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STAT3与SOCS3在子宫内膜腺癌中的表达及生物学行为相关性分析 被引量:6

Biological behavior analysis and expression of STAT3 and SOCS3 in endometrial carcinoma by using tissue chip technique
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摘要 目的探讨STAT3、SOCS3基因蛋白在子宫内膜腺癌中的表达及意义,以期了解这两种蛋白在子宫内膜腺癌癌变过程中的作用。方法收集46例手术切除的子宫内膜腺癌组织标本,同时取30例正常子宫内膜组织作为对照,运用组织芯片技术以及免疫组织化学的方法检测子宫内膜癌组织、正常子宫内膜组织中STAT3、SOCS3蛋白的表达。结果 46例子宫内膜癌组织中STAT3的阳性表达率为76.1%,SOCS3的阳性表达率为19.6%,两者在子宫内膜腺癌与正常子宫内膜组织之间的阳性率表达差异有显著的统计学意义(P<0.05)。二者的阳性表达与子宫内膜腺癌患者的肿瘤分化程度有关,与手术病理分期、肌层浸润及绝经情况等临床特征无相关性(P>0.05)。子宫内膜腺癌中STAT3与SOCS3呈负相关。结论子宫内膜腺癌中STAT3呈高表达,SOCS3呈低表达,提示STAT3促进了子宫内膜腺癌的发生发展,而SOCS3抑制子宫内膜腺癌癌变的作用。 Objective To investigate the expression of STAT3 and SOCS3 protein in endometrial cancer of uterine and its clinicopathologic significance in order to detect if these protein have effect on endometrial carcinoma. Methods Tissue chip technique and immunohistochemical staining method were used to examine the expression of STAT3 and SOCS3 in 46 cases of endometrial carcinoma and in 30 cases of the normal endometrium. The relationship of these subjects was analyzed with spearman rank correlation. Results The positive rates of STAT3 and SOCS3 in endometrial carcinoma were demonstrated significant difference compared with normal endometrial tissue. The expression of STAT3 and SOCS3 had relationship with histological grade in endometrial carcinoma. The differences reached significant value ( P 〈 0.05 ). Negative correlation was found between the expression of STAT3 and SOCS3 in endometrial carcinoma ( r = - 0. 494, P = 0. 004 〈 0.05 ). Conclusion The over - ex- pressions of STAT3 and the down - regulated expression of SOCS3 in endometrial carcinoma may play an important role in the carcinogenesis and progression of endometrial carcinoma.
出处 《临床和实验医学杂志》 2013年第17期1350-1352,1354,共4页 Journal of Clinical and Experimental Medicine
关键词 子宫内膜腺癌 STAT3 SOCS3 免疫组织化学 Endometrial carcinoma STAT3 SOCS3 Immunohistochemistry
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  • 1De Yun Feng,Hui Zheng,Yi Tan,Rui Xue Cheng Department of Pathology, Hunan Medical University, Changsha 410078, Hunan Province, China New England Biolab, MA, USA.Effect of phosphorylation of MAPK and Stat3 and expression of c-fos and c-jun proteins on hepatocarcinogenesis and their clinical significance[J].World Journal of Gastroenterology,2001,7(1):33-36. 被引量:76
  • 2Leong PL, Andrews GA, Johnson DE, et al. Targeted inhibition of STAT3 with a decoy oligonucleotide abrogates herd and neck cancer cell growth[ J ]. Proc Natl Acad SciUSA ,2003,100 ( 7 ) :4138-4143.
  • 3Mizoguchi M, Betensky RA, Batchelor TT, et al. Activation of STAT3, MAPK, and A KT in malignant ast rocytic gliomas: cot2 relation wit h EGFR status, tumor grade, and survival. J Neuro2 pat hol Exp Neurol, 2006, 65(12) :1181-1188.
  • 4Levy DE, Darnell J E J r. Stat s: transcriptional control and biological impact. Nat Rev Mol Cell Biol, 2002, 3(9) :651-662.
  • 5Niu G, Wright KL, Hung M, et al. Constitutive STAT3 activity upregulates VEGF expression and tumor angiogenesis [ J]. Oncogene, 2002, 21(13) :2000.
  • 6Sulkowska M, Golaszewska J, Wincewicz A, et al . Leptin 2From Regulation of fat Metabolism to Stimulation of BreastCancer Growth. Pathol Oncol Res, 2006,12(2) :69-72.
  • 7Ni Z, Lou W, Lee So, et al . Selective activation of members of the signal transdueers and activators of transcription family inprostate carcinoma. J Urol, 2002, 167(4) :1859-1862.
  • 8Rosen D G, M ercado U I, Yang G, et al. The role of constitutivelyactive signal transducer and activator of transcrip tion 3 in ovarian tumorigenesis and prognosis[ J]. Cancer,2006,107 ( 11 ) :2730-2740.
  • 9Sehulter C, Duchrow M,Wohlenberg C, et al. Molecular cloing of the cell proliferation associated nuclear antigen defined by antibody Ki67 : A very large rblquitous nulear protein with numerous repeated elements representing a new kind of cell cycle-maintaining protein[J].J Cell Biol,1993,123(3) :513-522.
  • 10Heintz AP,Odicino F,Maisonneuve P,et al.Carcinoma of the ovary[J].Int J Gynaecol Obstet,2003,83(10):135-166.

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  • 1张竹青,卢书明,陈美如,李春艳,刘丽娜,吕申.胃癌中STAT3、p-STAT3和Bcl-xL的表达及临床意义[J].肿瘤防治研究,2014,41(5):430-433. 被引量:9
  • 2邢长英,归绥琪,王海燕.人早孕母胎界面SOCS1、SOCS2、SOCS3表达[J].中国免疫学杂志,2006,22(6):538-544. 被引量:10
  • 3Coskun M, Salem M, Pedersen J, et al. Involvement of JAK/STAT signaling in the pathogenesis of inflammatory bowel disease C J ]. Pharmacol Res,2013,76 : 1 - 8.
  • 4Amoyel M, Andersen AM,Bach EA. JAK/STAT pathway dysregula- tion in tumors:A Drosophila perspective[J]. Semin Cell Dev Bio], 2014,28C :96 - 103.
  • 5Inagaki - Ohara K, Kondo T, Ito M et 81. SOCS, inflammation, and cancer[ J]. JAKSTAT,2013,2 (3) : e24053.
  • 6Fire A, Xu S, Montgomery MK, et al. Potent and specific genetic in- terference by double - stranded BNA in Caenorhabditis elegans [J]. Nature, 1998,391 (6669) :806 -811.
  • 7Ichim TE,Li M,Qian H,et al. RNA interference:a potent tool for gene - specific therapeutics [ J ]. Am J Transplant, 2004,4 ( 8 ) : 1227 - 1236.
  • 8Foued TM,Kogawa T,Reuben JM,et al. The role of inflammation in inflamntory breast cancer[J]. Adv Exp Med Biol,2014,816:53 -73.
  • 9Kumar J, Ward AC. Bole of the interleukin 6 receptor family in epi- thelial ovarian cancer and its clinical implications [ J ]. Biochim Biophys Acta,2014,1845(2) :117 -125.
  • 10Teramo A, Gattazzo C ,Passed F,et al. Intrinsic and extrinsic mech- anisms contribute to maintain the JAK/STAT pathway aberrantly activated in T -type large granular lymphocyte leukemia [ J ]. Blood,2013,121 (19) :3843 -3854.

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