Evidence map›Paper›PMID 41570022›Full record

ArticlePloS one2026

A screening strategy based on machine learning for diagnostic biomarkers in small cell lung cancer.

Yifeng Pan, Xuansheng Ding, Wenyun Duan, Liangbiao Wang, Yong Dai, Rongrong Han, Shubei Wang, Mingquan Guo

Abstract read
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Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yifeng PanSchool of Medicine, Anhui University of Science and Technology, Huainan, Anhui, China.
Xuansheng DingSchool of Medicine, Anhui University of Science and Technology, Huainan, Anhui, China.
Wenyun DuanSchool of Medicine, Anhui University of Science and Technology, Huainan, Anhui, China.
Liangbiao WangSchool of Medicine, Anhui University of Science and Technology, Huainan, Anhui, China.
Yong DaiSchool of Medicine, Anhui University of Science and Technology, Huainan, Anhui, China.
Rongrong HanSchool of Mechanics and Photoelectric Physics, Anhui University of Science and Technology, Huainan, Anhui, China.
Shubei WangSchool of Medicine, Anhui University of Science and Technology, Huainan, Anhui, China.
Mingquan GuoSchool of Medicine, Anhui University of Science and Technology, Huainan, Anhui, China.ORCID https://orcid.org/0009-0004-8152-657X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small cell lung cancer (SCLC) is the most aggressive subtype with high mortality rates due to the lack of specific diagnostic biomarkers to delay the optimal opportunity for treatment. Traditional biomarkers, such as neuron-specific enolase (NSE) or pro-gastrin-releasing peptide (ProGRP), have insufficient specificity and sensitivity to meet the demands of clinical diagnosis. Exosome and its contents have become burgeoning cancer biomarkers due to their diverse molecular cargo to achieve intercellular communication. Herein, a novel machine learning strategy was reported for rapid, efficient screening of biomarkers and identified an optimal exosome RNA combination as diagnostic biomarker of SCLC. Firstly, RNA sequencing data from 111 SCLC patients and 362 healthy controls were obtained from the exoRBase 2.0 and 3.0 databases. The machine learning methods were employed to select specific RNA by using 20 iterations with 10-fold nested cross-validation for SCLC diagnosis. Then, an optimal combination of three exosome RNAs (LINC00989, CXCL5, and MAP3K7CL) was confirmed and achieved excellent diagnostic performance (area under the curve (AUC) of 0.950, sensitivity of 0.936, and specificity of 0.892). Finally, an independent validation cohort containing tissue-based RNA expression data for two biomarkers (CXCL5 and MAP3K7CL) from 79 SCLC patients and 7 standard controls was used to evaluate the diagnostic performance of the selected RNAs. The results demonstrated modest diagnostic performance in tissue samples (AUC = 0.718) with two biomarkers, indicating potential cross-tissue applicability despite the limitations of incomplete biomarker coverage. In addition, a specificity analysis of exosome RNA data, including gastric cancer, hepatocellular carcinoma, and breast cancer, demonstrated significant specificity for SCLC. Therefore, the novel biomarker screening strategy integrating nested cross-validation with multiple machine learning algorithms successfully established to offer a potentially valuable protocol for early SCLC diagnosis and other cancers.

Indexed as

Biomarkers, TumorLung NeoplasmsMachine LearningSmall Cell Lung CarcinomaExosomesFemaleHumansMaleMiddle AgedSensitivity and SpecificityBiomarkers, Tumor

Identifiers

PMID41570022
PMCPMC12826499

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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.