Mangiferin suppresses human metastatic osteosarcoma cell growth by down-regulating the expression of metalloproteinases-1/2 and parathyroid hormone receptor 1

Abstract The study evaluates the protective effect of mangiferin on osteosarcoma cell proliferation and metastasis. Saos-2 and U2OS cells were treated with mangiferin (25, 50, 75 and 100 µM) for 72 h. Mangiferin reduced the cell viability, invasion, and cell adhesion and migration rate. Matrix metal...

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Main Authors: Jifeng Wen, Yong Qin, Chao Li, Xiankui Dai, Tong Wu, Wenzhe Yin
Format: Article
Language:English
Published: SpringerOpen 2020-01-01
Series:AMB Express
Subjects:
Online Access:https://doi.org/10.1186/s13568-020-0949-4
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spelling doaj-66764ca84b114234aaea5a016de214322021-01-17T12:26:36ZengSpringerOpenAMB Express2191-08552020-01-0110111010.1186/s13568-020-0949-4Mangiferin suppresses human metastatic osteosarcoma cell growth by down-regulating the expression of metalloproteinases-1/2 and parathyroid hormone receptor 1Jifeng Wen0Yong Qin1Chao Li2Xiankui Dai3Tong Wu4Wenzhe Yin5Department of Gastroenterology, The Second Affiliated Hospital of Harbin Medical UniversityDepartment of Orthopedics, The Second Affiliated Hospital of Harbin Medical UniversityDepartment of Orthopedics, The Second Affiliated Hospital of Harbin Medical UniversityDepartment of Orthopedics, The Second Affiliated Hospital of Harbin Medical UniversityDepartment of Orthopedics, The Second Affiliated Hospital of Harbin Medical UniversityDepartment of Orthopedics, The Second Affiliated Hospital of Harbin Medical UniversityAbstract The study evaluates the protective effect of mangiferin on osteosarcoma cell proliferation and metastasis. Saos-2 and U2OS cells were treated with mangiferin (25, 50, 75 and 100 µM) for 72 h. Mangiferin reduced the cell viability, invasion, and cell adhesion and migration rate. Matrix metalloproteinases-2/9 (MMP-2/9) mRNA expression was reduced significantly, while the levels of tissue inhibitors of metalloproteinases-1/2 (TIMP-1/2) were elevated in Saos-2 and U2OS cells. Mangiferin treatment significantly reduced parathyroid hormone receptor 1 (PTHR1) mRNA and protein expression by more than 0.5-fold in both osteosarcoma cells. In addition, the immunofluorescent analysis also showed decreased PTHR1 expression following treatment with mangiferin. In summary, we have demonstrated that treatment with mangiferin reduces cell viability, proliferation, invasion, adhesion and migration, and induces apoptosis of osteosarcoma cells. Therefore, treatment with mangiferin can be effective agent in inhibiting growth and inducing apoptosis in osteosarcoma cells. Our experimental results provide evidence for the therapeutic effect of mangiferin in osteosarcoma cells.https://doi.org/10.1186/s13568-020-0949-4MangiferinProliferationAdhesionOsteosarcomamRNA
collection DOAJ
language English
format Article
sources DOAJ
author Jifeng Wen
Yong Qin
Chao Li
Xiankui Dai
Tong Wu
Wenzhe Yin
spellingShingle Jifeng Wen
Yong Qin
Chao Li
Xiankui Dai
Tong Wu
Wenzhe Yin
Mangiferin suppresses human metastatic osteosarcoma cell growth by down-regulating the expression of metalloproteinases-1/2 and parathyroid hormone receptor 1
AMB Express
Mangiferin
Proliferation
Adhesion
Osteosarcoma
mRNA
author_facet Jifeng Wen
Yong Qin
Chao Li
Xiankui Dai
Tong Wu
Wenzhe Yin
author_sort Jifeng Wen
title Mangiferin suppresses human metastatic osteosarcoma cell growth by down-regulating the expression of metalloproteinases-1/2 and parathyroid hormone receptor 1
title_short Mangiferin suppresses human metastatic osteosarcoma cell growth by down-regulating the expression of metalloproteinases-1/2 and parathyroid hormone receptor 1
title_full Mangiferin suppresses human metastatic osteosarcoma cell growth by down-regulating the expression of metalloproteinases-1/2 and parathyroid hormone receptor 1
title_fullStr Mangiferin suppresses human metastatic osteosarcoma cell growth by down-regulating the expression of metalloproteinases-1/2 and parathyroid hormone receptor 1
title_full_unstemmed Mangiferin suppresses human metastatic osteosarcoma cell growth by down-regulating the expression of metalloproteinases-1/2 and parathyroid hormone receptor 1
title_sort mangiferin suppresses human metastatic osteosarcoma cell growth by down-regulating the expression of metalloproteinases-1/2 and parathyroid hormone receptor 1
publisher SpringerOpen
series AMB Express
issn 2191-0855
publishDate 2020-01-01
description Abstract The study evaluates the protective effect of mangiferin on osteosarcoma cell proliferation and metastasis. Saos-2 and U2OS cells were treated with mangiferin (25, 50, 75 and 100 µM) for 72 h. Mangiferin reduced the cell viability, invasion, and cell adhesion and migration rate. Matrix metalloproteinases-2/9 (MMP-2/9) mRNA expression was reduced significantly, while the levels of tissue inhibitors of metalloproteinases-1/2 (TIMP-1/2) were elevated in Saos-2 and U2OS cells. Mangiferin treatment significantly reduced parathyroid hormone receptor 1 (PTHR1) mRNA and protein expression by more than 0.5-fold in both osteosarcoma cells. In addition, the immunofluorescent analysis also showed decreased PTHR1 expression following treatment with mangiferin. In summary, we have demonstrated that treatment with mangiferin reduces cell viability, proliferation, invasion, adhesion and migration, and induces apoptosis of osteosarcoma cells. Therefore, treatment with mangiferin can be effective agent in inhibiting growth and inducing apoptosis in osteosarcoma cells. Our experimental results provide evidence for the therapeutic effect of mangiferin in osteosarcoma cells.
topic Mangiferin
Proliferation
Adhesion
Osteosarcoma
mRNA
url https://doi.org/10.1186/s13568-020-0949-4
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AT chaoli mangiferinsuppresseshumanmetastaticosteosarcomacellgrowthbydownregulatingtheexpressionofmetalloproteinases12andparathyroidhormonereceptor1
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AT tongwu mangiferinsuppresseshumanmetastaticosteosarcomacellgrowthbydownregulatingtheexpressionofmetalloproteinases12andparathyroidhormonereceptor1
AT wenzheyin mangiferinsuppresseshumanmetastaticosteosarcomacellgrowthbydownregulatingtheexpressionofmetalloproteinases12andparathyroidhormonereceptor1
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