4.3 Review

The Role of miR-378a in Metabolism, Angiogenesis, and Muscle Biology

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HINDAWI LTD
DOI: 10.1155/2015/281756

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  1. MAESTRO grant of the Polish National Science Centre [2012/06/A/NZ1/0004]
  2. OPUS grant of the Polish National Science Centre [2012/07/B/NZ1/0288]
  3. Iuventus Plus from the Ministry of Science and Higher Education [0244/IP1/2013/72]
  4. Ministry of Science and Higher Education

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MicroRNA-378a (miR-378a, previously known as miR-378) is one of the small noncoding RNA molecules able to regulate gene expression at posttranscriptional level. Its two mature strands, miR-378a-5p and miR-378a-5p, originate from the first intron of the peroxisome proliferator-activated receptor gamma, coactivator 1 beta (ppargc1b) gene encoding PGC-1 beta. Embedding in the sequence of this transcriptional regulator of oxidative energy metabolism implies involvement of miR-378a in metabolic pathways, mitochondrial energy homeostasis, and related biological processes such as muscle development, differentiation, and regeneration. On the other hand, modulating the expression of proangiogenic factors such as vascular endothelial growth factor, angiopoietin-1, or interleukin-8, influencing inflammatory reaction, and affecting tumor suppressors, such as SuFu and Fus-1, miR-378a is considered as a part of an angiogenic network in tumors. In the latter, miR-378a can evoke broader actions by enhancing cell survival, reducing apoptosis, and promoting cell migration and invasion. This review describes the current knowledge on miR378a linking oxidative/lipid metabolism, muscle biology, and blood vessel formation.

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