Evidence map›Paper›PMID 38429660›Full record

ArticleBMC cancer2024

Evaluating the comprehensive diagnosis efficiency of lung cancer, including measurement of SHOX2 and RASSF1A gene methylation.

Jian Liu, Tingting Bian, Bin She, Lei Liu, Hui Sun, Qing Zhang, Jun Zhu, Jianguo Zhang, Yifei Liu

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
4.9field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 21 citations in OpenAlex.

  1. Clinical value of combinedOncology reviews · 2026
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  13. Detection ofMolecular and clinical oncology · 2025
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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

9 authors at 1 institution in 1 country.

Jian Liu *Department of Oncology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Tingting Bian *Department of Pathology, Affiliated Hospital of Nantong University, No 20, Xisi Road, Nantong, 226001, China.
Bin SheAcademic Development, Shanghai Methyldia Technology Co. Ltd, Tellgen Corporation, No. 412 Huiqing Road, Shanghai, 201203, China.
Lei LiuDepartment of Pathology, Affiliated Hospital of Nantong University, No 20, Xisi Road, Nantong, 226001, China.
Hui SunDepartment of Pathology, Affiliated Hospital of Nantong University, No 20, Xisi Road, Nantong, 226001, China.
Qing ZhangDepartment of Pathology, Affiliated Hospital of Nantong University, No 20, Xisi Road, Nantong, 226001, China.
Jun ZhuDepartment of Cardio-Thoracic Surgery, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Jianguo ZhangDepartment of Pathology, Affiliated Hospital of Nantong University, No 20, Xisi Road, Nantong, 226001, China. 13815212431@163.com.
Yifei LiuDepartment of Pathology, Affiliated Hospital of Nantong University, No 20, Xisi Road, Nantong, 226001, China. ntdxliuyifei@sina.com.
Nantong University · CN

Funding

Jiangsu Provincial Research Hospital Hospital YJXYY202204 YSB01Jiangsu Provincial Research Hospital Hospital YJXYY202204 YSC01Nantong Basic Research Plan Project JC12022016Nantong Basic Research Plan Project JC2021029Nantong Basic Research Plan Project JC22022020Nantong Municipal Science and technology project JCZ0001National Natural Science Foundation of China No. 82273422Research project on cutting-edge tumor support therapy cphcf-2022-206Shanghai Pudong New District Foundation for Development of Science and Technology PKX2021-S09
6 · The paper itself

Abstract

Methylation of the promoters of SHOX2 and RASSF1A (LungMe®) exhibits promise as a potential molecular biomarker for diagnosing lung cancer. This study sought to assess the aberrant methylation of SHOX2 and RASSF1A in broncho-exfoliated cells (BEC) and compare it with conventional cytology, histology examination, immunohistochemistry, and serum tumor markers to evaluate the overall diagnostic efficiency for lung cancer. This study recruited 240 patients, including 185 malignant cases and 55 benign cases. In our observation, we noted a slight reduction in the detection sensitivity, however, the ΔCt method exhibited a significant enhancement in specificity when compared to Ct judgment. Consequently, the ΔCt method proves to be a more appropriate approach for interpreting methylation results. The diagnostic sensitivity of cytology and histology was in ranged from 20.0%-35.1% and 42.9%-80%, respectively, while the positive detection rate of LungMe® methylation ranged from 70.0% to 100%. Additionally, our findings indicate a higher prevalence of SHOX2( +) among patients exhibiting medium and high expression of Ki67 (P < 0.01), as opposed to those with low expression of Ki67, but RASSF1A methylation did not show this phenomenon (P = 0.35). Furthermore, CEA, SCCA, and CYFRA21-1 showed positive detection rates of 48.8%, 26.2%, and 55.8%, respectively. Finally, we present a comprehensive lung cancer diagnostic work-up, including LumgMe® methylation. The combined analysis of SHOX2 and RASSF1A methylation serves as a powerful complement and extension to conventional methods, enhancing the accuracy of a lung cancer diagnosis with satisfactory sensitivity and specificity.

Indexed as

Antigens, NeoplasmKeratin-19Lung NeoplasmsDNA MethylationHomeodomain ProteinsHumansKi-67 Antigenantigen CYFRA21.1Antigens, NeoplasmHomeodomain ProteinsKeratin-19Ki-67 AntigenSHOX2 protein, humanDiagnosisDNA methylationLung cancerRASSF1ASHOX2

Identifiers

PMID38429660
PMCPMC10908052
OpenAlexW4392346276

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.