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新型可视化定量表观遗传印记基因生物标志物可诊断十种癌症的恶性程度。

Novel visualized quantitative epigenetic imprinted gene biomarkers diagnose the malignancy of ten cancer types.

机构信息

Department of Pathology, Ohio State University Wexner Medical Center, Columbus, OH, 43210, USA.

Epigenetics Lab, Chinese Alliance Against Lung Cancer, 6th Floor, Building 5, No.66, Jinghuidongdao Road, Wuxi, 214135, Jiangsu, China.

出版信息

Clin Epigenetics. 2020 May 24;12(1):71. doi: 10.1186/s13148-020-00861-1.

Abstract

BACKGROUND

Epigenetic alterations are involved in most cancers, but its application in cancer diagnosis is still limited. More practical and intuitive methods to detect the aberrant expressions from clinical samples using highly sensitive biomarkers are needed. In this study, we developed a novel approach in identifying, visualizing, and quantifying the biallelic and multiallelic expressions of an imprinted gene panel associated with cancer status. We evaluated the normal and aberrant expressions measured using the imprinted gene panel to formulate diagnostic models which could accurately distinguish the imprinting differences of normal and benign cases from cancerous tissues for each of the ten cancer types.

RESULTS

The Quantitative Chromogenic Imprinted Gene In Situ Hybridization (QCIGISH) method developed from a 1013-case study which provides a visual and quantitative analysis of non-coding RNA allelic expressions identified the guanine nucleotide-binding protein, alpha-stimulating complex locus (GNAS), growth factor receptor-bound protein (GRB10), and small nuclear ribonucleoprotein polypeptide N (SNRPN) out of five tested imprinted genes as efficient epigenetic biomarkers for the early-stage detection of ten cancer types. A binary algorithm developed for cancer diagnosis showed that elevated biallelic expression (BAE), multiallelic expression (MAE), and total expression (TE) measurements for the imprinted gene panel were associated with cell carcinogenesis, with the formulated diagnostic models achieving consistently high sensitivities (91-98%) and specificities (86-98%) across the different cancer types.

CONCLUSIONS

The QCIGISH method provides an innovative way to visually assess and quantitatively analyze individual cells for cancer potential extending from hyperplasia and dysplasia until carcinoma in situ and invasion, which effectively supplements standard clinical cytologic and histopathologic diagnosis for early cancer detection. In addition, the diagnostic models developed from the BAE, MAE, and TE measurements of the imprinted gene panel GNAS, GRB10, and SNRPN could provide important predictive information which are useful in early-stage cancer detection and personalized cancer management.

摘要

背景

表观遗传改变涉及大多数癌症,但在癌症诊断中的应用仍然有限。需要使用高度敏感的生物标志物从临床样本中检测异常表达的更实用和直观的方法。在这项研究中,我们开发了一种新方法,用于识别、可视化和量化与癌症状态相关的印迹基因panel 的双等位基因和多等位基因表达。我们评估了使用印迹基因panel 测量的正常和异常表达,以制定诊断模型,这些模型可以准确地区分正常和良性病例与每种十种癌症类型的癌症组织之间的印迹差异。

结果

从 1013 例研究中开发的定量显色印迹基因原位杂交 (QCIGISH) 方法提供了非编码 RNA 等位基因表达的可视化和定量分析,鉴定出鸟嘌呤核苷酸结合蛋白、α-刺激复合物基因座 (GNAS)、生长因子受体结合蛋白 (GRB10) 和小核核糖核蛋白多肽 N (SNRPN) 作为五种测试印迹基因中的有效表观遗传生物标志物,用于十种癌症类型的早期检测。为癌症诊断开发的二进制算法表明,印迹基因panel 的双等位基因表达 (BAE)、多等位基因表达 (MAE) 和总表达 (TE) 测量与细胞癌变相关,所制定的诊断模型在不同癌症类型中均具有一致的高敏感性 (91-98%) 和特异性 (86-98%)。

结论

QCIGISH 方法提供了一种创新的方法,可以直观地评估和定量分析具有癌症潜力的单个细胞,从增生和发育不良到原位癌和浸润,有效地补充了标准的临床细胞学和组织病理学诊断,用于早期癌症检测。此外,从印迹基因panel GNAS、GRB10 和 SNRPN 的 BAE、MAE 和 TE 测量开发的诊断模型可以提供重要的预测信息,这些信息对于早期癌症检测和个性化癌症管理非常有用。

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