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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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 |
work_keys_str_mv |
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