Genes (Apr 2024)

G-Protein Signaling Modulator 2 as a Potential Biomarker in Colorectal Cancer: Integrative Analysis Using Genetic Profiling and Pan-Cancer Studies

  • Doaa Jawad Kadhim,
  • Hanieh Azari,
  • Saeideh Khorshid Sokhangouy,
  • Seyed Mahdi Hassanian,
  • Hawraa Ibrahim Alshekarchi,
  • Ladan Goshayeshi,
  • Lena Goshayeshi,
  • Mohammad Reza Abbaszadegan,
  • Fatemeh Khojasteh-Leylakoohi,
  • Majid Khazaei,
  • Ibrahim Saeed Gataa,
  • Godefridus J. Peters,
  • Gordon A. Ferns,
  • Jyotsna Batra,
  • Alfred King-Yin Lam,
  • Elisa Giovannetti,
  • Amir Avan

DOI
https://doi.org/10.3390/genes15040474
Journal volume & issue
Vol. 15, no. 4
p. 474

Abstract

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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.

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