MicroRNA expression profiling of mature ovarian teratomas

被引:14
作者
Ding, Ye [1 ]
Gu, Xiao-Yan [1 ]
Xu, Feng [1 ]
Shi, Xiao-Yan [1 ]
Yang, Da-Zheng [1 ]
Zhong, Jian [1 ]
Wang, Su-Min [1 ]
机构
[1] Nanjing Med Univ, Nanjing Maternal & Child Hlth Hosp, Dept Endoscop Diagnost & Treatment Ctr, Nanjing 210004, Peoples R China
关键词
microRNAs; mature ovarian teratomas; microarrays; DNA-DAMAGE; METHYLATION; GENES; ATM;
D O I
10.3892/ol.2011.438
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are a class of endogenous, small, non-coding RNAs that regulate gene expression by targeting mRNAs and inhibiting expression via translation repression or RNA degradation. Emerging evidence indicates that miRNAs play a crucial role in the pathogenesis of human diseases, including tumor development. We profiled the miRNA expression between mature ovarian teratoma samples and matched normal tissues using miRNA microarrays, followed by validation with quantitative RT-PCR (qRT-PCR). The most highly expressed miRNAs in mature ovarian teratoma tissues were miRNA-520a-5p, miRNA-26b*, miRNA-421, miRNA-492 and miRNA-555, with a 1.3- to 2.6-fold change, whereas the least expressed miRNAs were miRNA-142-3p, let-7a, miRNA-19a, miRNA-34a, miRNA-620, miRNA-934, miRNA-657, miRNA-720, miRNA-22, miRNA-629 and miRNA-214, with a decreased level of 55-87% compared with normal tissues. The findings of the present study are the first to provide an altered miRNA profile for mature ovarian teratomas and differentially expressed miRNAs, which, if validated in future studies, may be essential in the pathogenesis of mature ovarian teratomas.
引用
收藏
页码:35 / 38
页数:4
相关论文
共 25 条
  • [1] The functions of animal microRNAs
    Ambros, V
    [J]. NATURE, 2004, 431 (7006) : 350 - 355
  • [2] Mature cystic teratomas of the ovary: case series from one institution over 34 years
    Ayhan, A
    Bukulmez, O
    Genc, C
    Karamursel, BS
    Ayhan, A
    [J]. EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2000, 88 (02) : 153 - 157
  • [3] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [4] MiR-15a and MiR-16 Control Bmi-1 Expression in Ovarian Cancer
    Bhattacharya, Resham
    Nicoloso, Milena
    Arvizo, Rochelle
    Wang, Enfeng
    Cortez, Angelica
    Rossi, Simona
    Calin, George A.
    Mukherjee, Priyabrata
    [J]. CANCER RESEARCH, 2009, 69 (23) : 9090 - 9095
  • [5] MicroRNA signatures in human cancers
    Calin, George A.
    Croce, Carlo M.
    [J]. NATURE REVIEWS CANCER, 2006, 6 (11) : 857 - 866
  • [6] Frequent Downregulation of miR-34 Family in Human Ovarian Cancers
    Corney, David C.
    Hwang, Chang-Il
    Matoso, Andres
    Vogt, Markus
    Flesken-Nikitin, Andrea
    Godwin, Andrew K.
    Kamat, Aparna A.
    Sood, Anil K.
    Ellenson, Lora H.
    Hermeking, Heiko
    Nikitin, Alexander Yu.
    [J]. CLINICAL CANCER RESEARCH, 2010, 16 (04) : 1119 - 1128
  • [7] Tumor markers in mature cystic teratomas of the ovary
    Emin, Ustunyurt
    Tayfun, Gungor
    Cantekin, Iskender
    Ozlem, Ustunyurt Basak
    Umit, Bilge
    Leyla, Mollamahmutoglu
    [J]. ARCHIVES OF GYNECOLOGY AND OBSTETRICS, 2009, 279 (02) : 145 - 147
  • [8] ATM is down-regulated by N-Myc-regulated microRNA-421
    Hu, Hailiang
    Du, Liutao
    Nagabayashi, Gindy
    Seeger, Robert C.
    Gatti, Richard A.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (04) : 1506 - 1511
  • [9] Potential role of miR-9 and miR-223 in recurrent ovarian cancer
    Laios, Alexandros
    O'Toole, Sharon
    Flavin, Richard
    Martin, Cara
    Kelly, Lynne
    Ring, Martina
    Finn, Stephen P.
    Barrett, Ciara
    Loda, Massimo
    Gleeson, Noreen
    D'Arcy, Tom
    McGuinness, Eamonn
    Sheils, Orla
    Sheppard, Brian
    Leary, John O'
    [J]. MOLECULAR CANCER, 2008, 7 (1)
  • [10] LAKKIS WG, 1985, CAN J SURG, V28, P444