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Transformer 2β (Tra2β/SFRS10) positively regulates the progression of NSCLC via promoting cell proliferation
Lili Ji1, Tingting Ni, Yanbo Shen
1Department of Pathology, Medical College, Nantong University, Nantong, 226001, Jiangsu, China.
Abstract:
Transformer 2β (Tra2β), a member of the serine/arginine-rich-like protein family, is an important RNA-binding protein involved in alternative splice. Deregulation of Tra2β has been observed in several cancers. However, the detailed role of Tra2β in non-small cell lung cancer (NSCLC) has not been elucidated. In this study, the contribution of Tra2β to NSCLC development was investigated. On histological level, the expression of Tra2β was determined by Western and immunohistochemistry assays. It demonstrated that Tra2β was expressed higher in NSCLC tumor tissues compared with adjacent non-tumor tissues. In addition to confirm the association of Tra2β expression with histological differentiation and clinical stage (p < 0.05), we also confirmed significant positive correlation between the expression level of Tra2β and that of Ki67 (p < 0.05, r = 0.446) by Spearman rank correlation test. Moreover, high expression of Tra2β predicted poor prognosis by Kaplan-Meier survival analysis. And Tra2β among with other clinicopathologic variables was an independent prognostic indicator for patients' overall survival by multivariate analysis. On cellular level, Tra2β expression was demonstrated to promote proliferation of NSCLC cells through a series of assays, including serum starvation and release assay, Western blot assay and flow cytometry analysis. Moreover, knockdown of Tra2β was confirmed to inhibit proliferation and to induce apoptosis of NSCLC cells through flow cytometry analysis, western analysis, cell counting kit-8 assay and Tunnel assay. Our results indicated that Tra2β was involved in the tumorigenesis of NSCLC and might be a potential therapeutic target of NSCLC.
Insights
Transformer 2β (Tra2β) promotes non-small cell lung cancer (NSCLC) growth and is linked to poor prognosis. Targeting Tra2β may offer a new therapeutic strategy for NSCLC patients.
Area of Science:
- Molecular Biology
- Oncology
- RNA Biology
Background:
- Transformer 2β (Tra2β) is an RNA-binding protein implicated in alternative splicing.
- Dysregulation of Tra2β is observed in various cancers.
- The specific role of Tra2β in non-small cell lung cancer (NSCLC) remains unclear.
Purpose of the Study:
- To investigate the role of Transformer 2β (Tra2β) in the development and progression of non-small cell lung cancer (NSCLC).
- To evaluate Tra2β as a potential prognostic marker and therapeutic target in NSCLC.
Main Methods:
- Western blot and immunohistochemistry to assess Tra2β expression in NSCLC tissues.
- Correlation analysis (Spearman) to link Tra2β expression with clinicopathological features and Ki67.
- Kaplan-Meier and multivariate analyses for prognostic evaluation.
- Cellular assays (proliferation, apoptosis, Western blot, flow cytometry, CCK-8, TUNEL) to determine Tra2β's functional impact on NSCLC cells.
Main Results:
- Tra2β expression is significantly upregulated in NSCLC tissues compared to adjacent non-tumor tissues.
- High Tra2β expression correlates with poor histological differentiation, advanced clinical stage, and increased proliferation (Ki67).
- Elevated Tra2β predicts poor overall survival and serves as an independent prognostic indicator.
- Tra2β promotes NSCLC cell proliferation and inhibits apoptosis; its knockdown reduces proliferation and induces apoptosis.
Conclusions:
- Transformer 2β (Tra2β) plays a crucial role in non-small cell lung cancer (NSCLC) tumorigenesis.
- Tra2β is associated with aggressive tumor features and predicts poor prognosis in NSCLC patients.
- Tra2β represents a potential therapeutic target for NSCLC treatment.
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