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Comprehensive Analysis of the Oncogenic Role of Targeting Protein for Xklp2 (TPX2) in Human Malignancies
Ting Shao1, Xiling Jiang2,3, Guochang Bao4,5
1Department of Gynecology, Affiliated Hospital of Chifeng University, Chifeng 024000, China.
Abstract:
Mitosis and spindle assembly require the microtubule-associated protein Xenopus kinesin-like protein 2 (TPX2). Although TPX2 is highly expressed in several malignant tumor forms, little is known about its role in cancer. In this study, we performed the gene set enrichment analysis of TPX2 in 33 types of cancers and an extensive pan-cancer bioinformatic analysis using prognosis, tumor mutational burdens, microsatellite instability, tumor microenvironment, and immune cell infiltration data. According to the differential expression study, TPX2 was found to be overexpressed across all studied cancer types. Based on the survival analysis, increased TPX2 expression was associated with a poor prognosis for most cancers. The TPX2 expression level was confirmed to correlate with the clinical stage, microsatellite instability, and tumor mutational burden across all cancer types. Furthermore, TPX2 expression has been linked to tumor microenvironments and immune cell infiltration, particularly in bladder urothelial carcinoma, liver hepatocellular carcinoma, lung adenocarcinoma, stomach adenocarcinoma, and uterine corpus endometrial carcinoma. Finally, the gene set enrichment analysis implicated TPX2 in the regulation of aminoacyl tRNA biosynthesis, which is the most important tumor cell cycle signaling pathway. This comprehensive pan-cancer analysis shows that TPX2 is a prognostic molecular biomarker for most cancers and suggests its potential as an effective therapeutic target for the treatment of these diseases.
Insights
Xenopus kinesin-like protein 2 (TPX2) is overexpressed in most cancers and linked to poor prognosis. This study reveals TPX2 as a potential pan-cancer prognostic biomarker and therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Bioinformatics
Background:
- Mitosis and spindle assembly depend on the microtubule-associated protein Xenopus kinesin-like protein 2 (TPX2).
- TPX2 is highly expressed in several malignant tumors, but its precise role in cancer remains largely unknown.
- Understanding TPX2's function in cancer is crucial for developing new therapeutic strategies.
Purpose of the Study:
- To investigate the role of TPX2 in various cancer types using a comprehensive pan-cancer bioinformatic analysis.
- To evaluate TPX2 as a prognostic biomarker across 33 cancer types.
- To explore the association of TPX2 expression with tumor characteristics and the tumor microenvironment.
Main Methods:
- Differential gene expression analysis across 33 cancer types.
- Pan-cancer bioinformatic analysis including survival, tumor mutational burden, microsatellite instability, and immune cell infiltration data.
- Gene set enrichment analysis (GSEA) to identify associated signaling pathways.
Main Results:
- TPX2 was significantly overexpressed in all studied cancer types.
- Increased TPX2 expression correlated with poor prognosis in most cancers.
- TPX2 expression associated with clinical stage, microsatellite instability, tumor mutational burden, and immune cell infiltration in specific cancers.
- GSEA implicated TPX2 in aminoacyl tRNA biosynthesis, a key tumor cell cycle pathway.
Conclusions:
- TPX2 is a potential pan-cancer prognostic biomarker.
- TPX2 expression is linked to critical cancer hallmarks and the tumor microenvironment.
- TPX2 represents a promising therapeutic target for various cancers.
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