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Proteomic profiling and identification of significant markers from high-grade osteosarcoma after cryotherapy and irradiation
Biological reconstruction of allografts and recycled autografts have been widely implemented in high-grade osteogenic sarcoma. For treating tumor-bearing autografts, extracorporeal irradiation (ECIR) and liquid nitrogen (LN) freezing techniques are being used worldwide as a gold standard treatment p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005698/ https://www.ncbi.nlm.nih.gov/pubmed/32034162 http://dx.doi.org/10.1038/s41598-019-56024-7 |
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author | Madda, Rashmi Chen, Chao-Ming Wang, Jir-You Chen, Cheng-Fong Chao, Kuang-Yu Yang, Yu-Min Wu, Hsin-Yi Chen, Wei-Ming Wu, Po-Kuei |
author_facet | Madda, Rashmi Chen, Chao-Ming Wang, Jir-You Chen, Cheng-Fong Chao, Kuang-Yu Yang, Yu-Min Wu, Hsin-Yi Chen, Wei-Ming Wu, Po-Kuei |
author_sort | Madda, Rashmi |
collection | PubMed |
description | Biological reconstruction of allografts and recycled autografts have been widely implemented in high-grade osteogenic sarcoma. For treating tumor-bearing autografts, extracorporeal irradiation (ECIR) and liquid nitrogen (LN) freezing techniques are being used worldwide as a gold standard treatment procedure. Both the methods aim to eradicate the tumor cells from the local recurrence and restore the limb function. Therefore, it is essential and crucial to find, and compare the alterations at molecular and physiological levels of the treated and untreated OGS recycled autografts to obtain valuable clinical information for better clinical practice. Thus, we aimed to investigate the significantly expressed altered proteins from ECIR-and cryotherapy/freezing- treated OGS (n = 12) were compared to untreated OGS (n = 12) samples using LC-ESI-MS/MS analysis, and the selected proteins from this protein panel were verified using immunoblot analysis. From our comparative proteomic analysis identified a total of 131 differentially expressed proteins (DEPs) from OGS. Among these, 91 proteins were up-regulated (2.5 to 3.5-folds), and 40 proteins were down-regulated (0.2 to 0.5 folds) (p < 0.01 and 0.05). The functional enrichment analysis revealed that the identified DEPs have belonged to more than 10 different protein categories include cytoskeletal, extracellular matrix, immune, enzyme modulators, and cell signaling molecules. Among these, we have confirmed two potential candidates’ expressions levels such as Fibronectin and Protein S100 A4 using western blot analysis. Our proteomic study revealed that LN-freezing and ECIR treatments are effectively eradicating tumor cells, and reducing the higher expressions of DEPs at molecular levels which may help in restoring the limb functions of OGS autografts effectively. To the best of our knowledge, this is the first proteomic study that compared proteomic profiles among freezing, ECIR treated with untreated OGS in recycled autografts. Moreover, the verified proteins could be used as prognostic or diagnostic markers that reveal valuable scientific information which may open various therapeutic avenues in clinical practice to improve patient outcomes. |
format | Online Article Text |
id | pubmed-7005698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70056982020-02-18 Proteomic profiling and identification of significant markers from high-grade osteosarcoma after cryotherapy and irradiation Madda, Rashmi Chen, Chao-Ming Wang, Jir-You Chen, Cheng-Fong Chao, Kuang-Yu Yang, Yu-Min Wu, Hsin-Yi Chen, Wei-Ming Wu, Po-Kuei Sci Rep Article Biological reconstruction of allografts and recycled autografts have been widely implemented in high-grade osteogenic sarcoma. For treating tumor-bearing autografts, extracorporeal irradiation (ECIR) and liquid nitrogen (LN) freezing techniques are being used worldwide as a gold standard treatment procedure. Both the methods aim to eradicate the tumor cells from the local recurrence and restore the limb function. Therefore, it is essential and crucial to find, and compare the alterations at molecular and physiological levels of the treated and untreated OGS recycled autografts to obtain valuable clinical information for better clinical practice. Thus, we aimed to investigate the significantly expressed altered proteins from ECIR-and cryotherapy/freezing- treated OGS (n = 12) were compared to untreated OGS (n = 12) samples using LC-ESI-MS/MS analysis, and the selected proteins from this protein panel were verified using immunoblot analysis. From our comparative proteomic analysis identified a total of 131 differentially expressed proteins (DEPs) from OGS. Among these, 91 proteins were up-regulated (2.5 to 3.5-folds), and 40 proteins were down-regulated (0.2 to 0.5 folds) (p < 0.01 and 0.05). The functional enrichment analysis revealed that the identified DEPs have belonged to more than 10 different protein categories include cytoskeletal, extracellular matrix, immune, enzyme modulators, and cell signaling molecules. Among these, we have confirmed two potential candidates’ expressions levels such as Fibronectin and Protein S100 A4 using western blot analysis. Our proteomic study revealed that LN-freezing and ECIR treatments are effectively eradicating tumor cells, and reducing the higher expressions of DEPs at molecular levels which may help in restoring the limb functions of OGS autografts effectively. To the best of our knowledge, this is the first proteomic study that compared proteomic profiles among freezing, ECIR treated with untreated OGS in recycled autografts. Moreover, the verified proteins could be used as prognostic or diagnostic markers that reveal valuable scientific information which may open various therapeutic avenues in clinical practice to improve patient outcomes. Nature Publishing Group UK 2020-02-07 /pmc/articles/PMC7005698/ /pubmed/32034162 http://dx.doi.org/10.1038/s41598-019-56024-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Madda, Rashmi Chen, Chao-Ming Wang, Jir-You Chen, Cheng-Fong Chao, Kuang-Yu Yang, Yu-Min Wu, Hsin-Yi Chen, Wei-Ming Wu, Po-Kuei Proteomic profiling and identification of significant markers from high-grade osteosarcoma after cryotherapy and irradiation |
title | Proteomic profiling and identification of significant markers from high-grade osteosarcoma after cryotherapy and irradiation |
title_full | Proteomic profiling and identification of significant markers from high-grade osteosarcoma after cryotherapy and irradiation |
title_fullStr | Proteomic profiling and identification of significant markers from high-grade osteosarcoma after cryotherapy and irradiation |
title_full_unstemmed | Proteomic profiling and identification of significant markers from high-grade osteosarcoma after cryotherapy and irradiation |
title_short | Proteomic profiling and identification of significant markers from high-grade osteosarcoma after cryotherapy and irradiation |
title_sort | proteomic profiling and identification of significant markers from high-grade osteosarcoma after cryotherapy and irradiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005698/ https://www.ncbi.nlm.nih.gov/pubmed/32034162 http://dx.doi.org/10.1038/s41598-019-56024-7 |
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