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结直肠腺瘤及腺癌组织中FOXO1表达及其临床意义 被引量:5

Expression and clinical significance of FOXO1 in colorectal adenoma and adenocarcinoma
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摘要 目的检测结直肠腺瘤及腺癌组织中转录因子FOXO1的表达,在组织学水平上初步探讨FOXO1在结直肠腺瘤癌变过程中的作用及其与临床病理特征的关系。方法采用Western blot法免疫组化SP两步法检测146例结直肠腺瘤、48例结直肠腺癌及48例癌旁组织中FOXO1蛋白的表达水平。结果 FOXO1在结直肠腺瘤及腺癌组织中的表达明显低于正常组织,组间比较差异有统计学意义(P<0.01)。结直肠腺瘤组织中FOXO1表达与肿物大小相关,腺癌组织中FOXO1表达与肿瘤分化程度相关。结论 FOXO1在人类肠道癌前病变(腺瘤)及腺癌组织细胞核表达减少和缺失,可能是导致结肠腺癌发病的机制之一,其在结直肠癌的发生、发展过程中起抑癌基因的作用,有望成为下一个潜在的临床治疗靶点。 Purpose To investigate the expression level of transcriptional factor FOXO1 in colorectal adenoma and adenocarcinoma, and to explore its relationship with clinicopathological characteristics. Methods The protion of FOXO1 was detected by immnnohisto- chemistry of SP two-step and Western blot in 146 cases of colorectal adenoma, 48 cases of colorectal adenocarcinoma and 48 cases of the adjacent mucosa. Results The expression of FOXO1 in adenoma and adenocarcinoma was significantly lower than that in normal tissues, and the differences between the groups were statistically significant (P 〈 0. 01 ). The expression level of FOXO1 proteins was related to the size of the tumors in colorectal adenoma and the pathological grade of cancer tissues in colorectal adenocarcinoma. Con- dusion The findings of our study indicate that the decreased or deleted expression of FOXO1 in colorectal precancerous lesions ( ade- noma) and adenocarcinoma may be one of the reasons to cause colorectal adenocarcinoma. It acts as tumor suppressor gene and plays a vital role in the carcinogenesis and development of colorectal cancer. FOXO1 seems to become the next potential target of clinical treatment.
出处 《临床与实验病理学杂志》 CAS CSCD 北大核心 2016年第9期1009-1013,共5页 Chinese Journal of Clinical and Experimental Pathology
基金 甘肃省青年科技基金计划(145RJYA322) 新药临床前重点实验室开放课题(GSKFKT-1204)
关键词 结直肠肿瘤 结直肠腺癌 结直肠腺瘤 FOXO1 colorectal neoplasm colorectal adenocarcinoma colorectal adenoma FOXO1
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参考文献15

  • 1李道娟,李倩,贺宇彤.结直肠癌流行病学趋势[J].肿瘤防治研究,2015,42(3):305-310. 被引量:524
  • 2薛军,武雪亮,王立坤,屈明,贾光辉,赵秀芳.结直肠腺癌、腺瘤、正常黏膜中RUNX3的表达及意义[J].临床与实验病理学杂志,2014,30(6):605-609. 被引量:8
  • 3Weidinger C,Krause K,Klagge A,et al.Forkhead box-O transcription factor:critical conductors of cancer's fate[J].Endocr Relat Cancer,2008,15(4):917-29.
  • 4Anderson M J,Viars C S,Czekay S,et al.Cloning and characterization of three human forkhead genes that comprise an FKHR-like gene subfamily[J].Genomics,1998,47(2):187-99.
  • 5Nho R S,Hergert P.FoxO3a and disease progression[J].World Biol Chem,2014,5(3):346-54.
  • 6Birkenkamp K U,Cofferp J.FOXO transeription factors as regulators of immune homeostasis:molecules to die for?[J].Immunol,2003,171:1623-9.
  • 7Barthel A,Schmoll D,Unterman T G.FOXO Proteins in insulin action and Metabolism[J].Trends Endoerinol Metab,2005,16:183-9.
  • 8Dong X Y,Chen C S,Sun X D,et al.FOXOIA is candidate for the 13ql4 tumor suppressor gene inhibiting androgen receptor signaling in prostate cancer[J].Cancer Res,2006,66(14):6998-7000.
  • 9Sisci D,Maris P,Cesario M G,et al.The estrogen receptor αis the key regulator of the bifunctional role of FOXO3a transcription factor in breast cancer motility and invasiveness[J].Cell Cycle,2013,12(21):3405-20.
  • 10谭超,仇小强,谭盛葵,曾小云,刘顺,李岸花.叉形头转录因子O亚型相关基因位点多态性与肝细胞癌关系[J].中华疾病控制杂志,2014,18(4):281-285. 被引量:4

二级参考文献76

  • 1郑杰.结直肠息肉和结直肠癌[J].中华病理学杂志,2005,34(1):4-5. 被引量:65
  • 2张雪妍,张煦.抑癌基因Runx3的研究进展[J].临床与实验病理学杂志,2006,22(5):611-614. 被引量:1
  • 3Tang HY, Smith-Caldas MS, Driscoll MV, et al. FOXO regulates organ-specificphenotypic plasticity in Drosophila [ J ]. PLoS Gen- et, 2011,7(11) : e1002373.
  • 4Medema RH, Kops GJ, Bos JL, et al. AFXlike Forkhead tran- scription factors mediate cell cycle regulation by Ras and PKB through p27kipl [J]. Nature, 2000,404(6779) :782-787.
  • 5Wilk A, Urbanska K, Grabacka M, et al. Fenofibrate-induced nuclear translocation of FoxO3A triggers Bim-mediated apoptosis in glioblastoma cells in vitro [ J ]. Cell Cycle, 2012,11 ( 14 ) : 2660- 2671.
  • 6Muranen T, Selfors LM, Worster DT, et al. Inhibition of PI3K/ mTOR leads to adaptive resistance in matrix-attached cancer ceils [ J]. Cancer Cell, 2012,21 (2) :227-239.
  • 7Newton RH, Turka LA. Regulation of T cell homeostasis and re- sponses by pten [J]. Front Immunol, 2012,3:151.
  • 8Hagenbuchner J, Kuznetsov A, Hermann M, et al. FOXO3-in- duced reactive oxygen species are regulated by BCL2Lll (Bim) and SESN3 [J]. Cell Sci, 2012,125(Pt 5) :1191-1203.
  • 9Cantley LC. The phosphoinositide 3-kinase pathway [ J ]. Sci- ence, 2002,296(5573) :1655-1657.
  • 10Brunet A, Sweeney LB, Sturgill JF, et al. Stress-dependent regu- lation of FOXO transcription factors by the SIRT1 deacetylase [J]. Science, 2004,303(5666) :2011-2015.

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