Evidence map›Paper›PMID 40673815›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

MALMPS: A Machine Learning-Based Metabolic Gene Prognostic Signature for Stratifying Clinical Outcomes and Molecular Heterogeneity in Stage II/III Colorectal Cancer.

Hao Chen, Ze Wang, Chenglong Sun, Yang Zhong, Yuan Liu, Yikun Li, Tongchao Zhang, Yuan Zhang, Xingyu Zhu, Leping Li and 3 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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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

13 authors.

Hao ChenClinical Epidemiology Unit, Clinical Research Center of Shandong University, Qilu Hospital of Shandong University, Jinan, 250012, China.
Ze WangDepartment of Epidemiology and Health Statistics, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.
Chenglong SunKey Laboratory for Applied Technology of Sophisticated Analytical Instruments of Shandong Province, Shandong Analysis and Test Center, Qilu University of Technology, Shandong Academy of Sciences, Shandong, 250014, China.
Yang ZhongClinical Epidemiology Unit, Clinical Research Center of Shandong University, Qilu Hospital of Shandong University, Jinan, 250012, China.
Yuan LiuDepartment of Gastroenterological Surgery, Shandong Provincial Hospital, Shandong University, Jinan, Shandong, 250021, China.
Yikun LiDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, 250117, China.
Tongchao ZhangClinical Epidemiology Unit, Clinical Research Center of Shandong University, Qilu Hospital of Shandong University, Jinan, 250012, China.
Yuan ZhangClinical Epidemiology Unit, Clinical Research Center of Shandong University, Qilu Hospital of Shandong University, Jinan, 250012, China.
Xingyu ZhuDepartment of Gastrointestinal Surgery, Key Laboratory of Engineering of Shandong Province, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Medical Science and Technology Innovation Center, Shandong First Medical University, Shandong Academy of Medical Sciences, Jinan, Shandong, 250117, China.
Leping LiDepartment of Gastrointestinal Surgery, Key Laboratory of Engineering of Shandong Province, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Medical Science and Technology Innovation Center, Shandong First Medical University, Shandong Academy of Medical Sciences, Jinan, Shandong, 250117, China.
Feifei TengDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, 250117, China.
Ming LuClinical Epidemiology Unit, Clinical Research Center of Shandong University, Qilu Hospital of Shandong University, Jinan, 250012, China.
Wei ChongDepartment of Gastrointestinal Surgery, Key Laboratory of Engineering of Shandong Province, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Medical Science and Technology Innovation Center, Shandong First Medical University, Shandong Academy of Medical Sciences, Jinan, Shandong, 250117, China.ORCID https://orcid.org/0000-0002-1074-8595

Funding

Cultivation Plan of Shandong Provincial Hospital 2025PY204National Scientific Foundation of China 82102702National Scientific Foundation of China 82103322National Scientific Foundation of China 82173591National Scientific Foundation of China 82473112National Scientific Foundation of China 82473296Natural Science Foundation of Shandong Province of China ZR2021QH141Natural Science Foundation of Shandong Province of China ZR2024MH011Natural Science Foundation of Shandong Province of China ZR2024MH066Taishan Scholars Program of Shandong Province tsqn202306373Taishan Scholars Program of Shandong Province tstp20230654Young Talent of Lifting engineering for Science and Technology in Shandong SDAST2025QTA071Youth Innovation Science and Technology Program of Shandong Provincial Universities 2022KJ187Youth Innovation Science and Technology Program of Shandong Provincial Universities 2023KJ018
6 · The paper itself

Abstract

Colorectal cancer (CRC) is a frequently lethal disease, with stage II/III CRC accounting for ≈70%. Metabolic reprogramming plays a pivotal role in deciphering cancer heterogeneity and progression. Here, 9 datasets and 83 machine learning algorithm combinations are leveraged‌ to develop the Machine Learning-based Metabolic gene Prognostic Signature (MALMPS) model. The MALMPS model outperformed traditional clinical traits and molecular features in predicting prognosis for stage II/III CRC patients across training and validation datasets. COX7B, a key gene in MALMPS, is shown to promote CRC malignancy through multi-omics analysis and in vitro assays. CRC patients are stratified into high- and low-risk groups based on the median cutoff of MALMPS. Notably, the high-risk subgroup exhibited poor prognosis, activated inflammation, and enriched carbohydrate, glycosaminoglycan, and lipid metabolism, with therapeutic potential for IGF-1R and Wnt/β-catenin inhibitor. In contrast, the low-risk group displayed a TGF-β pathway inactivating mutation and enriched in nucleotides, cofactors, and amino acids metabolism. Metabolite profiling in the in-house SDCRC dataset validated the distinct metabolic alterations between the two groups. These findings indicate that MALMPS is a valuable instrument for predicting the recurrence risk of stage II/III colorectal cancer, particularly for identifying individuals at high risk.

Indexed as

Colorectal NeoplasmsMachine LearningBiomarkers, TumorFemaleHumansMaleNeoplasm StagingPrognosisBiomarkers, Tumorcolorectal cancermachine learningmetabolic‐related geneprognosistumor metabolism

Identifiers

PMID40673815
PMCPMC12499476

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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.