CCN6-mediated MMP-9 activation enhances metastatic potential of human chondrosarcoma

Huey En Tzeng, Chih Hsin Tang, Sz Hua Wu, Hsien Te Chen, Yi Chin Fong, Yung Chang Lu, Wei Cheng Chen, Hsien Da Huang, Chih Yang Lin, Shih Wei Wang

研究成果: 雜誌貢獻文章

3 引文 (Scopus)

摘要

Chondrosarcomas are primary malignant bone tumors that have a poor prognosis. WNT1-inducible signaling pathway protein-3 (WISP-3, also termed CCN6) belongs to the CCN family of proteins and is implicated in the regulation of various cellular functions, such as cell proliferation, differentiation, and migration. It is unknown as to whether CCN6 affects human chondrosarcoma metastasis. We show how CCN6 promotes chondrosarcoma cell migration and invasion via matrix metallopeptidase-9 (MMP)-9 expression. These effects were abolished by pretreatment of chondrosarcoma cells with PI3K, Akt, mTOR, and NF-κB inhibitors or short interfering (si)RNAs. Our investigations indicate that CCN6 facilitates metastasis through the PI3K/Akt/mTOR/NF-κB signaling pathway. CCN6 and MMP-9 expression was markedly increased in the highly migratory JJ012(S10) cell line compared with the primordial cell line (JJ012) in both in vitro and in vivo experiments. CCN6 knockdown suppressed MMP-9 production in JJ012(S10) cells and attenuated cell migration and invasion ability. Importantly, CCN6 knockdown profoundly inhibited chondrosarcoma cell metastasis to lung. Our findings reveal an important mechanism underlying CCN6-induced metastasis and they highlight the clinical significance between CCN6 and MMP-9 in regard to human chondrosarcoma. CCN6 appears to be a promising therapeutic target in chondrosarcoma metastasis.
原文英語
文章編號955
期刊Cell Death and Disease
9
發行號10
DOIs
出版狀態已發佈 - 十月 1 2018

指紋

Chondrosarcoma
Metalloproteases
Neoplasm Metastasis
S 10
Cell Movement
Phosphatidylinositol 3-Kinases
CCN Intercellular Signaling Proteins
Cell Line
Small Interfering RNA
Cell Differentiation
Cell Proliferation
Bone and Bones
Lung

ASJC Scopus subject areas

  • Immunology
  • Cellular and Molecular Neuroscience
  • Cell Biology
  • Cancer Research

引用此文

CCN6-mediated MMP-9 activation enhances metastatic potential of human chondrosarcoma. / Tzeng, Huey En; Tang, Chih Hsin; Wu, Sz Hua; Chen, Hsien Te; Fong, Yi Chin; Lu, Yung Chang; Chen, Wei Cheng; Huang, Hsien Da; Lin, Chih Yang; Wang, Shih Wei.

於: Cell Death and Disease, 卷 9, 編號 10, 955, 01.10.2018.

研究成果: 雜誌貢獻文章

Tzeng, HE, Tang, CH, Wu, SH, Chen, HT, Fong, YC, Lu, YC, Chen, WC, Huang, HD, Lin, CY & Wang, SW 2018, 'CCN6-mediated MMP-9 activation enhances metastatic potential of human chondrosarcoma', Cell Death and Disease, 卷 9, 編號 10, 955. https://doi.org/10.1038/s41419-018-1008-9
Tzeng, Huey En ; Tang, Chih Hsin ; Wu, Sz Hua ; Chen, Hsien Te ; Fong, Yi Chin ; Lu, Yung Chang ; Chen, Wei Cheng ; Huang, Hsien Da ; Lin, Chih Yang ; Wang, Shih Wei. / CCN6-mediated MMP-9 activation enhances metastatic potential of human chondrosarcoma. 於: Cell Death and Disease. 2018 ; 卷 9, 編號 10.
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abstract = "Chondrosarcomas are primary malignant bone tumors that have a poor prognosis. WNT1-inducible signaling pathway protein-3 (WISP-3, also termed CCN6) belongs to the CCN family of proteins and is implicated in the regulation of various cellular functions, such as cell proliferation, differentiation, and migration. It is unknown as to whether CCN6 affects human chondrosarcoma metastasis. We show how CCN6 promotes chondrosarcoma cell migration and invasion via matrix metallopeptidase-9 (MMP)-9 expression. These effects were abolished by pretreatment of chondrosarcoma cells with PI3K, Akt, mTOR, and NF-κB inhibitors or short interfering (si)RNAs. Our investigations indicate that CCN6 facilitates metastasis through the PI3K/Akt/mTOR/NF-κB signaling pathway. CCN6 and MMP-9 expression was markedly increased in the highly migratory JJ012(S10) cell line compared with the primordial cell line (JJ012) in both in vitro and in vivo experiments. CCN6 knockdown suppressed MMP-9 production in JJ012(S10) cells and attenuated cell migration and invasion ability. Importantly, CCN6 knockdown profoundly inhibited chondrosarcoma cell metastasis to lung. Our findings reveal an important mechanism underlying CCN6-induced metastasis and they highlight the clinical significance between CCN6 and MMP-9 in regard to human chondrosarcoma. CCN6 appears to be a promising therapeutic target in chondrosarcoma metastasis.",
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AU - Tzeng, Huey En

AU - Tang, Chih Hsin

AU - Wu, Sz Hua

AU - Chen, Hsien Te

AU - Fong, Yi Chin

AU - Lu, Yung Chang

AU - Chen, Wei Cheng

AU - Huang, Hsien Da

AU - Lin, Chih Yang

AU - Wang, Shih Wei

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AB - Chondrosarcomas are primary malignant bone tumors that have a poor prognosis. WNT1-inducible signaling pathway protein-3 (WISP-3, also termed CCN6) belongs to the CCN family of proteins and is implicated in the regulation of various cellular functions, such as cell proliferation, differentiation, and migration. It is unknown as to whether CCN6 affects human chondrosarcoma metastasis. We show how CCN6 promotes chondrosarcoma cell migration and invasion via matrix metallopeptidase-9 (MMP)-9 expression. These effects were abolished by pretreatment of chondrosarcoma cells with PI3K, Akt, mTOR, and NF-κB inhibitors or short interfering (si)RNAs. Our investigations indicate that CCN6 facilitates metastasis through the PI3K/Akt/mTOR/NF-κB signaling pathway. CCN6 and MMP-9 expression was markedly increased in the highly migratory JJ012(S10) cell line compared with the primordial cell line (JJ012) in both in vitro and in vivo experiments. CCN6 knockdown suppressed MMP-9 production in JJ012(S10) cells and attenuated cell migration and invasion ability. Importantly, CCN6 knockdown profoundly inhibited chondrosarcoma cell metastasis to lung. Our findings reveal an important mechanism underlying CCN6-induced metastasis and they highlight the clinical significance between CCN6 and MMP-9 in regard to human chondrosarcoma. CCN6 appears to be a promising therapeutic target in chondrosarcoma metastasis.

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