Related Experiment Video
Updated: Jan 4, 2026

06:32
Evaluation of Biomarkers in Glioma by Immunohistochemistry on Paraffin-Embedded 3D Glioma Neurosphere Cultures
Published on: January 9, 2019
8.2K
Glioma SOX2 expression decreased after adjuvant therapy
Wei Yu1,2, Xiaoqiu Ren1,2, Chunxiu Hu1,3
1Department of Radiation Oncology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Jiefang Road 88, Hangzhou, 310009, People's Republic of China.
BMC Cancer
|November 14, 2019
Summary
SOX2 expression, a key stem cell marker, often decreases in recurrent high-grade gliomas (HGG) after adjuvant therapy. This decrease is linked to poorer prognosis, highlighting SOX2's role in glioma progression.
Area of Science:
- Neuro-oncology
- Cancer Stem Cells
- Molecular Oncology
Background:
- SOX2 is a crucial stem cell marker.
- Its expression changes in high-grade glioma (HGG) after adjuvant therapy are not well understood.
- Recurrent HGG samples are scarce, limiting research.
Purpose of the Study:
- To analyze SOX2 protein expression in paired primary and recurrent HGG.
- To understand SOX2 expression changes following adjuvant therapy in HGG.
- To correlate SOX2 expression patterns with patient prognosis.
Main Methods:
- Immunohistochemistry used to assess SOX2 protein expression in 24 paired primary and recurrent HGG samples.
- Patients included those who underwent a second resection.
- Statistical analysis performed using IBM SPSS Statistics.
Main Results:
- SOX2 was highly expressed in primary HGG (83.3% cases showed 3+ expression).
- SOX2 expression significantly decreased in recurrent HGG compared to primary tumors (p=0.001).
- Decreased SOX2 expression was associated with prior chemotherapy and/or radiotherapy (p=0.003). High SOX2 expression in primary tumors correlated with longer progression-free survival (PFS).
- A decrease in SOX2 expression from primary to recurrent HGG indicated worse prognosis (PFS: 10.4 vs 14.9 months, OS: 27.0 vs 49.5 months).
Conclusions:
- This is the first study to compare SOX2 expression in paired primary and recurrent HGG.
- A tendency for decreased SOX2 expression in recurrent gliomas was observed, particularly after adjuvant therapy.
- Both low SOX2 expression in primary HGG and a decrease in expression upon recurrence are associated with poorer patient outcomes.
Related Concept Videos
Tumor Progression
7.2K
Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
7.2K
Loss of Tumor Suppressor Gene Functions
5.8K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
5.8K

