Categorized Serum miRNAs as Potential Biomarkers for Predicting the Progression and Prognosis of Colorectal Cancer

cancer patient area under the curve alcohol consumption overall survival 610 PI3K/AKT/PTEN colorectal cancer cancer prognosis Article cancer growth microRNA 92a reverse transcription polymerase chain reaction Colorectal cancer (CRC) male demographics Pi3K/Akt signaling microRNA 221 controlled study diagnostic test accuracy study human microRNA 103 microRNA 720 microRNA 19a clinical article emt signaling receiver operating characteristic microRNA 106a microRNAs (miRNAs) microRNA EMT bioinformatics prediction Prognosis biological marker cancer susceptibility WNT/CATENIN human tissue unclassified drug RNA isolation female microRNA 150 sensitivity and specificity KEGG canonical Wnt signaling histopathology mRNA expression level microRNA 107a Biomarkers signal transduction
DOI: 10.61186/ijbc.16.2.7 Publication Date: 2024-10-01T14:30:42Z
ABSTRACT
Background: Colorectal cancer (CRC), a common and aggressive gastrointestinal cancer, presents significant challenges in diagnosis and prognosis prediction despite available detection and treatment options. Many studies emphasized the crucial link between abnormal microRNA regulation and their potential role in cancer development and progression. These miRNAs are recognized as important non-invasive biomarkers for prognosis and overall survival prediction in various cancers, including CRC. Materials and Methods: In this study, we compared the expression patterns of eight miRNAs in the serum of 36 CRC patients with those of 37 healthy controls. The matching criteria included clinicodemographic factors and CRC susceptibility, and the analysis was performed using quantitative real-time PCR (qRT-PCR). Results: The serum miRNA levels of these eight miRNAs (miR-19a, miR-92a, miR-103, miR-106a, miR-107a, miR-150, miR-221, and miR-720) in the study groups are significantly higher compared to the control group. This analysis revealed eight specific miRNAs with varying expression levels in CRC patients. Furthermore, bioinformatic analysis using data collection and analytical tools has shown that these miRNAs may be associated with important aspects of colorectal cancer development and progression through the PI3K/AKT/PTEN, WNT/CATENIN, and EMT signaling pathways. Conclusion: Our analysis has identified a group of 8 overexpressed miRNAs (miR-19a, miR-92a, miR-103, miR-106a, miR-107a, miR-150, miR-221, and miR-720.) in serum samples of CRC patients.: Although further validation in larger and more diverse groups is necessary, these findings support a potential mechanism of action for these miRNAs in CRC and their association with essential signaling pathways, including PI3K/AKT/PTEN, WNT/CATENIN, and EMT. © 2024, Iranian Pediatric Hematology and Oncology Society. All rights reserved.
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