Department of Animal Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran.
Zimagene Medical Genetics Laboratory, Avicenna St, Hamedan, Iran.
J Gastrointest Cancer. 2022 Dec;53(4):1014-1019. doi: 10.1007/s12029-021-00744-5. Epub 2021 Nov 11.
Gastric cancer (GC) is a heterogeneous disease, and this heterogeneity significantly affects survival and treatment outcomes. Identification of molecular biomarkers specific for early-stage GC can help clinicians to choose more precise and effective treatment approaches. Long non-coding RNAs (lncRNAs) have the potential to be used as biomarkers because of their tissue specificity, stability, and availability in body fluids. In this study, we aimed to investigate changes in the expression levels of lncRNA KRT18P55 and to assess its biomarker potentials in patients with GC.
Tumor and non-tumor marginal tissues were collected from 102 patients at Noor-Nejat Hospital (Tabriz, Iran). RNA was isolated, and quantitative reverse transcriptase PCR (qRT-PCR) was performed to assess KRT18P55 expression levels in tumor and non-tumor tissue samples. The receiver operating characteristic (ROC) curve analysis was performed to evaluate potentials of KRT18P55 as a prognostic biomarker in GC. SPSS and GraphPad Prism software were used for data analysis.
We found that KRT18P55 is significantly overexpressed in tumor as compared to non-tumor tissues (p < 0.0001). We found a significant association between KRT18P55 overexpression and intestinal GC subtype (p < 0.0001), lymph node metastasis (p = 0.013), and Helicobacter pylori infection (p = 0.033). Based on the ROC analysis, KRT18P55 showed a sensitivity and specificity of 53.92% and 77.45%, respectively.
Overexpression of KRT18P55 in gastric tumors is suggestive of its oncogenic role in GC. In addition, KRT18P55 may be used as a potential prognosis biomarker and therapeutic target in intestinal GC subtype.
胃癌(GC)是一种异质性疾病,这种异质性显著影响生存和治疗结果。鉴定特定于早期 GC 的分子生物标志物可以帮助临床医生选择更精确和有效的治疗方法。长链非编码 RNA(lncRNA)具有成为生物标志物的潜力,因为它们具有组织特异性、稳定性和在体液中的可用性。在本研究中,我们旨在研究 lncRNA KRT18P55 表达水平的变化,并评估其在 GC 患者中的生物标志物潜力。
从诺尔-内贾特医院(伊朗大不里士)的 102 名患者中采集肿瘤和非肿瘤边缘组织。提取 RNA,通过定量逆转录 PCR(qRT-PCR)评估肿瘤和非肿瘤组织样本中 KRT18P55 的表达水平。进行受试者工作特征(ROC)曲线分析,以评估 KRT18P55 作为 GC 预后生物标志物的潜力。使用 SPSS 和 GraphPad Prism 软件进行数据分析。
我们发现 KRT18P55 在肿瘤组织中明显高于非肿瘤组织(p<0.0001)。我们发现 KRT18P55 过表达与肠型 GC 亚型(p<0.0001)、淋巴结转移(p=0.013)和幽门螺杆菌感染(p=0.033)显著相关。基于 ROC 分析,KRT18P55 的敏感性和特异性分别为 53.92%和 77.45%。
KRT18P55 在胃肿瘤中的过表达表明其在 GC 中具有致癌作用。此外,KRT18P55 可能作为肠型 GC 亚型的潜在预后生物标志物和治疗靶点。