Mesenchymal stem cell-derived interleukin-28 drives the selection of apoptosis resistant bone metastatic prostate cancer

The effects of bone-marrow derived MSCs on prostate cancer cells remain unknown. Here the authors show that MSC-derived IL-28 induces prostate cancer cell apoptosis via IL-28Rα-STAT1 signalling, while acquired resistance to apoptosis is associated with a shift in IL-28Rα signalling via STAT1 to STAT...

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Main Authors: Jeremy J. McGuire, Jeremy S. Frieling, Chen Hao Lo, Tao Li, Ayaz Muhammad, Harshani R. Lawrence, Nicholas J. Lawrence, Leah M. Cook, Conor C. Lynch
Format: Article
Language:English
Published: Nature Publishing Group 2021-02-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-021-20962-6
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spelling doaj-61b815bbfbe3485cb1696124b372aa502021-02-07T12:13:29ZengNature Publishing GroupNature Communications2041-17232021-02-0112111310.1038/s41467-021-20962-6Mesenchymal stem cell-derived interleukin-28 drives the selection of apoptosis resistant bone metastatic prostate cancerJeremy J. McGuire0Jeremy S. Frieling1Chen Hao Lo2Tao Li3Ayaz Muhammad4Harshani R. Lawrence5Nicholas J. Lawrence6Leah M. Cook7Conor C. Lynch8Cancer Biology Ph.D. Program, University of South FloridaTumor Biology Department, H. Lee Moffitt Cancer Center and Research InstituteCancer Biology Ph.D. Program, University of South FloridaTumor Biology Department, H. Lee Moffitt Cancer Center and Research InstituteDepartment of Drug Discovery, H. Lee Moffitt Cancer Center and Research InstituteDepartment of Drug Discovery, H. Lee Moffitt Cancer Center and Research InstituteDepartment of Drug Discovery, H. Lee Moffitt Cancer Center and Research InstituteDepartment of Pathology and Microbiology, University of Nebraska Medical CenterTumor Biology Department, H. Lee Moffitt Cancer Center and Research InstituteThe effects of bone-marrow derived MSCs on prostate cancer cells remain unknown. Here the authors show that MSC-derived IL-28 induces prostate cancer cell apoptosis via IL-28Rα-STAT1 signalling, while acquired resistance to apoptosis is associated with a shift in IL-28Rα signalling via STAT1 to STAT3.https://doi.org/10.1038/s41467-021-20962-6
collection DOAJ
language English
format Article
sources DOAJ
author Jeremy J. McGuire
Jeremy S. Frieling
Chen Hao Lo
Tao Li
Ayaz Muhammad
Harshani R. Lawrence
Nicholas J. Lawrence
Leah M. Cook
Conor C. Lynch
spellingShingle Jeremy J. McGuire
Jeremy S. Frieling
Chen Hao Lo
Tao Li
Ayaz Muhammad
Harshani R. Lawrence
Nicholas J. Lawrence
Leah M. Cook
Conor C. Lynch
Mesenchymal stem cell-derived interleukin-28 drives the selection of apoptosis resistant bone metastatic prostate cancer
Nature Communications
author_facet Jeremy J. McGuire
Jeremy S. Frieling
Chen Hao Lo
Tao Li
Ayaz Muhammad
Harshani R. Lawrence
Nicholas J. Lawrence
Leah M. Cook
Conor C. Lynch
author_sort Jeremy J. McGuire
title Mesenchymal stem cell-derived interleukin-28 drives the selection of apoptosis resistant bone metastatic prostate cancer
title_short Mesenchymal stem cell-derived interleukin-28 drives the selection of apoptosis resistant bone metastatic prostate cancer
title_full Mesenchymal stem cell-derived interleukin-28 drives the selection of apoptosis resistant bone metastatic prostate cancer
title_fullStr Mesenchymal stem cell-derived interleukin-28 drives the selection of apoptosis resistant bone metastatic prostate cancer
title_full_unstemmed Mesenchymal stem cell-derived interleukin-28 drives the selection of apoptosis resistant bone metastatic prostate cancer
title_sort mesenchymal stem cell-derived interleukin-28 drives the selection of apoptosis resistant bone metastatic prostate cancer
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2021-02-01
description The effects of bone-marrow derived MSCs on prostate cancer cells remain unknown. Here the authors show that MSC-derived IL-28 induces prostate cancer cell apoptosis via IL-28Rα-STAT1 signalling, while acquired resistance to apoptosis is associated with a shift in IL-28Rα signalling via STAT1 to STAT3.
url https://doi.org/10.1038/s41467-021-20962-6
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