MicroRNAs in ovarian cancer biology and therapy resistance

被引:141
|
作者
van Jaarsveld, Marijn T. M. [1 ]
Helleman, Jozien [1 ]
Berns, Els M. J. J. [1 ]
Wiemer, Erik A. C. [1 ]
机构
[1] Erasmus MC, Josephine Nefkens Inst, Dept Med Oncol, NL-3015 GE Rotterdam, Netherlands
关键词
Ovarian cancer; microRNA; miR-200; family; Let-7; Therapy resistance; EPITHELIAL-MESENCHYMAL TRANSITION; MIR-200; FAMILY; REPRESSORS ZEB1; STEM-CELLS; EXPRESSION; CHEMOTHERAPY; CARCINOMA; GROWTH; ADENOCARCINOMA; LET-7A-3;
D O I
10.1016/j.biocel.2010.01.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Epithelial ovarian cancer is the most common cause of death from gynecological malignancies in the Western world. The overall 5-year survival is only 30% due to late diagnosis and development of resistance to chemotherapy. There is, therefore, a strong need for prognostic and predictive markers to help optimize and personalize treatment hence ameliorating the prognosis of ovarian cancer patients. Since 2006, an increasing number of studies have indicated an essential role for microRNAs in ovarian cancer tumorigenesis. In this review, we provide an overview of the microRNAs that have been associated with different aspects of ovarian cancer, such as tumor subtype, stage, histological grade, germline mutations in BRCA genes, prognosis and therapy resistance. We highlight the role of the let-7 and miR-200 families, two major microRNA families that are frequently dysregulated in ovarian cancer and have been associated with poor prognosis. Interestingly, both have been implicated in the regulation of the epithelial-to-mesenchymal transition, a cellular transition associated with tumor aggressiveness, tumor invasion and chemoresistance. Furthermore, we discuss several other microRNAs that have been associated with chemotherapy resistance, such as miR-214, miR-130a, miR-27a and miR-451. In the final section, we speculate on the possibilities of microRNA-based therapies and the use of microRNAs as diagnostic tools. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1282 / 1290
页数:9
相关论文
共 50 条
  • [1] A systems biology approach to identify microRNAs contributing to cisplatin resistance in human ovarian cancer cells
    Liu, Weisha
    Wang, Shuyuan
    Zhou, Shunheng
    Yang, Feng
    Jiang, Wei
    Zhang, Qingyuan
    Wang, Lihong
    MOLECULAR BIOSYSTEMS, 2017, 13 (11) : 2268 - 2276
  • [2] Involvement of microRNAs in lung cancer biology and therapy
    Liu, Xi
    Sempere, Lorenzo F.
    Guo, Yongli
    Korc, Murray
    Kauppinen, Sakari
    Freemantle, Sarah J.
    Dmitrovsky, Ethan
    TRANSLATIONAL RESEARCH, 2011, 157 (04) : 200 - 208
  • [3] Significance of MicroRNAs in determining taxane resistance in ovarian cancer
    Sultan, A.
    Kiet, T.
    Chan, J.
    Wang, Y.
    Duran, G.
    Francisco, B.
    Sikic, B.
    GYNECOLOGIC ONCOLOGY, 2012, 125 : S131 - S131
  • [4] MicroRNAs in cancer biology and therapy: Current status and perspectives
    Price, Colles
    Chen, Jianjun
    GENES & DISEASES, 2014, 1 (01) : 53 - 63
  • [5] MicroRNAs as the critical regulators of Cisplatin resistance in ovarian cancer cells
    Meysam Moghbeli
    Journal of Ovarian Research, 14
  • [7] MicroRNAs in Ovarian Cancer
    Katz, Betina
    Trope, Claes G.
    Reich, Reuven
    Davidson, Ben
    HUMAN PATHOLOGY, 2015, 46 (09) : 1245 - 1256
  • [8] Therapy resistance on the RADar in ovarian cancer
    Schwickert, Jonas
    Zickgraf, Franziska M.
    Sprick, Martin R.
    EMBO MOLECULAR MEDICINE, 2021, 13 (05)
  • [9] Current status and implications of microRNAs in ovarian cancer diagnosis and therapy
    Zaman, Mohd Saif
    Maher, Diane M.
    Khan, Sheema
    Jaggi, Meena
    Chauhan, Subhash C.
    JOURNAL OF OVARIAN RESEARCH, 2012, 5
  • [10] Differential role of microRNAs in prognosis, diagnosis, and therapy of ovarian cancer
    Mahdian-shakib, Ahmad
    Dorostkar, Ruhollah
    Tat, Mahdi
    Hashemzadeh, Mohammad Sadegh
    Saidi, Navid
    BIOMEDICINE & PHARMACOTHERAPY, 2016, 84 : 592 - 600