Evidence map›Paper›PMID 39725937›Full record

ArticleBMC bioinformatics2024

Deep learning-based metabolomics data study of prostate cancer.

Liqiang Sun, Xiaojing Fan, Yunwei Zhao, Qi Zhang, Mingyang Jiang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

5 authors.

Liqiang SunCollege of Computer Science and Technology, Inner Mongolia Minzu University, Tongliao, 028000, China.
Xiaojing FanCollege of Engineering, Key Laboratory of Intelligent Manufacturing Technology, Inner Mongolia Minzu University, Tongliao, 028000, China.
Yunwei ZhaoCollege of Computer Science and Technology, Inner Mongolia Minzu University, Tongliao, 028000, China.
Qi ZhangDepartment of Immunology and Pathogenic Biology, Yanbian University Medical College, Yanji, China.
Mingyang JiangCollege of Computer Science and Technology, Inner Mongolia Minzu University, Tongliao, 028000, China. jiang_ming_yang@163.com.

Funding

National Natural Science Foundation of China 62162049
6 · The paper itself

Abstract

As a heterogeneous disease, prostate cancer (PCa) exhibits diverse clinical and biological features, which pose significant challenges for early diagnosis and treatment. Metabolomics offers promising new approaches for early diagnosis, treatment, and prognosis of PCa. However, metabolomics data are characterized by high dimensionality, noise, variability, and small sample sizes, presenting substantial challenges for classification. Despite the wide range of applications of deep learning methods, the use of deep learning in metabolomics research has not been extensively explored. In this study, we propose a hybrid model, TransConvNet, which combines transformer and convolutional neural networks for the classification of prostate cancer metabolomics data. We introduce a 1D convolution layer for the inputs to the dot-product attention mechanism, enabling the interaction of both local and global information. Additionally, a gating mechanism is incorporated to dynamically adjust the attention weights. The features extracted by multi-head attention are further refined through 1D convolution, and a residual network is introduced to alleviate the gradient vanishing problem in the convolutional layers. We conducted comparative experiments with seven other machine learning algorithms. Through five-fold cross-validation, TransConvNet achieved an accuracy of 81.03% and an AUC of 0.89, significantly outperforming the other algorithms. Additionally, we validated TransConvNet's generalization ability through experiments on the lung cancer dataset, with the results demonstrating its robustness and adaptability to different metabolomics datasets. We also proposed the MI-RF (Mutual Information-based random forest) model, which effectively identified key biomarkers associated with prostate cancer by leveraging comprehensive feature weight coefficients. In contrast, traditional methods identified only a limited number of biomarkers. In summary, these results highlight the potential of TransConvNet and MI-RF in both classification tasks and biomarker discovery, providing valuable insights for the clinical application of prostate cancer diagnosis.

Indexed as

Deep LearningMetabolomicsProstatic NeoplasmsAlgorithmsBiomarkers, TumorHumansMaleNeural Networks, ComputerBiomarkers, TumorBiomarker discoveryCNNHybrid deep learningMetabolomicsProstate cancerTransformer

Identifiers

PMID39725937
PMCPMC11674358

What OpenQuestion holds

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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.