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卵巢上皮性癌组织中miR-338-3p的表达 被引量:7

Expression of miR-338-3p in epithelial ovarian cancer tissue
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摘要 目的:检测微小RNA-338-3p(miR-338-3p)在卵巢上皮性癌组织中的表达情况,探讨其在卵巢癌发生发展中的作用。方法:采用qRT-PCR检测20例正常卵巢组织、20例良性卵巢上皮性肿瘤组织和65例卵巢上皮性癌组织中miR-338-3p的表达情况,分析卵巢上皮性癌与组织中miR-338-3p表达与临床病理指标的关系,Kaplan-Meier法分析miR-338-3p表达对卵巢癌患者生存的影响。结果:卵巢上皮性癌组织中miR-338-3p的表达显著低于正常卵巢组织和良性卵巢上皮性肿瘤组织(P<0.05)。临床分期晚、组织级别高、有淋巴结转移的卵巢上皮性癌组织中miR-338-3p表达低(P<0.05)。miR-338-3p表达水平相对较低的卵巢上皮性癌患者的总体生存率和无进展生存期明显短于miR-338-3p表达水平相对较高的患者(P<0.05)。结论:miR-338-3p低表达与卵巢癌患者预后不良有关,可作为卵巢癌预后的标记物。 Aim:To detect the expression of miR-338-3p in epithelial ovarian cancer tissue.Methods:The expressions of miR-338-3p in 20 specimens of normal ovary,20 specimens of benign epithelial ovarian tumor and 65 specimens of epithelial ovarian cancer tissues were detected by qRT-PCR,and its association with the clinicopathologic characteristics of epithelial ovarian cancer was analyzed.The relation between miR-338-3p expression and the survival of ovarian cancer patients was measured by Kaplan-Meier analysis.Results:The expression of miR-338-3p in epithelial ovarian cancer tissue was obviously lower than those in normal ovarian tissue and benign ovarian tumor(P<0.05).In epithelial ovarian cancer,lower expression of miR-338-3p was associated with more advanced FIGO stage,higher histological grade and lymph node metastasis(P<0.05).The overall survival rate and progression free survival rate of patients with lower miR-338-3p were obviously shorter(P<0.05).Conclusion:Low expression of miR-338-3p is related with poor prognosis of ovarian cancer patients,and miR-338-3p could be served as a biomarker for the prognosis of ovarian cancer.
作者 张瑞涛 史惠蓉 刘哲颖 张微微 姬鹏程 王文文 ZHANG Ruitao;SHI Huirong;LIU Zheying;ZHANG Weiwei;JI Pengcheng;WANG Wenwen(Department of Gynecology,the First Affiliated Hospital,Zhengzhou University,Zhengzhou 450052)
出处 《郑州大学学报(医学版)》 CAS 北大核心 2019年第5期780-783,共4页 Journal of Zhengzhou University(Medical Sciences)
关键词 卵巢上皮性癌 微小RNA-338-3p 复发 预后 ovarian epithelial cancer miR-338-3p recurrence prognosis
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  • 1Noman MZ, Buart S, Romero P, Ketari S, Janji B, Mari B, et al. Hypoxia-inducible miR-210 regulates the susceptibility of tumor cells to lysis by cytotoxic T cells. Cancer Res 2012; 72: 4629–41.
  • 2Vaupel P, Mayer A, Hockel M. Tumor hypoxia and malignant progression. Methods Enzymol 2004; 381: 335–54.
  • 3Semenza GL. HIF-1 and tumor progression: pathophysiology and therapeutics. Trends Mol Med 2002; 8: S62–7.
  • 4Pocock R. Invited review: decoding the microRNA response to hypoxia. Pflugers Arch 2011; 461: 307–15.
  • 5Huang X, Ding L, Bennewith KL, Tong RT, Welford SM, Ang KK, et al. Hypoxia-inducible mir-210 regulates normoxic gene expression involved in tumor initiation. Mol Cell 2009; 35: 856–67.
  • 6Bruning U, Cerone L, Neufeld Z, Fitzpatrick SF, Cheong A, Scholz CC, et al. MicroRNA-155 promotes resolution of hypoxia-inducible factor 1alpha activity during prolonged hypoxia. Mol Cell Biol 2011; 31: 4087–96.
  • 7Crosby ME, Kulshreshtha R, Ivan M, Glazer PM. MicroRNA regulation of DNA repair gene expression in hypoxic stress. Cancer Res 2009; 69: 1221–9.
  • 8Haque I, Banerjee S, Mehta S, De A, Majumder M, Mayo MS, et al. Cysteine-rich 61-connective tissue growth factor-nephroblastoma-overexpressed 5 (CCN5)/Wnt-1-induced signaling protein-2 (WISP-2) regulates microRNA-10b via hypoxia-inducible factor-1alpha-TWIST signaling networks in human breast cancer cells. J Biol Chem 2011; 286: 43475–85.
  • 9Mathieu J, Zhang Z, Zhou W, Wang AJ, Heddleston JM, Pinna CM, et al. HIF induces human embryonic stem cell markers in cancer cells. Cancer Res 2011; 71: 4640–52.
  • 10Neal CS, Michael MZ, Rawlings LH, Van der Hoek MB, Gleadle JM. The VHL-dependent regulation of microRNAs in renal cancer. BMC Med 2010; 8: 64.

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