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The local and circulating SOX9 as a potential biomarker for the diagnosis of primary bone cancer

PURPOSE: The status of the local and circulating SOX9, a master regulator of the tumor fate, and its relevance to tumor types, severity, invasion feature, response to therapy, and chemotherapy treatment were surveyed in bone cancer in the current study. METHODS: The SOX9 expression level was evaluat...

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Autores principales: Hosseini, Ameinh, Mirzaei, Alireza, Salimi, Vahid, Jamshidi, Khodamorad, Babaheidarian, Pegah, Fallah, Soudabeh, Rampisheh, Zahra, Khademian, Narges, Abdolvahabi, Zohreh, Bahrabadi, Mehrdad, Ibrahimi, Mostafa, Hosami, Fatemeh, Tavakoli-Yaraki, Masoumeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292907/
https://www.ncbi.nlm.nih.gov/pubmed/32551218
http://dx.doi.org/10.1016/j.jbo.2020.100300
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author Hosseini, Ameinh
Mirzaei, Alireza
Salimi, Vahid
Jamshidi, Khodamorad
Babaheidarian, Pegah
Fallah, Soudabeh
Rampisheh, Zahra
Khademian, Narges
Abdolvahabi, Zohreh
Bahrabadi, Mehrdad
Ibrahimi, Mostafa
Hosami, Fatemeh
Tavakoli-Yaraki, Masoumeh
author_facet Hosseini, Ameinh
Mirzaei, Alireza
Salimi, Vahid
Jamshidi, Khodamorad
Babaheidarian, Pegah
Fallah, Soudabeh
Rampisheh, Zahra
Khademian, Narges
Abdolvahabi, Zohreh
Bahrabadi, Mehrdad
Ibrahimi, Mostafa
Hosami, Fatemeh
Tavakoli-Yaraki, Masoumeh
author_sort Hosseini, Ameinh
collection PubMed
description PURPOSE: The status of the local and circulating SOX9, a master regulator of the tumor fate, and its relevance to tumor types, severity, invasion feature, response to therapy, and chemotherapy treatment were surveyed in bone cancer in the current study. METHODS: The SOX9 expression level was evaluated in tissue and peripheral blood mononuclear cells from patients with different types of malignant and benign bone tumors also tumor margin tissues using Real-Time PCR. The protein level of SOX9 was assessed using immunohistochemistry and western blot analysis. Also, the correlations of the SOX9 expression level with the patient’s clinical and pathological features were considered. RESULTS: The remarkable overexpression of SOX9 was detected in bone tumors compared to tumor margin tissues (P < 0.0001). Malignant bone tumors revealed a higher expression of SOX9 compared to benign tumors (P < 0.0001) while osteosarcoma tumors showed higher expression levels compared to Ewing sarcoma, and chondrosarcoma. Overexpression of SOX9 was observed in high grade, metastatic, recurrent tumors also tumors with poor response to therapy. Besides, the patients under the chemotherapy treatment demonstrated higher levels of SOX9 compared to the rest of malignant tumors (P = 0.02). The simultaneous up-regulation of circulating SOX9 in the patients with bone cancer was observed compared to healthy individuals (P < 0.0001) accompanying with overexpression of SOX9 in malignant tumors compared to benign tumors (P < 0.0001). The circulating SOX9 expression was up-regulated in the patients with malignant bone tumors who receive chemotherapy treatment also patients with high grade, metastatic, recurrent tumors. The protein level of SOX9 was in line with our data on the SOX9 gene expression. CONCLUSION: The simultaneous overexpression of local and circulating SOX9 in bone cancer besides its positive correlation with tumor severity, malignancy, size, and chemotherapy may deserve receiving more attention in bone cancer diagnosis and therapy.
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spelling pubmed-72929072020-06-17 The local and circulating SOX9 as a potential biomarker for the diagnosis of primary bone cancer Hosseini, Ameinh Mirzaei, Alireza Salimi, Vahid Jamshidi, Khodamorad Babaheidarian, Pegah Fallah, Soudabeh Rampisheh, Zahra Khademian, Narges Abdolvahabi, Zohreh Bahrabadi, Mehrdad Ibrahimi, Mostafa Hosami, Fatemeh Tavakoli-Yaraki, Masoumeh J Bone Oncol Research Article PURPOSE: The status of the local and circulating SOX9, a master regulator of the tumor fate, and its relevance to tumor types, severity, invasion feature, response to therapy, and chemotherapy treatment were surveyed in bone cancer in the current study. METHODS: The SOX9 expression level was evaluated in tissue and peripheral blood mononuclear cells from patients with different types of malignant and benign bone tumors also tumor margin tissues using Real-Time PCR. The protein level of SOX9 was assessed using immunohistochemistry and western blot analysis. Also, the correlations of the SOX9 expression level with the patient’s clinical and pathological features were considered. RESULTS: The remarkable overexpression of SOX9 was detected in bone tumors compared to tumor margin tissues (P < 0.0001). Malignant bone tumors revealed a higher expression of SOX9 compared to benign tumors (P < 0.0001) while osteosarcoma tumors showed higher expression levels compared to Ewing sarcoma, and chondrosarcoma. Overexpression of SOX9 was observed in high grade, metastatic, recurrent tumors also tumors with poor response to therapy. Besides, the patients under the chemotherapy treatment demonstrated higher levels of SOX9 compared to the rest of malignant tumors (P = 0.02). The simultaneous up-regulation of circulating SOX9 in the patients with bone cancer was observed compared to healthy individuals (P < 0.0001) accompanying with overexpression of SOX9 in malignant tumors compared to benign tumors (P < 0.0001). The circulating SOX9 expression was up-regulated in the patients with malignant bone tumors who receive chemotherapy treatment also patients with high grade, metastatic, recurrent tumors. The protein level of SOX9 was in line with our data on the SOX9 gene expression. CONCLUSION: The simultaneous overexpression of local and circulating SOX9 in bone cancer besides its positive correlation with tumor severity, malignancy, size, and chemotherapy may deserve receiving more attention in bone cancer diagnosis and therapy. Elsevier 2020-05-31 /pmc/articles/PMC7292907/ /pubmed/32551218 http://dx.doi.org/10.1016/j.jbo.2020.100300 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Hosseini, Ameinh
Mirzaei, Alireza
Salimi, Vahid
Jamshidi, Khodamorad
Babaheidarian, Pegah
Fallah, Soudabeh
Rampisheh, Zahra
Khademian, Narges
Abdolvahabi, Zohreh
Bahrabadi, Mehrdad
Ibrahimi, Mostafa
Hosami, Fatemeh
Tavakoli-Yaraki, Masoumeh
The local and circulating SOX9 as a potential biomarker for the diagnosis of primary bone cancer
title The local and circulating SOX9 as a potential biomarker for the diagnosis of primary bone cancer
title_full The local and circulating SOX9 as a potential biomarker for the diagnosis of primary bone cancer
title_fullStr The local and circulating SOX9 as a potential biomarker for the diagnosis of primary bone cancer
title_full_unstemmed The local and circulating SOX9 as a potential biomarker for the diagnosis of primary bone cancer
title_short The local and circulating SOX9 as a potential biomarker for the diagnosis of primary bone cancer
title_sort local and circulating sox9 as a potential biomarker for the diagnosis of primary bone cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292907/
https://www.ncbi.nlm.nih.gov/pubmed/32551218
http://dx.doi.org/10.1016/j.jbo.2020.100300
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