Natural melanoma-derived extracellular vesicles
- PMID: 31386906
- DOI: 10.1016/j.semcancer.2019.06.020
Natural melanoma-derived extracellular vesicles
Abstract
Melanoma cells produce a variety of extracellular vesicle (EV) types including shedding vesicles and exosomes (EXOs). These EVs are defined by their mechanism of cellular production. To date, the majority of EV investigations has centered around melanoma EXOs or small EVs (sEVs). Natural melanoma sEVs mediate pro-tumor processes including angiogenesis, immune regulation and modification of tissue microenvironments. A thorough examination of these processes reveals that they are interdependent. They work in concert to support tumor growth and survival. Pro-tumor functions attributed to melanoma cells are reproduced by melanoma sEVs. This ensures a certain degree of redundancy within the melanoma pathogenic process. It also allows for rapid adaptation of melanoma cells to changing microenvironments, anti-tumor immune responses, and therapeutic challenges. Further, as a result of their composition and inherent ability to engage the immune system, natural melanoma EVs possess excellent biomarker potential and might be used therapeutically as tumor vaccines.
Keywords: Ectosomes; Exosomes; Extracellular vesicles; Melanoma; Microvesicles; Shedding vesicles.
Copyright © 2019 Elsevier Ltd. All rights reserved.
Similar articles
-
Regulatory Role of Immune Cell-Derived Extracellular Vesicles in Cancer: The Message Is in the Envelope.Front Immunol. 2020 Jul 16;11:1525. doi: 10.3389/fimmu.2020.01525. eCollection 2020. Front Immunol. 2020. PMID: 32765528 Free PMC article. Review.
-
Immune Cell-Derived Extracellular Vesicles - Functions and Therapeutic Applications.Trends Mol Med. 2019 May;25(5):382-394. doi: 10.1016/j.molmed.2019.02.003. Epub 2019 Mar 7. Trends Mol Med. 2019. PMID: 30853173 Review.
-
Comparative proteomic analysis of three major extracellular vesicle classes secreted from human primary and metastatic colorectal cancer cells: Exosomes, microparticles, and shed midbody remnants.Proteomics. 2024 Jun;24(11):e2300057. doi: 10.1002/pmic.202300057. Epub 2023 Jul 28. Proteomics. 2024. PMID: 37507836
-
Focus on Extracellular Vesicles: New Frontiers of Cell-to-Cell Communication in Cancer.Int J Mol Sci. 2016 Feb 6;17(2):175. doi: 10.3390/ijms17020175. Int J Mol Sci. 2016. PMID: 26861306 Free PMC article. Review.
-
Extracellular Vesicles in Angiogenesis.Circ Res. 2017 May 12;120(10):1658-1673. doi: 10.1161/CIRCRESAHA.117.309681. Circ Res. 2017. PMID: 28495996 Free PMC article. Review.
Cited by
-
Advancements in melanoma immunotherapy: the emergence of Extracellular Vesicle Vaccines.Cell Death Discov. 2024 Aug 23;10(1):374. doi: 10.1038/s41420-024-02150-9. Cell Death Discov. 2024. PMID: 39174509 Free PMC article. Review.
-
The role and application of small extracellular vesicles in glioma.Cancer Cell Int. 2024 Jun 29;24(1):229. doi: 10.1186/s12935-024-03389-z. Cancer Cell Int. 2024. PMID: 38951882 Free PMC article. Review.
-
The Roles of Extracellular Vesicles in Malignant Melanoma.Cells. 2021 Oct 14;10(10):2740. doi: 10.3390/cells10102740. Cells. 2021. PMID: 34685720 Free PMC article. Review.
-
Three-dimensional multicellular cell culture for anti-melanoma drug screening: focus on tumor microenvironment.Cytotechnology. 2021 Feb;73(1):35-48. doi: 10.1007/s10616-020-00440-5. Epub 2020 Nov 20. Cytotechnology. 2021. PMID: 33505112 Free PMC article.
-
Rethinking the biology of metastatic melanoma: a holistic approach.Cancer Metastasis Rev. 2021 Jun;40(2):603-624. doi: 10.1007/s10555-021-09960-8. Epub 2021 Apr 19. Cancer Metastasis Rev. 2021. PMID: 33870460 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical