An Online Monitoring Method for Low-Frequency Dielectric Loss Angle of Mining Cables.

The dielectric loss angle can better reflect the overall insulation level of mining cables, so it is necessary to implement reliable and effective online monitoring of the dielectric loss angle of mining cables. In order to improve the monitoring accuracy of the dielectric loss angle tan δ of mining cables, a low-frequency dielectric loss angle online monitoring method combining signal injection method and double-end synchronous measurement method is proposed in this paper. Firstly, the superiority of the low-frequency signal in improving the detection accuracy of dielectric loss angle is explained, and the feasibility of the low-frequency signal injection method is analyzed. Secondly, the cable leakage is calculated using the double-terminal synchronous measurement method to measure the core current at the first and last ends of the cable, and the phase sum of the voltage at the first and last ends is selected as the reference phase quantity to realize the effective calculation of the dielectric loss angle tan δ of the cable. Then, the simulation model for online monitoring of dielectric loss angle of mining cable is built, and the feasibility of the online monitoring method proposed in this paper is verified by combining the simulation results. Finally, the theoretical and simulation analysis of the monitoring error of dielectric loss angle of mining cable is carried out.

New flavonoid and their anti-A549 cell activity from the bi-directional solid fermentation products of Astragalus membranaceus and Cordyceps kyushuensis.

Astragalus membranaceus and Cordyceps kyushuensis were used to obtain Astragalus membranaceus-Cordyceps kyushuensis bi-directional solid fermentation products using the bi-directional solid fermentation technique. The fermentation products were isolated and purified to obtain 20 individual compounds, of which compound 1 was a novel isoflavane, and compounds 2, 3, and 4 were novel isoflavones, along with 16 known compounds. In vitro experiments demonstrated that compounds 4, 5, 8, 10, and 20 exhibited significant inhibitory activity against A549 lung cancer cells. Specifically, the IC50 value of the novel compound 4 was 53.4 µM, while the IC50 value of cordycepin was 9.0 µM.

Identification of biomarker associated with Trop2 in breast cancer: implication for targeted therapy.

PURPOSE: Trop2, a cell membrane glycoprotein, is overexpressed in almost all epithelial cancers. This study aimed to explore the mutational characteristics and significance of Trop2 in breast cancer (BC). METHODS: Patients diagnosed with BC (n = 77) were enrolled to investigate expression level and clinical characteristics of Trop2. Database of cBioPortal and Kaplan-Meier Plotter were used to evaluate the effects of Trop2 (TACSTD2) genomic ateration and mRNA expression levels on disease-free survival (DFS) and relapse-free survival (RFS), respectively. Based on next generation sequencing analysis, the Trop2 mutation characteristics of BC patients were deeply depicted. In addition, Trop2 expression, mutation and methylation signature associated with Trop2 mutations were analyzed. RESULTS: Trop2 mutation and high expression of Trop2 were predictive biomarker for shorter DFS and RFS in BC. The positive rate of Trop2 expression in these 77 BC patients was 96.1% (74/77). Based on the Trop2 expression level, the patients were classified into Trop2 negative group, medium expression group and high expression group. The mutation frequencies of MAP3K1, NOTCH2, PTEN and MAGI2 were significantly higher in Trop2 medium expression group than high expression group. Moreover, we investigated the effect of the Trop2 mutations on other genes, including co-expressed genes, differentially mutated genes, differentially expressed genes, gene methylation and phosphorylation. We found that MED8, DPH2, KDM4A, EBNA1BP2, USP1, IPO13, CGAS, PRKAA2, NCOA7, ASCC3 and ABRACL were differentially expressed, mutated and methylated between Trop2 mutation group and wild group. CONCLUSION: MAP3K1, NOTCH2, PTEN and MAGI2 mutations were significantly different between Trop2 medium expression and Trop2 high expression BC patients. The effects of Trop2 mutation on the expression, variation, methylation, and phosphorylation of other genes were comprehensively revealed. High expression level of Trop2 and Trop2 mutation were predictive biomarker for poor prognosis and targeted therapy in BC.