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Rhotekin 2 silencing inhibits proliferation and induces apoptosis in human osteosarcoma cells

Human osteosarcoma is the most frequent primary malignant of bone, and often occurs in adolescents. However, molecular mechanism of this disease remains unclear. In the present study, we found that the level of Rhotekin 2 (RTKN2) was up-regulated in osteosarcoma tissues and cell lines. In addition,...

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Detalles Bibliográficos
Autores principales: Wang, Xiong, Zhang, Lei, Wang, Wenji, Wang, Yuchen, Chen, Ye, Xie, Ruimin, Li, Xiang, Wang, Yongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246767/
https://www.ncbi.nlm.nih.gov/pubmed/30389712
http://dx.doi.org/10.1042/BSR20181384
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author Wang, Xiong
Zhang, Lei
Wang, Wenji
Wang, Yuchen
Chen, Ye
Xie, Ruimin
Li, Xiang
Wang, Yongping
author_facet Wang, Xiong
Zhang, Lei
Wang, Wenji
Wang, Yuchen
Chen, Ye
Xie, Ruimin
Li, Xiang
Wang, Yongping
author_sort Wang, Xiong
collection PubMed
description Human osteosarcoma is the most frequent primary malignant of bone, and often occurs in adolescents. However, molecular mechanism of this disease remains unclear. In the present study, we found that the level of Rhotekin 2 (RTKN2) was up-regulated in osteosarcoma tissues and cell lines. In addition, silencing of RTKN2 of human osteosarcoma cell lines U2OS, inhibited proliferation, and induced G(1) phase cell cycle arrest via reducing the level of the cyclin-dependent kinase 2 (CDK2). Furthermore, RTKN2 knockdown in the U2OS cells induced apoptosis by increasing the level of Bax and decreasing the level of Bcl2. These results suggested that RTKN2 is involved in the progression of human osteosarcoma, and may be a potential therapeutic target.
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spelling pubmed-62467672018-11-28 Rhotekin 2 silencing inhibits proliferation and induces apoptosis in human osteosarcoma cells Wang, Xiong Zhang, Lei Wang, Wenji Wang, Yuchen Chen, Ye Xie, Ruimin Li, Xiang Wang, Yongping Biosci Rep Research Articles Human osteosarcoma is the most frequent primary malignant of bone, and often occurs in adolescents. However, molecular mechanism of this disease remains unclear. In the present study, we found that the level of Rhotekin 2 (RTKN2) was up-regulated in osteosarcoma tissues and cell lines. In addition, silencing of RTKN2 of human osteosarcoma cell lines U2OS, inhibited proliferation, and induced G(1) phase cell cycle arrest via reducing the level of the cyclin-dependent kinase 2 (CDK2). Furthermore, RTKN2 knockdown in the U2OS cells induced apoptosis by increasing the level of Bax and decreasing the level of Bcl2. These results suggested that RTKN2 is involved in the progression of human osteosarcoma, and may be a potential therapeutic target. Portland Press Ltd. 2018-11-21 /pmc/articles/PMC6246767/ /pubmed/30389712 http://dx.doi.org/10.1042/BSR20181384 Text en © 2018 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Wang, Xiong
Zhang, Lei
Wang, Wenji
Wang, Yuchen
Chen, Ye
Xie, Ruimin
Li, Xiang
Wang, Yongping
Rhotekin 2 silencing inhibits proliferation and induces apoptosis in human osteosarcoma cells
title Rhotekin 2 silencing inhibits proliferation and induces apoptosis in human osteosarcoma cells
title_full Rhotekin 2 silencing inhibits proliferation and induces apoptosis in human osteosarcoma cells
title_fullStr Rhotekin 2 silencing inhibits proliferation and induces apoptosis in human osteosarcoma cells
title_full_unstemmed Rhotekin 2 silencing inhibits proliferation and induces apoptosis in human osteosarcoma cells
title_short Rhotekin 2 silencing inhibits proliferation and induces apoptosis in human osteosarcoma cells
title_sort rhotekin 2 silencing inhibits proliferation and induces apoptosis in human osteosarcoma cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246767/
https://www.ncbi.nlm.nih.gov/pubmed/30389712
http://dx.doi.org/10.1042/BSR20181384
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