TRPV2 Calcium Channel Gene Expression and Outcomes in Gastric Cancer Patients: A Clinically Relevant Association.
Pietro ZoppoliGiovanni CaliceSimona LaurinoVitalba RuggieriFrancesco La RoccaGiuseppe La TorreMario CiuffiElena AmendolaFerdinando De VitaAngelica PetrilloGiuliana NapolitanoGeppino FalcoSabino RussiPublished in: Journal of clinical medicine (2019)
Gastric cancer (GC) is characterized by poor efficacy and the modest clinical impact of current therapies. Apoptosis evasion represents a causative factor for treatment failure in GC as in other cancers. Since intracellular calcium homeostasis regulation has been found to be associated with apoptosis resistance, the aberrant expression of intracellular calcium regulator genes (CaRGs) could have a prognostic value in GC patients. We analyzed the association of the expression levels of 98 CaRGs with prognosis by the log-rank test in a collection of 1524 GC samples from four gene expression profiling datasets. We also evaluated differential gene expression in comparison with normal stomach tissue, and then we crossed results with tissue microarrays from the Human Protein Atlas. Among the investigated CaRGs, patients with high levels of TRPV2 expression were characterized by a shorter overall survival. TRPV2 expression was found to increase according to tumor stage. Both mRNA and protein levels were significantly higher in tumor than normal stomach samples. TRPV2 was also associated with poor prognosis in the Lauren's intestinal type GC and in patients treated with adjuvant therapy. Overall, we highlighted the relevance of TRPV2 not only as a prognostic biomarker but also as a potential therapeutic target to improve GC treatment efficacy.
Keyphrases
- poor prognosis
- gene expression
- long non coding rna
- end stage renal disease
- binding protein
- neuropathic pain
- ejection fraction
- newly diagnosed
- genome wide
- oxidative stress
- dna methylation
- gas chromatography
- chronic kidney disease
- peritoneal dialysis
- endoplasmic reticulum stress
- cell death
- spinal cord
- single cell
- adipose tissue
- patient reported outcomes
- young adults
- rna seq
- protein protein
- combination therapy
- high resolution
- reactive oxygen species
- free survival
- patient reported
- genome wide analysis