期刊文献+

赖氨酸特异性去甲基化酶1在胃癌组织中的表达及意义 被引量:2

Expression and significance of the lysine-specific demethylase 1 in gastric cancer tissues
原文传递
导出
摘要 目的检测胃癌及癌旁组织中的赖氨酸特异性去甲基化酶1(LSDI)、E-钙黏蛋白的表达,探讨LSD1、E-钙黏蛋白与胃癌患者的临床病理特征、预后之间的关系,以及LSD1与E-钙黏蛋白表达的相关性。方法采用病例对照研究方法。收集2008年6月至2009年6月中南大学湘雅医院收治80例胃癌患者手术切除的胃癌组织及癌旁组织。采用免疫组织化学染色检测手术标本中LSD1、E-钙黏蛋白的表达情况。术后通过电话随访,了解患者生存情况。随访时间截至2015年6月。分析LSD1和E-钙黏蛋白的表达及其与胃癌患者临床病理特征的关系,LSD1和E-钙黏蛋白在胃癌组织中表达的相关性。分析LSD1、E-钙黏蛋白表达与胃癌患者预后的关系。计数资料的比较采用,检验,相关性采用Spearman等级相关分析,采用Kaplan—Meier法绘制生存曲线,Log-rank检验进行生存分析。结果LSDI在胃癌细胞及癌旁组织细胞中表达均定位于细胞核。其阳性表达率分别为67.5%(54/80)、43.8%(35/80),两者比较,差异有统计学意义(χ^2=9.141,P〈0.05)。E-钙黏蛋白在胃癌细胞及癌旁组织细胞中表达定位于细胞膜和细胞质。其阳性表达率分别为63.8%(51/80)、81.3%(65/80),两者比较,差异有统计学意义(χ^2=6.140,P〈0.05)。LSD1在不同的病理学分级的低、中、高分化的阳性表达率分别为83.3%(25/30)、76.0%(19/25)和40.0%(10/25),在TNM分期的Ⅰ、Ⅱ、Ⅲ、Ⅳ期中分别为37.5%(6/16)、72.7%(16/22)、71.9%(23/32)和90.0%(9/10),在无和有淋巴结转移中分别为36.4%(4/11)和72.5%(50/69),几者比较,差异均有统计学意义(χ^2=12.870,9.425,4.111,P〈0.05)。E-钙黏蛋白在低、中、高分化的阳性表达率分别为53.3%(16/30)、56.0%(14/25)和84.0� Objective To investigate the expressions and relationship between lysine-specific demethylase 1 ( LSD1 ) and E-cadherin protein in gastric cancer tissues and adjacent normal tissues, and the correlation with the clinicopathological features and prognosis of patients with gastric cancer. Methods The ease-control study was adopted. The gastric cancer tissues and adjacent normal tissues were collected by surgical resection from 80 patients with gastric cancer who were admitted to the Xiangya Hospital of Central South University from June 2008 to June 2009. Expressions of LSD1 and E-cadherin protein were detected by immunohistochemistry (IHC). The follow-up of telephone interview was performed to detect survival of patients till June 2015. Relationships between the expressions of LSD1 and E-eadherin protein and clinieopathologieal features or prognosis of patients were analyzed. Comparison of count data and correlation were analyzed by the chi-square test and Spearman rank correlation analysis. Survival curve was drawn using the Kaplan-Meier method, and survival analysis was done using the Log-rank test. Results Expressions of LSD1 in cancer tissues and adjacent normal tissues were located at the cell nucleus. The positive expression rate of LSD1 was 67.5% (54/80) and 43.8% (35/80) in cancer tissues and adjacent normal tissues, respectively, with a significant difference (χ^2= 9. 141, P 〈 0. 05). Expressions of E-cadherin protein in cancer tissues and adjacent normal tissues were located at the cell membrane and cytoplasm. The positive expression rate of E-eadherin was 63.8% (51/80) and 81.3% (65/80) in cancer tissues and adjacent normal tissues, respectively, with a significant difference (χ^2 = 6. 140, P 〈 0.05 ). The positive expression rate of LSD1 was 83.3% (25/30) , 76.0% ( 19/25 ) and 40.0% ( 10/25 ) in the low-, moderate- and high-differentiated tumors, 37. 5% ( 6/16), 72.7% ( 16/22), 71.9% (23/32) and 90.0% (9/10) in the Ⅰ, Ⅱ, Ⅲ and Ⅳ
出处 《中华消化外科杂志》 CAS CSCD 北大核心 2016年第3期271-276,共6页 Chinese Journal of Digestive Surgery
基金 湖南省发改委科研项目(湘发改投资[2014]658) 湖南省自然科学基金项目(08JJ5009)
关键词 胃肿瘤 表观遗传 赖氨酸特异性去甲基化酶1 E-钙黏蛋白 预后 Gastric neoplasms Epigenetic Lysine-specific demethylase 1 E-cadherin protein Prognosis
  • 相关文献

参考文献31

  • 1Jemal A, Bray F, Center MM, et al. Global cancer statistics[J]. CA Cancer J Clin, 2011,61 ( 2 ) : 69-90. 被引量:1
  • 2Boyer B, Vall6s AM, Edme N. Induction and regulation of epithe- lial-mesenchymal transitions [ J ]. Bioehem Pharmacol, 2000,60 ( 8 ) : 1091 - 1099. 被引量:1
  • 3Kang Y, Massagu6 J. Epithelial-mesenehymal transitions: twist in development and metastasis [ J ]. Cell, 2004, 118 ( 3 ) : 277-279. 被引量:1
  • 4Hajra KM, Chen DY, Fearon ER. The SLUG zinc-finger protein represses E-eadherin in breast cancer[ J]. Cancer Res,2002,62 (6) :1613-1618. 被引量:1
  • 5Chang ZG, Wei JM, Qin CF, et al. Suppression of the epidermal growth factor receptor inhibits epithelial-mesenchymal transition in human pancreatic cancer PANC- 1 cells [ J ]. Dig Dis Sci,2012,57 (5) :1181-1189. 被引量:1
  • 6Dai YH, Tang YP, Zhu HY, et al. ZEB2 promotes the metastasis of gastric cancer and modulates epithelial mesenchymal transition of gastric cancer cells [ J ]. Dig Dis Sei,2012,57 ( 5 ) : 1253-1260. 被引量:1
  • 7Batlle E, Sancho E, Franci C, et al. The transcription factor snail is a repressor of E-cadherin gene expression in epithelial tumour cells[ J ]. Nat Cell Biol, 2000,2 (2) : 84-89. 被引量:1
  • 8Lin T, Ponn A, Hu X, et al. Requirement of the histone demethy- lase LSD1 in Snail-mediated transcriptional repression during epi- thelial-nmsenchymal transition [J]. Oncogene, 2010, 29 ( 35 ) : 4896-4904. 被引量:1
  • 9Mosammaparast N, Shi Y. Reversal of histone methylation: bio- chemical and molecular mechanisms of histone demethylases [J].Annu Rev Biochem,2010,79 : 155-179. 被引量:1
  • 10Yang M, Culhane JC, Szewczuk LM, et al. Structural basis of his- tone demethylation by LSD1 revealed by suicide inactivation [J]. Nat Struct Mol Biol, 2007, 14 ( 6 ) : 535-539. 被引量:1

二级参考文献41

  • 1Yan Li Zhao-You Tang Sheng-Long Ye Yin-Kun Liu Jie Chen Qiong Xue Jun Chen Dong-Mei Gao Wei-Hua Bao Liver Cancer Institute and Zhongshan Hospital of Fudan University (Former Liver Cancer Institute of Shanghai Medical University),Shanghai 200032,China.Establishment of cell clones with different metastatic potential from the metastatic hepatocellular carcinoma cell line MHCC97[J].World Journal of Gastroenterology,2001,7(5):630-636. 被引量:111
  • 2Candido J, Hagemann T. Cancer related inflammalion [J]. J Clin Immunol, 2013,33 Suppl 1 :S79-84. 被引量:1
  • 3Thiery JP. Epithelial-mesenchymal transitions in tumour progression[J]. Nat Rev Cancer, 2002,2(6) :442-454. 被引量:1
  • 4Wu Y, Zhou BP. TNF-alpha/NF-kappaB/Snail pathway in cancer cell migration and invasion[J]. Br J Cancer, 2010, 102(4) :639-644. 被引量:1
  • 5Gao D, Vahdat LT, Wong S, et al. Microenvironmental regulation of epithelial-mesenchymal transitions in cancer[J]. Cancer Res, 2012,72(19) :4883-4889. 被引量:1
  • 6Chen XF, Zhang HJ, Wang HB, et al. Transforming growth factor-β1 induces epithelial-to-mesenchymal transition in human lung cancer ceils via PI3K/Akt and MEK/Erkl/2 signaling pathways[J]. Mol Biol Rep, 2012, 39(4):3549- 3556. 被引量:1
  • 7Maier HJ, Schmidt-Strassburger U, Huber MA, et al. NF-kappaB promotes epit helial-mesenchymal transition, migration and invasion of pancreatic carcinoma cells[J]. Cancer Lett, 2010,295(2) :214-228. 被引量:1
  • 8Giampieri S, Manning C, Hooper S, et al. Localized and reversible TGFheta signalling switches breast cancer ceils from cohesive to single cell motility[J]. Nat Cell BioI, 2009, 11(11) :1287-1296. 被引量:1
  • 9Chuang MJ, Sun KH, Tang SJ, et al. Tumor-derived tumor necrosis factor-alpha promotes progression and epithelial- mesenchymal transition in renal cell carcinoma cells[J]. Cancer Sci, 2008,99(5) :905-913. 被引量:1
  • 10Yamauchi Y, Kohyama T, Takizawa H,et al. Tumor necrosis factor-alpha enhances both epithelial-mesenchymal transition and cell contraction induced in A549 human alveolar epithelial cells by transforming growth factor-betal[J]. Exp Lung Res, 2010,36(1) : 12-24. 被引量:1

共引文献3

同被引文献23

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部