Serum IL-24 combined with CA125 as screening and prognostic biomarkers for NSCLC

IF 3.3 3区 生物学 Q3 CELL BIOLOGY
Kai Zhang, Jiao Qu, Shu Deng, Enwu Yuan
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Abstract

Noninvasive and effective methods for early screening of non-small cell lung cancer (NSCLC) still need to be developed. At present, a reasonable conclusion is that a combination of tumor markers is a superior predictor of screening. Cytokines, as important regulators of cancer development, have great potential for the screening and prognosis of NSCLC. This study screened novel biomarkers related to the early screening and prognosis of NSCLC. In the present study, the biological significance and immunoregulation of interleukin-24 (IL-24) were analyzed based on The Cancer Genome Atlas data. Next, 150 serum samples from initially treated patients with NSCLC and 70 controls were collected, and we obtained pathological sections from 60 patients with NSCLC. The ELISA and immunohistochemistry results showed the differential expression of IL-24 and carbohydrate antigen 125 (CA125). The results show that IL-24 is an important tumor suppressor in NSCLC that helps to improve the poor prognosis of these patients. A significantly negative correlation between IL-24 and CA125 levels was also found. Notably, serum IL-24 levels were significantly negatively correlated with the TNM stage of patients with NSCLC, consistent with an important role for tumor suppressors in NSCLC. The receiver operating characteristic curve analysis showed that a combination of IL-24 and CA125 was an effective panel for discriminating patients with NSCLC from HD, and individuals with other lung diseases. Serum IL-24 and CA125 levels were identified as independent prognostic markers for NSCLC. The IL-24 and CA125 panel exhibited good performance in the screening of NSCLC.

Abstract Image

血清 IL-24 与 CA125 结合作为 NSCLC 的筛查和预后生物标志物。
非小细胞肺癌(NSCLC)早期筛查的无创有效方法仍有待开发。目前,一个合理的结论是,肿瘤标志物的组合是一种更优越的筛查预测指标。细胞因子作为癌症发展的重要调控因子,在非小细胞肺癌的筛查和预后方面具有很大的潜力。本研究筛选了与 NSCLC 早期筛查和预后相关的新型生物标志物。本研究根据癌症基因组图谱数据分析了白细胞介素-24(IL-24)的生物学意义和免疫调节作用。接下来,我们收集了 150 份初步治疗的 NSCLC 患者和 70 份对照组患者的血清样本,并获得了 60 份 NSCLC 患者的病理切片。ELISA和免疫组化结果显示,IL-24和碳水化合物抗原125(CA125)的表达存在差异。结果表明,IL-24 是 NSCLC 中重要的肿瘤抑制因子,有助于改善这些患者的不良预后。研究还发现,IL-24与CA125水平呈明显负相关。值得注意的是,血清IL-24水平与NSCLC患者的TNM分期呈显著负相关,这与肿瘤抑制因子在NSCLC中的重要作用一致。接收器操作特征曲线分析表明,IL-24 和 CA125 的组合是区分 NSCLC 患者与 HD 及其他肺部疾病患者的有效面板。血清IL-24和CA125水平被确定为NSCLC的独立预后标志物。IL-24和CA125面板在筛查NSCLC方面表现出良好的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Biology International
Cell Biology International 生物-细胞生物学
CiteScore
7.60
自引率
0.00%
发文量
208
审稿时长
1 months
期刊介绍: Each month, the journal publishes easy-to-assimilate, up-to-the minute reports of experimental findings by researchers using a wide range of the latest techniques. Promoting the aims of cell biologists worldwide, papers reporting on structure and function - especially where they relate to the physiology of the whole cell - are strongly encouraged. Molecular biology is welcome, as long as articles report findings that are seen in the wider context of cell biology. In covering all areas of the cell, the journal is both appealing and accessible to a broad audience. Authors whose papers do not appeal to cell biologists in general because their topic is too specialized (e.g. infectious microbes, protozoology) are recommended to send them to more relevant journals. Papers reporting whole animal studies or work more suited to a medical journal, e.g. histopathological studies or clinical immunology, are unlikely to be accepted, unless they are fully focused on some important cellular aspect. These last remarks extend particularly to papers on cancer. Unless firmly based on some deeper cellular or molecular biological principle, papers that are highly specialized in this field, with limited appeal to cell biologists at large, should be directed towards journals devoted to cancer, there being very many from which to choose.
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