MicroRNA-222 Regulates Melanoma Plasticity

Melanoma is one of the most aggressive and highly resistant tumors. Cell plasticity in melanoma is one of the main culprits behind its metastatic capabilities. The detailed molecular mechanisms controlling melanoma plasticity are still not completely understood. Here we combine mathematical models o...

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Main Authors: Maria Chiara Lionetti, Filippo Cola, Oleksandr Chepizhko, Maria Rita Fumagalli, Francesc Font-Clos, Roberto Ravasio, Saverio Minucci, Paola Canzano, Marina Camera, Guido Tiana, Stefano Zapperi, Caterina A. M. La Porta
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/9/8/2573
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author Maria Chiara Lionetti
Filippo Cola
Oleksandr Chepizhko
Maria Rita Fumagalli
Francesc Font-Clos
Roberto Ravasio
Saverio Minucci
Paola Canzano
Marina Camera
Guido Tiana
Stefano Zapperi
Caterina A. M. La Porta
author_facet Maria Chiara Lionetti
Filippo Cola
Oleksandr Chepizhko
Maria Rita Fumagalli
Francesc Font-Clos
Roberto Ravasio
Saverio Minucci
Paola Canzano
Marina Camera
Guido Tiana
Stefano Zapperi
Caterina A. M. La Porta
author_sort Maria Chiara Lionetti
collection DOAJ
description Melanoma is one of the most aggressive and highly resistant tumors. Cell plasticity in melanoma is one of the main culprits behind its metastatic capabilities. The detailed molecular mechanisms controlling melanoma plasticity are still not completely understood. Here we combine mathematical models of phenotypic switching with experiments on IgR39 human melanoma cells to identify possible key targets to impair phenotypic switching. Our mathematical model shows that a cancer stem cell subpopulation within the tumor prevents phenotypic switching of the other cancer cells. Experiments reveal that hsa-mir-222 is a key factor enabling this process. Our results shed new light on melanoma plasticity, providing a potential target and guidance for therapeutic studies.
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spelling doaj.art-fe70d9ba882d4bcd8ef66ad79a7ed0652023-11-20T09:32:13ZengMDPI AGJournal of Clinical Medicine2077-03832020-08-0198257310.3390/jcm9082573MicroRNA-222 Regulates Melanoma PlasticityMaria Chiara Lionetti0Filippo Cola1Oleksandr Chepizhko2Maria Rita Fumagalli3Francesc Font-Clos4Roberto Ravasio5Saverio Minucci6Paola Canzano7Marina Camera8Guido Tiana9Stefano Zapperi10Caterina A. M. La Porta11Center for Complexity and Biosystems, Department of Environmental Science and Policy, University of Milan, via Celoria 26, 20133 Milano, ItalyCenter for Complexity and Biosystems, Department of Physics, University of Milan, via Celoria 16, 20133 Milano, ItalyInstitut für Theoretische Physik, Leopold-Franzens-Universität Innsbruck, Technikerstrasse 21a, A-6020 Innsbruck, AustriaCenter for Complexity and Biosystems, Department of Environmental Science and Policy, University of Milan, via Celoria 26, 20133 Milano, ItalyCenter for Complexity and Biosystems, Department of Physics, University of Milan, via Celoria 16, 20133 Milano, ItalyDepartment of Experimental Oncology, European Institute of Oncology, Via Adamello 16, 20139 Milano, ItalyDepartment of Experimental Oncology, European Institute of Oncology, Via Adamello 16, 20139 Milano, ItalyCentro Cardiologico Monzino I.R.C.C.S., Via Carlo Parea 4, 20138 Milano, ItalyCentro Cardiologico Monzino I.R.C.C.S., Via Carlo Parea 4, 20138 Milano, ItalyCenter for Complexity and Biosystems, Department of Physics, University of Milan, via Celoria 16, 20133 Milano, ItalyCenter for Complexity and Biosystems, Department of Physics, University of Milan, via Celoria 16, 20133 Milano, ItalyCenter for Complexity and Biosystems, Department of Environmental Science and Policy, University of Milan, via Celoria 26, 20133 Milano, ItalyMelanoma is one of the most aggressive and highly resistant tumors. Cell plasticity in melanoma is one of the main culprits behind its metastatic capabilities. The detailed molecular mechanisms controlling melanoma plasticity are still not completely understood. Here we combine mathematical models of phenotypic switching with experiments on IgR39 human melanoma cells to identify possible key targets to impair phenotypic switching. Our mathematical model shows that a cancer stem cell subpopulation within the tumor prevents phenotypic switching of the other cancer cells. Experiments reveal that hsa-mir-222 is a key factor enabling this process. Our results shed new light on melanoma plasticity, providing a potential target and guidance for therapeutic studies.https://www.mdpi.com/2077-0383/9/8/2573melanomatumor plasticityhsa-mir-222reaction diffusionkinetic equationscancer stem cells
spellingShingle Maria Chiara Lionetti
Filippo Cola
Oleksandr Chepizhko
Maria Rita Fumagalli
Francesc Font-Clos
Roberto Ravasio
Saverio Minucci
Paola Canzano
Marina Camera
Guido Tiana
Stefano Zapperi
Caterina A. M. La Porta
MicroRNA-222 Regulates Melanoma Plasticity
Journal of Clinical Medicine
melanoma
tumor plasticity
hsa-mir-222
reaction diffusion
kinetic equations
cancer stem cells
title MicroRNA-222 Regulates Melanoma Plasticity
title_full MicroRNA-222 Regulates Melanoma Plasticity
title_fullStr MicroRNA-222 Regulates Melanoma Plasticity
title_full_unstemmed MicroRNA-222 Regulates Melanoma Plasticity
title_short MicroRNA-222 Regulates Melanoma Plasticity
title_sort microrna 222 regulates melanoma plasticity
topic melanoma
tumor plasticity
hsa-mir-222
reaction diffusion
kinetic equations
cancer stem cells
url https://www.mdpi.com/2077-0383/9/8/2573
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