MicroRNAs in Ewing sarcoma

被引:31
作者
Dylla, Layne [1 ,2 ,3 ]
Moore, Colin [3 ,4 ,5 ,6 ]
Jedlicka, Paul [1 ,2 ,3 ,6 ,7 ]
机构
[1] Univ Colorado, Med Scientist Training Program, Denver, CO 80202 USA
[2] Univ Colorado, Canc Biol Grad Program, Denver, CO 80202 USA
[3] Univ Colorado, Anschutz Med Campus, Denver, CO 80202 USA
[4] Univ Colorado Denver, Ctr Canc & Blood Disorders, Aurora, CO USA
[5] Univ Colorado, Dept Pediat, Denver, CO 80202 USA
[6] Childrens Hosp Colorado, Aurora, CO USA
[7] Univ Colorado, Dept Pathol, Denver, CO 80202 USA
关键词
microRNAs; sarcoma; Ewing sarcoma; pathogenesis; prognosis; therapy;
D O I
10.3389/fonc.2013.00065
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRs) have emerged recently as important regulators of gene expression in the cell. Frequently dysregulated in cancer, miRs have shed new light on molecular mechanisms of oncogenesis, and have generated substantial interest as biomarkers, and novel therapeutic agents and targets. Recently, a number of studies have examined miR biology in Ewing sarcoma. Findings indicate that alterations in miR expression in Ewing Sarcoma are widespread, involve both EWS/Ets oncogenic fusion-dependent and independent mechanisms, and contribute to malignant phenotypes. miRs with prognostic potential have been identified, and several preclinical studies suggest that miR manipulation could be therapeutically useful in this aggressive disease. These and future studies of miR biology stand to expand our understanding of Ewing sarcoma pathogenesis, and may identify new biomarkers and treatment options.
引用
收藏
页数:6
相关论文
共 48 条
[41]   MicroRNAs as potential cancer therapeutics [J].
Trang P. ;
Weidhaas J.B. ;
Slack F.J. .
Oncogene, 2008, 27 (Suppl 2) :S52-S57
[42]   MiRNAs and Cancer [J].
Visone, Rosa ;
Croce, Carlo M. .
AMERICAN JOURNAL OF PATHOLOGY, 2009, 174 (04) :1131-1138
[43]   MicroRNAs: Synthesis, mechanism, function, and recent clinical trials [J].
Wahid, Fazli ;
Shehzad, Adeeb ;
Khan, Taous ;
Kim, You Young .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2010, 1803 (11) :1231-1243
[44]   Ewing's sarcoma cells with CD57-associated increase of tumorigenicity and with neural crest-like differentiation capacity [J].
Wahl, Joachim ;
Bogatyreva, Liubov ;
Boukamp, Petra ;
Rojewski, Markus ;
van Valen, Frans ;
Fiedler, Joerg ;
Hipp, Nora ;
Debatin, Klaus-Michael ;
Beltinger, Christian .
INTERNATIONAL JOURNAL OF CANCER, 2010, 127 (06) :1295-1307
[45]   MicroRNA-Based Therapeutics for Cancer [J].
Wang, Vivien ;
Wu, Wei .
BIODRUGS, 2009, 23 (01) :15-23
[46]   MicroRNAs as potential agents to alter resistance to cytotoxic anticancer therapy [J].
Weidhaas, Joanne B. ;
Babar, Lmran ;
Nallur, Sunitha M. ;
Trang, Phong ;
Roush, Sarah ;
Boehm, Nfichelle ;
Gillespie, Erin ;
Slack, Frank J. .
CANCER RESEARCH, 2007, 67 (23) :11111-11116
[47]   Many roads to maturity: microRNA biogenesis pathways and their regulation [J].
Winter, Julia ;
Jung, Stephanie ;
Keller, Sarina ;
Gregory, Richard I. ;
Diederichs, Sven .
NATURE CELL BIOLOGY, 2009, 11 (03) :228-234
[48]   Expression of the EWS/FLI-1 oncogene in murine primary bone-derived cells results in EWS/FLI-1-dependent, Ewing sarcoma-like tumors [J].
Yeny, CT ;
Eliazer, S ;
Xiang, LL ;
Richardson, JA ;
Ilaria, RL .
CANCER RESEARCH, 2005, 65 (19) :8698-8705