A stable gene set for prediction of prognosis and efficacy of chemotherapy in gastric cancer

Abstract Background Gastric cancer (GC) is a primary reason for cancer death in the world. At present, GC has become a public health issue urgently to be solved to. Prediction of prognosis is critical to the development of clinical treatment regimens. This work aimed to construct the stable gene set...

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Main Authors: Rui Wu, Sixuan Guo, Shuhui Lai, Guixing Pan, Linyi Zhang, Huanbing Liu
Format: Article
Language:English
Published: BMC 2021-06-01
Series:BMC Cancer
Subjects:
Online Access:https://doi.org/10.1186/s12885-021-08444-w
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spelling doaj-dadcea53e1ea4c40a6c24dd44f018d362021-06-13T11:55:09ZengBMCBMC Cancer1471-24072021-06-0121111210.1186/s12885-021-08444-wA stable gene set for prediction of prognosis and efficacy of chemotherapy in gastric cancerRui Wu0Sixuan Guo1Shuhui Lai2Guixing Pan3Linyi Zhang4Huanbing Liu5The First Affiliated Hospital of Nanchang UniversityThe Second Clinical College, Medical College of Nanchang UniversityThe First Clinical College, Medical College of Nanchang UniversityShangrao Maternity and Child Care HospitalSchool of Ophthalmology & Optometry, Nanchang UniversityThe First Affiliated Hospital of Nanchang UniversityAbstract Background Gastric cancer (GC) is a primary reason for cancer death in the world. At present, GC has become a public health issue urgently to be solved to. Prediction of prognosis is critical to the development of clinical treatment regimens. This work aimed to construct the stable gene set for guiding GC diagnosis and treatment in clinic. Methods A public microarray dataset of TCGA providing clinical information was obtained. Dimensionality reduction was carried out by selection operator regression on the stable prognostic genes discovered through the bootstrap approach as well as survival analysis. Findings A total of 2 prognostic models were built, respectively designated as stable gene risk scores of OS (SGRS-OS) and stable gene risk scores of PFI (SGRS-PFI) consisting of 18 and 21 genes. The SGRS set potently predicted the overall survival (OS) along with progression-free interval (PFI) by means of univariate as well as multivariate analysis, using the specific risk scores formula. Relative to the TNM classification system, the SGRS set exhibited apparently higher predicting ability. Moreover, it was suggested that, patients who had increased SGRS were associated with poor chemotherapeutic outcomes. Interpretation The SGRS set constructed in this study potentially serves as the efficient approach for predicting GC patient survival and guiding their treatment.https://doi.org/10.1186/s12885-021-08444-wGastric cancerMolecular typingPrognosisPrediction of efficacy of chemotherapyImmune infiltration
collection DOAJ
language English
format Article
sources DOAJ
author Rui Wu
Sixuan Guo
Shuhui Lai
Guixing Pan
Linyi Zhang
Huanbing Liu
spellingShingle Rui Wu
Sixuan Guo
Shuhui Lai
Guixing Pan
Linyi Zhang
Huanbing Liu
A stable gene set for prediction of prognosis and efficacy of chemotherapy in gastric cancer
BMC Cancer
Gastric cancer
Molecular typing
Prognosis
Prediction of efficacy of chemotherapy
Immune infiltration
author_facet Rui Wu
Sixuan Guo
Shuhui Lai
Guixing Pan
Linyi Zhang
Huanbing Liu
author_sort Rui Wu
title A stable gene set for prediction of prognosis and efficacy of chemotherapy in gastric cancer
title_short A stable gene set for prediction of prognosis and efficacy of chemotherapy in gastric cancer
title_full A stable gene set for prediction of prognosis and efficacy of chemotherapy in gastric cancer
title_fullStr A stable gene set for prediction of prognosis and efficacy of chemotherapy in gastric cancer
title_full_unstemmed A stable gene set for prediction of prognosis and efficacy of chemotherapy in gastric cancer
title_sort stable gene set for prediction of prognosis and efficacy of chemotherapy in gastric cancer
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2021-06-01
description Abstract Background Gastric cancer (GC) is a primary reason for cancer death in the world. At present, GC has become a public health issue urgently to be solved to. Prediction of prognosis is critical to the development of clinical treatment regimens. This work aimed to construct the stable gene set for guiding GC diagnosis and treatment in clinic. Methods A public microarray dataset of TCGA providing clinical information was obtained. Dimensionality reduction was carried out by selection operator regression on the stable prognostic genes discovered through the bootstrap approach as well as survival analysis. Findings A total of 2 prognostic models were built, respectively designated as stable gene risk scores of OS (SGRS-OS) and stable gene risk scores of PFI (SGRS-PFI) consisting of 18 and 21 genes. The SGRS set potently predicted the overall survival (OS) along with progression-free interval (PFI) by means of univariate as well as multivariate analysis, using the specific risk scores formula. Relative to the TNM classification system, the SGRS set exhibited apparently higher predicting ability. Moreover, it was suggested that, patients who had increased SGRS were associated with poor chemotherapeutic outcomes. Interpretation The SGRS set constructed in this study potentially serves as the efficient approach for predicting GC patient survival and guiding their treatment.
topic Gastric cancer
Molecular typing
Prognosis
Prediction of efficacy of chemotherapy
Immune infiltration
url https://doi.org/10.1186/s12885-021-08444-w
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