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循环无细胞 circRNA panel 预测结直肠癌的发生和发展。

Circulating cell-free circRNA panel predicted tumorigenesis and development of colorectal cancer.

机构信息

Department of Gastroenterology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.

Department of Gastroenterology, The Fourth Affiliated Hospital of Anhui Medical University, Hefei, China.

出版信息

J Clin Lab Anal. 2022 May;36(5):e24431. doi: 10.1002/jcla.24431. Epub 2022 Apr 14.

Abstract

BACKGROUND

Colorectal cancer (CRC) is reported with high morbidity and mortality. Currently, the sensitivity of diagnostic markers for colorectal cancer is low. Therefore, further exploration of new plasma diagnostic markers for early detection of colorectal cancer is of great value. We aimed to explore potential circRNAs in plasma as biomarkers for early diagnosis of CRC.

METHODS

We employed the circRNA microarray to investigate dysregulated circRNAs in plasma samples of CRC patients, colorectal adenoma patients (CRA), and healthy controls. Through in-depth analysis, significantly differentially expressed circRNAs were screened as candidate targets.

RESULTS

Eight circRNAs (hsa_circ_104885, hsa_circ_100185, hsa_circ_103171, hsa_circ_001978, hsa_circ_105039, hsa_circ_103627, hsa_circ_101717, and hsa_circ_104192) were obtained as candidate circRNAs with upregulation in CRC comparing with both CRA and healthy control. Through detecting the plasma expression levels of eight candidate targets, we identified three circRNA (hsa_circ_001978, hsa_circ_105039, and hsa_circ_103627) with increased level which were consistent with the microarray results in training set. Further validation found the circRNA panel was consistent with training set. The ROC curve also revealed a high diagnostic ability of hsa_circ_001978, hsa_circ_105039, and hsa_circ_103627 in predicted the CRC from CRA patients (AUC = 0.966) as well as healthy controls (AUC = 0.969).

CONCLUSION

Our data suggest that hsa_circ_001978, hsa_circ_105039, and hsa_circ_103627 might be a CRC-specific biomarker for early diagnosis.

摘要

背景

结直肠癌(CRC)发病率和死亡率均较高。目前,用于结直肠癌诊断的标记物的敏感性较低。因此,进一步探索用于早期检测结直肠癌的新型血浆诊断标记物具有重要价值。本研究旨在探索血浆中潜在的 circRNA 作为 CRC 早期诊断的生物标志物。

方法

我们采用 circRNA 微阵列分析 CRC 患者、结直肠腺瘤患者(CRA)和健康对照者的血浆样本中失调的 circRNA。通过深入分析,筛选出差异显著的 circRNA 作为候选靶标。

结果

与 CRA 和健康对照组相比,CRC 患者的血浆中有 8 个 circRNA(hsa_circ_104885、hsa_circ_100185、hsa_circ_103171、hsa_circ_001978、hsa_circ_105039、hsa_circ_103627、hsa_circ_101717 和 hsa_circ_104192)表达上调,被确定为候选 circRNA。通过检测 8 个候选靶标的血浆表达水平,我们发现 3 个 circRNA(hsa_circ_001978、hsa_circ_105039 和 hsa_circ_103627)的水平升高,与训练集的微阵列结果一致。进一步验证发现 circRNA 谱与训练集一致。ROC 曲线也显示 hsa_circ_001978、hsa_circ_105039 和 hsa_circ_103627 对预测 CRC 患者(AUC=0.966)和健康对照者(AUC=0.969)具有较高的诊断能力。

结论

本研究数据表明,hsa_circ_001978、hsa_circ_105039 和 hsa_circ_103627 可能是用于早期诊断 CRC 的特异性生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f70/9102498/e70536460ffa/JCLA-36-e24431-g007.jpg

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