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卵巢浆液性癌组织中microRNA表达谱分析 被引量:2

Expression Profile of MicroRNA in Ovarian Serous Carcinoma
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摘要 目的寻找与卵巢浆液性癌相关的microRNA,积累以国内患者为数据来源的microRNA表达谱资料,并初步探讨其临床意义。方法利用microRNA芯片,筛查卵巢浆液性癌组织及正常卵巢组织中差异表达的microRNA,用实时荧光定量PCR在58份卵巢组织标本中进行验证,并分析microRNA表达水平与卵巢浆液性癌临床病理特征之间的关系。结果与正常卵巢组织比较,芯片结果显示卵巢浆液性癌有9个microRNA明显上调,分别是hsa-mi R-141-3p、hsa-mi R-200a-3p、hsa-mi R-200b-3p、hsa-mi R-200c-3p、hsa-mi R-224-5p、hsa-mi R-7-5p、hsa-mi R-142-3p、hsa-mi R-21-5p、hsa-mi R-142-5p,6个microRNA明显下调,分别是hsa-mi R-424-5p、hsa-mi R-214-3p、hsa-mi R-125b-5p、hsa-let-7b-5p、hsa-mi R-199a-5p、hsa-mi R-100-5p。实时荧光定量PCR验证结果与芯片结果一致。对差异microRNA进行分层分析发现,与卵巢浆液性癌Ⅰ-Ⅱ期、淋巴结未转移患者比较,Ⅲ-Ⅳ期、淋巴结有转移患者的hsa-mi R-21-5p表达均增高,hsa-mi R-125b-5p表达均降低(P<0.05);而在高级别与低级别卵巢癌患者之间microRNA的表达水平差异均无统计学意义(P均>0.05)。结论卵巢浆液性癌中异常表达的microRNA可能与肿瘤的发生发展相关。 Objective To search for microRNA associated with ovarian serous carcinoma, and to accumulate the microRNA expression profile data from domestic patients, and to make a preliminary study of its clinical significance. Methods Microarray was used to screen the differentially expressed microRNA in ovarian serous carcinoma and normal ovarian tissues, and the real-time fluorescence quantitative PCR was used to verify the expression in 58 samples of ovarian tissues. The relationship between microRNA expression and clinicopathological features of ovarian serous carcinoma was analyzed. Results Compared with the normal ovarian tissue, nine microRNA were up-regulated in ovarian serous carcinoma by microarray and they were hsa-miR-141-3p, hsa-miR-200a-3p,hsa-miR-200b-3p,hsa-miR-200c-3p,hsa-miR-224-Sp, hsa-miR-7-Sp, hsa-miR- 142- 3p, hsa-miR-21-Sp,hsa-miR-142-Sp, respectively. Six microRNA was significantly down-regnlated and they werehsa-miR-424-Sp, hsa-miR-214-3p, hsa-miR- 125b-Sp, let-7b-Sp, hsa-miR- 199a-Sp, hsa-miR- 100- 5p, respectively. The results of real-time fluorescence quantitative PCR were consistent with the chips. And in the stratified analysis of different microRNA,compared with no lymph node metastasis and I-II stage, hsa-miR-21-5p expression increased in III-IV stage lymph node metastasis patients, and hsa-miR-125b-Sp expression decreased (P〈0.05). Conclusion The abnormal expression of microRNA in ovarian serous carcinoma is related to the occurrence and development of tumor.
作者 马丽 马会明 崔娇 张雪玉 MA Li MA Huiming CUI Jiao ZHANG Xueyu(Ningxia Medical University, Yinchuan 750004 Department of Gynecology, the General Hospital of Ningxia Medical University, Yinchuan 750004)
出处 《宁夏医科大学学报》 2017年第2期149-153,F0004,共6页 Journal of Ningxia Medical University
基金 宁夏自然科学基金(NZ15140)
关键词 浆液性卵巢癌 micro RNA 微阵列芯片技术 实时定量反转录聚合酶链反应 ovarian serous carcinoma microRNA microarray chip technology real-time quantitative reverse transcription polymerase chain reaction
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  • 1Shen J, Hung MC. Signaling-mediated regulation of MicroRNA processing[J]. Cancer Res, 2015, 75(5) : 783-791.
  • 2Kim S, Lee UJ, Kim MN, et al. MicroRNA miR-199a * regulates the MET proto-oncogene and the downstream extracellular signal-regulated kinase 2 ( ERK2 ) [ J ]. J Biol Chem, 2008, 283(26) : 18158-18166.
  • 3Ergun S, Tayeb TS, Arslan A, et al. The investigation of miR- 221-3p and PAK1 gene expressions in breast cancer cell lines[ J]. Gene, 2015, 555(2) : 377-381.
  • 4Park EY, Chang E, Lee EJ, et al. Targeting of miR34a-NOTCH1 axis reduced breast cancer stemness and chemoresistance [ J ]. Cancer Res, 2014, 74(24) : 7573-7582.
  • 5Luo ML, Gong C, Chen CH, et al. Prolyl isomerase Pinl acts downstream of miR200c to promote cancer stem-like cell traits in breast cancer[J]. Cancer Res, 2014, 74(13) : 3603-3616.
  • 6Borralho PM, Kren BT, Castro RE, et al. MicroRNA-143 reducesviability and increases sensitivity to 5-fluorouracil in HCTll6 human colorectal cancer ceils [ J ]. FEBS J, 2009, 276 (22) : 6689-6700.
  • 7O'Brien NA, McDonald K, Tong L, et al. Targeting PI3K/mTOR overcomes resistance to HER2-targeted therapy independent of feedback activation of AKT [ J ]. Clin Cancer Res, 2014, 20 (13) : 3507-3520.
  • 8Zoncu R, Efeyan A, Sabatini DM. mTOR: from growth signal integration to cancer, diabetes and ageing[ J]. Nat Rev Mol Cell Biol, 2011, 12(1): 21-35.
  • 9Hay N. The Akt-mTOR tango and its relevance to cancer [J]. Cancer Cell, 2005, 8(3) : 179-183.
  • 10Hisamatsu T, Mabuchi S, Matsumoto Y, et al. Potential role of mTORC2 as a therapeutic target in clear cell carcinoma of the ovary[J]. Mol Cancer Ther, 2013, 12(7) : 1367-1377.

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