Evidence map›Paper›PMID 42238034›Full record

ArticlePhenomics (Cham, Switzerland)2026

Identification of High-Performing Blood Metabolite Biomarkers of Lung Cancer in a Chinese Population.

Zhenpu Chen, Lun Zhang, Kaining Mao, Jia Li, Yongchun Zhou, Jiamin Zheng, Marcia LeVatte, David S Wishart, Youguang Huang, Yunchao Huang and 1 more

Abstract read
In one paragraph

Article in Phenomics (Cham, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

11 authors.

Zhenpu Chen *Cancer Institute, The Third Affiliated Hospital of Kunming Medical University,Yunnan Cancer Hospital,Peking University Cancer Hospital Yunnan, Kunming, 650118 Yunnan China.
Lun Zhang *Department of Biological Sciences, University of Alberta, Edmonton, AB T6G 2E9 Canada.ORCID 0009-0000-9506-1612
Kaining Mao *Department of Electrical Engineering, University of Alberta, Edmonton, AB T6G 2R3 Canada.
Jia LiCancer Institute, The Third Affiliated Hospital of Kunming Medical University,Yunnan Cancer Hospital,Peking University Cancer Hospital Yunnan, Kunming, 650118 Yunnan China.
Yongchun ZhouCancer Institute, The Third Affiliated Hospital of Kunming Medical University,Yunnan Cancer Hospital,Peking University Cancer Hospital Yunnan, Kunming, 650118 Yunnan China.
Jiamin ZhengDepartment of Biological Sciences, University of Alberta, Edmonton, AB T6G 2E9 Canada.
Marcia LeVatteDepartment of Biological Sciences, University of Alberta, Edmonton, AB T6G 2E9 Canada.ORCID 0000-0002-5657-6661
David S WishartDepartment of Biological Sciences, University of Alberta, Edmonton, AB T6G 2E9 Canada.ORCID 0000-0002-3207-2434
Youguang HuangCancer Institute, The Third Affiliated Hospital of Kunming Medical University,Yunnan Cancer Hospital,Peking University Cancer Hospital Yunnan, Kunming, 650118 Yunnan China.
Yunchao HuangCancer Institute, The Third Affiliated Hospital of Kunming Medical University,Yunnan Cancer Hospital,Peking University Cancer Hospital Yunnan, Kunming, 650118 Yunnan China.
Jie ChenDepartment of Electrical Engineering, University of Alberta, Edmonton, AB T6G 2R3 Canada.ORCID 0000-0001-7925-3729

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is the world's leading cause of cancer deaths. Early detection through low-cost metabolite screening approaches could reduce lung cancer mortality. Here we report the results of a large-scale, quantitative metabolomics study aimed at identifying plasma biomarkers for lung cancer detection in a Chinese population. A cohort of 410 patients, including 137 healthy controls, 189 biopsy-confirmed individuals with stage I/II lung cancer, and 84 individuals with biopsy-confirmed stage III/IV cancer, were studied. Plasma samples were collected and analyzed using an in-house-developed, targeted liquid chromatography-mass spectrometry (LC-MS) metabolomics method that detects and quantifies 138 metabolites. Logistic regression was used to develop an optimal biomarker panel that could distinguish all-stage lung cancer patients from healthy controls. The resulting six-metabolite panel achieved an area under the curve (AUC) of 95.0%. A second biomarker panel was developed to distinguish early-stage lung cancer from healthy controls and reached an AUC of 94.3%. All models were developed on an initial training set and then fully validated on a separate holdout set. Our proposed biomarker models show significant improvements over previously published models for metabolite-based lung cancer diagnosis and detection. These metabolite biomarker panels are intended for the development of a low-cost, minimally invasive blood test for lung cancer screening in China. Supplementary Information: The online version contains supplementary material available at 10.1007/s43657-024-00206-5.

Indexed as

Early detectionLiquid chromatography- mass spectrometryLung cancerMetabolomics

Identifiers

PMID42238034
PMCPMC13226740

What OpenQuestion holds

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Registered trials

None linked

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.