The review articles in this issue provide an improved appreciation for microRNA (miRNA)
as an essential feature of lineage commitment and regulatory guidance during tissue
development that, when absent or hampered, often lead to disease states. In the coming
years, there is much to be learned about adaptive (and maladaptive) states by examining
how the expression of miRNAs is influenced by the genetic architecture of miR genes,
clusters, and mirtrons, as well as miRNA polymorphism and polymorphism in their mRNA
targets. We are also introduced to several modes of miRNA regulation (negative feedback,
positive feedback, and cross regulatory) that monitor, modulate, or resolve signaling
pathways in a variety of biologic processes that include sepsis response, fibrosis,
acute exercise, and steroid biology. Perhaps the homeostasis or micromanagement of
these miRNA regulatory systems, when perturbed, arrive at new stable networked interactions
that have an undesired effect of promoting or antagonizing disease severity and cancer
progression. Clearly, a better understanding of these miRNA regulatory networks, as
well as improved therapeutic tools for guiding miRNA expression and their targets
toward desired outcomes, will be the subject of many advances in miRNA biology over
the coming years.
Abbreviations:
IGF-1 (insulin growth factor-1), IRAK1 (interleukin-1 receptor associated kinase 1), LNA (locked nucleic acid), LPS (lipopolysaccharide), MKP-1 (MAP kinase phosphatase-1), miRNA (microRNA), RA (rheumatoid arthritis), RISC (RNA inducing silencing complex), SNP (single-nucleotide polymorphism), TGF-β (tumor necrosis factor β), TRAF6 (TNF receptor-associated factor 6), UTR (untranslated region)To read this article in full you will need to make a payment
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Article info
Publication history
Published online: February 11, 2011
Identification
Copyright
© 2011 Mosby, Inc. Published by Elsevier Inc. All rights reserved.