The Multifunctional Protein Syntenin-1: Regulator of Exosome Biogenesis, Cellular Function, and Tumor Progressionopen access
- Authors
- Lee, Kwang-Min; Seo, Eun-Chan; Lee, Jeong-Hyung; Kim, Hyo-Jin; Hwangbo, Cheol
- Issue Date
- May-2023
- Publisher
- MDPI
- Keywords
- exosome; microRNA; syntenin-1; trafficking; tumor microenvironment
- Citation
- International Journal of Molecular Sciences, v.24, no.11
- Indexed
- SCIE
SCOPUS
- Journal Title
- International Journal of Molecular Sciences
- Volume
- 24
- Number
- 11
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/59667
- DOI
- 10.3390/ijms24119418
- ISSN
- 1661-6596
1422-0067
- Abstract
- Syntenin acts as an adaptor and scaffold protein through its two PSD-95, Dlg, and ZO-1 (PDZ) domains, participating in multiple signaling pathways and modulating cellular physiology. It has been identified as an oncogene, promoting cancer development, metastasis, and angiogenesis in various carcinomas. Syntenin-1 is also associated with the production and release of exosomes, small extracellular vesicles that play a significant role in intercellular communication by containing bioactive molecules such as proteins, lipids, and nucleic acids. The trafficking of exosomes involves a complex interplay of various regulatory proteins, including syntenin-1, which interacts with its binding partners, syndecan and activated leukocyte cell adhesion molecule (ALIX). Exosomal transfer of microRNAs, a key cargo, can regulate the expression of various cancer-related genes, including syntenin-1. Targeting the mechanism involving the regulation of exosomes by syntenin-1 and microRNAs may provide a novel treatment strategy for cancer. This review highlights the current understanding of syntenin-1’s role in regulating exosome trafficking and its associated cellular signaling pathways. © 2023 by the authors.
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