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RNF213 gene mutation in circulating tumor DNA detected by targeted next‐generation sequencing in the assisted discrimination of early‐stage lung cancer from pulmonary nodules

BACKGROUND: To distinguish early‐stage lung cancer from benign disease in pulmonary nodules, especially lesions with ground‐glass opacity (GGO), we assessed gene mutations of ctDNA in peripheral blood using targeted next‐generation sequencing (NGS). METHODS: Single pulmonary nodule patients without...

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Autores principales: Jiang, Ning, Zhou, Jie, Zhang, Wenhao, Li, Peichao, Liu, Yu, Shi, Hubo, Zhang, Chengke, Wang, Yunshan, Zhou, Chengjun, Peng, Chuanliang, Zhang, Weiquan, Hao, Yingtao, Sun, Qifeng, Li, Yuliang, Zhao, Xiaogang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812078/
https://www.ncbi.nlm.nih.gov/pubmed/33200540
http://dx.doi.org/10.1111/1759-7714.13741
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author Jiang, Ning
Zhou, Jie
Zhang, Wenhao
Li, Peichao
Liu, Yu
Shi, Hubo
Zhang, Chengke
Wang, Yunshan
Zhou, Chengjun
Peng, Chuanliang
Zhang, Weiquan
Hao, Yingtao
Sun, Qifeng
Li, Yuliang
Zhao, Xiaogang
author_facet Jiang, Ning
Zhou, Jie
Zhang, Wenhao
Li, Peichao
Liu, Yu
Shi, Hubo
Zhang, Chengke
Wang, Yunshan
Zhou, Chengjun
Peng, Chuanliang
Zhang, Weiquan
Hao, Yingtao
Sun, Qifeng
Li, Yuliang
Zhao, Xiaogang
author_sort Jiang, Ning
collection PubMed
description BACKGROUND: To distinguish early‐stage lung cancer from benign disease in pulmonary nodules, especially lesions with ground‐glass opacity (GGO), we assessed gene mutations of ctDNA in peripheral blood using targeted next‐generation sequencing (NGS). METHODS: Single pulmonary nodule patients without mediastinal lymph nodes and symptoms that were hard to diagnose by chest CT and lung cancer biomarker measurement in multiple medical centers were enrolled into the study. All patients accepted minimally invasive surgery but refused preoperative biopsy. Gene mutations in preoperative blood samples were detected by targeted NGS. Mutations with significant differences between lung tumors and benign lesions, as grouped by postoperative pathology, were screened. Protein expression was determined by immunohistochemistry. Highly expressed genes were selected as biomarkers to verify the mutations in peripheral blood. RESULTS: In the training set, the RNF213, KMT2D, CSMD3 and LRP1B genes were mutated more frequently in early‐stage lung cancer (27 cases) than in benign nodules (15 cases) (P < 0.05). High expression of the RNF213 gene in lung cancers and low expression in benign diseases were seen by immunohistochemistry. The RNF213 gene was mutated in 25% of lung cancer samples in the validation set of 28 samples and showed high specificity (100%). In GGO patients, RNF213 was mutated more frequently in early‐stage lung cancer compared to benign diseases (P < 0.05). CONCLUSIONS: RNF213 gene mutations were observed more frequently in early‐stage lung cancer, but not in benign nodules. Mutation of the RNF213 gene in peripheral blood may be a high specificity biomarker for the assisted early diagnosis of lung cancer in pulmonary nodules. KEY POINTS: Significant findings of the study: In peripheral venous blood and tumor tissue, RNF213 gene mutated more frequently in lung cancer than benign pulmonary nodules. What this study adds: Detection mutation of the RNF213 gene in peripheral blood may be a high specificity method for the assisted early diagnosis of lung cancer in pulmonary nodules.
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spelling pubmed-78120782021-01-22 RNF213 gene mutation in circulating tumor DNA detected by targeted next‐generation sequencing in the assisted discrimination of early‐stage lung cancer from pulmonary nodules Jiang, Ning Zhou, Jie Zhang, Wenhao Li, Peichao Liu, Yu Shi, Hubo Zhang, Chengke Wang, Yunshan Zhou, Chengjun Peng, Chuanliang Zhang, Weiquan Hao, Yingtao Sun, Qifeng Li, Yuliang Zhao, Xiaogang Thorac Cancer Original Articles BACKGROUND: To distinguish early‐stage lung cancer from benign disease in pulmonary nodules, especially lesions with ground‐glass opacity (GGO), we assessed gene mutations of ctDNA in peripheral blood using targeted next‐generation sequencing (NGS). METHODS: Single pulmonary nodule patients without mediastinal lymph nodes and symptoms that were hard to diagnose by chest CT and lung cancer biomarker measurement in multiple medical centers were enrolled into the study. All patients accepted minimally invasive surgery but refused preoperative biopsy. Gene mutations in preoperative blood samples were detected by targeted NGS. Mutations with significant differences between lung tumors and benign lesions, as grouped by postoperative pathology, were screened. Protein expression was determined by immunohistochemistry. Highly expressed genes were selected as biomarkers to verify the mutations in peripheral blood. RESULTS: In the training set, the RNF213, KMT2D, CSMD3 and LRP1B genes were mutated more frequently in early‐stage lung cancer (27 cases) than in benign nodules (15 cases) (P < 0.05). High expression of the RNF213 gene in lung cancers and low expression in benign diseases were seen by immunohistochemistry. The RNF213 gene was mutated in 25% of lung cancer samples in the validation set of 28 samples and showed high specificity (100%). In GGO patients, RNF213 was mutated more frequently in early‐stage lung cancer compared to benign diseases (P < 0.05). CONCLUSIONS: RNF213 gene mutations were observed more frequently in early‐stage lung cancer, but not in benign nodules. Mutation of the RNF213 gene in peripheral blood may be a high specificity biomarker for the assisted early diagnosis of lung cancer in pulmonary nodules. KEY POINTS: Significant findings of the study: In peripheral venous blood and tumor tissue, RNF213 gene mutated more frequently in lung cancer than benign pulmonary nodules. What this study adds: Detection mutation of the RNF213 gene in peripheral blood may be a high specificity method for the assisted early diagnosis of lung cancer in pulmonary nodules. John Wiley & Sons Australia, Ltd 2020-11-16 2021-01 /pmc/articles/PMC7812078/ /pubmed/33200540 http://dx.doi.org/10.1111/1759-7714.13741 Text en © 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, 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 Original Articles
Jiang, Ning
Zhou, Jie
Zhang, Wenhao
Li, Peichao
Liu, Yu
Shi, Hubo
Zhang, Chengke
Wang, Yunshan
Zhou, Chengjun
Peng, Chuanliang
Zhang, Weiquan
Hao, Yingtao
Sun, Qifeng
Li, Yuliang
Zhao, Xiaogang
RNF213 gene mutation in circulating tumor DNA detected by targeted next‐generation sequencing in the assisted discrimination of early‐stage lung cancer from pulmonary nodules
title RNF213 gene mutation in circulating tumor DNA detected by targeted next‐generation sequencing in the assisted discrimination of early‐stage lung cancer from pulmonary nodules
title_full RNF213 gene mutation in circulating tumor DNA detected by targeted next‐generation sequencing in the assisted discrimination of early‐stage lung cancer from pulmonary nodules
title_fullStr RNF213 gene mutation in circulating tumor DNA detected by targeted next‐generation sequencing in the assisted discrimination of early‐stage lung cancer from pulmonary nodules
title_full_unstemmed RNF213 gene mutation in circulating tumor DNA detected by targeted next‐generation sequencing in the assisted discrimination of early‐stage lung cancer from pulmonary nodules
title_short RNF213 gene mutation in circulating tumor DNA detected by targeted next‐generation sequencing in the assisted discrimination of early‐stage lung cancer from pulmonary nodules
title_sort rnf213 gene mutation in circulating tumor dna detected by targeted next‐generation sequencing in the assisted discrimination of early‐stage lung cancer from pulmonary nodules
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812078/
https://www.ncbi.nlm.nih.gov/pubmed/33200540
http://dx.doi.org/10.1111/1759-7714.13741
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