Evidence map›Paper›PMID 41880007›Full record

ArticleDie Naturwissenschaften2026

A tissue-to-blood mRNA classifier enables early detection of gastric cancer risk in precancerous lesions.

Wenqian Ma, Honghai Guo, Tao Zheng, Mingchang Miao, Shuo Guo, Jiangao Yu, Ping'an Ding, Qun Zhao

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Article in Die Naturwissenschaften, 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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5 · Who and what money

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8 authors.

Wenqian MaDepartment of Endoscopy, The Fourth Hospital of Hebei Medical University, Shijiazhuang, 050011, Hebei, China.
Honghai GuoHebei Key Laboratory of Precision Diagnosis and Comprehensive Treatment of Gastric Cancer, Shijiazhuang, 050011, Hebei, China.
Tao ZhengHebei Key Laboratory of Precision Diagnosis and Comprehensive Treatment of Gastric Cancer, Shijiazhuang, 050011, Hebei, China.
Mingchang MiaoDepartment of Radiation Oncology, the Fourth Hospital of Hebei Medical University, Shijiazhuang, 050011, Hebei, China.
Shuo GuoDepartment of Endoscopy, The Fourth Hospital of Hebei Medical University, Shijiazhuang, 050011, Hebei, China.
Jiangao YuDepartment of Endoscopy, The Fourth Hospital of Hebei Medical University, Shijiazhuang, 050011, Hebei, China.
Ping'an DingHebei Key Laboratory of Precision Diagnosis and Comprehensive Treatment of Gastric Cancer, Shijiazhuang, 050011, Hebei, China.
Qun ZhaoHebei Key Laboratory of Precision Diagnosis and Comprehensive Treatment of Gastric Cancer, Shijiazhuang, 050011, Hebei, China. zhaoqun@hebmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly identification of gastric cancer (GC) risk among patients with precancerous lesions remains a major clinical challenge. This study aimed to develop and validate a minimally invasive mRNA-based classifier for predicting malignant transformation.

methodsThree differentially expressed mRNAs (CCL3, CCL4, CXCL2) were identified through transcriptomic analyses of precancerous and cancerous gastric tissues and were further validated in tissue and serum samples. A logistic regression–based model which named risk signature assessment (RSA), was constructed using mRNA expression and key clinical variables.

resultsIn tissue biopsy samples from 229 patients, the RSA model achieved excellent predictive performance, with an AUC of 0.853 in the training set and 0.836 in the validation set. Sensitivity and specificity reached 82.6% and 79.7%, respectively. The RSA model outperformed clinical models (AUC = 0.695) and provided better net clinical benefit across thresholds. In serum samples (n = 210), the model remained robust, yielding an AUC of 0.846 in the training cohort and 0.843 in the validation cohort, with consistent sensitivity (81.3%) and specificity (77.1%). Risk reclassification improved markedly: low-risk patients identified by the RSA model had a cancer conversion rate of only 2.9% (vs. 4.3% using clinical models), while high-risk patients had rates of 12.9% (vs. 12.2%).

conclusionThis dual-platform mRNA classifier demonstrates strong potential for early, noninvasive identification of high-risk individuals with precancerous gastric lesions, offering a valuable tool for precision screening and clinical decision-making.

Indexed as

Early Detection of CancerPrecancerous ConditionsRNA, MessengerStomach NeoplasmsFemaleHumansMaleMiddle AgedRNA, MessengerGastric CancerLiquid biopsyMRNA biomarkersPrecancerous gastric lesions

Identifiers

PMID41880007

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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.