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Bone Marrow Mesenchymal Stem Cells-Derived Extracellular Vesicles Promote Proliferation, Invasion and Migration of Osteosarcoma Cells via the lncRNA MALAT1/miR-143/NRSN2/Wnt/[beta]-Catenin Axis

Introduction: Osteosarcoma is a malignant primary bone tumor. Bone marrow- derived mesenchymal stem cells-derived extracellular vesicles (BMSC-EVs) bear repair function for bone and cartilage. This study investigated the mechanism of BMSC-EVs in osteosarcoma cell proliferation, migration and invasio...

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Published in:OncoTargets and therapy 2021-04, Vol.14, p.737
Main Authors: Li, Fujiang, Chen, Xin, Shang, Cong, Ying, Qinglong, Zhou, Xianjun, Zhu, Rongkun, Lu, Hongting, Hao, Xiwei, Dong, Qian, Jiang, Zhong
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container_title OncoTargets and therapy
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creator Li, Fujiang
Chen, Xin
Shang, Cong
Ying, Qinglong
Zhou, Xianjun
Zhu, Rongkun
Lu, Hongting
Hao, Xiwei
Dong, Qian
Jiang, Zhong
description Introduction: Osteosarcoma is a malignant primary bone tumor. Bone marrow- derived mesenchymal stem cells-derived extracellular vesicles (BMSC-EVs) bear repair function for bone and cartilage. This study investigated the mechanism of BMSC-EVs in osteosarcoma cell proliferation, migration and invasion. Methods: BMSC-EVs were isolated and identified. The effects of different concentrations of EVs on osteosarcoma cell proliferation, migration and invasion were evaluated. LncRNA MALAT1 expression in osteosarcoma cells was detected. BMSCs were transfected with siMALAT1 or si-NC. The binding relationships between MALAT1 and miR-143, and miR-143 and NRSN2 were verified. Levels of NRSN2 and Wnt/[beta]-catenin pathway key proteins were detected. miR-143 mimic was transfected into EVs-treated osteosarcoma cells. Nude mice were injected with MG63 cells to verify the effect of EVs on osteosarcoma growth in vivo. Results: BMSC-EVs facilitated proliferation, invasion and migration of osteosarcoma cells. BMSC-EVs carried MALAT1 into osteosarcoma cells. BMSC-EVs-treated osteosarcoma cells showed increased MALAT1 and NRSN2 expressions, decreased miR-143 expression, and activated Wnt/[beta]-catenin pathway. miR-143 mimic or si-MALATl reversed the effects of BMSC-EVs on osteosarcoma cells. In vivo experiment confirmed that BMSC-EVs promoted tumor growth in nude mice. Discussion: BMSC-EVs promoted proliferation, invasion and migration of osteosarcoma cells via the MALAT1/miR-143/NRSN2/Wnt/[beta]-catenin axis. This study might offer new insights into osteosarcoma management. Keywords: osteosarcoma, bone marrow-derived mesenchymal stem cells, extracellular vesicles, lncRNA MALAT1, miR-143, NRSN2, Wnt/[beta]-catenin pathway
doi_str_mv 10.2147/OTT.S283459
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Bone marrow- derived mesenchymal stem cells-derived extracellular vesicles (BMSC-EVs) bear repair function for bone and cartilage. This study investigated the mechanism of BMSC-EVs in osteosarcoma cell proliferation, migration and invasion. Methods: BMSC-EVs were isolated and identified. The effects of different concentrations of EVs on osteosarcoma cell proliferation, migration and invasion were evaluated. LncRNA MALAT1 expression in osteosarcoma cells was detected. BMSCs were transfected with siMALAT1 or si-NC. The binding relationships between MALAT1 and miR-143, and miR-143 and NRSN2 were verified. Levels of NRSN2 and Wnt/[beta]-catenin pathway key proteins were detected. miR-143 mimic was transfected into EVs-treated osteosarcoma cells. Nude mice were injected with MG63 cells to verify the effect of EVs on osteosarcoma growth in vivo. Results: BMSC-EVs facilitated proliferation, invasion and migration of osteosarcoma cells. BMSC-EVs carried MALAT1 into osteosarcoma cells. BMSC-EVs-treated osteosarcoma cells showed increased MALAT1 and NRSN2 expressions, decreased miR-143 expression, and activated Wnt/[beta]-catenin pathway. miR-143 mimic or si-MALATl reversed the effects of BMSC-EVs on osteosarcoma cells. In vivo experiment confirmed that BMSC-EVs promoted tumor growth in nude mice. Discussion: BMSC-EVs promoted proliferation, invasion and migration of osteosarcoma cells via the MALAT1/miR-143/NRSN2/Wnt/[beta]-catenin axis. This study might offer new insights into osteosarcoma management. Keywords: osteosarcoma, bone marrow-derived mesenchymal stem cells, extracellular vesicles, lncRNA MALAT1, miR-143, NRSN2, Wnt/[beta]-catenin pathway</description><identifier>ISSN: 1178-6930</identifier><identifier>EISSN: 1178-6930</identifier><identifier>DOI: 10.2147/OTT.S283459</identifier><language>eng</language><publisher>Dove Medical Press Limited</publisher><subject>Osteosarcoma ; Proteins ; Stem cells</subject><ispartof>OncoTargets and therapy, 2021-04, Vol.14, p.737</ispartof><rights>COPYRIGHT 2021 Dove Medical Press Limited</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Li, Fujiang</creatorcontrib><creatorcontrib>Chen, Xin</creatorcontrib><creatorcontrib>Shang, Cong</creatorcontrib><creatorcontrib>Ying, Qinglong</creatorcontrib><creatorcontrib>Zhou, Xianjun</creatorcontrib><creatorcontrib>Zhu, Rongkun</creatorcontrib><creatorcontrib>Lu, Hongting</creatorcontrib><creatorcontrib>Hao, Xiwei</creatorcontrib><creatorcontrib>Dong, Qian</creatorcontrib><creatorcontrib>Jiang, Zhong</creatorcontrib><title>Bone Marrow Mesenchymal Stem Cells-Derived Extracellular Vesicles Promote Proliferation, Invasion and Migration of Osteosarcoma Cells via the lncRNA MALAT1/miR-143/NRSN2/Wnt/[beta]-Catenin Axis</title><title>OncoTargets and therapy</title><description>Introduction: Osteosarcoma is a malignant primary bone tumor. Bone marrow- derived mesenchymal stem cells-derived extracellular vesicles (BMSC-EVs) bear repair function for bone and cartilage. This study investigated the mechanism of BMSC-EVs in osteosarcoma cell proliferation, migration and invasion. Methods: BMSC-EVs were isolated and identified. The effects of different concentrations of EVs on osteosarcoma cell proliferation, migration and invasion were evaluated. LncRNA MALAT1 expression in osteosarcoma cells was detected. BMSCs were transfected with siMALAT1 or si-NC. The binding relationships between MALAT1 and miR-143, and miR-143 and NRSN2 were verified. Levels of NRSN2 and Wnt/[beta]-catenin pathway key proteins were detected. miR-143 mimic was transfected into EVs-treated osteosarcoma cells. Nude mice were injected with MG63 cells to verify the effect of EVs on osteosarcoma growth in vivo. Results: BMSC-EVs facilitated proliferation, invasion and migration of osteosarcoma cells. BMSC-EVs carried MALAT1 into osteosarcoma cells. BMSC-EVs-treated osteosarcoma cells showed increased MALAT1 and NRSN2 expressions, decreased miR-143 expression, and activated Wnt/[beta]-catenin pathway. miR-143 mimic or si-MALATl reversed the effects of BMSC-EVs on osteosarcoma cells. In vivo experiment confirmed that BMSC-EVs promoted tumor growth in nude mice. Discussion: BMSC-EVs promoted proliferation, invasion and migration of osteosarcoma cells via the MALAT1/miR-143/NRSN2/Wnt/[beta]-catenin axis. This study might offer new insights into osteosarcoma management. 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Bone marrow- derived mesenchymal stem cells-derived extracellular vesicles (BMSC-EVs) bear repair function for bone and cartilage. This study investigated the mechanism of BMSC-EVs in osteosarcoma cell proliferation, migration and invasion. Methods: BMSC-EVs were isolated and identified. The effects of different concentrations of EVs on osteosarcoma cell proliferation, migration and invasion were evaluated. LncRNA MALAT1 expression in osteosarcoma cells was detected. BMSCs were transfected with siMALAT1 or si-NC. The binding relationships between MALAT1 and miR-143, and miR-143 and NRSN2 were verified. Levels of NRSN2 and Wnt/[beta]-catenin pathway key proteins were detected. miR-143 mimic was transfected into EVs-treated osteosarcoma cells. Nude mice were injected with MG63 cells to verify the effect of EVs on osteosarcoma growth in vivo. Results: BMSC-EVs facilitated proliferation, invasion and migration of osteosarcoma cells. BMSC-EVs carried MALAT1 into osteosarcoma cells. BMSC-EVs-treated osteosarcoma cells showed increased MALAT1 and NRSN2 expressions, decreased miR-143 expression, and activated Wnt/[beta]-catenin pathway. miR-143 mimic or si-MALATl reversed the effects of BMSC-EVs on osteosarcoma cells. In vivo experiment confirmed that BMSC-EVs promoted tumor growth in nude mice. Discussion: BMSC-EVs promoted proliferation, invasion and migration of osteosarcoma cells via the MALAT1/miR-143/NRSN2/Wnt/[beta]-catenin axis. This study might offer new insights into osteosarcoma management. Keywords: osteosarcoma, bone marrow-derived mesenchymal stem cells, extracellular vesicles, lncRNA MALAT1, miR-143, NRSN2, Wnt/[beta]-catenin pathway</abstract><pub>Dove Medical Press Limited</pub><doi>10.2147/OTT.S283459</doi></addata></record>
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subjects Osteosarcoma
Proteins
Stem cells
title Bone Marrow Mesenchymal Stem Cells-Derived Extracellular Vesicles Promote Proliferation, Invasion and Migration of Osteosarcoma Cells via the lncRNA MALAT1/miR-143/NRSN2/Wnt/[beta]-Catenin Axis
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