Serum miR-23 and miR-150 Profiles as Biomarkers for Predicting Recurrence following Surgical Intervention in Colorectal Cancer Patients

被引:0
|
作者
Mahmoudivar, Saeid [1 ]
Zarredar, Habib [1 ]
Asadi, Milad [2 ]
Zafari, Venus [2 ]
Hashemzadeh, Shahriyar [1 ]
Farzaneh, Rojin [1 ]
Kermani, Touraj Asvadi [1 ]
机构
[1] Tabriz Univ Med Sci, TB & Lung Dis Res Ctr, Tabriz, Iran
[2] Ege Univ, Inst Hlth Sci, Dept Basic Oncol, Izmir, Turkiye
来源
关键词
Biomarker; Colorectal cancer; micro-RNAs; Tumorigenesis; EXPRESSION; INVASION; MIR-374; BLOOD;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: MicroRNAs (miRNAs) play pivotal roles in post-transcriptional regulation of gene expression and have emerged as crucial regulators in cancer development, progression, and metastasis. This study aimed to assess the expression profiles of miR-23, miR-223, miR-1246, and miR-150 in serum samples obtained from colorectal cancer (CRC) patients before and three months after surgery, in comparison to a healthy control group, to explore their biomarker potential. Methods: A total of 50 blood samples were collected from patients with CRC (pre- and post-surgery), along with 50 samples from healthy controls. The relative expression levels of miR-23, miR-223, miR1246, and miR-150 in the serum were quantified using quantitative real-time PCR. Results: Our findings revealed upregulated expression levels of miR-23, miR-1246, and miR-223, while miR-150 exhibited significant downregulation in the serum of CRC subjects compared to healthy controls. Receiver operating characteristic (ROC) analysis indicated that miR-23 and miR-150 could distinguish CRC cases from controls with relatively high accuracy. Moreover, three months postsurgery, miR-23, miR-1246, and miR-223 serum levels were downregulated, and miR-150 was significantly upregulated. However, no significant correlations were observed between serum levels of the studied genes and the clinical features of our patients. Conclusions: The serum levels of miR-23 and miR-150 hold promise as potential biomarkers for the diagnosis and prognosis of CRC.
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页码:540 / 549
页数:10
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