Cargando…
Identification of Novel Target for Osteosarcoma by Network Analysis
BACKGROUND: Osteosarcoma (OS) is a highly complicated bone cancer involving imbalance of signaling transduction networks in cells. Development of new anti-osteosarcoma drugs is very challenging, mainly due to lack of known key targets. MATERIAL/METHOD: In this study, we attempted to reveal more prom...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120164/ https://www.ncbi.nlm.nih.gov/pubmed/30144309 http://dx.doi.org/10.12659/MSM.909973 |
_version_ | 1783352220310306816 |
---|---|
author | Zhi, Li-Qiang Yang, Yi-Xin Yao, Shu-Xin Qing, Zhong Ma, Jian-Bing |
author_facet | Zhi, Li-Qiang Yang, Yi-Xin Yao, Shu-Xin Qing, Zhong Ma, Jian-Bing |
author_sort | Zhi, Li-Qiang |
collection | PubMed |
description | BACKGROUND: Osteosarcoma (OS) is a highly complicated bone cancer involving imbalance of signaling transduction networks in cells. Development of new anti-osteosarcoma drugs is very challenging, mainly due to lack of known key targets. MATERIAL/METHOD: In this study, we attempted to reveal more promising targets for drug design by “Target-Pathway” network analysis, providing the new therapeutic strategy of osteosarcoma. The potential targets used for the treatment of OS were selected from 4 different sources: DrugBank, TCRD database, dbDEMC database, and recent scientific literature papers. Cytoscape was used for the establishment of the “Target-Pathway” network. RESULTS: The obtained results suggest that tankyrase 2 (TNKS2) might be a very good potential protein target for the treatment of osteosarcoma. An in vitro MTT assay proved that it is an available option against OS by targeting the TNKS2 protein. Subsequently, cell cycle and apoptosis assay by flow cytometry showed the TNKS2 inhibitor can obviously induce cell cycle arrest, apoptosis, and mitotic cell death. CONCLUSIONS: Tankyrase 2 (TNKS2), a member of the multifunctional poly(ADP-ribose) polymerases (PARPs), could be a very useful protein target for the treatment of osteosarcoma. |
format | Online Article Text |
id | pubmed-6120164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61201642018-09-04 Identification of Novel Target for Osteosarcoma by Network Analysis Zhi, Li-Qiang Yang, Yi-Xin Yao, Shu-Xin Qing, Zhong Ma, Jian-Bing Med Sci Monit Lab/In Vitro Research BACKGROUND: Osteosarcoma (OS) is a highly complicated bone cancer involving imbalance of signaling transduction networks in cells. Development of new anti-osteosarcoma drugs is very challenging, mainly due to lack of known key targets. MATERIAL/METHOD: In this study, we attempted to reveal more promising targets for drug design by “Target-Pathway” network analysis, providing the new therapeutic strategy of osteosarcoma. The potential targets used for the treatment of OS were selected from 4 different sources: DrugBank, TCRD database, dbDEMC database, and recent scientific literature papers. Cytoscape was used for the establishment of the “Target-Pathway” network. RESULTS: The obtained results suggest that tankyrase 2 (TNKS2) might be a very good potential protein target for the treatment of osteosarcoma. An in vitro MTT assay proved that it is an available option against OS by targeting the TNKS2 protein. Subsequently, cell cycle and apoptosis assay by flow cytometry showed the TNKS2 inhibitor can obviously induce cell cycle arrest, apoptosis, and mitotic cell death. CONCLUSIONS: Tankyrase 2 (TNKS2), a member of the multifunctional poly(ADP-ribose) polymerases (PARPs), could be a very useful protein target for the treatment of osteosarcoma. International Scientific Literature, Inc. 2018-08-25 /pmc/articles/PMC6120164/ /pubmed/30144309 http://dx.doi.org/10.12659/MSM.909973 Text en © Med Sci Monit, 2018 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Lab/In Vitro Research Zhi, Li-Qiang Yang, Yi-Xin Yao, Shu-Xin Qing, Zhong Ma, Jian-Bing Identification of Novel Target for Osteosarcoma by Network Analysis |
title | Identification of Novel Target for Osteosarcoma by Network Analysis |
title_full | Identification of Novel Target for Osteosarcoma by Network Analysis |
title_fullStr | Identification of Novel Target for Osteosarcoma by Network Analysis |
title_full_unstemmed | Identification of Novel Target for Osteosarcoma by Network Analysis |
title_short | Identification of Novel Target for Osteosarcoma by Network Analysis |
title_sort | identification of novel target for osteosarcoma by network analysis |
topic | Lab/In Vitro Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120164/ https://www.ncbi.nlm.nih.gov/pubmed/30144309 http://dx.doi.org/10.12659/MSM.909973 |
work_keys_str_mv | AT zhiliqiang identificationofnoveltargetforosteosarcomabynetworkanalysis AT yangyixin identificationofnoveltargetforosteosarcomabynetworkanalysis AT yaoshuxin identificationofnoveltargetforosteosarcomabynetworkanalysis AT qingzhong identificationofnoveltargetforosteosarcomabynetworkanalysis AT majianbing identificationofnoveltargetforosteosarcomabynetworkanalysis |