TY - JOUR
T1 - G-Protein Signaling Modulator 2 as a Potential Biomarker in Colorectal Cancer:Integrative Analysis Using Genetic Profiling and Pan-Cancer Studies
AU - Kadhim, Doaa Jawad
AU - Azari, Hanieh
AU - Sokhangouy, Saeideh Khorshid
AU - Hassanian, Seyed Mahdi
AU - Alshekarchi, Hawraa Ibrahim
AU - Goshayeshi, Ladan
AU - Goshayeshi, Lena
AU - Abbaszadegan, Mohammad Reza
AU - Khojasteh-Leylakoohi, Fatemeh
AU - Khazaei, Majid
AU - Gataa, Ibrahim Saeed
AU - Peters, Godefridus J.
AU - Ferns, Gordon A.
AU - Batra, Jyotsna
AU - Lam, Alfred King Yin
AU - Giovannetti, Elisa
AU - Avan, Amir
PY - 2024/4/9
Y1 - 2024/4/9
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/85191633756
U2 - 10.3390/genes15040474
DO - 10.3390/genes15040474
M3 - Article
C2 - 38674408
SN - 2073-4425
VL - 15
SP - 1
EP - 25
JO - Genes
JF - Genes
IS - 4
ER -