Tayae Eman, Osman Eman M, Tawfik Marwa R, Hegazy Neamat, Moaaz Marwa, Ghazala Rasha A
Clinical Pathology Department, Alexandria University, Alexandria, Egypt.
Faculty of Medicine, Champollion Street, Alexandria, Egypt.
J Gastrointest Cancer. 2025 Mar 19;56(1):81. doi: 10.1007/s12029-025-01197-w.
Colorectal cancer (CRC) is identified as the second leading cause of cancer-associated deaths worldwide. Therefore, there is ongoing research to discover new potential biomarkers enabling early and noninvasive diagnosis of the disease. YRNAs, a novel class of non-coding RNAs, have been identified as a new player in carcinogenesis and an independent class of clinical biomarkers in various malignancies. Nevertheless, the role of plasma YRNAs in CRC diagnosis and prognosis remains unknown. Therefore, the current study aimed to investigate the clinical significance of plasma YRNAs as a noninvasive biomarker for CRC.
Plasma YRNAs expression was assessed in 50 newly diagnosed CRC patients as well as 50 age- and sex-matched healthy controls using quantitative reverse transcription polymerase chain reaction.
All plasma YRNAs expression levels were significantly higher in CRC patients than in controls. A significant correlation was observed between YRNA1 and YRNA3, and between YRNA1 and YRNA4. However, no significant correlation between YRNA1 and YRNA5 was identified. Plasma YRNA1 expression showed the highest diagnostic performance for the detection of CRC using the receiver operating characteristic curve analysis, with a sensitivity of 92% and a specificity of 90%. Nevertheless, when the four YRNAs were combined in a single ROC analysis, sensitivity decreased to 80%, while the specificity remained virtually unchanged. Moreover, significant association was observed between plasma YRNA1 and YRNA3 and tumor stage, grade, lymph node presence, metastasis, and lymphovascular invasion.
Plasma YRNA may serve as a potential noninvasive biomarker for the diagnosis and prognosis of CRC with high sensitivity and specificity vs. healthy controls.
结直肠癌(CRC)被认为是全球癌症相关死亡的第二大主要原因。因此,正在进行研究以发现能够实现该疾病早期和非侵入性诊断的新的潜在生物标志物。YRNAs是一类新型的非编码RNA,已被确定为致癌过程中的新参与者以及各种恶性肿瘤中一类独立的临床生物标志物。然而,血浆YRNAs在CRC诊断和预后中的作用仍不清楚。因此,本研究旨在探讨血浆YRNAs作为CRC非侵入性生物标志物的临床意义。
使用定量逆转录聚合酶链反应评估50例新诊断的CRC患者以及50例年龄和性别匹配的健康对照者的血浆YRNAs表达。
CRC患者的所有血浆YRNAs表达水平均显著高于对照组。观察到YRNA1与YRNA3之间以及YRNA1与YRNA4之间存在显著相关性。然而,未发现YRNA1与YRNA5之间存在显著相关性。使用受试者工作特征曲线分析,血浆YRNA1表达在检测CRC方面表现出最高的诊断性能,敏感性为92%,特异性为90%。然而,当将这四种YRNAs组合进行单一ROC分析时,敏感性降至80%,而特异性基本保持不变。此外,观察到血浆YRNA1和YRNA3与肿瘤分期、分级、淋巴结存在情况、转移和淋巴管浸润之间存在显著关联。
与健康对照相比,血浆YRNA可能作为CRC诊断和预后的潜在非侵入性生物标志物,具有高敏感性和特异性。