期刊文献+

人结肠癌中AKT2和PTEN蛋白表达的意义及相关性 被引量:6

Significance of AKT2 and PTEN protein expressions and their correlation with human colon cancer
下载PDF
导出
摘要 目的检测AKT2蛋白在人结肠癌组织中的表达及其与PTEN的相关性。方法应用免疫组织化学SP法检测30例正常结肠、30例腺瘤和64例结肠癌组织中AKT2和PTEN的表达。结果从正常组织、腺瘤组织到结肠癌组织,PTEN的阳性表达率呈递减趋势,AKT2呈递增趋势;PTEN在正常结肠组织中的表达明显高于结肠腺瘤和结肠癌组织中的表达,差异有统计学意义(χ2=68.855,P<0.05),而AKT2在结肠腺瘤和结肠癌组织中的表达明显高于正常结肠组织中的表达,差异有统计学意义(χ2=37.574,P<0.05);随结肠癌分化程度降低、淋巴结的转移、Dukes分期的增加,AKT2的阳性表达率升高(P<0.05);PTEN与AKT2的表达呈负相关(r=-0.143,n=64,P<0.05)。结论由于PTEN表达下调或缺失而导致AKT2的异常高表达,AKT2的高表达与结肠癌的发生发展有关。 Objective To detect the expression of AKT2 in human colon cancer and understand its relationship with PTEN. Methods The expressions of AKT2 and PTEN were detected in 30 patients with normal colonic tissues, 30 patients with colon adenoma tissues, and 64 patients with colon carcinoma tissues by immunohistochemical SP staining method. Results The positive expressive rate of PTEN presented a trend of progressive decrease from normal tissues, adenoma tissues to colon carcinoma tissues, while the positive expression rate of AKT2 presented a trend of progressive increase. PTEN expression was obviously higher in normal colon tissues than in colon adenoma tissues and colon cancer tissues ( x2 =68. 855, P〈O. 05). However, the expression of AKT2 in colon adenoma tissues and colon cancer tissues was significantly higher than that in normal colon tissues ( x2 =37. 574, P〈0.01). With the decrease of differentiation degree in colon cancer, metastasis of lymph node and increase of Dukes staging, the positive expression rate of AKT2 increased (P〈O. 05). AKT2 and PTEN expressions were negatively correlated ( r = 0. 143, n = 64, P 〈 0.05). Conclusion The results demonstrate that down- regulation or loss of PTEN expression may lead to abnormally high expression of AKT2, which is related to the genesis and progression of colon cancer.
出处 《西安交通大学学报(医学版)》 CAS CSCD 北大核心 2009年第5期592-595,共4页 Journal of Xi’an Jiaotong University(Medical Sciences)
关键词 结肠癌 PTEN AKT2 免疫组织化学法 colon cancer PTEN AKT2 immunohistochemistry
  • 相关文献

参考文献11

  • 1LIM WT,ZHANG WH,MILLER CR,et al.PTEN and phosphorylated AKT expression and prognosis in early-and late-stage non-small cell lung cancer[J].Oncol Rep,2007,17(4):853-857.
  • 2RYCHAHOU PG,KANG J,GULHATI P,et al.Akt2 overexpression plays a critical role in the establishment of colorectal cancer metastasis[J].Proc Natl Acad Sci USA,2008,105(51):20315-20320.
  • 3CARNERO A,BLANCO-APARICIO C,RENNER O,et al.The PTEN/PI3K/AKT signalling pathway in cancer,therapeutic implications[J].Curr Cancer Drug Targets,2008,8(3):187-198.
  • 4CICENAS J.The potential role of Akt phosphorylation in human cancers[J].Int J Biol Markers,2008,23(1):1-9.
  • 5ARBOLEDA MJ,LYONS JF,KABBINAVAR FF,et al.Overexpression of AKT2/protein kinase Bbeta leads to up-regulation of beta1integrins,increased invasion,and metastasis of human breast and ovarian cancer cells[J].Cancer Res,2003,63(1):196-206.
  • 6苗丽君,王静.Akt与肿瘤的研究进展[J].国外医学(生理病理科学与临床分册),2004,24(5):406-409. 被引量:38
  • 7SHIRATSUCHI H,BASSON MD.Akt2,but not Akt1 or Akt3 mediates pressure-stimulated serum-opsonized latex bead phagocytosis through activating mTOR and p70 S6 kinase[J].J Cell Biochem,2007,102(2):353-367.
  • 8CHENG GZ,ZHANG W,WANG LH,et al.Regulation of cancer cell survival,migration,and invasion by Twist:AKT2 comes to interplay[J].Cancer Res,2008,68(4):957-960.
  • 9ABBOTT RT,TRIPP S,PERKINS SL,et al.Analysis of the PI-3-Kinase-PTEN-AKT pathway in human lymphoma and leukemia using a cell line microarray[J].Mod Pathol,2003,16(6):607-612.
  • 10SUN M,PACIGA JE,FELDMAN RI,et al.Phosphatidylinositol-3-OH Kinase (PI3K)/AKT2,activated in breast cancer,regulates and is induced by estrogen receptor alpha (ERalpha) via interaction between ERalpha and PI3K[J].Cancer Res,2001,61(16):5985-5991.

二级参考文献20

  • 1Potter C J, Pedraza LG, Xu T. Akt regulates growth by directly phosphorylating Tsc2 [ J ]. Nat Cell Biol, 2002,4 (9) :658-665.
  • 2Vander Heiden MG, Plas DR, Rathmell JC, et al . Growth factors can influence cell growth and survival through effects on glucose metabolism[J]. Mol Cell Biol, 2001 ,21 (17) :5899-5912.
  • 3Edinger AL, Thompson CB. Akt maintains cell size and survival by increasing mTOR-dependent nutrient uptake [ J ]. Mol Biol Cell,2002 , 13 (7) : 2276-2288.
  • 4West KA, Brognard J, Clark AS, et al. Rapid Akt activation by nicotine and a tobacco carcinogen modulates the phenotype of normal human airway epithelial cells [ J]. J Clin Invest, 2003,111(1) :81-90.
  • 5Nam SY, Jung GA, Hur GC, et al. Upregulation of FLIP(S) by Akt, a possible inhibition mechanism of TRAIL-induced apoptosis in human gastric cancers [ J ]. Cancer Sci, 2003,94 ( 12 ) : 1066-1073.
  • 6Gagnon V, St-Germain ME, Parent S, et al. Akt activity in endometrial cancer cells: regulation of cell survival through cIAP-1 [ J].Int J Oncol, 2003 ,23(3) :803-810.
  • 7Dan HC, Sun M, Kaneko S, et al. Akt Phosphorylation and Stabilization of X-linked Inhibitor of Apoptosis Protein (XIAP) [ J ]. J Biol Chem, 2004,279(7) :5405-5412.
  • 8Zhang D, Brodt P. Type 1 insulin-like growth factor regulates MT1-MMP synthesis and tumor invasion via PI3-kinase/Akt signaling[J]. Oncogene, 2003,22(7) :974-982.
  • 9Qian Y, Corum L, Meng Q, et al. PI3K induced actin filament remodeling through Akt and p70S6K1 : implication of essential role in cell migration [ J ]. Am J Physiol Cell Physiol, 2004,286 ( 1 ) :C153-C163.
  • 10Kim D, Kim S, Koh H, et al. Akt/PKB promotes cancer cell invasion via increased motility and metalloproteinase production [ J ].FASEB J, 2001,15 ( 11 ) : 1953-1962.

共引文献37

同被引文献67

引证文献6

二级引证文献29

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