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Extracellular vesicle proteomic analysis leads to the discovery of HDGF as a new factor in multiple myeloma biology
Identifying factors secreted by multiple myeloma (MM) cells that may contribute to MM tumor biology and progression is of the utmost importance. In this study, hepatoma-derived growth factor (HDGF) was identified as a protein present in extracellular vesicles (EVs) released from human MM cell lines...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Hematology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198912/ https://www.ncbi.nlm.nih.gov/pubmed/35395072 http://dx.doi.org/10.1182/bloodadvances.2021006187 |
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author | Hoelzinger, Dominique B. Quinton, Sophia J. Walters, Denise K. Vardam-Kaur, Trupti Tschumper, Renee C. Borges da Silva, Henrique Jelinek, Diane F. |
author_facet | Hoelzinger, Dominique B. Quinton, Sophia J. Walters, Denise K. Vardam-Kaur, Trupti Tschumper, Renee C. Borges da Silva, Henrique Jelinek, Diane F. |
author_sort | Hoelzinger, Dominique B. |
collection | PubMed |
description | Identifying factors secreted by multiple myeloma (MM) cells that may contribute to MM tumor biology and progression is of the utmost importance. In this study, hepatoma-derived growth factor (HDGF) was identified as a protein present in extracellular vesicles (EVs) released from human MM cell lines (HMCLs). Investigation of the role of HDGF in MM cell biology revealed lower proliferation of HMCLs following HDGF knockdown and AKT phosphorylation following the addition of exogenous HDGF. Metabolic analysis demonstrated that HDGF enhances the already high glycolytic levels of HMCLs and significantly lowers mitochondrial respiration, indicating that HDGF may play a role in myeloma cell survival and/or act in a paracrine manner on cells in the bone marrow (BM) tumor microenvironment (ME). Indeed, HDGF polarizes macrophages to an M1-like phenotype and phenotypically alters naïve CD14(+) monocytes to resemble myeloid-derived suppressor cells which are functionally suppressive. In summary, HDGF is a novel factor in MM biology and may function to both maintain MM cell viability as well as modify the tumor ME. |
format | Online Article Text |
id | pubmed-9198912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-91989122022-06-15 Extracellular vesicle proteomic analysis leads to the discovery of HDGF as a new factor in multiple myeloma biology Hoelzinger, Dominique B. Quinton, Sophia J. Walters, Denise K. Vardam-Kaur, Trupti Tschumper, Renee C. Borges da Silva, Henrique Jelinek, Diane F. Blood Adv Lymphoid Neoplasia Identifying factors secreted by multiple myeloma (MM) cells that may contribute to MM tumor biology and progression is of the utmost importance. In this study, hepatoma-derived growth factor (HDGF) was identified as a protein present in extracellular vesicles (EVs) released from human MM cell lines (HMCLs). Investigation of the role of HDGF in MM cell biology revealed lower proliferation of HMCLs following HDGF knockdown and AKT phosphorylation following the addition of exogenous HDGF. Metabolic analysis demonstrated that HDGF enhances the already high glycolytic levels of HMCLs and significantly lowers mitochondrial respiration, indicating that HDGF may play a role in myeloma cell survival and/or act in a paracrine manner on cells in the bone marrow (BM) tumor microenvironment (ME). Indeed, HDGF polarizes macrophages to an M1-like phenotype and phenotypically alters naïve CD14(+) monocytes to resemble myeloid-derived suppressor cells which are functionally suppressive. In summary, HDGF is a novel factor in MM biology and may function to both maintain MM cell viability as well as modify the tumor ME. American Society of Hematology 2022-06-09 /pmc/articles/PMC9198912/ /pubmed/35395072 http://dx.doi.org/10.1182/bloodadvances.2021006187 Text en © 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. |
spellingShingle | Lymphoid Neoplasia Hoelzinger, Dominique B. Quinton, Sophia J. Walters, Denise K. Vardam-Kaur, Trupti Tschumper, Renee C. Borges da Silva, Henrique Jelinek, Diane F. Extracellular vesicle proteomic analysis leads to the discovery of HDGF as a new factor in multiple myeloma biology |
title | Extracellular vesicle proteomic analysis leads to the discovery of HDGF as a new factor in multiple myeloma biology |
title_full | Extracellular vesicle proteomic analysis leads to the discovery of HDGF as a new factor in multiple myeloma biology |
title_fullStr | Extracellular vesicle proteomic analysis leads to the discovery of HDGF as a new factor in multiple myeloma biology |
title_full_unstemmed | Extracellular vesicle proteomic analysis leads to the discovery of HDGF as a new factor in multiple myeloma biology |
title_short | Extracellular vesicle proteomic analysis leads to the discovery of HDGF as a new factor in multiple myeloma biology |
title_sort | extracellular vesicle proteomic analysis leads to the discovery of hdgf as a new factor in multiple myeloma biology |
topic | Lymphoid Neoplasia |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198912/ https://www.ncbi.nlm.nih.gov/pubmed/35395072 http://dx.doi.org/10.1182/bloodadvances.2021006187 |
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