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一种用于大规模鉴定食管癌相关基因的计算方法。

A computational method for large-scale identification of esophageal cancer-related genes.

作者信息

He Xin, Li Wei-Song, Qiu Zhen-Gang, Zhang Lei, Long He-Ming, Zhang Gui-Sheng, Huang Yang-Wen, Zhan Yun-Mei, Meng Fan

机构信息

Department of Respiratory and Critical Care, The First Affiliated Hospital of Gannan Medical University, Ganzhou, China.

Department of pathology, The First Affiliated Hospital of Gannan Medical University, Ganzhou, China.

出版信息

Front Oncol. 2022 Aug 16;12:982641. doi: 10.3389/fonc.2022.982641. eCollection 2022.

DOI:10.3389/fonc.2022.982641
PMID:36052230
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9425068/
Abstract

The incidence of esophageal cancer has obvious genetic susceptibility. Identifying esophageal cancer-related genes plays a huge role in the prevention and treatment of esophageal cancer. Through various sequencing methods, researchers have found only a small number of genes associated with esophageal cancer. In order to improve the efficiency of esophageal cancer genetic susceptibility research, this paper proposes a method for large-scale identification of esophageal cancer-related genes by computational methods. In order to improve the efficiency of esophageal cancer genetic susceptibility research, this paper proposes a method for large-scale identification of esophageal cancer-related genes by computational methods. This method fuses graph convolutional network and logical matrix factorization to effectively identify esophageal cancer-related genes through the association between genes. We call this method GCNLMF which achieved AUC as 0.927 and AUPR as 0.86. Compared with other five methods, GCNLMF performed best. We conducted a case study of the top three predicted genes. Although the association of these three genes with esophageal cancer has not been reported in the database, studies by other reseachers have shown that these three genes are significantly associated with esophageal cancer, which illustrates the accuracy of the prediction results of GCNLMF.

摘要

食管癌的发病率具有明显的遗传易感性。识别与食管癌相关的基因在食管癌的防治中发挥着巨大作用。通过各种测序方法,研究人员仅发现了少数与食管癌相关的基因。为了提高食管癌遗传易感性研究的效率,本文提出了一种通过计算方法大规模识别食管癌相关基因的方法。为了提高食管癌遗传易感性研究的效率,本文提出了一种通过计算方法大规模识别食管癌相关基因的方法。该方法融合了图卷积网络和逻辑矩阵分解,通过基因之间的关联有效地识别食管癌相关基因。我们将这种方法称为GCNLMF,其AUC为0.927,AUPR为0.86。与其他五种方法相比,GCNLMF表现最佳。我们对预测排名前三的基因进行了案例研究。虽然数据库中尚未报道这三个基因与食管癌的关联,但其他研究人员的研究表明这三个基因与食管癌显著相关,这说明了GCNLMF预测结果的准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6fc/9425068/ffb598c228fd/fonc-12-982641-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6fc/9425068/cdd56f24f799/fonc-12-982641-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6fc/9425068/5e34fe0d0464/fonc-12-982641-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6fc/9425068/a4d61f6e9167/fonc-12-982641-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6fc/9425068/ffb598c228fd/fonc-12-982641-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6fc/9425068/cdd56f24f799/fonc-12-982641-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6fc/9425068/5e34fe0d0464/fonc-12-982641-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6fc/9425068/a4d61f6e9167/fonc-12-982641-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6fc/9425068/ffb598c228fd/fonc-12-982641-g004.jpg

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本文引用的文献

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ETV5 overexpression promotes progression of esophageal squamous cell carcinoma by upregulating SKA1 and TRPV2.ETV5 过表达通过上调 SKA1 和 TRPV2 促进食管鳞癌细胞的进展。
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Actual Sarcopenia Reflects Poor Prognosis in Patients with Esophageal Cancer.
实际的肌肉减少症反映了食管癌患者的预后不良。
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Modern Diagnosis of Early Esophageal Cancer: From Blood Biomarkers to Advanced Endoscopy and Artificial Intelligence.早期食管癌的现代诊断:从血液生物标志物到先进的内镜检查与人工智能
Cancers (Basel). 2021 Jun 24;13(13):3162. doi: 10.3390/cancers13133162.
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V-Raf murine sarcoma viral oncogene homolog B1 (BRAF) as a prognostic biomarker of poor outcomes in esophageal cancer patients.V-Raf 鼠肉瘤病毒癌基因同源物 B1(BRAF)作为食管癌患者预后不良的生物标志物。
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