Novel Prognostic Biomarkers in Gastric Cancer: CGB5, MKNK2, and PAPPA2

IntroductionGastric cancer is one of the most common malignant tumors of the digestive tract. However, there are no adequate prognostic markers available for this disease. The present study used bioinformatics to identify prognostic markers for gastric cancer that would guide the clinical diagnosis...

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Main Authors: Min Qin, Zhihai Liang, Heping Qin, Yifang Huo, Qing Wu, Huiying Yang, Guodu Tang
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2021.683582/full
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author Min Qin
Zhihai Liang
Heping Qin
Yifang Huo
Qing Wu
Huiying Yang
Guodu Tang
author_facet Min Qin
Zhihai Liang
Heping Qin
Yifang Huo
Qing Wu
Huiying Yang
Guodu Tang
author_sort Min Qin
collection DOAJ
description IntroductionGastric cancer is one of the most common malignant tumors of the digestive tract. However, there are no adequate prognostic markers available for this disease. The present study used bioinformatics to identify prognostic markers for gastric cancer that would guide the clinical diagnosis and treatment of this disease.Materials and MethodsGene expression data and clinical information of gastric cancer patients along with the gene expression data of 30 healthy samples were downloaded from the TCGA database. The initial screening was performed using the WGCNA method combined with the analysis of differentially expressed genes, which was followed by univariate analysis, multivariate COX regression analysis, and Lasso regression analysis for screening the candidate genes and constructing a prognostic model for gastric cancer. Subsequently, immune cell typing was performed using CIBERSORT to analyze the expression of immune cells in each sample. Finally, we performed laboratory validation of the results of our analyses using immunohistochemical analysis.ResultsAfter five screenings, it was revealed that only three genes fulfilled all the screening requirements. The survival curves generated by the prognostic model revealed that the survival rate of the patients in the high-risk group was significantly lower compared to the patients in the low-risk group (P-value < 0.001). The immune cell component analysis revealed that the three genes were differentially associated with the corresponding immune cells (P-value < 0.05). The results of immunohistochemistry also support our analysis.ConclusionCGB5, MKNK2, and PAPPA2 may be used as novel prognostic biomarkers for gastric cancer.
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spelling doaj.art-185997c19aef4737a08524a3c27a18eb2022-12-21T18:58:04ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2021-06-011110.3389/fonc.2021.683582683582Novel Prognostic Biomarkers in Gastric Cancer: CGB5, MKNK2, and PAPPA2Min Qin0Zhihai Liang1Heping Qin2Yifang Huo3Qing Wu4Huiying Yang5Guodu Tang6The First Clinical Affiliated Hospital of Guangxi Medical University, Nanning, ChinaThe First Clinical Affiliated Hospital of Guangxi Medical University, Nanning, ChinaGastroenterology, Liuzhou People’s Hospital, Liuzhou, ChinaGastroenterology, Wuzhou Workers’ Hospital, Wuzhou, ChinaThe Second Clinical Affiliated Hospital of Guangxi Medical University, Nanning, ChinaThe First Clinical Affiliated Hospital of Guangxi Medical University, Nanning, ChinaThe First Clinical Affiliated Hospital of Guangxi Medical University, Nanning, ChinaIntroductionGastric cancer is one of the most common malignant tumors of the digestive tract. However, there are no adequate prognostic markers available for this disease. The present study used bioinformatics to identify prognostic markers for gastric cancer that would guide the clinical diagnosis and treatment of this disease.Materials and MethodsGene expression data and clinical information of gastric cancer patients along with the gene expression data of 30 healthy samples were downloaded from the TCGA database. The initial screening was performed using the WGCNA method combined with the analysis of differentially expressed genes, which was followed by univariate analysis, multivariate COX regression analysis, and Lasso regression analysis for screening the candidate genes and constructing a prognostic model for gastric cancer. Subsequently, immune cell typing was performed using CIBERSORT to analyze the expression of immune cells in each sample. Finally, we performed laboratory validation of the results of our analyses using immunohistochemical analysis.ResultsAfter five screenings, it was revealed that only three genes fulfilled all the screening requirements. The survival curves generated by the prognostic model revealed that the survival rate of the patients in the high-risk group was significantly lower compared to the patients in the low-risk group (P-value < 0.001). The immune cell component analysis revealed that the three genes were differentially associated with the corresponding immune cells (P-value < 0.05). The results of immunohistochemistry also support our analysis.ConclusionCGB5, MKNK2, and PAPPA2 may be used as novel prognostic biomarkers for gastric cancer.https://www.frontiersin.org/articles/10.3389/fonc.2021.683582/fullgastric cancerWGCNAtumor immunityLasso regressionprognostic biomarkersimmunohistochemistry
spellingShingle Min Qin
Zhihai Liang
Heping Qin
Yifang Huo
Qing Wu
Huiying Yang
Guodu Tang
Novel Prognostic Biomarkers in Gastric Cancer: CGB5, MKNK2, and PAPPA2
Frontiers in Oncology
gastric cancer
WGCNA
tumor immunity
Lasso regression
prognostic biomarkers
immunohistochemistry
title Novel Prognostic Biomarkers in Gastric Cancer: CGB5, MKNK2, and PAPPA2
title_full Novel Prognostic Biomarkers in Gastric Cancer: CGB5, MKNK2, and PAPPA2
title_fullStr Novel Prognostic Biomarkers in Gastric Cancer: CGB5, MKNK2, and PAPPA2
title_full_unstemmed Novel Prognostic Biomarkers in Gastric Cancer: CGB5, MKNK2, and PAPPA2
title_short Novel Prognostic Biomarkers in Gastric Cancer: CGB5, MKNK2, and PAPPA2
title_sort novel prognostic biomarkers in gastric cancer cgb5 mknk2 and pappa2
topic gastric cancer
WGCNA
tumor immunity
Lasso regression
prognostic biomarkers
immunohistochemistry
url https://www.frontiersin.org/articles/10.3389/fonc.2021.683582/full
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