期刊文献+

喉鳞状细胞癌组织中血管内皮生长因子和环氧化酶-2 mRNA检测 被引量:2

Expression of VEGF and COX-2 mRNA in laryngeal squamous cell carcinoma tissue
下载PDF
导出
摘要 目的:探讨喉鳞状细胞癌组织中血管内皮生长因子(VEGF)和环氧化酶(COX-2)mRNA的表达情况及与癌组织生长、浸润及转移的关系。方法:应用RT-PCR方法检测62例喉鳞状细胞癌、54例癌旁和9例正常喉黏膜组织中VEGF mRNA及COX-2 mRNA的表达。结果:喉鳞癌组织中VEGF mRNA和COX-2 mRNA的表达量高于癌旁和正常喉黏膜组织(P<0.01),Ⅰ、Ⅱ期喉鳞癌组织2者的表达量低于Ⅲ、Ⅳ期(P<0.01)。喉鳞癌组织中VEGF mRNA和COX-2 mRNA的表达呈正相关(r=0.756,P<0.01)。结论:VEGF和COX-2与喉鳞癌的生长、浸润及转移有密切关系,2者有协同作用。 Aim : To study the expressions of vascular endothelial growth factor (VEGF) and cyclooxygenase-2 ( COX- 2) mRNA in human laryngeal squamous cell carcinoma (LSCC) tissue and its significance. Methods: The expression of VEGF mRNA and COX-2 mRNA in 62 cases of LSCC, 54 cases of adjacent to tumor tissue, and 9 normal human laryngeal mucous membrane were detected using techniques of semi-quantify RT-PCR. Results: The expression level of VEGF mRNA and COX-2 mRNA in LSCC tissue were significantly higher than those in the normal human laryngeal mucous membrane and adjacent to tumor tissue (P 〈 0.01 ). The expression level of VEGF mRNA and COX-2 mRNA in Ⅲ and Ⅳ stage tissues were significantly higher than those of Ⅰ and Ⅱ stage tissues of LSCC (P 〈0.01 ). There was a high positive correlation between VEGF and COX-2 mRNA expression in LSCC (r = 0. 756,P 〈 0.01 ). Conclusion: VEGF and COX-2 may play key roles in the growth, invasion and metastasis of LSCC.
出处 《郑州大学学报(医学版)》 CAS 北大核心 2007年第2期239-242,共4页 Journal of Zhengzhou University(Medical Sciences)
基金 第四届教育部"高校青年教师奖"资助项目
关键词 喉肿瘤 鳞状细胞癌 VEGF COX-2 laryngeal neoplasm squamous cell carcinoma VEGF COX-2
  • 相关文献

参考文献1

二级参考文献1

共引文献36

同被引文献14

  • 1顾龙君.儿童急性淋巴细胞白血病诊疗建议(第三次修订草案)[J].中华儿科杂志,2006,44(5):392-395. 被引量:472
  • 2许子亮,韩中朝.VEGF与血液学恶性疾病[J].国际病理科学与临床杂志,2006,26(4):318-320. 被引量:8
  • 3曾军杰,李颖琰,崔玉青,闫明.VEGF COX-2表达对肺腺癌预后生存期影响[J].医药论坛杂志,2007,28(4):29-30. 被引量:3
  • 4DURON JJ, SILVA NJ, DU MONTCEL ST, et al. Adhesive postoperative small bowel obstruction, incidence and risk factors of recurrence after surgical treatment: a multicenter prospective study [J]. Ann Surg, 2006, 244(5) :750-757.
  • 5KATADA J, SAITO H, OHASHI A. Significance of cyclooxygenase-2 induced via p38 mitogen-activated protein kinase in mechanical stimulus-induced peritoneal adhesion in mice [J]. J Pharmacol Exp Ther, 2005, 313(1):286-292.
  • 6SAED GM, MUNKARAH AR, ABU-SOUD HM, et al. Hypoxia upregulates cyclooxygenase-2 and prostaglandin E(2) levels in human peritoneal fibroblasts[J].Fertil Steril, 2005, 83 (Suppl 1) :1216-1219.
  • 7SAED GM, MUNKARAH AR, DIAMOND MP. Cyclooxygenase-2 is expressed in human fibroblasts isolated from intraperitoneal adhesions but not from normal peritoneal tissues[J]. Fertil Steril, 2003, 79(6):1404-1408.
  • 8WICZYK HP, GROW DR, ADAMS LA, et al. Pelvic adhesions contain sex steroid receptors and produce angiogenesis growth factors[J]. Fertil Steril, 1998, 69(3) :511-516.
  • 9CHEGINI N. The role of growth factors in peritoneal healing: transforming growth factor beta (TGF-beta) [J].Eur J Surg, 1997, (577):17-23.
  • 10KUSUNOKI N, YAMAZAKI R, KAWAI S. Induction of apoptosis in rheumatoid synovial fibroblasts by celecoxib, but not by other selective cyclooxygenase 2 inhibitors [J]. Arthritis Rheum, 2002, 46(12) :3159-3167.

引证文献2

二级引证文献8

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