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Published on: March 30, 2019
SUMO4 small interfering RNA attenuates invasion and migration via the JAK2/STAT3 pathway in non-small cell lung
Jin-Xiao Liang1, Wei Gao2, Xiao-Wei Zeng1,3
1Department of Thoracic Surgery, Zhejiang Cancer Hospital, Hangzhou, Zhejiang 310022, P.R. China.
Abstract:
Small ubiquitin-like modifier 4 (SUMO4) is the latest member of the sumoylation family, which enhances the stability of protein, regulates the distribution and localization of the protein, and affects the transcription activity of the protein. However, the role of SUMO4 in non-small cell lung cancer (NSCLC) has not yet been reported. The present study first demonstrated that SUMO4 was upregulated in a number of tissues from patients with NSCLC. Immunohistochemistry was performed to demonstrate the expression level of SUMO4 in lung cancer tumor tissues. Following the transfection, The EMT status and signaling pathway activation regulated by SUMO4-siRNA was assessed by western blotting. The Transwell and wound healing assays were performed to investigate the regulatory effect of SUMO4-siRNA on cell migration and invasion. Cell Counting Kit-8 assay was performed to investigate whether SUMO4-siRNA affected the chemosensitivity of the NSCLC cells to cisplatin. Statistical analysis of immunohistochemical results from the tissues showed that the overexpression of SUMO4 was significantly associated with sex, tumor type, history of smoking, T stage and poor prognosis. It was also identified that SUMO4 small interfering RNA attenuated invasion and migration in NSCLC cell lines, as well chemosensitivity to cisplatin via the inhibition of the JAK2/STAT3 pathway. In conclusion, SUMO4 may play an important role in the poor prognosis of patients with NSCLC. The present study indicates that SUMO4 may be a potential therapeutic target for NSCLC.
Insights
Small ubiquitin-like modifier 4 (SUMO4) is upregulated in non-small cell lung cancer (NSCLC), correlating with poor prognosis. Inhibiting SUMO4 reduces NSCLC cell invasion, migration, and enhances cisplatin sensitivity by targeting the JAK2/STAT3 pathway.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Small ubiquitin-like modifier 4 (SUMO4) is a key regulator of protein stability and function.
- The role of SUMO4 in non-small cell lung cancer (NSCLC) remains largely unexplored.
- Understanding SUMO4's function is crucial for developing novel cancer therapies.
Purpose of the Study:
- To investigate the expression and function of SUMO4 in NSCLC.
- To determine the correlation between SUMO4 expression and clinical characteristics in NSCLC patients.
- To explore SUMO4's potential as a therapeutic target in NSCLC.
Main Methods:
- Immunohistochemistry was used to assess SUMO4 expression in NSCLC tissues.
- SUMO4 small interfering RNA (siRNA) was utilized to inhibit SUMO4 expression in NSCLC cell lines.
- Western blotting, Transwell, wound healing, and Cell Counting Kit-8 assays were performed to evaluate cellular processes and signaling pathways.
Main Results:
- SUMO4 was found to be upregulated in NSCLC tissues and associated with sex, tumor type, smoking history, T stage, and poor prognosis.
- SUMO4-siRNA significantly attenuated cell invasion and migration in NSCLC cell lines.
- SUMO4 inhibition enhanced NSCLC cell chemosensitivity to cisplatin by suppressing the JAK2/STAT3 pathway.
Conclusions:
- SUMO4 plays a significant role in the progression and poor prognosis of NSCLC.
- SUMO4 may serve as a potential diagnostic biomarker and therapeutic target for NSCLC.
- Targeting SUMO4 offers a promising strategy for improving NSCLC treatment outcomes.
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