Lin Ping, Qin Xiuju, Yi Caiyun, Jiang Man, Yi Lili, Liang Yuemian
Department of General Surgery, Minimally Invasive Surgery Center, Second People's Hospital of Hunan Province (Hunan Brain Hospital), Changsha, China.
Department of Oncology, No. 971 Navy Hospital of the Chinese People's Liberation Army, Qingdao, China.
Folia Biol (Praha). 2025;71(1):18-28. doi: 10.14712/fb2025071010018.
The poor prognosis of colorectal cancer (CRC) contributes to a yearly increase in CRC mortality, while microRNAs (miRNAs) were found to play a regulatory function in diversiform cancers, including CRC. The objective of this research was to evaluate the clinical value and possible regulatory mechanisms of miR-767-5p in CRC. The expression level of miR-767-5p in CRC tissues and cells was examined. The Kaplan-Meier curve was utilized to analyse the function of miR-767-5p in CRC prognosis. The independent prognostic factors in CRC were assessed by a multivariate COX regression analysis. Additionally, the regulatory mechanism of miR-767-5p in CRC was determined through an in vitro cell experiment. The miR-767-5p expression was down-regulated in CRC tumour tissues and CRC cells. Indicators such as tumour differentiation, TNM, LNM and miR-767-5p were identified as independent prognostic factors for a poor CRC prognosis. The regulatory relationship between miR-767-5p and nuclear factor I A (NFIA) was verified by the dual-luciferase reporter assay, and the NFIA expression level was significantly suppressed by over-expressed miR-767-5p. The proliferation, migration and invasion of CRC cells were inhibited by over-expressing miR-767-5p, while the inhibition effect could be reversed by over-expressing NFIA. The over-expressed miR-767-5p could serve as a tumour suppressor to inhibit the progression of CRC by suppressing the expression level of NFIA.
结直肠癌(CRC)的不良预后导致其死亡率逐年上升,而微小RNA(miRNA)在包括CRC在内的多种癌症中发挥调节作用。本研究的目的是评估miR-767-5p在CRC中的临床价值及可能的调控机制。检测了miR-767-5p在CRC组织和细胞中的表达水平。利用Kaplan-Meier曲线分析miR-767-5p在CRC预后中的作用。通过多因素COX回归分析评估CRC的独立预后因素。此外,通过体外细胞实验确定miR-767-5p在CRC中的调控机制。miR-767-5p在CRC肿瘤组织和CRC细胞中表达下调。肿瘤分化、TNM、LNM和miR-767-5p等指标被确定为CRC预后不良的独立预后因素。通过双荧光素酶报告基因实验验证了miR-767-5p与核因子IA(NFIA)之间的调控关系,过表达miR-767-5p可显著抑制NFIA的表达水平。过表达miR-767-5p可抑制CRC细胞的增殖、迁移和侵袭,而过表达NFIA可逆转这种抑制作用。过表达的miR-767-5p可作为肿瘤抑制因子,通过抑制NFIA的表达水平来抑制CRC的进展。