The Ceramide-Dependent EV Secretome Differentially Affects Prostate Cancer Cell Migration

Tumor-derived extracellular vesicles (EVs) play an important role in cancer progression. Neutral sphingomyelinases (nSMases) are lipid-modifying enzymes that modulate the secretion of EVs from cells. How nSMase activity and therefore ceramide generation affect the composition and functionality of se...

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Main Authors: Dolma Choezom, Jan-Moritz Plum, Pradhipa Karuna M., Adi Danieli-Mackay, Christof Lenz, Phillipp Brockmeyer, Julia Christina Gross
Format: Article
Language:English
Published: MDPI AG 2025-04-01
Series:Cells
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Online Access:https://www.mdpi.com/2073-4409/14/7/547
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author Dolma Choezom
Jan-Moritz Plum
Pradhipa Karuna M.
Adi Danieli-Mackay
Christof Lenz
Phillipp Brockmeyer
Julia Christina Gross
author_facet Dolma Choezom
Jan-Moritz Plum
Pradhipa Karuna M.
Adi Danieli-Mackay
Christof Lenz
Phillipp Brockmeyer
Julia Christina Gross
author_sort Dolma Choezom
collection DOAJ
description Tumor-derived extracellular vesicles (EVs) play an important role in cancer progression. Neutral sphingomyelinases (nSMases) are lipid-modifying enzymes that modulate the secretion of EVs from cells. How nSMase activity and therefore ceramide generation affect the composition and functionality of secreted EVs is not fully understood. Here, we aimed to investigate the expression of nSMases 1 and 2 in prostate cancer (PCa) tissue and their role in EV composition and secretion for prostate cancer cell migration. Reduced nSMase 1 and 2 expression was found in prostate cancer and correlated with the age of the patient. When nSMase 2 was inhibited by GW4869 in PCa cells (PC3 and DU145), the EV secretome was significantly altered, while the number of EVs and the total protein content of released EVs were not significantly changed. Using proteomic analysis, we found that extracellular matrix proteins, such as SDC4 (Syndecan-4) and SRPX-2, were differentially secreted on EVs from GW4869-treated PC3 cells. In scratch wound migration assays, GW4869 significantly increased migration compared to control PC3 cells but not DU145 cells, while SDC4 knockdown significantly reduced the migration of PC3 cells. These and other nSMase-2-dependent secreted proteins are interesting candidates for understanding the role of stress-induced EVs in the progression of prostate cancer.
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spelling doaj-art-854544b70fcc4321afed3963f03469bd2025-08-20T02:17:00ZengMDPI AGCells2073-44092025-04-0114754710.3390/cells14070547The Ceramide-Dependent EV Secretome Differentially Affects Prostate Cancer Cell MigrationDolma Choezom0Jan-Moritz Plum1Pradhipa Karuna M.2Adi Danieli-Mackay3Christof Lenz4Phillipp Brockmeyer5Julia Christina Gross6Department of Hematology and Oncology, University Medical Center Goettingen, 37075 Goettingen, GermanyDepartment of Hematology and Oncology, University Medical Center Goettingen, 37075 Goettingen, GermanyDepartment of Hematology and Oncology, University Medical Center Goettingen, 37075 Goettingen, GermanyDepartment of Hematology and Oncology, University Medical Center Goettingen, 37075 Goettingen, GermanyDepartment of Clinical Chemistry, University Medical Center Goettingen, 37075 Goettingen, GermanyDepartment of Oral and Maxillofacial Surgery, University Medical Center Goettingen, 37075 Goettingen, GermanyInstitute of Molecular Medicine, Department Medicine, HMU Health and Medical University Potsdam, 14471 Potsdam, GermanyTumor-derived extracellular vesicles (EVs) play an important role in cancer progression. Neutral sphingomyelinases (nSMases) are lipid-modifying enzymes that modulate the secretion of EVs from cells. How nSMase activity and therefore ceramide generation affect the composition and functionality of secreted EVs is not fully understood. Here, we aimed to investigate the expression of nSMases 1 and 2 in prostate cancer (PCa) tissue and their role in EV composition and secretion for prostate cancer cell migration. Reduced nSMase 1 and 2 expression was found in prostate cancer and correlated with the age of the patient. When nSMase 2 was inhibited by GW4869 in PCa cells (PC3 and DU145), the EV secretome was significantly altered, while the number of EVs and the total protein content of released EVs were not significantly changed. Using proteomic analysis, we found that extracellular matrix proteins, such as SDC4 (Syndecan-4) and SRPX-2, were differentially secreted on EVs from GW4869-treated PC3 cells. In scratch wound migration assays, GW4869 significantly increased migration compared to control PC3 cells but not DU145 cells, while SDC4 knockdown significantly reduced the migration of PC3 cells. These and other nSMase-2-dependent secreted proteins are interesting candidates for understanding the role of stress-induced EVs in the progression of prostate cancer.https://www.mdpi.com/2073-4409/14/7/547cell migrationextracellular matrixneutral sphingomyelinases<i>SMPD2</i>SMPD3
spellingShingle Dolma Choezom
Jan-Moritz Plum
Pradhipa Karuna M.
Adi Danieli-Mackay
Christof Lenz
Phillipp Brockmeyer
Julia Christina Gross
The Ceramide-Dependent EV Secretome Differentially Affects Prostate Cancer Cell Migration
Cells
cell migration
extracellular matrix
neutral sphingomyelinases
<i>SMPD2</i>
SMPD3
title The Ceramide-Dependent EV Secretome Differentially Affects Prostate Cancer Cell Migration
title_full The Ceramide-Dependent EV Secretome Differentially Affects Prostate Cancer Cell Migration
title_fullStr The Ceramide-Dependent EV Secretome Differentially Affects Prostate Cancer Cell Migration
title_full_unstemmed The Ceramide-Dependent EV Secretome Differentially Affects Prostate Cancer Cell Migration
title_short The Ceramide-Dependent EV Secretome Differentially Affects Prostate Cancer Cell Migration
title_sort ceramide dependent ev secretome differentially affects prostate cancer cell migration
topic cell migration
extracellular matrix
neutral sphingomyelinases
<i>SMPD2</i>
SMPD3
url https://www.mdpi.com/2073-4409/14/7/547
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