Exp Mol Med.  2017 Jan;49(1):e285. 10.1038/emm.2016.153.

Exosome-derived microRNAs in cancer metabolism: possible implications in cancer diagnostics and therapy

Affiliations
  • 1Department of Clinical and Molecular Sciences, Polytechnic University of Marche, Ancona, Italy. m.tomasetti@univpm.it
  • 2Department of Biochemistry, Dongguk University College of Medicine, Gyeongju, Korea.
  • 3Mitochondria, Apoptosis and Cancer Research Group, School of Medical Science and Menzies Health Institute Queensland, Griffith University, Southport, Queensland, Australia. j.neuzil@griffith.edu.au
  • 4Molecular Therapy Group, Institute of Biotechnology, Czech Academy of Sciences, Prague-West, Czech Republic.

Abstract

Malignant progression is greatly affected by dynamic cross-talk between stromal and cancer cells. Exosomes are secreted nanovesicles that have key roles in cell-cell communication by transferring nucleic acids and proteins to target cells and tissues. Recently, MicroRNAs (miRs) and their delivery in exosomes have been implicated in physiological and pathological processes. Tumor-delivered miRs, interacting with stromal cells in the tumor microenvironment, modulate tumor progression, angiogenesis, metastasis and immune escape. Altered cell metabolism is one of the hallmarks of cancer. A number of different types of tumor rely on mitochondrial metabolism by triggering adaptive mechanisms to optimize their oxidative phosphorylation in relation to their substrate supply and energy demands. Exogenous exosomes can induce metabolic reprogramming by restoring the respiration of cancer cells and supress tumor growth. The exosomal miRs involved in the modulation of cancer metabolism may be potentially utilized for better diagnostics and therapy.


MeSH Terms

Exosomes
Metabolism*
MicroRNAs*
Neoplasm Metastasis
Nucleic Acids
Oxidative Phosphorylation
Pathologic Processes
Respiration
Stromal Cells
Tumor Microenvironment
United Nations
MicroRNAs
Nucleic Acids
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