干细胞标志物Oct-4 Sox-2表达与结肠癌术后复发转移的关系

李宁 张力 陈小兵 马怡晖 罗素霞 邓文英

李宁, 张力, 陈小兵, 马怡晖, 罗素霞, 邓文英. 干细胞标志物Oct-4 Sox-2表达与结肠癌术后复发转移的关系[J]. 中国肿瘤临床, 2012, 39(9): 574-577. doi: 10.3969/j.issn.1000-8179.2012.09.022
引用本文: 李宁, 张力, 陈小兵, 马怡晖, 罗素霞, 邓文英. 干细胞标志物Oct-4 Sox-2表达与结肠癌术后复发转移的关系[J]. 中国肿瘤临床, 2012, 39(9): 574-577. doi: 10.3969/j.issn.1000-8179.2012.09.022
Ning LI, Li ZHANG, Xiaobing CHEN, Yihui MA, Suxia LUO, Wenying DENG. Relationship of Oct-4 and Sox-2 Expression in Colon Carcinoma with Recurrence and Metastasis[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2012, 39(9): 574-577. doi: 10.3969/j.issn.1000-8179.2012.09.022
Citation: Ning LI, Li ZHANG, Xiaobing CHEN, Yihui MA, Suxia LUO, Wenying DENG. Relationship of Oct-4 and Sox-2 Expression in Colon Carcinoma with Recurrence and Metastasis[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2012, 39(9): 574-577. doi: 10.3969/j.issn.1000-8179.2012.09.022

干细胞标志物Oct-4 Sox-2表达与结肠癌术后复发转移的关系

doi: 10.3969/j.issn.1000-8179.2012.09.022
基金项目: 

河南省卫生厅项目 2011020171

详细信息
    通讯作者:

    罗素霞  lining97@126.com

Relationship of Oct-4 and Sox-2 Expression in Colon Carcinoma with Recurrence and Metastasis

Funds: 

the Key Project of Henan Provincial Health Department 2011020171

More Information
  • 摘要:   目的  探讨结肠癌组织中Oct-4、Sox-2表达情况及其对术后复发转移的预测作用。  方法  采用免疫组织化学方法检测手术切除的80例结肠癌术后标本中Oct-4、Sox-2表达情况,并且对两指标的表达同肿瘤分化程度、分期和术后复发转移关系进行分析。采用RT-PCR检测20例冰冻肿瘤组织及癌旁组织中Sox-2、Oct-4表达情况。  结果  80例患者中35例出现复发转移,Sox-2、Oct-4在转移组中表达率分别为48.57%(17/35)、51.43%(18/35),在非转移组中表达率分别为17.78%(8/45)、13.33%(6/ 45),差异有统计学意义(P=0.001)。原发病灶分化程度、T分期和N分期同Oct-4和Sox-2表达无显著性差异。均为阳性表达者其转移发生率高,生存分析显示不同表达状态转移出现时间差异有统计学意义(P=0.001)。RT-PCR分析显示20例肿瘤组织中Sox-2、Oct-4阳性表达率分别为40%(8/20)、45%(9/20),明显高于癌旁正常组织5%(1/20)。  结论  肿瘤组织中Sox-2、Oct-4表达同结肠癌术后转移相关,两者联合检测有助于评估结肠癌术后复发转移的可能。

     

  • 图  1  Oct-4、Sox-2在结肠癌组织中表达(S-P×400)

    A:Oct-4阳性;B:Sox-2阳性

    Figure  1.  Expression of Oct-4 and Sox-2 in colon cancer

    图  2  RT-PCR检测Oct-4、Sox-2在结肠癌组织及癌旁组织中的表达

    T:肿瘤组织;N:癌旁组织;B:空白对照

    Figure  2.  Expression of Oct-4 and Sox-2 in colon cancer and normal paraneoplastic tissues

    图  3  Oct-4、Sox-2阳性表达和阴性表达患者转移出现时间比较(以转移为截点)

    Figure  3.  Comparison of metastasis between patients with Oct-4 and Sox-2 expression and those without Oct-4 and Sox-2 expression(P=0.001)(metastasis was censored)

    表  1  引物序列

    Table  1.   Primer sequences

    表  2  组织中Sox-2、Oct-4表达同临床特征间关系

    Table  2.   Relationship of Sox-2 and Oct-4 expression with clinical characteristics

  • [1] 张楠, 连鹏, 时永香, 等. Oct-4/Sox-2协同调控下游基因表达的分子机制[J]. 生物物理学报, 2007, 23(6): 420-426. doi: 10.3321/j.issn:1000-6737.2007.06.002
    [2] 王海威, 王家东. Oct-4蛋白在甲状腺肿瘤中的表达及意义[J]. J Clin Otorhinolaryngol Head Neck Surg(China), 2010, 24(15): 682-685. https://www.cnki.com.cn/Article/CJFDTOTAL-LCEH201015006.htm
    [3] Ben-Porath I, Thomson MW, Carey VJ, et al. An embryonic stem cell-like gene expresson signature in poorly differentiated aggressive human tumors[J]. Nat Genet, 2008, 40(5): 499-507. doi: 10.1038/ng.127
    [4] 曹婧, 樊青霞, 索振河. 靛玉红对膀胱癌ScaBer细胞株增殖的影响及机制[J]. 山东医药, 2008, 48(14): 61-62. doi: 10.3969/j.issn.1002-266X.2008.14.031
    [5] 曹浩哲, 冀静, 郑鹏生. Oct4基因在宫颈癌中的表达及其意义[J]. 西安交通大学学报(医学版), 2010, 31(1): 17-21. https://www.cnki.com.cn/Article/CJFDTOTAL-XAYX201001006.htm
    [6] 宋娟, 严宁, 张汉东, 等. 口腔鳞癌组织中干细胞转录因子Oct-4的表达及意义[J]. 临床口腔医学杂志, 2010, 26(7): 390-393. doi: 10.3969/j.issn.1003-1634.2010.07.002
    [7] 侯轶, 赵晓昆, 蒋宏毅, 等. 膀胱移行细胞癌组织中PSCA和Oct-4表达及其意义[J]. 实用肿瘤杂志, 2010, 25(5): 531-533. https://www.cnki.com.cn/Article/CJFDTOTAL-SYZZ201005010.htm
    [8] Attasi Y, Mowla SJ, Ziaee SA, et al. Oct-4, an embryonic stem cell marker, is highly expressed in bladder cancer[J]. Int J Cancer, 2007, 120(7): 1598-1602. doi: 10.1002/ijc.22508
    [9] Li XL, Eishi YB, Bai YQ, et al. Expression of the SRY-related HMG box protein SOX2 in human gastric carcinoma[J]. Int J Oncol, 2004, 24(2): 257-263. http://www.spandidos-publications.com/ijo/24/2/257/download
    [10] Sattler HP, Lensch R, Rohde V, et al. Novel amplification unit at chromosome 3q25-q27 in human prostate cancer[J]. Prostate, 2000, 45(3): 207-215. doi: 10.1002/1097-0045(20001101)45:3<207::AID-PROS2>3.0.CO;2-H
    [11] Jung M, Peterson H, Chavez L, et al. A data integration approach to mapping OCT4 gene regulatory networks operative in embryonic stem cells and embryonal carcinoma cells[J]. PloS One, 2010, 5(5): e10709. doi: 10.1371/journal.pone.0010709
    [12] Yamaguchi S, Kurimoto K, Yabuta Y, et al. Conditional knockdown of Nanog induces apoptotic cell death in mouse migrating primordial germ cells[J]. Development, 2009, 136(23): 4011-4020. doi: 10.1242/dev.041160
    [13] Park IH, Zhao R, West JA, et al. Reprogramming of human somatic cells to pluripotency with defined factors[J]. Nature, 2008, 451 (7175): 141-146. doi: 10.1038/nature06534
    [14] Lengerke C, Fehm T, Kurth R, et al. Expression of the embryonic stem cell marker SOX-2 in early-stage breast carcinoma[J]. BMC cancer, 2011, 11: 42. doi: 10.1186/1471-2407-11-42
    [15] Fong H, Hohenstein KA, Donovan PJ. Regulation of self-renewal and pluripotency by Sox2 in human embryonic stem cell[J]. Stem Cells, 2008, 26(8): 1931-1938. doi: 10.1634/stemcells.2007-1002
  • 加载中
图(3) / 表(2)
计量
  • 文章访问数:  15
  • HTML全文浏览量:  2
  • PDF下载量:  0
  • 被引次数: 0
出版历程
  • 收稿日期:  2011-10-15
  • 修回日期:  2011-12-20

目录

    /

    返回文章
    返回