Evidence map›Paper›PMID 36176402›Full record

ArticleFrontiers in oncology2022

A detection panel of novel methylated DNA markers for malignant pleural effusion.

Chaonan Liang, Nan Liu, Qin Zhang, Mingming Deng, Jiangwei Ma, Jingwen Lu, Yan Yin, Jian Wang, Yuan Miao, Bin She and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
2.9field-weighted citation impact, top 8% 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 citations in OpenAlex.

  1. Clinical value of combinedOncology reviews · 2026
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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

12 authors at 5 institutions in 1 country.

Chaonan LiangDepartment of Cardio-Pulmonary Function, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Henan University People's Hospital, Zhengzhou, Henan, China.
Nan LiuDepartment of Pathology, The First Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China.
Qin ZhangDepartment of Pulmonary and Critical Care Medicine, The First Hospital of China Medical University, Shenyang, China.
Mingming DengDepartment of Pulmonary and Critical Care Medicine, China-Japan Friendship Hospital, National Center of Respiratory Medicine, Institute of Respiratory Medicine, Chinese Academy of Medical Sciences, National Clinical Research Center for Respiratory Diseases, Beijing, China.
Jiangwei MaDepartment of Pulmonary and Critical Care Medicine, The First Hospital of China Medical University, Shenyang, China.
Jingwen LuDepartment of Pulmonary and Critical Care Medicine, The First Hospital of China Medical University, Shenyang, China.
Yan YinDepartment of Pulmonary and Critical Care Medicine, The First Hospital of China Medical University, Shenyang, China.
Jian WangDepartment of Pathology, The First Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China.
Yuan MiaoDepartment of Pathology, The First Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China.
Bin SheAcademic Development, Tellgen Corporation, Shanghai, China.
Qingchang LiDepartment of Pathology, The First Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China.
Gang HouDepartment of Pulmonary and Critical Care Medicine, China-Japan Friendship Hospital, National Center of Respiratory Medicine, Institute of Respiratory Medicine, Chinese Academy of Medical Sciences, National Clinical Research Center for Respiratory Diseases, Beijing, China.
China Medical University · CNFirst Hospital of China Medical University · CNChina-Japan Friendship Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNZhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cytology remains the gold standard for the detection of malignant cells in pleural effusion. However, its sensitivity is limited. The aim of this study was to establish a novel panel of cancer-specific methylated genes for the differential diagnosis of malignant pleural effusion (MPE). Methods: A cohort of 100 cancer patients (68 lung cancer, 32 other malignant tumors) and 48 patients with benign disease presenting with pleural effusion was prospectively enrolled. Pleural effusion was evaluated by means of cytopathological investigation and DNA methylation of SHOX2, RASSF1A, SEPTIN9 and HOXA9 in the cellular fraction. DNA methylation in bisulfite-converted DNA was determined using quantitative methylation-specific real-time PCR (MS-PCR). Cytopathological and DNA methylation results were evaluated with regard to the final clinical diagnosis. Results: The LungMe Conclusion: OncoMe has potential for use as a biomarker for the detection of MPE, even not limited to lung cancer.

Indexed as

biomarkersDNA methylationHOXA9pleural effusionRASSF1ASEPTIN9SHOX2

Identifiers

PMID36176402
PMCPMC9513209
OpenAlexW4296011358

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.