Circulating Pre-microRNA-488 in Blood Is a Potential Prognostic Biomarker in Gastric Cancer.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
환자: gastric cancer (GC)
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
pre-miR-488 was detected in exosomes isolated from the plasma of patients with GC. [CONCLUSION] Circulating pre-miR-488 and miR-488-5p expression in the blood may serve as novel prognostic biomarkers for patients with GC, predicting clinical outcomes and guiding therapeutic strategies.
[BACKGROUND/AIM] MicroRNAs (miRNAs) have been highlighted as non-invasive clinical biomarkers in liquid biopsy.
APA
Tsuruda Y, Masuda T, et al. (2025). Circulating Pre-microRNA-488 in Blood Is a Potential Prognostic Biomarker in Gastric Cancer.. Anticancer research, 45(1), 123-133. https://doi.org/10.21873/anticanres.17399
MLA
Tsuruda Y, et al.. "Circulating Pre-microRNA-488 in Blood Is a Potential Prognostic Biomarker in Gastric Cancer.." Anticancer research, vol. 45, no. 1, 2025, pp. 123-133.
PMID
39740846
Abstract
[BACKGROUND/AIM] MicroRNAs (miRNAs) have been highlighted as non-invasive clinical biomarkers in liquid biopsy. This study aimed to investigate the clinical significance of circulating tumor suppressors, precursor-miR-488 (pre-miR-488) and miR-488-5p, in the blood of patients with gastric cancer (GC).
[MATERIALS AND METHODS] The expression levels of pre-miR-488 and miR-488-5p in tumor tissues and blood were measured using RT-qPCR, and the clinicopathological and prognostic significance of their expression was assessed in patients with GC. Next, pathway analysis of miR-488-5p expression in GC tissues was performed by gene set enrichment analysis (GSEA) using the TCGA dataset. Finally, pre-miR-488 in exosomes from the plasma of GC patients was analyzed using RT-qPCR.
[RESULTS] Both pre-miR-488 and miR-488-5p were down-regulated in tumor tissues, whereas their expression in the blood was significantly higher in patients with GC than in healthy controls. Low expression of pre-miR-488 or miR-488-5p in the blood was associated with poor prognosis in patients with GC. Furthermore, low pre-miR-488 expression in the blood was an independent poor prognostic factor for overall survival. miR-488-5p expression tended to be negatively correlated with the expression of gene sets involved in epithelial-mesenchymal transition and hypoxia. pre-miR-488 was detected in exosomes isolated from the plasma of patients with GC.
[CONCLUSION] Circulating pre-miR-488 and miR-488-5p expression in the blood may serve as novel prognostic biomarkers for patients with GC, predicting clinical outcomes and guiding therapeutic strategies.
[MATERIALS AND METHODS] The expression levels of pre-miR-488 and miR-488-5p in tumor tissues and blood were measured using RT-qPCR, and the clinicopathological and prognostic significance of their expression was assessed in patients with GC. Next, pathway analysis of miR-488-5p expression in GC tissues was performed by gene set enrichment analysis (GSEA) using the TCGA dataset. Finally, pre-miR-488 in exosomes from the plasma of GC patients was analyzed using RT-qPCR.
[RESULTS] Both pre-miR-488 and miR-488-5p were down-regulated in tumor tissues, whereas their expression in the blood was significantly higher in patients with GC than in healthy controls. Low expression of pre-miR-488 or miR-488-5p in the blood was associated with poor prognosis in patients with GC. Furthermore, low pre-miR-488 expression in the blood was an independent poor prognostic factor for overall survival. miR-488-5p expression tended to be negatively correlated with the expression of gene sets involved in epithelial-mesenchymal transition and hypoxia. pre-miR-488 was detected in exosomes isolated from the plasma of patients with GC.
[CONCLUSION] Circulating pre-miR-488 and miR-488-5p expression in the blood may serve as novel prognostic biomarkers for patients with GC, predicting clinical outcomes and guiding therapeutic strategies.
MeSH Terms
Humans; Stomach Neoplasms; MicroRNAs; Biomarkers, Tumor; Prognosis; Female; Male; Middle Aged; Exosomes; Gene Expression Regulation, Neoplastic; Aged; Epithelial-Mesenchymal Transition