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

Author:

Kadhim Doaa Jawad1,Azari Hanieh1ORCID,Sokhangouy Saeideh Khorshid2,Hassanian Seyed Mahdi1,Alshekarchi Hawraa Ibrahim3,Goshayeshi Ladan45,Goshayeshi Lena5,Abbaszadegan Mohammad Reza2,Khojasteh-Leylakoohi Fatemeh1,Khazaei Majid1,Gataa Ibrahim Saeed6,Peters Godefridus J.78ORCID,A. Ferns Gordon9ORCID,Batra Jyotsna10ORCID,Lam Alfred King-Yin11ORCID,Giovannetti Elisa812ORCID,Avan Amir110ORCID

Affiliation:

1. Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad 91779-48564, Iran

2. Medical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad 91886-17871, Iran

3. Al-Zahraa Center for Medical and Pharmaceutical Research Sciences (ZCMRS), Al-Zahraa University for Women, Kerbala 56001, Iraq

4. Department of Gastroenterology and Hepatology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad 91779-48564, Iran

5. Surgical Oncology Research Center, Mashhad University of Medical Sciences, Mashhad 91779-48954, Iran

6. College of Medicine, University of Warith Al-Anbiyaa, Karbala 56001, Iraq

7. Department of Biochemistry, Medical University of Gdansk, 80-211 Gdansk, Poland

8. Cancer Center Amsterdam, Cancer Biology and Immunology, Amsterdam UMC, Vrije Universiteit, Department of Medical Oncology, 1081 HV Amsterdam, The Netherlands

9. Department of Medical Education, Brighton & Sussex Medical School, Falmer, Brighton BN1 9PH, UK

10. Faculty of Health, School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia

11. Pathology, School of Medicine and Dentistry, Gold Coast Campus, Griffith University, Gold Coast, QLD 4222, Australia

12. Cancer Pharmacology Laboratory, AIRC Start Up Unit, Fondazione Pisana per La Scienza, 56017 Pisa, Italy

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.

Funder

National Institute for Medical Research and Development

Publisher

MDPI AG

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