Glioma SOX2 expression decreased after adjuvant therapy

Abstract Background SOX2 is regarded as an important marker in stem cell. The change of SOX2 expression after adjuvant therapy in high grade glioma (HGG) remains unknown so far. Few patients with recurrent glioma have opportunity to undergo operation once again, so the recurrent glioma samples are s...

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Main Authors: Wei Yu, Xiaoqiu Ren, Chunxiu Hu, Yinuo Tan, Yongjie Shui, Zexin Chen, Lili Zhang, Jiaping Peng, Qichun Wei
Format: Article
Language:English
Published: BMC 2019-11-01
Series:BMC Cancer
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12885-019-6292-y
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spelling doaj-b32ee94a2fdc40fe830fc7717df356fa2020-11-25T04:01:04ZengBMCBMC Cancer1471-24072019-11-011911910.1186/s12885-019-6292-yGlioma SOX2 expression decreased after adjuvant therapyWei Yu0Xiaoqiu Ren1Chunxiu Hu2Yinuo Tan3Yongjie Shui4Zexin Chen5Lili Zhang6Jiaping Peng7Qichun Wei8Department of Radiation Oncology, the Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Radiation Oncology, the Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Radiation Oncology, the Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Medical Oncology, the Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Radiation Oncology, the Second Affiliated Hospital, Zhejiang University School of MedicineCenter of Clinical Epidemiology and Biostatistics for statistical analysis, the Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Radiation Oncology, the Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Radiation Oncology, the Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Radiation Oncology, the Second Affiliated Hospital, Zhejiang University School of MedicineAbstract Background SOX2 is regarded as an important marker in stem cell. The change of SOX2 expression after adjuvant therapy in high grade glioma (HGG) remains unknown so far. Few patients with recurrent glioma have opportunity to undergo operation once again, so the recurrent glioma samples are scarce. This study tries to analyze SOX2 expression in paired primary and recurrent HGG, aims to better understand the transformation law of SOX2 after adjuvant therapy in HGG. Methods Twenty-four recurrent HGG patients who undergone a second resection were included. 16 patients received adjuvant therapy, the remaining 8 patients didn’t receive any adjuvant therapy at all. The protein expression of SOX2 in paired primary and recurrent HGG was tested by immunohistochemistry. The statistical analysis was conducted by IBM SPSS Statistics 19.0. Results In primary HGG, SOX2 expression of 3 + , 2 + , 1+ and 0+ were seen in 20 (83.3%), 1 (4.2%), 1 (4.2%) and 2 cases (8.3%), respectively. The expression of SOX2 was decreased in recurrent HGG compared to the paired primary sample (p = 0.001). The decrease of SOX2 was often seen in patients received chemotherapy, radiotherapy or both (p = 0.003). Patients with SOX2 high expression in primary glioma had a longer median PFS than those with SOX2 low expression with marginal statistic significance (12.7 vs. 5.4 months, p = 0.083). For cases with SOX2 high expression in the primary glioma, those had SOX2 low expression after recurrence seemed to have worse prognosis as compared to patients with stable SOX2 high expression (PFS: 10.4 vs. 14.9 months, p = 0.036; OS: 27.0 vs 49.5 months, p = 0.005). Conclusions This is the first study comparing the protein expression of SOX2 in recurrent HGG and its paired primary tumor. SOX2 high expression is common in brain HGG, a tendency of decreased SOX2 expression in recurrent gliomas was evidenced. Lower SOX2 expression was seen in those patients who received adjuvant chemotherapy and/or radiotherapy. Patients with low SOX2 expression in primary HGG usually have poorer prognosis, those with SOX2 expression decreased in recurrent HGG had worse outcome.http://link.springer.com/article/10.1186/s12885-019-6292-yGliomaRecurrencePrognosisSOX2
collection DOAJ
language English
format Article
sources DOAJ
author Wei Yu
Xiaoqiu Ren
Chunxiu Hu
Yinuo Tan
Yongjie Shui
Zexin Chen
Lili Zhang
Jiaping Peng
Qichun Wei
spellingShingle Wei Yu
Xiaoqiu Ren
Chunxiu Hu
Yinuo Tan
Yongjie Shui
Zexin Chen
Lili Zhang
Jiaping Peng
Qichun Wei
Glioma SOX2 expression decreased after adjuvant therapy
BMC Cancer
Glioma
Recurrence
Prognosis
SOX2
author_facet Wei Yu
Xiaoqiu Ren
Chunxiu Hu
Yinuo Tan
Yongjie Shui
Zexin Chen
Lili Zhang
Jiaping Peng
Qichun Wei
author_sort Wei Yu
title Glioma SOX2 expression decreased after adjuvant therapy
title_short Glioma SOX2 expression decreased after adjuvant therapy
title_full Glioma SOX2 expression decreased after adjuvant therapy
title_fullStr Glioma SOX2 expression decreased after adjuvant therapy
title_full_unstemmed Glioma SOX2 expression decreased after adjuvant therapy
title_sort glioma sox2 expression decreased after adjuvant therapy
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2019-11-01
description Abstract Background SOX2 is regarded as an important marker in stem cell. The change of SOX2 expression after adjuvant therapy in high grade glioma (HGG) remains unknown so far. Few patients with recurrent glioma have opportunity to undergo operation once again, so the recurrent glioma samples are scarce. This study tries to analyze SOX2 expression in paired primary and recurrent HGG, aims to better understand the transformation law of SOX2 after adjuvant therapy in HGG. Methods Twenty-four recurrent HGG patients who undergone a second resection were included. 16 patients received adjuvant therapy, the remaining 8 patients didn’t receive any adjuvant therapy at all. The protein expression of SOX2 in paired primary and recurrent HGG was tested by immunohistochemistry. The statistical analysis was conducted by IBM SPSS Statistics 19.0. Results In primary HGG, SOX2 expression of 3 + , 2 + , 1+ and 0+ were seen in 20 (83.3%), 1 (4.2%), 1 (4.2%) and 2 cases (8.3%), respectively. The expression of SOX2 was decreased in recurrent HGG compared to the paired primary sample (p = 0.001). The decrease of SOX2 was often seen in patients received chemotherapy, radiotherapy or both (p = 0.003). Patients with SOX2 high expression in primary glioma had a longer median PFS than those with SOX2 low expression with marginal statistic significance (12.7 vs. 5.4 months, p = 0.083). For cases with SOX2 high expression in the primary glioma, those had SOX2 low expression after recurrence seemed to have worse prognosis as compared to patients with stable SOX2 high expression (PFS: 10.4 vs. 14.9 months, p = 0.036; OS: 27.0 vs 49.5 months, p = 0.005). Conclusions This is the first study comparing the protein expression of SOX2 in recurrent HGG and its paired primary tumor. SOX2 high expression is common in brain HGG, a tendency of decreased SOX2 expression in recurrent gliomas was evidenced. Lower SOX2 expression was seen in those patients who received adjuvant chemotherapy and/or radiotherapy. Patients with low SOX2 expression in primary HGG usually have poorer prognosis, those with SOX2 expression decreased in recurrent HGG had worse outcome.
topic Glioma
Recurrence
Prognosis
SOX2
url http://link.springer.com/article/10.1186/s12885-019-6292-y
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