Evidence map›Paper›PMID 33200540›Full record

ArticleThoracic cancer2021

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.

Ning Jiang, Jie Zhou, Wenhao Zhang, Peichao Li, Yu Liu, Hubo Shi, Chengke Zhang, Yunshan Wang, Chengjun Zhou, Chuanliang Peng and 5 more

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 1 country.

Ning JiangDepartment of Thoracic Surgery, The Second Hospital of Shandong University, Jinan, China.ORCID 0000-0002-4613-5029
Jie ZhouCheeloo College of Medicine, Shandong University, Jinan, China.
Wenhao ZhangCheeloo College of Medicine, Shandong University, Jinan, China.
Peichao LiCheeloo College of Medicine, Shandong University, Jinan, China.
Yu LiuDepartment of Thoracic Surgery, The 960th Hospital of People's Liberation Army of China, Jinan, China.
Hubo ShiDepartment of Thoracic Surgery, Shandong Provincial Chest Hospital, Jinan, China.
Chengke ZhangDepartment of Thoracic Surgery, The Second Hospital of Shandong University, Jinan, China.
Yunshan WangDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, China.
Chengjun ZhouPathology Department, The Second Hospital of Shandong University, Jinan, China.
Chuanliang PengDepartment of Thoracic Surgery, The Second Hospital of Shandong University, Jinan, China.ORCID 0000-0003-2275-4789
Weiquan ZhangDepartment of Thoracic Surgery, The Second Hospital of Shandong University, Jinan, China.
Yingtao HaoDepartment of Thoracic Surgery, The Second Hospital of Shandong University, Jinan, China.
Qifeng SunDepartment of Thoracic Surgery, Shandong Provincial Hospital, Jinan, China.
Yuliang LiDepartment of Interventional Medicine, The Second Hospital of Shandong University, Jinan, China.ORCID 0000-0002-0634-7035
Xiaogang ZhaoDepartment of Thoracic Surgery, The Second Hospital of Shandong University, Jinan, China.ORCID 0000-0002-5521-1628
Shandong University · CNSecond Hospital of Shandong University · CN117th Hospital of People's Liberation Army · CNShandong Chest Hospital · CNShandong Provincial Hospital · CN

Funding

Key Research and Development Program of Shandong Province 2016ZDJS07A15Key Research and Development Program of Shandong Province 2017G006028Key Research and Development Program of Shandong Province 2017GSF22107
6 · The paper itself

Abstract

backgroundTo 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).

methodsSingle 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.

resultsIn 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).

conclusionsRNF213 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.

Indexed as

MutationAdenosine TriphosphatasesAdultAgedBiomarkers, TumorCirculating Tumor DNAFemaleHigh-Throughput Nucleotide SequencingHumansLung NeoplasmsMaleMiddle AgedMultiple Pulmonary NodulesUbiquitin-Protein LigasesAdenosine TriphosphatasesBiomarkers, TumorCirculating Tumor DNARNF213 protein, humanUbiquitin-Protein LigasesCirculating tumor DNA (ctDNA)early diagnosislung cancerRNF213 genetargeted next generation sequencing (NGS)

Identifiers

PMID33200540
PMCPMC7812078
OpenAlexW3099616553

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.