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CT-based machine learning radiomics predicts CCR5 expression level and survival in ovarian cancer
OBJECTIVE: We aimed to evaluate the prognostic value of C-C motif chemokine receptor type 5 (CCR5) expression level for patients with ovarian cancer and to establish a radiomics model that can predict CCR5 expression level using The Cancer Imaging Archive (TCIA) and The Cancer Genome Atlas (TCGA) da...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9809527/ https://www.ncbi.nlm.nih.gov/pubmed/36597144 http://dx.doi.org/10.1186/s13048-022-01089-8 |
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author | Wan, Sheng Zhou, Tianfan Che, Ronghua Li, Ying Peng, Jing Wu, Yuelin Gu, Shengyi Cheng, Jiejun Hua, Xiaolin |
author_facet | Wan, Sheng Zhou, Tianfan Che, Ronghua Li, Ying Peng, Jing Wu, Yuelin Gu, Shengyi Cheng, Jiejun Hua, Xiaolin |
author_sort | Wan, Sheng |
collection | PubMed |
description | OBJECTIVE: We aimed to evaluate the prognostic value of C-C motif chemokine receptor type 5 (CCR5) expression level for patients with ovarian cancer and to establish a radiomics model that can predict CCR5 expression level using The Cancer Imaging Archive (TCIA) and The Cancer Genome Atlas (TCGA) database. METHODS: A total of 343 cases of ovarian cancer from the TCGA were used for the gene-based prognostic analysis. Fifty seven cases had preoperative computed tomography (CT) images stored in TCIA with genomic data in TCGA were used for radiomics feature extraction and model construction. 89 cases with both TCGA and TCIA clinical data were used for radiomics model evaluation. After feature extraction, a radiomics signature was constructed using the least absolute shrinkage and selection operator (LASSO) regression analysis. A prognostic scoring system incorporating radiomics signature based on CCR5 expression level and clinicopathologic risk factors was proposed for survival prediction. RESULTS: CCR5 was identified as a differentially expressed prognosis-related gene in tumor and normal sample, which were involved in the regulation of immune response and tumor invasion and metastasis. Four optimal radiomics features were selected to predict overall survival. The performance of the radiomics model for predicting the CCR5 expression level with 10-fold cross- validation achieved Area Under Curve (AUCs) of 0.770 and of 0.726, respectively, in the training and validation sets. A predictive nomogram was generated based on the total risk score of each patient, the AUCs of the time-dependent receiver operating characteristic (ROC) curve of the model was 0.8, 0.673 and 0.792 for 1-year, 3-year and 5-year, respectively. Along with clinical features, important imaging biomarkers could improve the overall survival accuracy of the prediction model. CONCLUSION: The expression levels of CCR5 can affect the prognosis of patients with ovarian cancer. CT-based radiomics could serve as a new tool for prognosis prediction. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13048-022-01089-8. |
format | Online Article Text |
id | pubmed-9809527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98095272023-01-04 CT-based machine learning radiomics predicts CCR5 expression level and survival in ovarian cancer Wan, Sheng Zhou, Tianfan Che, Ronghua Li, Ying Peng, Jing Wu, Yuelin Gu, Shengyi Cheng, Jiejun Hua, Xiaolin J Ovarian Res Research OBJECTIVE: We aimed to evaluate the prognostic value of C-C motif chemokine receptor type 5 (CCR5) expression level for patients with ovarian cancer and to establish a radiomics model that can predict CCR5 expression level using The Cancer Imaging Archive (TCIA) and The Cancer Genome Atlas (TCGA) database. METHODS: A total of 343 cases of ovarian cancer from the TCGA were used for the gene-based prognostic analysis. Fifty seven cases had preoperative computed tomography (CT) images stored in TCIA with genomic data in TCGA were used for radiomics feature extraction and model construction. 89 cases with both TCGA and TCIA clinical data were used for radiomics model evaluation. After feature extraction, a radiomics signature was constructed using the least absolute shrinkage and selection operator (LASSO) regression analysis. A prognostic scoring system incorporating radiomics signature based on CCR5 expression level and clinicopathologic risk factors was proposed for survival prediction. RESULTS: CCR5 was identified as a differentially expressed prognosis-related gene in tumor and normal sample, which were involved in the regulation of immune response and tumor invasion and metastasis. Four optimal radiomics features were selected to predict overall survival. The performance of the radiomics model for predicting the CCR5 expression level with 10-fold cross- validation achieved Area Under Curve (AUCs) of 0.770 and of 0.726, respectively, in the training and validation sets. A predictive nomogram was generated based on the total risk score of each patient, the AUCs of the time-dependent receiver operating characteristic (ROC) curve of the model was 0.8, 0.673 and 0.792 for 1-year, 3-year and 5-year, respectively. Along with clinical features, important imaging biomarkers could improve the overall survival accuracy of the prediction model. CONCLUSION: The expression levels of CCR5 can affect the prognosis of patients with ovarian cancer. CT-based radiomics could serve as a new tool for prognosis prediction. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13048-022-01089-8. BioMed Central 2023-01-03 /pmc/articles/PMC9809527/ /pubmed/36597144 http://dx.doi.org/10.1186/s13048-022-01089-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wan, Sheng Zhou, Tianfan Che, Ronghua Li, Ying Peng, Jing Wu, Yuelin Gu, Shengyi Cheng, Jiejun Hua, Xiaolin CT-based machine learning radiomics predicts CCR5 expression level and survival in ovarian cancer |
title | CT-based machine learning radiomics predicts CCR5 expression level and survival in ovarian cancer |
title_full | CT-based machine learning radiomics predicts CCR5 expression level and survival in ovarian cancer |
title_fullStr | CT-based machine learning radiomics predicts CCR5 expression level and survival in ovarian cancer |
title_full_unstemmed | CT-based machine learning radiomics predicts CCR5 expression level and survival in ovarian cancer |
title_short | CT-based machine learning radiomics predicts CCR5 expression level and survival in ovarian cancer |
title_sort | ct-based machine learning radiomics predicts ccr5 expression level and survival in ovarian cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9809527/ https://www.ncbi.nlm.nih.gov/pubmed/36597144 http://dx.doi.org/10.1186/s13048-022-01089-8 |
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