Carbajal-López Berenice, Martínez-Gutierrez Antonio Daniel, Madrigal-Santillán Eduardo O, Calderillo-Ruiz Germán, Morales-González José Antonio, Coronel-Hernández Jossimar, Lockhart Joey, Millan-Catalan Oliver, Mendoza-Rodriguez Monica G, Lino-Silva Leonardo S, Calderillo-Trejo Germán, Sumagin Ronen, Pérez-Plasencia Carlos, Pérez-Yépez Eloy Andrés
Programa de Doctorado en Investigación en Medicina, Escuela Superior de Medicina, Instituto Politécnico Nacional, Ciudad de México 11340, Mexico.
Laboratorio de Genómica, Instituto Nacional de Cancerología, Tlalpan 14080, Mexico.
Cancers (Basel). 2024 Oct 29;16(21):3649. doi: 10.3390/cancers16213649.
: The prognosis of colorectal cancer (CRC) is mainly based on the clinical stage; however, CRC is considered a complex disease due to its molecular heterogeneity. The development of novel biomarkers to improve patients' diagnosis and prognosis remains fundamental. : A cohort of forty-nine CRC patients from the National Cancer Institute of Mexico was included to collect clinical and miRNA expression data. The expression of a group of miRNAs was compared between CRC and non-tumoral adjacent tissues. Prognosis assessment considering each miRNA expression was tested using Kaplan-Meier survival curves and Cox regressions. Statistical significance was defined as ≤ 0.05. Trial registration: Retrospective study No.2021/046. : miR-3065-5p and miR-26a-5p expression differed between non-tumoral adjacent and tumoral tissues ( = 0.02). In terms of overall survival (OS), patients with low expression of miR-3065-5p had a median OS of 70 months, while patients with high levels did not reach the median OS ( = 0.041). Male patients with low expression of this miRNA had an OS of 70 months, whereas patients with high levels did not reach the median OS ( = 0.050). Under uni-multivariate analysis, clinical stage (HR: 1.30, CI 1.23-2.30; : 0.001) and low levels of miR-3065-5p (HR: 1.30, CI 1.23-2.30; : 0.001) were determined as predictor factors of OS. To this end, we designed the "Prognosis miRNAs assessment in cancer" (PROMIR-C) algorithm, which integrated clinical features with miR-3065-5p expression levels. : These findings support the clinical utility of miR-26a-5p and miR-3065-5p in the diagnosis and prognosis of CRC. PROMIR-C is a fundamental tool for clinicians in treatment decision-making, prognosis assessment, and outcome of CRC.
结直肠癌(CRC)的预后主要基于临床分期;然而,由于其分子异质性,CRC被认为是一种复杂的疾病。开发新型生物标志物以改善患者的诊断和预后仍然至关重要。:纳入了来自墨西哥国家癌症研究所的49名CRC患者队列,以收集临床和miRNA表达数据。比较了CRC组织与非肿瘤相邻组织中一组miRNA的表达情况。使用Kaplan-Meier生存曲线和Cox回归对考虑每种miRNA表达的预后评估进行了测试。统计学显著性定义为P≤0.05。试验注册:回顾性研究编号2021/046。:miR-3065-5p和miR-26a-5p在非肿瘤相邻组织和肿瘤组织中的表达存在差异(P = 0.02)。在总生存期(OS)方面,miR-3065-5p低表达的患者中位OS为70个月,而高表达的患者未达到中位OS(P = 0.041)。该miRNA低表达的男性患者OS为70个月,而高表达的患者未达到中位OS(P = 0.050)。在单变量和多变量分析中,临床分期(HR:1.30,CI 1.23 - 2.30;P:0.001)和低水平的miR-3065-5p(HR:1.30,CI 1.23 - 2.30;P:0.001)被确定为OS的预测因素。为此,我们设计了“癌症预后miRNA评估”(PROMIR-C)算法,该算法将临床特征与miR-3065-5p表达水平相结合。:这些发现支持了miR-26a-5p和miR-3065-5p在CRC诊断和预后中的临床应用价值。PROMIR-C是临床医生在CRC治疗决策、预后评估和结果判断方面的重要工具。