期刊文献+

miR-155在妇科恶性肿瘤中的研究进展 被引量:2

Research Progress of miR-155 in Gynecological Malignant Tumor
下载PDF
导出
摘要 微小RNA(microRNAs,miRNA)是参与基因转录后水平调控的非编码内源性小分子RNA,参与细胞周期、细胞分化、生长、新陈代谢以及细胞寿命等多个生物过程。miR-155是目前研究较多的miRNA中的1种,在卵巢癌、宫颈癌和子宫内膜癌中miR-155表达存在明显异常,提示其可能在调控妇科肿瘤的发生和发展中扮演着重要角色。综述miR-155在宫颈癌、子宫内膜癌、卵巢癌等妇科恶性肿瘤中表达情况,及其对肿瘤的早期发现、临床诊断、治疗和预后评估的意义及在妇科恶性肿瘤中的研究现状。 MicroRNAs(miRNAs) are small endogenous non-coding RNA molecules capable of regulating gene expression in posttranscriptional level, miRNAs are involved in a variety of biological processes such as cell cycle regulation,differentiation, growth, metabolism and aging. miR-155 is one of the most studied miRNA, which is expressed in many human cancers. Recent studies have shown that the expression profiling of miR-155 shows evidently abnormal in ovarian cancer,cervical cancer and endometrial cancer which indicated that miR-155 might play an important role in regulate the occurrence and development of gynecological tumors. Here is to summarize the expression of miR-155 in ovarian cancer, cervical cancer and endometrial cancer and its significance in the early detection, clinical diagnosis, treatment and prognosis of tumour, as well as their research status in gynecologic malignant tumor.
出处 《国际妇产科学杂志》 CAS 2016年第2期128-130,共3页 Journal of International Obstetrics and Gynecology
关键词 微RNAS 生殖器肿瘤 女(雌)性 宫颈肿瘤 子宫内膜肿瘤 卵巢肿瘤 MicroRNAs Genital neoplasms female Uterine cervical neoplasms Endometrial neoplasms Ovarian neoplasms
  • 相关文献

参考文献10

二级参考文献113

  • 1Kluiver J,Poppema S,de Jong D,et al.BIC and miR-155 are highly expressed in Hodgkin,primary mediastinal and diffuse large B cell lymphomas.J Pathol,2005,207(2):243-249. 被引量:1
  • 2Lawrie CH,Soneji S,Marafioti T,et al.MicroRNA expression distinguishes between germinal center B cell-like and activated B cell-like subtypes of diffuse large B cell lymphoma.Int J Cancer,2007,121(5):1156-1161. 被引量:1
  • 3Costinean S,Zanesi N,Pekarsky Y,et al.Pre-B cell proliferation and lymphoblastic leukemia/high-grade lymphoma in E (mu)-miR155 transgenic mice.Proc Natl Acad Sci USA,2006,103(18):7024-7029. 被引量:1
  • 4Pedersen IM,Otero D,Kao E,et al.Onco-miR-155 targets SHIP1 to promote TNFa-dependent growth of B cell lymphomas.EMBO Mol Med,2009,1(5):288-295. 被引量:1
  • 5Fulci V,Chiaretti S,Goldoni M,et al.Quantitative technologies establish a novel microRNA profile of chronic lymphocytic leukaemia.Blood,2007,109(11):4944-4951. 被引量:1
  • 6O'Connell RM,Rao DS,Chaudhuri AA,et al.Sustained expression of microRNA-155 in hematopoietic stem cells causes a myeloproliferative disorder.J Exp Med,2008,205(3):585-594. 被引量:1
  • 7Metcalf D,Dakic A,Mifsud S,et al.Inactivation of PU.1 in adult mice leads to the development of myeloid leukaemia.Proc Natl Acad Sci USA,2006,103(5):1486-1491. 被引量:1
  • 8Costinean S,Sandhu SK,Pedersen IM,et al.Src homology 2 domain-containing inositol-5-phosphatase and CCAAT enhancer-binding protein beta are targeted by miR-155 in B cells of Emicro-MiR-155 transgenic mice.Blood,2009,114(7):1374-1382. 被引量:1
  • 9Yan LX,Huang XF,Shao Q,et al.MicroRNA miR-21 overexpression in human breast cancer is associated with advanced clinical stage,lymph node metastasis and patient poor prognosis.RNA,2008,14(11):2348-2360. 被引量:1
  • 10Kong W,He L,Coppola M,et al.MicroRNA-155 regulates cell survival,growth and chemosensitivity by targeting FOXO3a in breast cancer.J Biol Chem,2010,285(23):17869-17879. 被引量:1

共引文献218

同被引文献27

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