高级搜索

STAT-3与 Enolase-1在乳腺癌组织中的表达及意义

杨洁, 叶双梅, 蒋学锋, 马全富, 阚淳一, 杨丽兰, 卢运萍, 王世宣, 马丁, 吴明富

杨洁, 叶双梅, 蒋学锋, 马全富, 阚淳一, 杨丽兰, 卢运萍, 王世宣, 马丁, 吴明富. STAT-3与 Enolase-1在乳腺癌组织中的表达及意义[J]. 肿瘤防治研究, 2012, 39(12): 1451-1455. DOI: 10.3971/j.issn.1000-8578.2012.12.011
引用本文: 杨洁, 叶双梅, 蒋学锋, 马全富, 阚淳一, 杨丽兰, 卢运萍, 王世宣, 马丁, 吴明富. STAT-3与 Enolase-1在乳腺癌组织中的表达及意义[J]. 肿瘤防治研究, 2012, 39(12): 1451-1455. DOI: 10.3971/j.issn.1000-8578.2012.12.011
Yang Jie, Ye Shuangmei, Jiang Xuefeng, Ma Quanfu, Kan Chunyi, Yang Lilan, Lu Yunping, Wang Shixuan, Ma Ding, Wu Mingfu. Expression and Clinical Signifiance of STAT-3 and Enolase-1 in Breast Cancer[J]. Cancer Research on Prevention and Treatment, 2012, 39(12): 1451-1455. DOI: 10.3971/j.issn.1000-8578.2012.12.011
Citation: Yang Jie, Ye Shuangmei, Jiang Xuefeng, Ma Quanfu, Kan Chunyi, Yang Lilan, Lu Yunping, Wang Shixuan, Ma Ding, Wu Mingfu. Expression and Clinical Signifiance of STAT-3 and Enolase-1 in Breast Cancer[J]. Cancer Research on Prevention and Treatment, 2012, 39(12): 1451-1455. DOI: 10.3971/j.issn.1000-8578.2012.12.011

STAT-3与 Enolase-1在乳腺癌组织中的表达及意义

基金项目: 教育部新教师基金资助项目(200804871056)
详细信息
    作者简介:

    杨洁(1987-),女,博士在读,主要从事肿瘤侵袭转移的研究

    通讯作者:

    吴明富,wumingfuwh@yahoo.com.cn

  • 中图分类号: R737.9

Expression and Clinical Signifiance of STAT-3 and Enolase-1 in Breast Cancer

  • 摘要: 目的 探讨乳腺癌组织中信号转导及转录活化因子3(STAT-3)和糖酵解酶烯醇化酶(Enolase-1)的表达与雌孕激素受体、淋巴结转移、临床分期、病理分级等的关系。方法免疫组织化学SP法检测126例乳腺癌和26例乳腺良性病变组织中STAT-3与 Enolase-1的表达情况,并分析他们与临床病理参数之间的关系。结果乳腺癌组织中STAT-3和 Enolase-1的阳性表达率分别为82.5%和77.8%,明显高于乳腺良性病变组织(11.5%和7.7%),差异均有统计学意义(χ2=42.416,P<0.05;χ2=57.211, P<0.05);在有淋巴结转移的乳腺癌组织中阳性表达率分别为85.7%和90.5%,高于无淋巴结转移组,差异均有统计学意义(χ2=9.184,P<0.05;χ2=11.014,P<0.05)。相关分析表明STAT-3和 Enolase-1的表达呈正相关。在雌激素受体阳性(ER+)和/或孕激素受体阳性(PR+)或表皮生长因子受体2阳性(HER-2+)乳腺癌组织中,有淋巴结转移组中STAT-3和Enolase-1的表达水平均明显高于无淋巴结转移组,差异均有统计学意义(P<0.05)。结论STAT-3与Enolase-1的表达与乳腺癌的发生发展及侵袭转移相关,且二者有协同作用(r=0.379,P<0.05)。在ER+和(或)PR+或HER-2+乳腺癌组织中,STAT-3和Enolase-1的高表达与淋巴结转移相关。在高表达STAT-3的乳腺癌组织中Enolase-1表达也较高,其联合检测可作为判断乳腺癌恶性程度、评价预后及指导治疗的一项评估指标。

     

    Abstract: Objective To investigate the expression of STAT-3 and Enolase-1 in breast cancer and its relationship with Estrogen receptor status,Progesterone receptor status,lymph node metastasis,clinical stages and histological grading. Methods The expression of STAT-3 and Enolase-1 were examined by immunohistochemical streptavid-peroxidase(S-P)assay in 126 cases of breast cancer and 26 cases of benign breast disease.And the significance of its expression was analyzed with clinicopathologic parameters. Results The expression rates of STAT-3(77.8%)and Enolase-1(82.5%)in breast cancer were significantly higher than that in benign breast disease(11.5% vs.7.7%)and the expression of two proteins were positively correlated(χ2=42.416,P<0.05;χ2=57.211,P<0.05).The expression of STAT-3 and Enolase-1 in breast cancer has no significant difference in age,tumor size,histologic grading and clinical stages.Epression of STAT-3(85.7%)and Enolase-1(90.5%)in breast cancer with metastasis is significantly higher than that without metastasis (χ2=9.184,P<0.05;χ2=11.014,P<0.05).There was a significant correlation between the high expression of STAT-3 and axillary lymphatic metastasis in comparisons between positive estrogen and/or progesterone receptor expression and Her-2 positive expression(P<0.05).And there was a significant correlation between the high expression of Enolase-1 and axillary lymphatic metastasis in comparisons with positive estrogen or positive progesterone receptor expression and Her-2 positive expression(P<0.05). Conclusion Both STAT-3 and Enolase-1 may be involved in the tumorgenesis development and metastasis of breast cancer.The high expression of STAT-3 and Enolase-1 in estrogen receptor or/and progesterone receptor or Her-2 positive breast cancer was associated with a high possibility of lymph node metastasis.The detection of STAT-3 and Enolase-1 may be helpful in the diagnosis and prognosis of breast cancer.

     

  • [1] Bromberg JF,Wrzeszczynska MH,Devgan G.STAT3 as an oncogene[J].Cell,1999,98(3):295-303.
    [2] Yang L,Li LD,Chen YD,et al.Parkin.Estimates of chinese breast cancer incidence and mortality trends[J].Zhonghua Zhong Liu Za Zhi,2006,28(6):438-40. [杨玲,李连弟,陈育德, 等.中国乳腺癌发病死亡趋势的估计与预测[J].中华肿瘤杂志,2006,28(6):438-40.]
    [3] Xu BH.The progress and future of breast cancer clinic research[J].Zhonghua Zhong Liu Za Zhi,2007,29(12):881-3.[徐兵河.乳腺癌临床研究的进展与未来[J].中华肿瘤杂志,2007,29(12):881-3.]
    [4] Song H,Wang R,Wang S,et al.A low-molecular-weight compound discovered through virtual database screening inhibits STAT3 function in breast cancer cells[J].Proc Natl Acad Sci U S A,2005,102(13):4700-5.
    [5] Yeh YT,Ou-Yang F,Chen IF,et al.STAT3 ser727 phosphorylation and its association with negative estrogen receptor STATus in breast infiltrating ductal carcinoma[J].Int J Cancer,2006,118(12):2943-7.
    [6] Sheen-Chen SM,Huang CC,Tang RP,et al.Prognostic value of signal transducers and activators of transcription 3 in breast cancer[J].Cancer Epidemiol Biomarkers Prev,2008,17(9):2286-90.
    [7] Takashima M,Kuramitsu Y,Yokoyama Y,et al.Overexpression of alpha enolase in hepatitis C virus-related hepatocellular carcinoma:association with tumor progression as determined by proteomic analysis[J].Proteomics,2005,5(6):1686-92.
    [8] Chen G,Gharib TG,Wang H,et al.Protein profiles associated with survival in lung adenocarcinoma[J].Proc Natl Acad Sci U S A,2003,100(23):13537-42.
    [9] Chang GC,Liu KJ,Hsieh CL,et al.Identification of alpha-enolase as an autoantigen in lung cancer:its overexpression is associated with clinical outcomes[J].Clin Cancer Res,2006,12(19):5746-54.
    [10] Tu SH,Chang CC,Chen CS,et al.Increased expression of enolase alpha in human breast cancer confers tamoxifen resistance in human breast cancer cells[J].Breast Cancer Res Treat,2010,121(3):539-53.
    [11] Warburg O.On respiratory impairment in cancer cells[J].Science,1956,124(3215):269-70.
    [12] Altenberg B,Greulich KO.Genes of glycolysis are ubiquitously overexpressed in 24 cancer classes[J].Genomics,2004,84(6):1014-20.
    [13] Dang CV,Lewis BC,Dolde C,et al.Oncogenes in tumor metabolism,tumorigenesis,and apoptosis[J].J Bioenerg Biomembr,1997,29(4):345-54.
    [14] Xu Q,Briggs J,Park S,et al.Targeting STAT3 blocks both HIF-1 and VEGF expression induced by multiple oncogenic growth signaling pathways[J].Oncogene,2005,24(36):5552-60.
    [15] Semenza GL.Targeting HIF-1 for cancer therapy[J].Nat Rev Cancer,2003,3(10):721-32.
计量
  • 文章访问数:  2070
  • HTML全文浏览量:  30
  • PDF下载量:  512
  • 被引次数: 0
出版历程
  • 收稿日期:  2012-01-09
  • 修回日期:  2012-05-03
  • 刊出日期:  2012-12-24

目录

    /

    返回文章
    返回
    x 关闭 永久关闭