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Omics Overview of the SPARC Gene in Mesothelioma
Licun Wu1, Marc de Perrot1,2,3
1Latner Thoracic Surgery Research Laboratories, Division of Thoracic Surgery, Toronto General Hospital, Toronto General Hospital Research Institute, University Health Network (UHN), 9N-961, 200 Elizabeth Street, Toronto, ON M5G 2C4, Canada.
Abstract:
The SPARC gene plays multiple roles in extracellular matrix synthesis and cell shaping, associated with tumor cell migration, invasion, and metastasis. The SPARC gene is also involved in the epithelial-mesenchymal transition (EMT) process, which is a critical phenomenon leading to a more aggressive cancer cell phenotype. SPARC gene overexpression has shown to be associated with poor survival in the mesothelioma (MESO) cohort from the TCGA database, indicating that this gene may be a powerful prognostic factor in MESO. Its overexpression is correlated with the immunosuppressive tumor microenvironment. Here, we summarize the omics advances of the SPARC gene, including the summary of SPARC gene expression associated with prognosis in pancancer and MESO, the immunosuppressive microenvironment, and cancer cell stemness. In addition, SPARC might be targeted by microRNAs. Notably, despite the controversial functions on angiogenesis, SPARC may directly or indirectly contribute to tumor angiogenesis in MESO. In conclusion, SPARC is involved in tumor invasion, metastasis, immunosuppression, cancer cell stemness, and tumor angiogenesis, eventually impacting patient survival. Strategies targeting this gene may provide novel therapeutic approaches to the treatment of MESO.
Insights
The SPARC gene is linked to aggressive cancer traits like invasion and metastasis. Targeting SPARC may offer new therapeutic strategies for mesothelioma (MESO) patients.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- The SPARC gene influences extracellular matrix synthesis and cell shape, impacting tumor progression.
- SPARC is implicated in epithelial-mesenchymal transition (EMT), promoting a more aggressive cancer phenotype.
- Overexpression of SPARC correlates with poor survival in mesothelioma (MESO) and an immunosuppressive tumor microenvironment.
Purpose of the Study:
- To review omics advances related to the SPARC gene in cancer.
- To explore SPARC's association with prognosis, the tumor microenvironment, and cancer stemness.
- To investigate SPARC's role in mesothelioma (MESO) progression and angiogenesis.
Main Methods:
- Literature review and analysis of omics data.
- Examination of SPARC gene expression in pancancer and MESO cohorts (TCGA database).
- Assessment of SPARC's correlation with tumor microenvironment, stemness, and angiogenesis.
Main Results:
- SPARC gene overexpression is associated with poor prognosis in MESO and pancancer.
- SPARC contributes to tumor invasion, metastasis, and an immunosuppressive microenvironment.
- SPARC influences cancer cell stemness and may promote tumor angiogenesis in MESO.
Conclusions:
- SPARC plays a significant role in multiple facets of cancer progression, including invasion, metastasis, and immunosuppression.
- SPARC gene targeting presents a potential therapeutic avenue for mesothelioma treatment.
- Further research into SPARC's functions, including its controversial role in angiogenesis, is warranted.
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