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前列腺癌组织中miR-21的表达及临床意义 被引量:4

Expression of miR-21 in prostate cancer and its clinical significance
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摘要 目的探讨miR-21在前列腺癌组织中的表达及临床意义。方法采用原位分子杂交技术检测90例前列腺癌组织及69例良性前列腺增生组织中miR-21的表达,并复习相关文献。结果 miR-21在90例前列腺癌及69例良性前列腺增生中的阳性率分别为71.1%、24.6%。miR-21在前列腺癌组织中的表达明显高于良性前列腺增生组织(P<0.05)。miR-21表达与Gleason评分有关(P<0.05),与其他临床病理学因素无关。结论 miR-21在前列腺癌组织中表达上调,提示miR-21可能在前列腺癌的发生、发展过程中发挥重要作用。 Purpose To investigate the expression and clinical significance of microRNA-21 ( miR-21 ) in patients with prostate cancer (PCa). Methods The human tissue specimens were paraffin-embedded blocks which were collected from the Department of Pathology. miR-21 was detected by in situ hybridization (ISH) in 90 cases of PCa and 69 cases of benign prostatic hyperplasia (BPH). Results The ISH data showed that the positive rate of miR-21 in PCa (71.1% ) was significantly higher than that in BPH (24. 6% ) (P 〈 0. 05 ), the expression of miR-21 correlated with the Gleason grade (P 〈 0. 05 ), and no relationship was observed with other clinicpathological features (P 〉0. 05). Conclusion The miR-21 plays an important role in the pathogenesis of PCa, which can be a new diagnostic target for PCa.
出处 《临床与实验病理学杂志》 CAS CSCD 北大核心 2016年第12期1365-1367,共3页 Chinese Journal of Clinical and Experimental Pathology
基金 安徽省自然科学基金(KJ2013A150)
关键词 前列腺肿瘤 良性前列腺增生 MIR-21 原位分子杂交 prostate neoplasm benign prostatic hyperplasia miR-21 in situ hybridization
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  • 1Campo E, Swerdlow S H, Harris N L, et al. The 2008 WHO clas- sification of lymphoid neoplasms and beyond: evolving concepts and practical applications [ J ]. Blood, 2011,117 ( 19 ) :5019 - 32.
  • 2Wu Z, Wu Q, Wang C, et al. MiR-339-5p inhibits breast cancer cell migration and invasion in vitro and may be a potential biomar- ker for breast cancer prognosis [ J ]. BMC Cancer, 2010,10 (6) : 542 -51.
  • 3Sehn L H, Berry B, Chhanabhai M, et al. The revised Interna- tional Prognostic Index (R-IPI) is a better predictor of outcome than the standard IPI for patients with diffuse large B-cell lympho- ma treated with R-CHOP [ J ]. Blood, 2007,109 (5) : 1857 - 61.
  • 4Zhou Z, Sehn L H, Rademaker A W, et al. An enhanced intema- tional prognostic index (NCCN-IPI) for patients with diffuse large B-cell lymphoma treated in the rituximab era[ J]. Blood, 2014, 123(6) :837 -42.
  • 5Pfreundschuh M, Schubert J, Ziepert M, et al. Six versus eight cycles of bi-weekly CHOP-14 with or without rituximab in elderly patients with aggressive CD20 + B-cell lymphomas : a randomised controlled trial (RICOVER-60) [ J ]. Lancet Oncol, 2008,9 ( 1 ) : 105 - 16.
  • 6De Jong D, Rosenwald A, Chhanabhai M, et al. Immunohisto- chemical prognostic markers in diffuse large B-cell lymphoma: val- idation of tissue microarray as a prerequisite for broad clinical ap- plications-a study from the lunenburg lymphoma biomarker con- sortium[ J]. J Clin Oncol, 2007,25(7):805 -12.
  • 7Tang G. siRNA and miRNA: an insight into RISCs[ J]. Trends Biochem Sci, 2005,30(2) :106 - 14.
  • 8Vasilatou D, Papageorgiou S, Pappa V, et al. The role of microR- NAs in normal and malignant hematopoiesis [ J ]. Eur J Haematol, 2010,84(1) :1 - 16.
  • 9Kloosterman W P, Plasterk R H. The diverse functions of microR- NAs in animal development and disease [ J ]. Dev Cell, 2006,11 (4) :441 -50.
  • 10Lawrie C H, Gal S, Dunlop H M, et al. Detection of elevated lev- els of tumour-associated microRNAs in serum of patients with dif- fuse large B-cell lymphoma[ ]]. Br J Haematol, 2008,141 (5) : 672 - 5.

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