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Validated limited gene predictor for cervical cancer lymph node metastases

Purpose: Recognizing the prognostic significance of lymph node (LN) involvement for cervical cancer, we aimed to identify genes that are differentially expressed in LN+ versus LN- cervical cancer and to potentially create a validated predictive gene signature for LN involvement. Materials and Method...

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Autores principales: Bloomstein, Joshua D., von Eyben, Rie, Chan, Andy, Rankin, Erinn B., Fregoso, Daniel R., Wang-Chiang, Jing, Lee, Lisa, Xie, Liang-Xi, David, Shannon MacLaughlan, Stehr, Henning, Esfahani, Mohammad S., Giaccia, Amato J., Kidd, Elizabeth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299532/
https://www.ncbi.nlm.nih.gov/pubmed/32595829
http://dx.doi.org/10.18632/oncotarget.27632
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author Bloomstein, Joshua D.
von Eyben, Rie
Chan, Andy
Rankin, Erinn B.
Fregoso, Daniel R.
Wang-Chiang, Jing
Lee, Lisa
Xie, Liang-Xi
David, Shannon MacLaughlan
Stehr, Henning
Esfahani, Mohammad S.
Giaccia, Amato J.
Kidd, Elizabeth A.
author_facet Bloomstein, Joshua D.
von Eyben, Rie
Chan, Andy
Rankin, Erinn B.
Fregoso, Daniel R.
Wang-Chiang, Jing
Lee, Lisa
Xie, Liang-Xi
David, Shannon MacLaughlan
Stehr, Henning
Esfahani, Mohammad S.
Giaccia, Amato J.
Kidd, Elizabeth A.
author_sort Bloomstein, Joshua D.
collection PubMed
description Purpose: Recognizing the prognostic significance of lymph node (LN) involvement for cervical cancer, we aimed to identify genes that are differentially expressed in LN+ versus LN- cervical cancer and to potentially create a validated predictive gene signature for LN involvement. Materials and Methods: Primary tumor biopsies were collected from 74 cervical cancer patients. RNA was extracted and RNA sequencing was performed. The samples were divided by institution into a training set (n = 57) and a testing set (n = 17). Differentially expressed genes were identified among the training cohort and used to train a Random Forest classifier. Results: 22 genes showed > 1.5 fold difference in expression between the LN+ and LN- groups. Using forward selection 5 genes were identified and, based on the clinical knowledge of these genes and testing of the different combinations, a 2-gene Random Forest model of BIRC3 and CD300LG was developed. The classification accuracy of lymph node (LN) status on the test set was 88.2%, with an Area under the Receiver Operating Characteristic curve (ROC-AUC) of 98.6%. Conclusions: We identified a 2 gene Random Forest model of BIRC3 and CD300LG that predicted lymph node involvement in a validation cohort. This validated model, following testing in additional cohorts, could be used to create a reverse transcription-quantitative polymerase chain reaction (RT-qPCR) tool that would be useful for helping to identify patients with LN involvement in resource-limited settings.
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spelling pubmed-72995322020-06-25 Validated limited gene predictor for cervical cancer lymph node metastases Bloomstein, Joshua D. von Eyben, Rie Chan, Andy Rankin, Erinn B. Fregoso, Daniel R. Wang-Chiang, Jing Lee, Lisa Xie, Liang-Xi David, Shannon MacLaughlan Stehr, Henning Esfahani, Mohammad S. Giaccia, Amato J. Kidd, Elizabeth A. Oncotarget Research Paper Purpose: Recognizing the prognostic significance of lymph node (LN) involvement for cervical cancer, we aimed to identify genes that are differentially expressed in LN+ versus LN- cervical cancer and to potentially create a validated predictive gene signature for LN involvement. Materials and Methods: Primary tumor biopsies were collected from 74 cervical cancer patients. RNA was extracted and RNA sequencing was performed. The samples were divided by institution into a training set (n = 57) and a testing set (n = 17). Differentially expressed genes were identified among the training cohort and used to train a Random Forest classifier. Results: 22 genes showed > 1.5 fold difference in expression between the LN+ and LN- groups. Using forward selection 5 genes were identified and, based on the clinical knowledge of these genes and testing of the different combinations, a 2-gene Random Forest model of BIRC3 and CD300LG was developed. The classification accuracy of lymph node (LN) status on the test set was 88.2%, with an Area under the Receiver Operating Characteristic curve (ROC-AUC) of 98.6%. Conclusions: We identified a 2 gene Random Forest model of BIRC3 and CD300LG that predicted lymph node involvement in a validation cohort. This validated model, following testing in additional cohorts, could be used to create a reverse transcription-quantitative polymerase chain reaction (RT-qPCR) tool that would be useful for helping to identify patients with LN involvement in resource-limited settings. Impact Journals LLC 2020-06-16 /pmc/articles/PMC7299532/ /pubmed/32595829 http://dx.doi.org/10.18632/oncotarget.27632 Text en http://creativecommons.org/licenses/by/3.0/ Copyright: Bloomstein et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Bloomstein, Joshua D.
von Eyben, Rie
Chan, Andy
Rankin, Erinn B.
Fregoso, Daniel R.
Wang-Chiang, Jing
Lee, Lisa
Xie, Liang-Xi
David, Shannon MacLaughlan
Stehr, Henning
Esfahani, Mohammad S.
Giaccia, Amato J.
Kidd, Elizabeth A.
Validated limited gene predictor for cervical cancer lymph node metastases
title Validated limited gene predictor for cervical cancer lymph node metastases
title_full Validated limited gene predictor for cervical cancer lymph node metastases
title_fullStr Validated limited gene predictor for cervical cancer lymph node metastases
title_full_unstemmed Validated limited gene predictor for cervical cancer lymph node metastases
title_short Validated limited gene predictor for cervical cancer lymph node metastases
title_sort validated limited gene predictor for cervical cancer lymph node metastases
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299532/
https://www.ncbi.nlm.nih.gov/pubmed/32595829
http://dx.doi.org/10.18632/oncotarget.27632
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