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检测sFas、sCD137和IL-27细胞因子作为肝细胞癌诊断的潜在生物标志物。

Detection of sFas, sCD137, and IL-27 Cytokines as Potential Biomarkers for Hepatocellular Carcinoma Diagnosis.

作者信息

Do Xuan-Hai, Le Mai Thi, Nguyen Thu Huyen, Le Thanh Thien, Nguyen Xuan-Hung, Mai Thanh Binh, Hoang Thi My Nhung, Than Uyen Thi Trang

机构信息

Department of Practical and Experimental Surgery, Vietnam Military Medical University, Hanoi, Vietnam.

Center of Applied Sciences, Regenerative Medicine and Advance Technologies, Vinmec Healthcare System, Hanoi, Vietnam.

出版信息

J Hepatocell Carcinoma. 2023 May 26;10:783-793. doi: 10.2147/JHC.S409649. eCollection 2023.

Abstract

PURPOSE

Hepatocellular carcinoma (HCC), a prevalent type of liver cancer, is mainly diagnosed in the advanced stage, leading to a high mortality rate. Recent advances have identified peripheral cytokines as a potential tool to predict disease outcomes and inform therapeutic decisions. Hence, in this study, we aim to build a predictive model for HCC based on serum levels of different cytokines.

PATIENTS AND METHODS

We used immunoassay to quantify the concentrations of IL-27, MIP-1β, Perforin, sCD137, sFas, and TNF-α in the serum of 38 HCC patients and 15 healthy controls. Logistic regression was then used to construct classification models detecting HCC based on these cytokines. A nomogram of the best-performing model was generated to visualize HCC prediction.

RESULTS

sFas and MIP-1β were found to be significantly higher in HCC patients compared to controls. Predictive models based on cytokine levels combining sFas, sCD137, and IL-27 performed the best in distinguishing HCC patients from healthy controls. This model has a bias-corrected area under the receiver operating characteristic (ROC) curve (AUC) of 0.948, a sensitivity of 92.11%, a specificity of 93.33%, and an accuracy of 0.925.

CONCLUSION

Our findings suggest that serum cytokines have the potential to be utilized in HCC screening to improve detection rates.

摘要

目的

肝细胞癌(HCC)是一种常见的肝癌类型,主要在晚期被诊断出来,导致高死亡率。最近的进展已将外周细胞因子确定为预测疾病预后和指导治疗决策的潜在工具。因此,在本研究中,我们旨在基于不同细胞因子的血清水平建立HCC预测模型。

患者与方法

我们使用免疫测定法对38例HCC患者和15名健康对照者血清中的IL-27、MIP-1β、穿孔素、sCD137、sFas和TNF-α浓度进行定量。然后使用逻辑回归基于这些细胞因子构建检测HCC的分类模型。生成表现最佳模型的列线图以可视化HCC预测。

结果

发现HCC患者的sFas和MIP-1β明显高于对照组。基于细胞因子水平结合sFas、sCD137和IL-27的预测模型在区分HCC患者和健康对照方面表现最佳。该模型在受试者工作特征(ROC)曲线下的偏差校正面积(AUC)为0.948,灵敏度为92.11%,特异性为93.33%,准确性为0.925。

结论

我们的研究结果表明,血清细胞因子有可能用于HCC筛查以提高检出率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eb3/10228584/a96493d8b544/JHC-10-783-g0001.jpg

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