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Colorectal Cancer Cell Surface Protein Profiling Using an Antibody Microarray and Fluorescence Multiplexing
Published on: September 25, 2011
G-Protein Signaling Modulator 2 as a Potential Biomarker in Colorectal Cancer: Integrative Analysis Using Genetic
Doaa Jawad Kadhim1, Hanieh Azari1, Saeideh Khorshid Sokhangouy2
1Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad 91779-48564, Iran.
Abstract:
Colorectal cancer (CRC) imposes a significant healthcare burden globally, prompting the quest for innovative biomarkers to enhance diagnostic and therapeutic strategies. This study investigates the G-protein signaling modulator (GPSM) family across several cancers and presents a comprehensive pan-cancer analysis of the GPSM2 gene across several gastrointestinal (GI) cancers. Leveraging bioinformatics methodologies, we investigated GPSM2 expression patterns, protein interactions, functional enrichments, prognostic implications, genetic alterations, and immune infiltration associations. Furthermore, the expression of the GPSM2 gene was analyzed using real-time analysis. Our findings reveal a consistent upregulation of GPSM2 expression in all GI cancer datasets analyzed, suggesting its potential as a universal biomarker in GI cancers. Functional enrichment analysis underscores the involvement of GPSM2 in vital pathways, indicating its role in tumor progression. The prognostic assessment indicates that elevated GPSM2 expression correlates with adverse overall and disease-free survival outcomes across multiple GI cancer types. Genetic alteration analysis highlights the prevalence of mutations, particularly missense mutations, in GPSM2. Furthermore, significant correlations between GPSM2 expression and immune cell infiltration are observed, suggesting its involvement in tumor immune evasion mechanisms. Collectively, our study underscores the multifaceted role of GPSM2 in GI cancers, particularly in CRC, emphasizing its potential as a promising biomarker for prognosis and therapeutic targeting. Further functional investigations are warranted to elucidate its clinical utility and therapeutic implications in CRC management.
Insights
G-protein signaling modulator 2 (GPSM2) is upregulated in gastrointestinal cancers, including colorectal cancer (CRC). Elevated GPSM2 expression correlates with poor prognosis and immune evasion, suggesting its potential as a biomarker.
Area of Science:
- Oncology
- Molecular Biology
- Bioinformatics
Background:
- Colorectal cancer (CRC) presents a global health challenge, necessitating novel biomarkers for improved diagnostics and therapeutics.
- The G-protein signaling modulator (GPSM) family's role in cancer remains incompletely understood, particularly GPSM2 in gastrointestinal (GI) malignancies.
Purpose of the Study:
- To conduct a comprehensive pan-cancer analysis of the GPSM2 gene in GI cancers.
- To investigate GPSM2 expression, protein interactions, functional roles, prognostic value, genetic alterations, and immune infiltration associations.
Main Methods:
- Bioinformatic analysis of publicly available datasets.
- Investigation of GPSM2 expression patterns, protein-protein interactions, and functional enrichment.
- Prognostic assessment, analysis of genetic alterations, and correlation with immune cell infiltration.
Main Results:
- Consistent upregulation of GPSM2 expression observed across all analyzed GI cancer datasets.
- GPSM2 is implicated in critical pathways involved in tumor progression.
- Elevated GPSM2 expression is linked to poorer overall and disease-free survival.
- GPSM2 exhibits genetic alterations and correlates with immune cell infiltration, suggesting a role in immune evasion.
Conclusions:
- GPSM2 is a promising pan-GI cancer biomarker, particularly for colorectal cancer (CRC).
- Its upregulation, prognostic implications, and association with immune evasion highlight its potential for therapeutic targeting.
- Further research is needed to confirm its clinical utility in CRC management.
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