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STAT3、Survivin在胆囊癌中的表达及意义 被引量:3

Significance and expression of STAT3 in survivin primary gallbladder carcinoma
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摘要 目的探讨胆囊癌中STAT3、p-STAT3和Survivin蛋白表达及其在胆囊癌发生、发展中的意义。方法采用免疫组织化学SP法检测45例胆囊癌及相应45例癌旁胆囊组织、20例慢性胆囊炎组织中STAT3、p-STAT3及Survivin蛋白的表达,并分析其与临床病理特征、预后的关系。结果本组45例胆囊癌组织中STAT3、p-STAT3和Survivin蛋白阳性率分别为66.7%(30/45)、55.6%(25/45)、64%(29/45),明显高于癌旁正常组织(P<0.01)和慢性胆囊炎组织(P<0.01)。在胆囊癌组织中STAT3、p-STAT3的表达与Survivin表达均呈正相关(r=0.558,0.830;P<0.01)。STAT3、p-STAT3和Survivin蛋白的表达与胆囊癌病理组织分级、Nevin分期、有无淋巴结转移和3年生存率有关(P<0.01)。结论 STAT3、p-STAT3、Survivin参与了胆囊癌的发生、发展,可能作为判断胆囊癌转移、预后的临床指标。 Objective To detect the expression of STAT3,p-STAT3 and Survivin in primary gallbladder carcinoma(PGC) and explore its significance in the occurrence and development of PGC.Methods The expression of STAT3,p-STAT3 and Survivin were determined in samples from 45 PGC tissues and corresponding nontumor tissues,20 chronic cholecystitis by immunohistochemistry.The relationship between expressions of these proteins and clinicopathological factors,and its prognosis were analysed.Results The positive rates of STAT3,p-STAT3 and Survivin in 45 PGC tissues were 66.7%(30/45),55.6%(29/45)and 64%(25/45)respectively,which was significantly higher than those in 45 corresponding PGC nontumor tissues(P0.01) and 20 chronic cholecystitis tissues(P0.01).The expression of survivin were positively correlated with STAT3(r=0.558,P0.01),p-STAT3(r=0.830,P0.01).The expressions of STAT3,p-STAT3 and Survivin were significantly associated with histopathological grades,lymph node metastasis,nevin stages and 3-year survival rate.Conclusion STAT3,p-STAT3 and Survivin may play a vital role in the occurrence and development of PGC.The expressions of STAT3,p-STAT3 or Survivin are the metastatic and prognostic factors in PGC.
出处 《临床肝胆病杂志》 CAS 2011年第9期939-943,共5页 Journal of Clinical Hepatology
基金 南京市科技发展项目(YKK09193)
关键词 胆囊肿瘤 STAT3转录因子 凋亡抑制蛋白质类 gallbladder neoplasms STAT3 transcription factor inhibitor of apoptosis
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  • 1Kunnumakkara AB, Nair AS, Sung B, et al, Boswellic acid blocks signal transducers and activators of transcription 3 signaling, proliferation,and survival of multiple myeloma vis the protein tyrosine phosphatase SliP - I[ J ]. Mol Cancer Res, 2009.7(11 : 118 -128.
  • 2Gu L, Chiang KY, Zhu N, et al. Contribution of STAT3 to the activation of surviving by GM -CSF in CD34^+ cell lines[ J ]. Exp Hematol, 2007, 35(6) .. 957 -966.
  • 3Dien J, Amin HM, Chiu N, et al. Signal transducers and activator of transcription -3 up -regulates tissue inhibitor of metalloproteinase-1 expression and decreases invasiveness of breast cancer[J]. Am J Pathol, 2006, 169(5): 633 - 642.
  • 4Qu P, Roberts J, Li Y, et al. STAT3 downstream genes serve as biomarkers in human lung carcinomas and chronic obstructive pulmonary disease[J]. Lung Cancer, 2009, 63 (8): 341 -347.
  • 5Mita AC, Mita MM, Nawrocki ST, et al. Survivin.. key regulator of mitosis and apoptosis and novel target for cancer therapeutics[ J ]. Clin Cancer Res, 2008, 14 (4): 5000 - 5005.
  • 6Gritsko T, Williams A, Turkson J, et at. Persistent activation of Stat3 signaling induces surviving gene expression and confers resistance to apoptosis in human breast cancer cells [J]. Clin Cancer Res, 2006, 12(8): 11 -19.
  • 7Aoki Y, Feldman GM, Tosato G. Inhibition of STAT3 signaling induces apoptosis and decreases survivin expression in primary effusion lymphoma [ J ]. Blood, 2003, 101 (4): 1535 - 1542.
  • 8沈汉斌,吴耀辉,龙浩成,郑启昌,龚建平.胆囊癌组织Survivin表达及临床意义[J].中华实验外科杂志,2009,26(3):393-393. 被引量:3

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  • 1王俊阁,李晓明,路秀英.JAK激酶抑制剂AG490联合顺铂对喉癌细胞STAT3信号转导通路的抑制作用[J].第四军医大学学报,2007,28(21):1930-1932. 被引量:3
  • 2Kisseleva T, Bhattacharya S, Braunstein J , et al. Signaling through the JAK/STAT pathway, recent advances and future challenges[J]. Gene, 2002,285 (1-2) : 1-24.
  • 3Caldera V, Mellai M, Annovazzi L, et al. Stat3 expression and its correlation with proliferation and apoptosis/autophagy in gliomas[J]. J Oncol, 2008,2008: 219241.
  • 4Mora LB, Buettner R, Seigne J, et al. Constitutive activation of Stat3 in human prostate tumors and cell lines., direct in- hibition of Stat3 signaling induces apoptosis of prostate cancer cells[J]. Cancer Res, 2002,62(22) : 6659-6666.
  • 5Yan S, Zhou C, Zhang W, et al. beta-Catenin/TCF pathway upregulates STAT3 expression in human esophageal squa- mous cell carcinoma[J]. Cancer Lett, 2008,271 (1) : 85-97.
  • 6Chang CJ, Chiang CH, Song WS, et al. Inhibition of phospho- rylated STAT3 by eueurbitacin Ⅰ enhances chemoradiosensi-tivity in medulloblastoma-derived cancer stem cells[J]. Childs Nerv Syst,2012,28(3) :363-373.
  • 7Yasuda S, Yogosawa S, Izutani Y, et al. Cucurbitacin B induces Gz arrest and apoptosis via a reactive oxygen species- dependent mechanism in human colon adenocarcinoma SW480 cells[J]. Mol Nutr Food Res,2010,54(4) ,559-565.
  • 8Chan KT, Li K,Liu SL, et al. Cucurbitacin B inhibits STAT3 and the Raf/MEK/ERK pathway in leukemia cell line K562 [J]. Cancer Lett,2010,289(1) :46-52.
  • 9Chan KT,Meng FY,Li Q,et al. Cucurbitacin B induces apop- tosis and S phase cell cycle arrest in BEL-7402 human hepato- cellular carcinoma cells and is effective via oral administration [J]. Cancer Lett, 2010,294(1) : 118-124.
  • 10Blaskovich MA, Sun J, Cantor A, et al. Discovery of JSI-124 (cucurbitacin I), a selective Janus kinase/signal transducer and activator of transcription 3 signaling pathway inhibitor with potent antitumor activity against human and murine cancer cells in mice[J]. Cancer Res, 2003,63(6) : 1270-1279.

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