Similarities and Differences in the Protein Composition of Cutaneous Melanoma Cells and Their Exosomes Identified by Mass Spectrometry

Intercellular transport of proteins mediated by extracellular vesicles (EVs)—exosomes and ectosomes—is one of the factors facilitating carcinogenesis. Therefore, the research on protein cargo of melanoma-derived EVs may provide a better understanding of the mechanisms involved in melanoma progressio...

Full description

Bibliographic Details
Main Authors: Magdalena Surman, Urszula Jankowska, Magdalena Wilczak, Małgorzata Przybyło
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/15/4/1097
_version_ 1797621964539428864
author Magdalena Surman
Urszula Jankowska
Magdalena Wilczak
Małgorzata Przybyło
author_facet Magdalena Surman
Urszula Jankowska
Magdalena Wilczak
Małgorzata Przybyło
author_sort Magdalena Surman
collection DOAJ
description Intercellular transport of proteins mediated by extracellular vesicles (EVs)—exosomes and ectosomes—is one of the factors facilitating carcinogenesis. Therefore, the research on protein cargo of melanoma-derived EVs may provide a better understanding of the mechanisms involved in melanoma progression and contribute to the development of alternative biomarkers. Proteomic data on melanoma-derived EVs are very limited. The shotgun nanoLC-MS/MS approach was applied to analyze the protein composition of primary (WM115, WM793) and metastatic (WM266-4, WM1205Lu) cutaneous melanoma cells and exosomes released by them. All cells secreted homogeneous populations of exosomes that shared a characteristic set of proteins. In total, 3514 and 1234 unique proteins were identified in melanoma cells and exosomes, respectively. Gene ontology analysis showed enrichment in several cancer-related categories, including cell proliferation, migration, negative regulation of apoptosis, and angiogenesis. The obtained results broaden our knowledge on the role of selected proteins in exosome biology, as well as their functional role in the development and progression of cutaneous melanoma. The results may also inspire future studies on the clinical potential of exosomes.
first_indexed 2024-03-11T09:03:33Z
format Article
id doaj.art-f7a74b63c06f4850b4943c9e6031c104
institution Directory Open Access Journal
issn 2072-6694
language English
last_indexed 2024-03-11T09:03:33Z
publishDate 2023-02-01
publisher MDPI AG
record_format Article
series Cancers
spelling doaj.art-f7a74b63c06f4850b4943c9e6031c1042023-11-16T19:36:07ZengMDPI AGCancers2072-66942023-02-01154109710.3390/cancers15041097Similarities and Differences in the Protein Composition of Cutaneous Melanoma Cells and Their Exosomes Identified by Mass SpectrometryMagdalena Surman0Urszula Jankowska1Magdalena Wilczak2Małgorzata Przybyło3Department of Glycoconjugate Biochemistry, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, 30-387 Krakow, PolandProteomics and Mass Spectrometry Core Facility, Malopolska Centre of Biotechnology, Jagiellonian University, 30-387 Krakow, PolandDepartment of Glycoconjugate Biochemistry, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, 30-387 Krakow, PolandDepartment of Glycoconjugate Biochemistry, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, 30-387 Krakow, PolandIntercellular transport of proteins mediated by extracellular vesicles (EVs)—exosomes and ectosomes—is one of the factors facilitating carcinogenesis. Therefore, the research on protein cargo of melanoma-derived EVs may provide a better understanding of the mechanisms involved in melanoma progression and contribute to the development of alternative biomarkers. Proteomic data on melanoma-derived EVs are very limited. The shotgun nanoLC-MS/MS approach was applied to analyze the protein composition of primary (WM115, WM793) and metastatic (WM266-4, WM1205Lu) cutaneous melanoma cells and exosomes released by them. All cells secreted homogeneous populations of exosomes that shared a characteristic set of proteins. In total, 3514 and 1234 unique proteins were identified in melanoma cells and exosomes, respectively. Gene ontology analysis showed enrichment in several cancer-related categories, including cell proliferation, migration, negative regulation of apoptosis, and angiogenesis. The obtained results broaden our knowledge on the role of selected proteins in exosome biology, as well as their functional role in the development and progression of cutaneous melanoma. The results may also inspire future studies on the clinical potential of exosomes.https://www.mdpi.com/2072-6694/15/4/1097cancerextracellular vesiclesexosomesLC-MS/MSmelanomaproteomics
spellingShingle Magdalena Surman
Urszula Jankowska
Magdalena Wilczak
Małgorzata Przybyło
Similarities and Differences in the Protein Composition of Cutaneous Melanoma Cells and Their Exosomes Identified by Mass Spectrometry
Cancers
cancer
extracellular vesicles
exosomes
LC-MS/MS
melanoma
proteomics
title Similarities and Differences in the Protein Composition of Cutaneous Melanoma Cells and Their Exosomes Identified by Mass Spectrometry
title_full Similarities and Differences in the Protein Composition of Cutaneous Melanoma Cells and Their Exosomes Identified by Mass Spectrometry
title_fullStr Similarities and Differences in the Protein Composition of Cutaneous Melanoma Cells and Their Exosomes Identified by Mass Spectrometry
title_full_unstemmed Similarities and Differences in the Protein Composition of Cutaneous Melanoma Cells and Their Exosomes Identified by Mass Spectrometry
title_short Similarities and Differences in the Protein Composition of Cutaneous Melanoma Cells and Their Exosomes Identified by Mass Spectrometry
title_sort similarities and differences in the protein composition of cutaneous melanoma cells and their exosomes identified by mass spectrometry
topic cancer
extracellular vesicles
exosomes
LC-MS/MS
melanoma
proteomics
url https://www.mdpi.com/2072-6694/15/4/1097
work_keys_str_mv AT magdalenasurman similaritiesanddifferencesintheproteincompositionofcutaneousmelanomacellsandtheirexosomesidentifiedbymassspectrometry
AT urszulajankowska similaritiesanddifferencesintheproteincompositionofcutaneousmelanomacellsandtheirexosomesidentifiedbymassspectrometry
AT magdalenawilczak similaritiesanddifferencesintheproteincompositionofcutaneousmelanomacellsandtheirexosomesidentifiedbymassspectrometry
AT małgorzataprzybyło similaritiesanddifferencesintheproteincompositionofcutaneousmelanomacellsandtheirexosomesidentifiedbymassspectrometry