miRNA - Therapeutic tool in breast cancer? Where are we now?

被引:11
作者
Zaleska, Karolina [1 ]
机构
[1] Greater Poland Canc Ctr, Med Phys Dept, Radiobiol Lab, Poznan, Poland
关键词
Breast cancer; miRNA; Tumourigenesis; Biomarkers;
D O I
10.1016/j.rpor.2014.10.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The aim of this study was to review the current knowledge about involvement of microRNAs in breast cancer, and their potential in the clinic, published in scientific journals searched in Pubmed/Medline database until March 2014. Results: MicroRNAs (miRNAs) are a family of 21-25 nucleotide small RNAs molecules. Currently, it is well known that miRNA plays a key role in all cellular processes of the organism including tumour initiation and progression. Many studies have shown that circulating miRNAs are attractive, easily detectable tumour biomarkers. Breast cancer is one of the most common cancers in the world. It is clinically established that different subtypes may respond differently to therapies, give metastases and present drug resistance. MicroRNAs have a potential as diagnostic, prognostic and therapeutic tools in breast cancer. Conclusion: Molecular knowledge is crucial for choosing the most effective therapy for individual patients. MicroRNAs holds a great potential in anticancer therapy. (C) 2014 Greater Poland Cancer Centre. Published by Elsevier Urban & Partner Sp. z o.o. All rights reserved.
引用
收藏
页码:79 / 86
页数:8
相关论文
共 100 条
  • [1] Ahmad A., 2013, ISRN VIRAL, V2013
  • [2] Radiation resistance due to high expression of miR-21 and G2/M checkpoint arrest in breast cancer cells
    Anastasov, Natasa
    Hoefig, Ines
    Vasconcellos, Iria Gonzalez
    Rappl, Kristina
    Braselmann, Herbert
    Ludyga, Natalie
    Auer, Gert
    Aubele, Michaela
    Atkinson, Michael J.
    [J]. RADIATION ONCOLOGY, 2012, 7
  • [3] MicroRNA-21 (miR-21) post-transcriptionally downregulates tumor suppressor Pdcd4 and stimulates invasion, intravasation and metastasis in colorectal cancer
    Asangani, I. A.
    Rasheed, S. A. K.
    Nikolova, D. A.
    Leupold, J. H.
    Colburn, N. H.
    Post, S.
    Allgayer, H.
    [J]. ONCOGENE, 2008, 27 (15) : 2128 - 2136
  • [4] MicroRNAs: Target Recognition and Regulatory Functions
    Bartel, David P.
    [J]. CELL, 2009, 136 (02) : 215 - 233
  • [5] 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
  • [6] A mammalian microRNA cluster controls DNA methylation and telomere recombination via Rbl2-dependent regulation of DNA methyltransferases
    Benetti, Roberta
    Gonzalo, Susana
    Jaco, Isabel
    Munoz, Purificacion
    Gonzalez, Susana
    Schoeftner, Stefan
    Murchison, Elizabeth
    Andl, Thomas
    Chen, Taiping
    Klatt, Peter
    Li, En
    Serrano, Manuel
    Millar, Sarah
    Hannon, Gregory
    Blasco, Maria A.
    [J]. NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2008, 15 (03) : 268 - 279
  • [7] The microRNA.org resource: targets and expression
    Betel, Doron
    Wilson, Manda
    Gabow, Aaron
    Marks, Debora S.
    Sander, Chris
    [J]. NUCLEIC ACIDS RESEARCH, 2008, 36 : D149 - D153
  • [8] miR-10b*, a master inhibitor of the cell cycle, is down-regulated in human breast tumours
    Biagioni, Francesca
    Ben-Moshe, Noa Bossel
    Fontemaggi, Giulia
    Canu, Valeria
    Mori, Federica
    Antoniani, Barbara
    Di Benedetto, Anna
    Santoro, Raffaela
    Germoni, Sabrina
    De Angelis, Fernanda
    Cambria, Anna
    Avraham, Roi
    Grasso, Giuseppe
    Strano, Sabrina
    Muti, Paola
    Mottolese, Marcella
    Yarden, Yosef
    Domany, Eytan
    Blandino, Giovanni
    [J]. EMBO MOLECULAR MEDICINE, 2012, 4 (11) : 1214 - 1229
  • [9] Bitterman A, 2012, ISR MED ASSOC J, V14, P256
  • [10] MicroRNA-30c inhibits human breast tumour chemotherapy resistance by regulating TWF1 and IL-11
    Bockhorn, Jessica
    Dalton, Rachel
    Nwachukwu, Chika
    Huang, Simo
    Prat, Aleix
    Yee, Kathy
    Chang, Ya-Fang
    Huo, Dezheng
    Wen, Yujia
    Swanson, Kaitlin E.
    Qiu, Tyler
    Lu, Jun
    Park, Seo Young
    Dolan, M. Eileen
    Perou, Charles M.
    Olopade, Olufunmilayo I.
    Clarke, Michael F.
    Greene, Geoffrey L.
    Liu, Huiping
    [J]. NATURE COMMUNICATIONS, 2013, 4