Extracellular Vesicles and Epigenetic Modifications Are Hallmarks of Melanoma Progression

被引:40
作者
Mannavola, Francesco [1 ]
D'Oronzo, Stella [1 ,2 ]
Cives, Mauro [1 ]
Stucci, Luigia Stefania [1 ]
Ranieri, Girolamo [2 ]
Silvestris, Franco [1 ]
Tucci, Marco [1 ,2 ]
机构
[1] Univ Bari Aldo Moro, Dept Biomed Sci & Clin Oncol, I-70121 Bari, Italy
[2] Natl Canc Res Ctr, Ist Tumori Giovanni Paolo 2, I-70121 Bari, Italy
关键词
melanoma; extracellular vesicles; epigenetic modifications; miRNAs; LONG NONCODING RNA; EPITHELIAL-MESENCHYMAL TRANSITION; CELL-DERIVED EXOSOMES; TUMOR PROGRESSION; MACROH2A SUPPRESSES; CUTANEOUS MELANOMA; MICROVESICLES; METHYLATION; INHIBITION; EXPRESSION;
D O I
10.3390/ijms21010052
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cutaneous melanoma shows a high metastatic potential based on its ability to overcome the immune system's control. The mechanisms activated for these functions vary extremely and are also represented by the production of a number of extracellular vesicles including exosomes. Other vesicles showing a potential role in the melanoma progression include oncosomes and melanosomes and the majority of them mediate tumor processes including angiogenesis, immune regulation, and modifications of the micro-environment. Moreover, a number of epigenetic modifications have been described in melanoma and abundant production of altered microRNAs (mi-RNAs), non-coding RNAs, histones, and abnormal DNA methylation have been associated with different phases of melanoma progression. In addition, exosomes, miRNAs, and other molecular factors have been used as potential biomarkers reflecting disease evolution while others have been suggested to be potential druggable molecules for therapeutic application.
引用
收藏
页数:16
相关论文
共 115 条
[1]   Selective targeting of point-mutated KRAS through artificial microRNAs [J].
Acunzo, Mario ;
Romano, Giulia ;
Nigita, Giovanni ;
Veneziano, Dario ;
Fattore, Luigi ;
Lagana, Alessandro ;
Zanesi, Nicola ;
Fadda, Paolo ;
Fassan, Matteo ;
Rizzotto, Lara ;
Kladney, Raleigh ;
Coppola, Vincenzo ;
Croce, Carlo M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2017, 114 (21) :E4203-E4212
[2]   Microenvironment-Driven Dynamic Heterogeneity and Phenotypic Plasticity as a Mechanism of Melanoma Therapy Resistance [J].
Ahmed, Farzana ;
Haass, Nikolas K. .
FRONTIERS IN ONCOLOGY, 2018, 8
[3]   Genomic Classification of Cutaneous Melanoma [J].
Akbani, Rehan ;
Akdemir, Kadir C. ;
Aksoy, B. Arman ;
Albert, Monique ;
Ally, Adrian ;
Amin, Samirkumar B. ;
Arachchi, Harindra ;
Arora, Arshi ;
Auman, J. Todd ;
Ayala, Brenda ;
Baboud, Julien ;
Balasundaram, Miruna ;
Balu, Saianand ;
Barnabas, Nandita ;
Bartlett, John ;
Bartlett, Pam ;
Bastian, Boris C. ;
Baylin, Stephen B. ;
Behera, Madhusmita ;
Belyaev, Dmitry ;
Benz, Christopher ;
Bernard, Brady ;
Beroukhim, Rameen ;
Bir, Natalie ;
Black, Aaron D. ;
Bodenheimer, Tom ;
Boice, Lori ;
Boland, Genevieve M. ;
Bono, Riccardo ;
Bootwalla, Moiz S. ;
Bosenberg, Marcus ;
Bowen, Jay ;
Bowlby, Reanne ;
Bristow, Christopher A. ;
Brockway-Lunardi, Laura ;
Brooks, Denise ;
Brzezinski, Jakub ;
Bshara, Wiam ;
Buda, Elizabeth ;
Burns, William R. ;
Butterfield, Yaron S. N. ;
Button, Michael ;
Calderone, Tiffany ;
Cappellini, Giancarlo Antonini ;
Carter, Candace ;
Carter, Scott L. ;
Cherney, Lynn ;
Cherniack, Andrew D. ;
Chevalier, Aaron ;
Chin, Lynda .
CELL, 2015, 161 (07) :1681-1696
[4]   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
[5]   EZH2 expression is associated with high proliferation rate and aggressive tumor subgroups in cutaneous melanoma and cancers of the endometrium, prostate, and breast [J].
Bachmann, IM ;
Halvorsen, OJ ;
Collett, K ;
Stefansson, IM ;
Straume, O ;
Haukaas, SA ;
Salvesen, HB ;
Otte, AP ;
Akslen, LA .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (02) :268-273
[6]   Regulation of chromatin by histone modifications [J].
Bannister, Andrew J. ;
Kouzarides, Tony .
CELL RESEARCH, 2011, 21 (03) :381-395
[7]   An operational definition of epigenetics [J].
Berger, Shelley L. ;
Kouzarides, Tony ;
Shiekhattar, Ramin ;
Shilatifard, Ali .
GENES & DEVELOPMENT, 2009, 23 (07) :781-783
[8]   Assessment of circulating tumor cells and serum markers for progression-free survival prediction in metastatic breast cancer: a prospective observational study [J].
Bidard, Francois-Clement ;
Hajage, David ;
Bachelot, Thomas ;
Delaloge, Suzette ;
Brain, Etienne ;
Campone, Mario ;
Cottu, Paul ;
Beuzeboc, Philippe ;
Rolland, Emilie ;
Mathiot, Claire ;
Pierga, Jean-Yves .
BREAST CANCER RESEARCH, 2012, 14 (01)
[9]   Exosomes derived from B16F0 melanoma cells alter the transcriptome of cytotoxic T cells that impacts mitochondrial respiration [J].
Bland, Cassidy L. ;
Byrne-Hoffman, Christina N. ;
Fernandez, Audry ;
Rellick, Stephanie L. ;
Deng, Wentao ;
Klinke, David J., II .
FEBS JOURNAL, 2018, 285 (06) :1033-1050
[10]   Oncogenic BRAF mutation induces DNA methylation changes in a murine model for human serrated colorectal neoplasia [J].
Bond, Catherine E. ;
Liu, Cheng ;
Kawamata, Futoshi ;
McKeone, Diane M. ;
Fernando, Winnie ;
Jamieson, Saara ;
Pearson, Sally-Ann ;
Kane, Alexandra ;
Woods, Susan L. ;
Lannagan, Tamsin R. M. ;
Somashekar, Roshini ;
Lee, Young ;
Dumenil, Troy ;
Hartel, Gunter ;
Spring, Kevin J. ;
Borowsky, Jennifer ;
Fennell, Lochlan ;
Bettington, Mark ;
Lee, Jason ;
Worthley, Daniel L. ;
Leggett, Barbara A. ;
Whitehall, Vicki L. J. .
EPIGENETICS, 2018, 13 (01) :40-48