• 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

维生素E琥珀酸酯对人胃癌细胞中Fas和PCNA蛋白表达的影响及其临床意义

Effects of vitamin E succinate on the expression of Fas and PCNA proteins in human gastric carcinoma cells and its clinical significance.

作者信息

Wu Kun, Zhao Lan, Li Yao, Shan Yu-Juan, Wu Li-Jie

机构信息

Department of Nutrition and Food Hygiene, School of Public Health, Harbin Medical University, Harbin 150001, Heilongjiang Province, China.

出版信息

World J Gastroenterol. 2004 Apr 1;10(7):945-9. doi: 10.3748/wjg.v10.i7.945.

DOI:10.3748/wjg.v10.i7.945
PMID:15052671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4717109/
Abstract

AIM

To investigate the effects of vitamin E succinate (VES) on the expression of Fas and PCNA proteins as well as its clinical significance in human gastric carcinoma, and to explore the mechanism of VES-induced inhibition of gastric carcinoma cell growth.

METHODS

Immunohistochemical methods were used to detect Fas and PCNA expression both in human gastric cancer SGC-7901 cells treated with VES at different doses and in human gastric carcinoma tissues.

RESULTS

After the SGC-7901 cells were treated with VES at 5, 10, 20 mg/L for 48 h, the positive rates of Fas expression were 16%, 27% and 48%, respectively, significantly increased compared to that of control group (P< 0.05); while the positive rates of PCNA expression in groups treated with different doses of VES were 20%, 18% and 7%, respectively, which were significantly decreased compared to that of the control group (P<0.05). In human gastric carcinoma tissues, the Fas positive expression rate was 42.4%(25/59), which declined with the decrease in the degree of tumor differentiation (P<0.05) and with the existence of lymph node metastasis (P<0.001). While the PCNA positive expression rate was 91.5%(54/59), no relationship was observed between PCNA expression and clinicopathologic parameters.

CONCLUSION

VES inhibited the growth of gastric cancer cells by inducing Fas expression and inhibiting PCNA expression. It is, therefore, considered that the expression of Fas and PCNA genes, through tumor cell apoptosis and proliferation, respectively, may be useful as a clinical predictive index in the application of VES to gastric carcinoma therapy, where as Fas may be of more value than PCNA.

摘要

目的

探讨琥珀酸维生素E(VES)对人胃癌中Fas和PCNA蛋白表达的影响及其临床意义,探讨VES诱导胃癌细胞生长抑制的机制。

方法

采用免疫组化方法检测不同剂量VES处理的人胃癌SGC-7901细胞及人胃癌组织中Fas和PCNA的表达。

结果

SGC-7901细胞分别用5、10、20mg/L的VES处理48h后,Fas表达阳性率分别为16%、27%和48%,与对照组相比显著升高(P<0.05);而不同剂量VES处理组PCNA表达阳性率分别为20%、18%和7%,与对照组相比显著降低(P<0.05)。在人胃癌组织中,Fas阳性表达率为42.4%(25/59),随肿瘤分化程度降低(P<0.05)及有淋巴结转移(P<0.001)而下降。而PCNA阳性表达率为91.5%(54/59),PCNA表达与临床病理参数之间无相关性。

结论

VES通过诱导Fas表达和抑制PCNA表达抑制胃癌细胞生长。因此,认为Fas和PCNA基因的表达分别通过肿瘤细胞凋亡和增殖,可能作为VES应用于胃癌治疗的临床预测指标,而Fas可能比PCNA更有价值。

相似文献

1
Effects of vitamin E succinate on the expression of Fas and PCNA proteins in human gastric carcinoma cells and its clinical significance.维生素E琥珀酸酯对人胃癌细胞中Fas和PCNA蛋白表达的影响及其临床意义
World J Gastroenterol. 2004 Apr 1;10(7):945-9. doi: 10.3748/wjg.v10.i7.945.
2
Roles of Fas signaling pathway in vitamin E succinate-induced apoptosis in human gastric cancer SGC-7901 cells.Fas信号通路在维生素E琥珀酸酯诱导人胃癌SGC-7901细胞凋亡中的作用
World J Gastroenterol. 2002 Dec;8(6):982-6. doi: 10.3748/wjg.v8.i6.982.
3
RRR-alpha-tocopheryl succinate inhibits human gastric cancer SGC-7901 cell growth by inducing apoptosis and DNA synthesis arrest.RRR-α-生育酚琥珀酸酯通过诱导细胞凋亡和DNA合成阻滞来抑制人胃癌SGC-7901细胞的生长。
World J Gastroenterol. 2002 Feb;8(1):26-30. doi: 10.3748/wjg.v8.i1.26.
4
c-Jun N-terminal kinase is required for vitamin E succinate-induced apoptosis in human gastric cancer cells.人胃癌细胞中维生素E琥珀酸酯诱导的细胞凋亡需要c-Jun氨基末端激酶。
World J Gastroenterol. 2004 Apr 15;10(8):1110-4. doi: 10.3748/wjg.v10.i8.1110.
5
The effects of vitamin E succinate on the expression of c-jun gene and protein in human gastric cancer SGC-7901 cells.维生素E琥珀酸酯对人胃癌SGC-7901细胞中c-jun基因及蛋白表达的影响
World J Gastroenterol. 2002 Oct;8(5):782-6. doi: 10.3748/wjg.v8.i5.782.
6
[Study on vitamin E succinate inducing apoptosis of human gastric carcinoma cell].
Wei Sheng Yan Jiu. 2000 Jul;29(4):234-6.
7
Protective Macroautophagy Is Involved in Vitamin E Succinate Effects on Human Gastric Carcinoma Cell Line SGC-7901 by Inhibiting mTOR Axis Phosphorylation.保护性巨自噬通过抑制mTOR轴磷酸化参与维生素E琥珀酸酯对人胃癌细胞系SGC-7901的作用。
PLoS One. 2015 Jul 13;10(7):e0132829. doi: 10.1371/journal.pone.0132829. eCollection 2015.
8
Clinical significance of expression of proliferating cell nuclear antigen and E-cadherin in gastric carcinoma.增殖细胞核抗原和 E-钙黏蛋白在胃癌中的表达及其临床意义。
World J Gastroenterol. 2017 May 28;23(20):3721-3729. doi: 10.3748/wjg.v23.i20.3721.
9
[The expression and activity of caspase-8 in the process of vitamin E succinate-induced apoptosis in human gastric carcinoma SGC-7901 cells].[维生素E琥珀酸酯诱导人胃癌SGC-7901细胞凋亡过程中caspase-8的表达及活性]
Zhonghua Yu Fang Yi Xue Za Zhi. 2003 Mar;37(2):112-4.
10
[Inhibition of human gastric carcinoma cell growth by vitamin E succinate].[维生素E琥珀酸酯对人胃癌细胞生长的抑制作用]
Wei Sheng Yan Jiu. 2000 May 30;29(3):172-4.

引用本文的文献

1
Prognostic value and clinicopathological significance of proliferating cell nuclear antigen expression in gastric cancer: a systematic review and meta-analysis.增殖细胞核抗原表达在胃癌中的预后价值及临床病理意义:一项系统评价与Meta分析
Onco Targets Ther. 2017 Jan 10;10:319-327. doi: 10.2147/OTT.S126551. eCollection 2017.
2
ATRA promotes alpha tocopherol succinate-induced apoptosis in freshly isolated leukemic cells from chronic myeloid leukemic patients.全反式维甲酸促进α-生育酚琥珀酸酯诱导慢性髓性白血病患者新鲜分离的白血病细胞凋亡。
Mol Cell Biochem. 2008 Jan;307(1-2):109-19. doi: 10.1007/s11010-007-9590-7. Epub 2007 Sep 15.

本文引用的文献

1
Detection of HBV, PCNA and GST-pi in hepatocellular carcinoma and chronic liver diseases.肝细胞癌及慢性肝病中乙肝病毒、增殖细胞核抗原和谷胱甘肽S转移酶π的检测
World J Gastroenterol. 2003 Mar;9(3):459-62. doi: 10.3748/wjg.v9.i3.459.
2
Expression of p57kip2, Rb protein and PCNA and their relationships with clinicopathology in human pancreatic cancer.p57kip2、Rb蛋白和增殖细胞核抗原在人胰腺癌中的表达及其与临床病理的关系。
World J Gastroenterol. 2003 Feb;9(2):377-80. doi: 10.3748/wjg.v9.i2.377.
3
Effects of TNP-470 on proliferation and apoptosis in human colon cancer xenografts in nude mice.TNP - 470对裸鼠人结肠癌异种移植瘤增殖和凋亡的影响。
World J Gastroenterol. 2003 Feb;9(2):281-3. doi: 10.3748/wjg.v9.i2.281.
4
Alterations of p53 and PCNA in cancer and adjacent tissues from concurrent carcinomas of the esophagus and gastric cardia in the same patient in Linzhou, a high incidence area for esophageal cancer in northern China.中国北方食管癌高发地区林州同一患者食管和贲门同时发生的癌组织及癌旁组织中p53和增殖细胞核抗原(PCNA)的变化。
World J Gastroenterol. 2003 Jan;9(1):16-21. doi: 10.3748/wjg.v9.i1.16.
5
Effects of tachyplesin on proliferation and differentiation of human hepatocellular carcinoma SMMC-7721 cells.鲎素对人肝癌SMMC - 7721细胞增殖和分化的影响。
World J Gastroenterol. 2002 Dec;8(6):1053-8. doi: 10.3748/wjg.v8.i6.1053.
6
Roles of Fas signaling pathway in vitamin E succinate-induced apoptosis in human gastric cancer SGC-7901 cells.Fas信号通路在维生素E琥珀酸酯诱导人胃癌SGC-7901细胞凋亡中的作用
World J Gastroenterol. 2002 Dec;8(6):982-6. doi: 10.3748/wjg.v8.i6.982.
7
The effects of vitamin E succinate on the expression of c-jun gene and protein in human gastric cancer SGC-7901 cells.维生素E琥珀酸酯对人胃癌SGC-7901细胞中c-jun基因及蛋白表达的影响
World J Gastroenterol. 2002 Oct;8(5):782-6. doi: 10.3748/wjg.v8.i5.782.
8
Tumour Fas ligand:Fas ratio greater than 1 is an independent marker of relative resistance to tamoxifen therapy in hormone receptor positive breast cancer.肿瘤Fas配体与Fas的比值大于1是激素受体阳性乳腺癌中对他莫昔芬治疗相对耐药的独立标志物。
Breast Cancer Res. 2002;4(5):R9. doi: 10.1186/bcr456. Epub 2002 Jun 21.
9
The Fas-FasL system and colorectal tumours.Fas-FasL系统与结直肠肿瘤
J Clin Pathol. 2002 Jul;55(7):559; author reply 559-60. doi: 10.1136/jcp.55.7.559.
10
The prognostic molecular markers in hepatocellular carcinoma.肝细胞癌的预后分子标志物
World J Gastroenterol. 2002 Jun;8(3):385-92. doi: 10.3748/wjg.v8.i3.385.