MicroRNA-mediated posttranscriptional mechanisms of gene expression in proliferating and quiescent cancer cells

被引:13
作者
LeTonqueze, Olivier [1 ]
Lee, Ju Huck [1 ]
Vasudevan, Shobha [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Ctr Canc, Sch Med, Boston, MA 02114 USA
关键词
microRNA; RNA-binding proteins; cancer; quiescence; regulation; RNA-BINDING PROTEIN; TUMOR-ASSOCIATED MACROPHAGES; 3' UNTRANSLATED REGIONS; MESSENGER-RNA; TRANSLATIONAL REPRESSION; BREAST-CANCER; GW BODIES; TRANSCRIPT STABILITY; MAMMALIAN MICRORNAS; RIBOSOMAL-SUBUNITS;
D O I
10.4161/rna.20806
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
MicroRNAs are small non-coding RNA regulators of gene expression that play important roles in critical biological processes, including cell division, self-renewal and cell state maintenance. Their deregulation leads to extensive clinical consequences in tumorigenesis. Cancers demonstrate heterogeneity in their cell states implicated in their resistance and resurgence. Apart from proliferating cells, cancers harbor a small proportion of assorted quiescent cells that resist conventional therapeutics and contribute to cancer recurrence. MicroRNA expression, targets, microRNPs (microRNA-protein complexes) and their functions have been demonstrated to be regulated in distinct tumor cell states and as an adaptive response to stress signals in tumor-unfavorable environments. In turn, altered microRNPs and their modified post-transcriptional mechanisms of gene expression may contribute to tumor resistance and influence tumor progression. An understanding of distinct microRNA mechanisms in cancer cells would provide extensive insights into the versatile roles of microRNAs in the perpetuation of tumors and indicate potential therapeutic avenues.
引用
收藏
页码:871 / 880
页数:10
相关论文
共 149 条
[1]
TEMPORAL REGULATION OF LIN-14 BY THE ANTAGONISTIC ACTION OF 2 OTHER HETEROCHRONIC GENES, LIN-4 AND LIN-28 [J].
ARASU, P ;
WIGHTMAN, B ;
RUVKUN, G .
GENES & DEVELOPMENT, 1991, 5 (10) :1825-1833
[2]
MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[3]
microRNA-Mediated Messenger RNA Deadenylation Contributes to Translational Repression in Mammalian Cells [J].
Beilharz, Traude H. ;
Humphreys, David T. ;
Clancy, Jennifer L. ;
Thermann, Rolf ;
Martin, David I. K. ;
Hentze, Matthias W. ;
Preiss, Thomas .
PLOS ONE, 2009, 4 (08)
[4]
Cancer Stem Cells: The Emerging Challenge of Drug Targeting [J].
Besancon, Roger ;
Valsesia-Wittmann, Sandrine ;
Puisieux, Alain ;
de Fromentel, Claude Caron ;
Maguer-Satta, Veronique .
CURRENT MEDICINAL CHEMISTRY, 2009, 16 (04) :394-416
[5]
Relief of microRNA-mediated translational repression in human cells subjected to stress [J].
Bhattacharyya, Suvendra N. ;
Habermacher, Regula ;
Martine, Ursula ;
Closs, Ellen I. ;
Filipowicz, Witold .
CELL, 2006, 125 (06) :1111-1124
[6]
Cell fate determination during G1 phase progression [J].
Blomen, V. A. ;
Boonstra, J. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2007, 64 (23) :3084-3104
[7]
GW182 Proteins Directly Recruit Cytoplasmic Deadenylase Complexes to miRNA Targets [J].
Braun, Joerg E. ;
Huntzinger, Eric ;
Fauser, Maria ;
Izaurralde, Elisa .
MOLECULAR CELL, 2011, 44 (01) :120-133
[8]
CPEB and two poly(A) polymerases control miR-122 stability and p53 mRNA translation [J].
Burns, David M. ;
D'Ambrogio, Andrea ;
Nottrott, Stephanie ;
Richter, Joel D. .
NATURE, 2011, 473 (7345) :105-U125
[9]
Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia [J].
Calin, GA ;
Dumitru, CD ;
Shimizu, M ;
Bichi, R ;
Zupo, S ;
Noch, E ;
Aldler, H ;
Rattan, S ;
Keating, M ;
Rai, K ;
Rassenti, L ;
Kipps, T ;
Negrini, M ;
Bullrich, F ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (24) :15524-15529
[10]
Origins and Mechanisms of miRNAs and siRNAs [J].
Carthew, Richard W. ;
Sontheimer, Erik J. .
CELL, 2009, 136 (04) :642-655