Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/163101
Title: Actin-related protein 2/3 complex subunit 2-enriched extracellular vesicles drive liver cancer metastasis
Authors: Mei, Piaorong
Tey, Sze Keong
Wong, Samuel Wan Ki
Ng, Tung Him
Mao, Xiaowen
Yeung, Cherlie Lot Sum
Xu, Yi
Yu, Liang
Huang, Qianhua
Cao, Peihua
Yam, Judy Wai Ping
Gao, Yi
Keywords: Science::Biological sciences
Issue Date: 2022
Source: Mei, P., Tey, S. K., Wong, S. W. K., Ng, T. H., Mao, X., Yeung, C. L. S., Xu, Y., Yu, L., Huang, Q., Cao, P., Yam, J. W. P. & Gao, Y. (2022). Actin-related protein 2/3 complex subunit 2-enriched extracellular vesicles drive liver cancer metastasis. Hepatology International, 16(3), 603-613. https://dx.doi.org/10.1007/s12072-022-10338-3
Journal: Hepatology International
Abstract: Background: Extracellular vesicles (EVs) play pivotal roles in tumor growth, cancer metastasis and angiogenesis. Here, we aimed to identify proteins that contribute to the functionality of EVs derived from metastatic hepatocellular carcinoma (HCC) cells. Methods: Proteins of EVs derived from metastatic HCC cells and normal liver cells were analyzed by mass spectrometry. Proteomic profiling identified actin-related protein 2/3 complex subunit 2 (ARPC2) to be highly expressed in EVs of metastatic HCC cells. The expression of ARPC2 in EVs and HCC tissues was examined using immunoblotting and TCGA database, respectively. The functional roles of EV-ARPC2 were investigated by knockout approach and various in vitro and in vivo assays. Results: ARPC2 was highly expressed in EVs of metastatic cells but barely detected in non-metastatic HCC cells and normal liver cells. Immunogold labeling showed the presence of APRC2 on the surface of EVs. Analysis of TCGA database of liver cancer revealed ARPC2 overexpression was correlated with poor prognosis of patients. ARPC2 was knockout in metastatic HCC cells. EVs derived from knockout cells displayed compromised activity in enhancing cell growth, motility and metastasis compared to EVs of control cells. Pimozide, an inhibitor of APRC2, also inhibited the promoting effect of EVs of metastatic cells in lung colonization of tumor cells in mice. Conclusion: This study reveals previously unreported expression and function of ARPC2 in EVs. EVs with highly expressed ARPC2 enhance cancer cell growth and metastasis. ARPC2 may provide a prospective target for the novel treatment of HCC patients.
URI: https://hdl.handle.net/10356/163101
ISSN: 1936-0533
DOI: 10.1007/s12072-022-10338-3
Rights: © 2022 Asian Pacific Association for the Study of the Liver. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SBS Journal Articles

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