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趋化因子受体CCR3在上皮性卵巢癌中的表达及临床意义

Expression and Clinical Significance of CCR3 in Human Epithelial Ovarian Cancer
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摘要 目的:探讨趋化因子受体CCR3在上皮性卵巢癌组织中的表达情况,以及其与卵巢癌临床病理特征的关系。方法:收集上皮性卵巢癌组织、良性上皮性卵巢肿瘤组织以及正常卵巢组织标本各30例,采用多聚腺苷酸加尾实时荧光定量反转录聚合酶链反应[poly(A)-RT-qPCR]检测其CCR3的表达,并分析上皮性卵巢癌组织中CCR3的表达与患者临床病理特征之间的关系。结果:上皮性卵巢癌组织中CCR3的表达显著高于良性卵巢肿瘤组和正常卵巢组,差异有统计学意义(P<0.05);且上皮性卵巢癌组织中CCR3的表达与患者的分期、组织分级及淋巴结转移均显著相关(P<0.05)。结论:CCR3在上皮性卵巢癌组织中呈高表达,且在上皮性卵巢癌的发生和发展过程中均起着十分重要的作用。 Objective: To investigate the expression of chemokine receptor CCR3 in epithelial ovarian carcinoma, and the relationship with the clinicopathological characteristics. Methods: Tissue samples of epithelial ovarian cancer(30 cases), benign ovarian tumor(30 cases) and normal ovarian(30 cases) were collected, the polyadenylation real-time fluorescent quantitative reverse transcription polymerase chain reaction(A [poly)-RT-qPCR] were used to detect the expression of CCR3, and analyze the correlation of CCR3 expression with the clinicopathological characteristics. Results: The expression of CCR3 in ovarian cancer group was significantly higher than those in the benign ovarian tumors and normal ovarian group(P〈0.05), which was also markedly correlated with the staging,histological grade and lymph node metastasis of epithelial ovarian carcinoma(P〈0.05). Conclusion: The upregulation of CCR3 expression played an important role in the development of epithelial ovarian carcinoma.
出处 《现代生物医学进展》 CAS 2014年第23期4494-4496,共3页 Progress in Modern Biomedicine
基金 黑龙江省卫生厅科研项目(2010132)
关键词 卵巢癌 趋化因子受体 CCR3 逆转录聚合酶反应 Ovarian cancer Chemokine receptor CCR3 Reverse transcriptase polymerase chain reaction
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参考文献19

  • 1Rescigno P, Cerillo I, Ruocco R, et al. New hypothesis on pathogenesis of ovarian cancer lead to future tailored approaches[J]. Biomed Res Int, 2013, 2013: 852839.
  • 2Kigawa J. New strategy for overcoming resistance to chemotherapy of ovarian cancer[J].Yonago Acta Med, 2013, 56(2): 43-50.
  • 3王景苗,靳卫国.卵巢癌靶向基因治疗研究进展[J].泰山医学院学报,2010,31(8):640-642. 被引量:2
  • 4Horuk R. Chemokines[J]. Scientific World Journal, 2007, 7: 224-232.
  • 5Guergnon J, Combadie re C. Role of chemokines polymorphisms in diseases[J]. Immunol Lett, 2012,145(1-2): 15-22.
  • 6Raman D, Sobolik-Delmaire T, Richmond A. Chemokines in health and disease[J]. Exp Cell Res, 2011, 317(5): 575-589.
  • 7Fusi A, Liu Z, Ku mmerlen V, et al. Expression of chemokine receptors on circulating tumor cells in patients with solid tumors [J].J Transl Med, 2012,10: 52.
  • 8Mii ller A, Homey B, Soto H, et al. Involvement of chemokine receptors in breast cancer metastasis[J]. Nature, 2001, 410(6824): 50- 56.
  • 9Liu Y, Ji R, Li J, et al. Correlation effect of EGFR and CXCR4 and CCR 7 chemokine receptors in predicting breast cancer metastasisand prognosis[J]. J Exp Clin Cancer Res, 20 I 0, 29: 16.
  • 10Takeuchi H, Fujimoto A, Tanaka M, et al. CCL21 chemokine regulates chemokine receptor CCR7 bearing malignant melanoma cells[J]. Clin Cancer Res, 2004, 10: 2351-2358.

二级参考文献20

  • 1汤军桥,葛海良.卵巢癌基因治疗的研究现状及进展[J].国外医学(妇产科学分册),2006,33(4):259-263. 被引量:2
  • 2陈煜,谢小芳.RNAi的作用机制及抗病毒研究进展[J].世界华人消化杂志,2006,14(21):2123-2129. 被引量:11
  • 3席勇,邓燕杰.卵巢癌基因治疗研究与进展[J].国外医学(妇产科学分册),2007,34(3):196-199. 被引量:3
  • 4Kramm CM,Niehues T,Rainov NG.Experimental strategies for combined suicide and immune cancer gene therapy[J].Methods Mol Biol,2003,215(6):137-152.
  • 5Caracciolo G,Pozzi D,Caminiti R,et al.Structural characterization of a new lipid /DNA complex showing a selective transfection efficiency in ovarian cancer cells[J].Eur Phys J E Soft Matter,2003,10(4):331-336.
  • 6Dachs GU,Tupper J,Tozer GM.From bench to bedside for gene directed enzyme prodrug therapy of cancer[J].Anticancer Drugs,2005,16(4):349-359.
  • 7Ziller C,Lincet H,Muller CD,et al.The cyclin-dependent kinase inhibitor p21cipl /waf1 enhances the cytotoxicity of gancielovir in HSV-tk transfected ovarian carcinoma cells[J].Cancer Lett,2004,212(1):43-52.
  • 8Song Y,Kong B,Ma D,et al.Procaspase-3 enhances the in vitro effect cytosine deam inase-thymidine kinase disuicide gene therapy on human ovarian cancer[J].Int J Gynecol Cancer,2006,16(1):156-164.
  • 9Hamstra DA,Lee KC,Tychewicz JM,et al.The use of 19F spectroscopy and diffusion-weighted MRI to evaluate differences in gene-dependent enzyme prodrug therapies[J].Mol Ther,2004,10(5):916-928.
  • 10Noske A,Kaszubiak A,Weichert W,et al.Specific inhibition of AKT2 by RNA interference results in reduction of ovarian cancer cell proliferation:increased expression of AKT in advanced ovarian cancer[J].Cancer Lett,2007,246(1-2):190-200.

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