are little known in gastric cancer in Indian context. In this study, we detected mRNA expression of VEGF, E-cadherin, and MMPs (MMP-1, MMP-2, and MMP-9) in 73 gastric cancer tissues and 27 normal controls by reverse-transcriptase polymerase chain reaction (RT-PCR). Receiver operator characteristics analysis was done for determining the diagnostic utility of VEGF, MMPs and E-cadherin with respect to the sensitivity and specificity. The association of VEGF, MMPs, and E-cadherin expression with the clinicopathological characteristics and the prognosis was subsequently analyzed. The mRNA expression results showed that E-cadherin was significantly downregulated in 47.9% of GC in comparison to control. There was no change in VEGF expression observed in 90.4% GC cases. MMP-1, MMP-2, and MMP-9 were overexpressed in 13.7%, 28.8%, and 11% of GC, respectively, with significant change in MMP-2 ( ≤ 0.0001) and MMP-9 ( = 0.027) in comparison to control. Our results strengthen the necessity of more studies to elucidate the prophetic role of these genes in the development of gastric cancer.

摘要

胃癌(GC)在全球范围内是一种严重的致命癌症,因为其多在晚期出现。其他癌症中血管内皮生长因子(VEGF)、E-钙黏蛋白和基质金属蛋白酶(MMPs)的表达已有报道。然而,在印度背景下,其在胃癌中的表达及潜在机制却鲜为人知。在本研究中,我们通过逆转录聚合酶链反应(RT-PCR)检测了73例胃癌组织和27例正常对照中VEGF、E-钙黏蛋白和MMPs(MMP-1、MMP-2和MMP-9)的mRNA表达。进行了受试者工作特征分析,以确定VEGF、MMPs和E-钙黏蛋白在敏感性和特异性方面的诊断效用。随后分析了VEGF、MMPs和E-钙黏蛋白表达与临床病理特征及预后的关系。mRNA表达结果显示,与对照相比,47.9%的胃癌中E-钙黏蛋白显著下调。90.4%的胃癌病例中未观察到VEGF表达变化。MMP-1、MMP-2和MMP-9分别在13.7%、28.8%和11%的胃癌中过表达,与对照相比,MMP-2(≤0.0001)和MMP-9(=0.027)有显著变化。我们的结果强化了开展更多研究以阐明这些基因在胃癌发生中预测作用的必要性。