期刊文献+

miR-181a在卵巢癌组织中的表达及临床意义 被引量:2

Expression of miR-181a in Ovarian Cancer and Its Clinical Significance
原文传递
导出
摘要 目的:分析miR-181a在卵巢癌组织中的表达并探究其与临床特征之间的关系。方法:选取我院妇科2011-2013年治疗的30例卵巢癌恶性肿瘤患者的卵巢组织为卵巢癌组,选取同期术中诊断卵囊巢浆液性或黏液性囊腺瘤行卵巢切除的卵巢组织为对照组。提取两组患者卵巢组织中的总RNA后通过microRNA茎环引物进行逆转录,实时荧光定量PCR(q-PCR)技术检测正常组织与卵巢癌组织中miR-181a的表达,并分析不同临床特征中miR-181a的表达差异。结果:miR-181a在卵巢癌中表达显著升高,相对正常组表达量(2-ΔΔCt值)为20.620±1.242。上皮性卵巢癌组织中,高分化卵巢癌miR-181a的表达明显低于中、低分化组织;病理分期Ⅰ、Ⅱ期的卵巢癌患者miR-181a表达明显低于Ⅲ、Ⅳ;存在淋巴转移的患者miR-181a表达明显高于无淋巴转移的患者;术前CA-125<1 000μmol/L的患者miR-181a表达明显低于CA-125>1 000μmol/L的患者;腹水量<1 000ml的患者miR-181a的表达明显低于腹水量>1 000ml的患者,以上差异均有统计学意义(P<0.05)。结论:miR-181a在卵巢癌组织中表达差异明显,并与患者FIGO分期、组织分级、淋巴转移、术前CA-125等临床特征相关,提示它可能参与调节卵巢癌的发生、发展并可能成为卵巢癌治疗的一个潜在靶点。 Objective: To analyze the miR-181a expression in ovarian cancer and to explore its relationship to the clinical features. Methods: Thirty cases of ovarian cancer and another group of benign ovarian tumor tissues including oocysts nest serous or mucinous cystadenoma were involved in this study. Pathological and clinical features were reviewed in ovarian cancer group. Q-PCR was adopted to detect miR-181a expression. Results: Expression of miR-181a was significantly in- creased in ovarian cancer. The expression level of miR-181a was lower in well differentiated, low- er pathological staged, and non lymph node metastasis ovarian cancer. And the expression was also lower in the cases with CA-125〈1 000 tamol/L before operation and ascites volume 〈1 000 ml (P〈0.05). Conclusion: miR-181a is differentially expressed in ovarian cancer with different clinical and pathological characteristics. It may be involved in the regulation of ovarian cancer development and may become a potential target for the treatment of ovarian cancer.
出处 《武汉大学学报(医学版)》 CAS 北大核心 2014年第2期232-235,共4页 Medical Journal of Wuhan University
基金 广东省科技计划项目(编号:2011B031800203)
关键词 卵巢癌 miR-181a 实时荧光定量聚合酶链反应 Ovarian Carcinomal miR-181a Real-time Fluorescence Quantitative PolymeraseChain Reaction
  • 相关文献

参考文献7

  • 1Iorio MV, Visone R, Di Leva G, et al. MicroRNA sig- natures in human ovarian cancer [J]. Cancer Research, 2007, 67(18): 8 699-8 707.
  • 2陈熙,聂玉强,叶敏,杜艳蕾,林泳.胃癌组织中miR-181a和miR-27a高表达及意义[J].广州医学院学报,2011,39(4):13-16. 被引量:4
  • 3Guo LJ, Zhang QY. Decreased serum miR-181a is a potential new tool for breast cancer screening [J]. Int J Mnl MH. 17. N(. 680.
  • 4Oliverasferraros C, Curl S, Vazquez-Martin A, et al. Micro(mi)RNA expression profile of breast cancer epi- thelial cells treated with the anti-diabetic drug metform- in: induction of the tumor suppressor miRNA let-7a and suppression of the TGFbeta-induced oncomiR miR- NA-181a[J]. Cell Cycle, 2011, 10(7).. 1 144-1 151.
  • 5Shi L, Cheng Z, Zhang J, et al. hsa-mir-181a and hsa- mir-181b function as tumor suppressors in human glio- ma cells[J]. Brain Res, 2008, 1 236 185-193.
  • 6Bhattacharya SD, Garrison J, Guo H, et al. Micro- RNA-181a regulates osteopontin-dependent metastatic function in hepatocellular cancer cell lines[J]. Surgery, 2010, 148(2).. 291-297.
  • 7谭同焕,关婷,况玉兰,张伟.骨桥蛋白在卵巢肿瘤组织中的表达及其临床意义[J].肿瘤防治研究,2009,36(1):47-50. 被引量:4

二级参考文献23

  • 1朱耀魁,王晓玉,夏明翰,罗惠娟,罗新.骨桥蛋白在卵巢肿瘤组织的表达及其与恶性肿瘤侵袭转移的关系[J].暨南大学学报(自然科学与医学版),2006,27(2):251-256. 被引量:7
  • 2Xic H, Song J, Du R, et al. Prognostic significance of osteopontin in hepatitis B virus related hepatocellular carcinoma [J]. Dig Liver Dis, 2007, 39(2) : 167-172.
  • 3Kita Y, Natsugoe S, Okumura H. Expression of osteopontin in oesophagcal squamous cell carcinoma[J]. Br J Cancer, 2006, 95(5) :634-638.
  • 4Hu Z, Lin D, Yuan J, et al. Overexpression of osteopontin is associated with more aggressive phenotypes in human non-small cell lung cacer[J]. Clin Cancer Res, 2005, 11 (13): 4646-4652.
  • 5Mattem J, Koomagi R, Volmm. Association of vascular endothelial PTBE growth factor expression with intratumoral microvessel density and tumor cell proliferation in human epidermoid lung carcinoma[J]. British J of Cancer, 1996, 73 (7) :931-934.
  • 6Standal T, Borset M, Sundan A. Role of osteopontin in adhesion, migration, cell survival and bone remodeling [J].Exp Wncol, 2004, 26(3) : 179-184.
  • 7Das R, Mahabeleshwar GH, Krndu GC. Osteopontin induces APE-mediated secretion of urokinase-type plasminogen activator through c-Src-dependent epidermal growth factor receptor transactivation in breast cancer cells[J]. J Biol Chem, 2004,19,279(12) : 11051-11064.
  • 8Tahara E. Molecular aspects of invasion and metastasis of stomach cancer[J]. Verb Dtsch Ges Pathol,2000,84:43-49.
  • 9Fruger KA, Allan AL, Wilson SM, et al. Beta(3) integrin expression increase breast carcinoma cell responsive to the malignancy-enhancing effects of osteopontin[J]. Mol-Cancer-Res, 2003, 1 (11) :810-819.
  • 10Sulzbacher I, Bimer P, Trieb K, et al. Expression of osteopontin and vascular endothelial growth factor in benign and malignant bone tumors[J].Virchows Arch,2002, 441 (4):345-349.

共引文献6

同被引文献17

引证文献2

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部