Compound Kushen injection (CKI) has been extensively used in treating breast cancer (BC). However, the molecular mechanism remains unclear. In this study, 16 active compounds of CKI were obtained from 3 articles for target prediction. Then, a compound-predicted target network and a compound-BC target network were conducted by Cytoscape 3.6.1. The gene ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis were performed on the DAVID database. The binding energy between the key targets of CKI and the active compounds was studied by molecular docking. As a result, 16 active compounds of CKI were identified, corresponding to 285 putative targets. The key targets of CKI for BC are HSD11B1, DPP4, MMP9, CDK1, MMP2, PTGS2, and CA14. The function enrichment analysis obtained 13 GO entries and 6 KEGG pathways, including bladder cancer, cancer pathways, chemical carcinogenesis, estrogen signaling pathway, TNF signaling pathway, and leukocyte transendothelial migration. The result of molecular docking indicated that DPP4 had strong binding activity with matrine, alicyclic protein, and sophoridine, and MMP9 had strong binding activity with adenine and sophoridine. In conclusion, the therapeutic effect of CKI on BC is based on the overall pharmacological effect formed by the combined effects of multiple components, multiple targets, and multiple pathways. This study provides a theoretical basis for further experimental research in the future.
To introduce a dual-domain reconstruction network with V-Net and K-Net for accurate MR image reconstruction from undersampled k-space data.Methods: Most state-of-the-art reconstruction methods apply U-Net or cascaded U-Nets in the image domain and/or k-space domain. Nevertheless, these methods have the following problems: (1) directly applying U-Net in the k-space domain is not optimal for extracting features; (2) classical image-domain-oriented U-Net is heavyweighted and hence inefficient when cascaded many times to yield good reconstruction accuracy; (3) classical image-domain-oriented U-Net does not make full use of information of the encoder network for extracting features in the decoder network; and (4) existing methods are ineffective in simultaneously extracting and fusing features in the image domain and its dual k-space domain. To tackle these problems, we present 3 different methods: (1) V-Net, an image-domain encoder-decoder subnetwork that is more lightweight for cascading and effective in fully utilizing features in the encoder for decoding; (2) K-Net, a k-space domain subnetwork that is more suitable for extracting hierarchical features in the k-space domain, and (3) KV-Net, a dual-domain reconstruction network in which V-Nets and K-Nets are effectively combined and cascaded. Results: Extensive experimental results on the fastMRI dataset demonstrate that the proposed KV-Net can reconstruct high-quality images and outperform state-of-the-art approaches with fewer parameters. Conclusions: To reconstruct images effectively and efficiently from incomplete k-space data, we have presented a dual-domain KV-Net to combine K-Nets and V-Nets. The KV-Net achieves better results with 9% and 5% parameters than comparable methods (XPD-Net and i-RIM).
The pathogenesis of pheochromocytoma and paraganglioma (PCPG) catecholamine-producing tumors is exceedingly complicated. Here, we sought to identify important genes affecting the prognosis and survival rate of patients suffering from PCPG. We analyzed 95 samples obtained from two microarray data series, GSE19422 and GSE60459, from the Gene Expression Omnibus (GEO) repository. First, differentially expressed genes (DEGs) were identified by comparing 87 PCPG tumor samples and eight normal adrenal tissue samples using R language. The GEO2R tool and Venn diagram software were applied to the Database for Annotation, Visualization and Integrated Discovery (DAVID) to analyze Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways and Gene Ontology (GO). We further employed Cytoscape with the Molecular Complex Detection (MCODE) tool to make protein-protein interactions visible for the Search Tool for Retrieval of Interacting Genes (STRING). These procedures resulted in 30 candidate DEGs, which were subjected to Kaplan-Meier analysis and validated by Gene Expression Profiling Interactive Analysis (GEPIA) to determine their influence on overall survival rate. Finally, we identified ALDH3A2 and AKR1B1, two genes in the glycerolipid metabolism pathway, as being particularly enriched in PCPG tumors and correlated with T and B tumor-infiltrating immune cells. Our results suggest that these two DEGs are closely associated with the prognosis of malignant PCPG tumors.
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