期刊文献+

P-p38和uPA蛋白在大肠癌中的表达及临床意义 被引量:7

The expression and significance of P- p38 and uPA in colorectal cancer
在线阅读 下载PDF
导出
摘要 目的:研究P-p38和uPA蛋白的表达与大肠癌生物学行为及预后的关系。方法:应用免疫组织化学(SP)法检测P-p38和uPA在62例大肠癌、25例大肠腺瘤及18例正常大肠黏膜组织中的表达。结果:大肠癌组织中P-p38和uPA阳性表达率分别为79.0%和74.2%,均明显高于大肠腺瘤及正常大肠黏膜组织,差异有显著统计学意义(P<0.05)。P-p38和uPA表达与大肠癌的分化程度、淋巴结转移、Duke's分期及浸润肌层的深度密切相关(P<0.05),且两者表达成明显正相关(P<0.05)。P-p38和uPA表达阳性者术后5年生存率明显低于阴性者,差异有显著意义(P<0.05)。结论:P-p38和uPA的高表达预示着大肠癌的低分化,并共同促进了肿瘤的侵袭、转移。联合检测P-p38和uPA的表达情况对于评估大肠癌的发展及预后具有重要意义。 Objective:To study the expression of P-p38 and uPA in colorectal carcinoma and their relationship with the biological behavior and prognosis. Methods:SP immunochemical method was performed to detect the expres-sion of P-p38 and uPA in 62 cases of colorectal carcinoma,25 cases of colorectal adenomas,and 18 cases of normal colorectal tissues. Results:The positive rates of P-p38 and uPA in colorectal cancers(79. 0%,74. 2% respectively) were significantly higher than those in the colorectal adenomas and normal colorectal tissues group(P〈0.05).Theex-pressions of P-p38 and uPA were closely related to pathological differentiation,lymph node metastasis,Duke&#39;s stages and the deepnessofinvasion(P〈0.05).The expression of P-p38 was significantly correlated with uPA(P〈0.05). The 5 years survival rates after operation in positive expression groups of P-p38 and uPA were significantly lower than those in negative expression groups. Conclusion:Overexpression of P -p38 and uPA in colorectal carcinoma were associated with poorly histological grades,cell migration,tumormetastases and poor prognosis. It is very signifi-cant to investigate the expression of P-p38 and uPA combinedly in colorectal carcinoma.
出处 《现代肿瘤医学》 CAS 2014年第10期2374-2377,共4页 Journal of Modern Oncology
  • 相关文献

参考文献15

  • 1Wang XF,Zhou QM,Du J,et al. Baicalin suppresses migration,in-vasion and metastasis of breast cancer via p38MAPK signalingpathway[ J] . Anticancer Agents Med Chem, 2013 ,13(6) : 923 -931.
  • 2Yousif NG, Al - Amran FG, Hadi N, et al. Expression of IL - 32modulates NF - kB and p38 MAP kinase pathways in human e-sophageal cancer[ J]. Cytokine,2013 ,61 (1) :223 -227.
  • 3Santibanez JF. Transforming growth factor - Beta and urokinase -type plasminogen activator : Dangerous partners in tumorigenesis -implications in skin cancer [ J ]. ISRN Dermatol, 2013,18(7):597927.
  • 4Tjomsland V,Bojmar L,SandstrOm P,et al. IL - la expression inpancreatic ductal adenocarcinoma affects the tumor cell migrationand is regulated by the p38MAPK signaling pathway [ J ]. PLoSOne,2013,8(8) :e70874.
  • 5Tovar - Y - Romo LB,Tapia R. VEGF protects spinal motor neu-rons against chronic excitotoxic degeneration in vivo by activation ofPI3 - K pathway and inhibition of p38MAPK [ J ]. J Neurochem,2010,115(5) :1090-1101.
  • 6Kim ES,Sohn YW,Moon A. TGF - beta - induced transcriptionalactivation of MMP -2 is mediated by activating transcription factor(ATF)2 in human breast epithelial cells[ J]. Cancer Lett,2007,252(1) :147 -156.
  • 7Xu L,Chen S,Bergan RC. MAPKAPK2 and HSP27 are downstreameffectors of p38 MAP kinase 一 mediated matrix metalloproteinasetype 2 activation and cell invasion in human prostate cancer[ J].Oncogene,2006,25(21) :2987 -2998.
  • 8Lee SJ, Park SS,Cho YH,et al. Activation of matrix metalloprotein-ase -9 by TNF - alpha in human urinary bladder cancer HT1376cells: The role of MAP kinase signaling pathways [ J ]. Oncol Rep,2008,19(4) :1007 -1013.
  • 9Rousseau S,Dolado I,Beardmore V,et al. CXCL12 and C5a triggercell migration via a PAK1/2 - p3 8 alpha MAPK - MAPKAP 一 K2-HSP27 pathway [J]. Cell Signal,2006,18( 11) :1897 - 1905.
  • 10Horvatic Herceg G, Herceg D. Urokinase plasminogen activatorand its inhibitor type - 1 as prognostic factors in differentiatedthyroid carcinoma patients [ J ]. Otolaryngol Head Neck Surg,2013,149(4):533 -540.

同被引文献78

引证文献7

二级引证文献33

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