miRNAs in melanoma: a defined role in tumor progression and metastasis

被引:43
作者
Mannavola, Francesco [1 ]
Tucci, Marco [1 ]
Felici, Claudia [1 ]
Stucci, Stefania [1 ]
Silvestris, Franco [1 ]
机构
[1] Univ Bari Aldo Moro, Dept Internal Med & Clin Oncol, DIMO, Bari, Italy
关键词
miRNA; melanoma; tumor microenvironment; metastasis; exosomes; REGULATORY T-CELLS; TRANSCRIPTION FACTOR; E-CADHERIN; TARGET GENES; MALIGNANT-MELANOMA; CUTANEOUS MELANOMA; SUPPRESSOR-CELLS; MICRORNA PROFILE; DOWN-REGULATION; EXPRESSION;
D O I
10.1586/1744666X.2016.1100965
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The crosstalk of melanoma cells with components of the microenvironment promotes malignant cell proliferation and spread to distant tissues. Although the major pathogenetic events have already been elucidated, the mechanisms that drive the metastatic behavior of tumor cells are still undefined. MicroRNAs (miRNAs) are small non-coding RNAs that control post-transcriptional gene expression through interconnected kinases upstream of functional genes involved in tumor progression. Here, we review the biological relevance of melanoma-related miRNAs and focus on their potential role in propagating signals that may cause tumor microenvironment rearrangements, as well as disablement of the immune system and melanoma cell proliferation.
引用
收藏
页码:79 / 89
页数:11
相关论文
共 124 条
[1]  
Ahmad A, 2014, AM J TRANSL RES, V6, P384
[2]   Biogenesis of extracellular vesicles (EV): exosomes, microvesicles, retrovirus-like vesicles, and apoptotic bodies [J].
Akers, Johnny C. ;
Gonda, David ;
Kim, Ryan ;
Carter, Bob S. ;
Chen, Clark C. .
JOURNAL OF NEURO-ONCOLOGY, 2013, 113 (01) :1-11
[3]   Exosome-delivered microRNAs modulate the inflammatory response to endotoxin [J].
Alexander, Margaret ;
Hu, Ruozhen ;
Runtsch, Marah C. ;
Kagele, Dominique A. ;
Mosbruger, Timothy L. ;
Tolmachova, Tanya ;
Seabra, Miguel C. ;
Round, June L. ;
Ward, Diane M. ;
O'Connell, Ryan M. .
NATURE COMMUNICATIONS, 2015, 6
[4]   Peripherally Induced Treg: Mode, Stability, and Role in Specific Tolerance [J].
Apostolou, Irina ;
Verginis, Panos ;
Kretschmer, Karsten ;
Polansky, Julia ;
Huehn, Jochen ;
von Boehmer, Harald .
JOURNAL OF CLINICAL IMMUNOLOGY, 2008, 28 (06) :619-624
[5]   Genetic and epigenetic loss of microRNA-31 leads to feed-forward expression of EZH2 in melanoma [J].
Asangani, Irfan A. ;
Harms, Paul W. ;
Dodson, Lois ;
Pandhi, Mithil ;
Kunju, Lakshmi P. ;
Maher, Christopher A. ;
Fullen, Douglas R. ;
Johnson, Timothy M. ;
Giordano, Thomas J. ;
Palanisamy, Nallasivam ;
Chinnaiyan, Arul M. .
ONCOTARGET, 2012, 3 (09) :1011-1025
[6]   A Novel miR-451a isomiR, Associated with Amelanotypic Phenotype, Acts as a Tumor Suppressor in Melanoma by Retarding Cell Migration and Invasion [J].
Babapoor, Sankhiros ;
Fleming, Elizabeth ;
Wu, Rong ;
Dadras, Soheil S. .
PLOS ONE, 2014, 9 (09) :e120
[7]   Integrin CD11b Negatively Regulates TLR9-Triggered Dendritic Cell Cross-Priming by Upregulating microRNA-146a [J].
Bai, Yi ;
Qian, Cheng ;
Qian, Li ;
Ma, Feng ;
Hou, Jin ;
Chen, Yongjian ;
Wang, Qingqing ;
Cao, Xuetao .
JOURNAL OF IMMUNOLOGY, 2012, 188 (11) :5293-5302
[8]   Differentially Expressed miRNAs in Cancer-Stem-Like Cells: Markers for Tumor Cell Aggressiveness of Pancreatic Cancer [J].
Bao, Bin ;
Ali, Shadan ;
Ahmad, Aamir ;
Li, Yiwei ;
Banerjee, Sanjeev ;
Kong, Dejuan ;
Aboukameel, Amro ;
Mohammad, Ramzi ;
Van Buren, Eric ;
Azmi, Asfar S. ;
Sarkar, Fazlul H. .
STEM CELLS AND DEVELOPMENT, 2014, 23 (16) :1947-1958
[9]   MicroRNA-137 targets microphthalmia-associated transcription factor in melanoma cell lines [J].
Bemis, Lynne T. ;
Chen, Robert ;
Amato, Carol M. ;
Classen, Elizabeth H. ;
Robinson, Steven E. ;
Coffey, David G. ;
Erickson, Paul F. ;
Shellman, Yiqun G. ;
Robinson, William A. .
CANCER RESEARCH, 2008, 68 (05) :1362-1368
[10]   Transforming growth factor beta (TGF-β) and inflammation in cancer [J].
Bierie, Brian ;
Moses, Harold L. .
CYTOKINE & GROWTH FACTOR REVIEWS, 2010, 21 (01) :49-59