Cargando…
Identification of a 9‐gene prognostic signature for breast cancer
Breast cancer (BRCA) is the most common cancer among women and is the second leading cause of cancer death in women. In this study, we developed a 9‐gene prognostic signature to predict the prognosis of patients with BRCA. GSE20685, GSE42568, GSE20711, and GSE88770 were used as training sets. The Ka...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774725/ https://www.ncbi.nlm.nih.gov/pubmed/33090721 http://dx.doi.org/10.1002/cam4.3523 |
_version_ | 1783630322206769152 |
---|---|
author | Tian, Zelin Tang, Jianing Liao, Xing Yang, Qian Wu, Yumin Wu, Gaosong |
author_facet | Tian, Zelin Tang, Jianing Liao, Xing Yang, Qian Wu, Yumin Wu, Gaosong |
author_sort | Tian, Zelin |
collection | PubMed |
description | Breast cancer (BRCA) is the most common cancer among women and is the second leading cause of cancer death in women. In this study, we developed a 9‐gene prognostic signature to predict the prognosis of patients with BRCA. GSE20685, GSE42568, GSE20711, and GSE88770 were used as training sets. The Kaplan–Meier plot was constructed to assess survival differences and log‐rank test was performed to evaluate the statistical significance. The overall survival (OS) of patients in the low‐risk group was significantly higher than that in the high‐risk group. ROC analysis indicated that this 9‐gene signature shows good diagnostic efficiency both in OS and disease‐free survival (DFS). The 9‐gene signature was further validated through GSE16446, GSE7390, and TCGA‐BRCA datasets. We also established a nomogram that integrates clinicopathological features and 9‐gene signature. The analysis of the calibration plot showed that the nomogram has good prognostic performance. More convincingly, real‐time reverse transcription‐polymerase chain reaction (RT‐PCR) results indicated that the protective prognostic factors in BRCA patients were downregulated, whereas the dangerous prognostic factors were upregulated. The innovation of this article is not only constructing a prognostic gene signature, but also combining with clinical information to further establish a nomogram to better predict the survival probability of patients. It is worth mentioning that this signature also does not depend on other clinical factors or variables. |
format | Online Article Text |
id | pubmed-7774725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77747252021-01-05 Identification of a 9‐gene prognostic signature for breast cancer Tian, Zelin Tang, Jianing Liao, Xing Yang, Qian Wu, Yumin Wu, Gaosong Cancer Med Cancer Biology Breast cancer (BRCA) is the most common cancer among women and is the second leading cause of cancer death in women. In this study, we developed a 9‐gene prognostic signature to predict the prognosis of patients with BRCA. GSE20685, GSE42568, GSE20711, and GSE88770 were used as training sets. The Kaplan–Meier plot was constructed to assess survival differences and log‐rank test was performed to evaluate the statistical significance. The overall survival (OS) of patients in the low‐risk group was significantly higher than that in the high‐risk group. ROC analysis indicated that this 9‐gene signature shows good diagnostic efficiency both in OS and disease‐free survival (DFS). The 9‐gene signature was further validated through GSE16446, GSE7390, and TCGA‐BRCA datasets. We also established a nomogram that integrates clinicopathological features and 9‐gene signature. The analysis of the calibration plot showed that the nomogram has good prognostic performance. More convincingly, real‐time reverse transcription‐polymerase chain reaction (RT‐PCR) results indicated that the protective prognostic factors in BRCA patients were downregulated, whereas the dangerous prognostic factors were upregulated. The innovation of this article is not only constructing a prognostic gene signature, but also combining with clinical information to further establish a nomogram to better predict the survival probability of patients. It is worth mentioning that this signature also does not depend on other clinical factors or variables. John Wiley and Sons Inc. 2020-10-14 /pmc/articles/PMC7774725/ /pubmed/33090721 http://dx.doi.org/10.1002/cam4.3523 Text en © 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cancer Biology Tian, Zelin Tang, Jianing Liao, Xing Yang, Qian Wu, Yumin Wu, Gaosong Identification of a 9‐gene prognostic signature for breast cancer |
title | Identification of a 9‐gene prognostic signature for breast cancer |
title_full | Identification of a 9‐gene prognostic signature for breast cancer |
title_fullStr | Identification of a 9‐gene prognostic signature for breast cancer |
title_full_unstemmed | Identification of a 9‐gene prognostic signature for breast cancer |
title_short | Identification of a 9‐gene prognostic signature for breast cancer |
title_sort | identification of a 9‐gene prognostic signature for breast cancer |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774725/ https://www.ncbi.nlm.nih.gov/pubmed/33090721 http://dx.doi.org/10.1002/cam4.3523 |
work_keys_str_mv | AT tianzelin identificationofa9geneprognosticsignatureforbreastcancer AT tangjianing identificationofa9geneprognosticsignatureforbreastcancer AT liaoxing identificationofa9geneprognosticsignatureforbreastcancer AT yangqian identificationofa9geneprognosticsignatureforbreastcancer AT wuyumin identificationofa9geneprognosticsignatureforbreastcancer AT wugaosong identificationofa9geneprognosticsignatureforbreastcancer |