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Indirect matrix converters (IMC) feature an AC-AC configuration without an intermediate DC link and wide application prospects in wind power generation, AC transmission, and various other fields, known for their sinusoidal input/output, high power density, and superior operating efficiency. However, these converters inevitably generate common-mode voltages during modulation operations, causing motor damage and affecting the reliable functioning of the systems. This paper aims to enhance the operational reliability of IMCs by suppressing common-mode voltage output, and focuses on five classical modulation methods for suppressing common-mode voltage peaks by 42.3% in IMCs, including the modulation method for synthesizing reference output voltage vectors using adjacent four effective voltage vectors at the inverter stage, that for synthesizing reference output voltage vectors using adjacent three effective voltage vectors at the inverter stage, that for synthesizing reference current vectors using adjacent three effective current vectors at the rectifier stage, that for synthesizing reference current vectors using two adjacent 120° effective current vectors plus a zero-current vector at the rectifier stage, and that for synthesizing reference current vectors using weighted three effective current vectors at the rectifier stage. By modeling the effective value (root mean square, rms) of output common-mode voltages, which incorporates the influence of voltage transfer ratios on these values, a quantitative analysis was conducted to explore the variation patterns of the rms value of common-mode voltages. Following this, an evaluation was performed on the suppression capability of different modulation methods on common-mode voltages. The comparative analysis results indicated that the space vector modulation method of synthesizing reference voltage using adjacent four effective voltage vectors at the inverter stage exhibited the best suppression effect on the rms value of common-mode voltages in IMCs. Additionally, the correctness of the theoretical analysis results was verified through simulations and experiments.

Abstract Background Hormone receptor‐positive (HR+)/human epidermal growth factor receptor 2‐positive (HER2+) breast cancer exhibits considerable heterogeneity, and it is of great interest whether patients with premenopausal HR+/HER2+ breast cancer treated with trastuzumab can benefit from ovarian function suppression (OFS) therapy similarly to HR+/HER2‐ breast cancer. Here, we conducted a real‐world study in this population to identify both who would derive substantial benefits from the addition of OFS and clinicopathological factors with potential prognostic value. Methods Multicenter data from 253 premenopausal patients with HR+/HER2+ early‐stage breast cancer who received trastuzumab from October 2009 to October 2018 were retrospectively included. The Kaplan–Meier method was used for survival analysis, while the log‐rank test was used to compare the survival rates. Univariate and multifactor Cox regression analyses were performed to analyze the independent risk factors affecting invasive disease‐free survival (IDFS). Results After a median follow‐up of 98.50 months, compared with tamoxifen/toremifene alone, tamoxifen/toremifene/aromatase inhibitors plus OFS demonstrated significant benefits in the overall study population (HR = 0.289, 95% CI: 0.100–0.835, p = 0.022, 8‐year IDFS rate: 90.78% vs. 95.54%), especially in the lymph node‐positive subgroup and age ≤40 years subgroup. Age ≤40 years, histological grade >2, lymph node involvement, PR ≤50%, and tamoxifen alone were independent prognostic factors. Conclusions For premenopausal HR+ breast cancer patients, HER2 positivity alone is an indication for the addition of OFS in adjuvant endocrine therapy. Age, histological grade, lymph node status, the expression of PR, and OFS treatment were independent prognostic factors in this population.

This study utilized meta-analysis and Mendelian randomization (MR) to identify risk factors for endocrine-related immune-related adverse events (EirAEs) and to ascertain whether EirAEs confer better prognosis of immunotherapy. The meta-analysis identified several risk factors for EirAEs, including elevated baseline TSH (OR = 1.30, 95% CI 1.10–1.53), positive TgAb (OR = 14.23, p

Abstract In recent decades, using circulating tumor cell (CTC), circulating tumor DNA (ctDNA), circulating tumor RNA (ctRNA), exosomes and etc. as liquid biomarkers has received enormous attention in various tumors, including breast cancer (BC). To date, efforts in the area of liquid biopsy predominantly focus on the analysis of blood-based markers. It is worth noting that the identifications of markers from non-blood sources provide unique advantages beyond the blood and these alternative sources may be of great significance in offering supplementary information in certain settings. Here, we outline the latest advances in the analysis of non-blood biomarkers, predominantly including urine, saliva, cerebrospinal fluid, pleural fluid, stool and etc. The unique advantages of such testings, their current limitations and the appropriate use of non-blood assays and blood assays in different settings are further discussed. Finally, we propose to highlight the challenges of these alternative assays from basic to clinical implementation and explore the areas where more investigations are warranted to elucidate its potential utility.

For the problem that the abnormal circulation of bipolar double twelve-pulse ultra high voltage direct current (UHVDC) line permanent grounding fault can not be effectively isolated, an optimized scheme for suppressing the abnormal fault circulation is proposed. Firstly, the influencing factors of abnormal circulating current value for DC line permanent grounding fault are analyzed. Secondly, combined with the existing removal strategies of DC line fault in China, the causes of abnormal circulation are analyzed, which are caused by restarting the high-end valve group with communication condition, unsuccessful restart with communication condition or without communication condition after DC line grounding fault happens. Then, a circulating current suppression scheme for DC line permanent ground fault based on pole isolation and blocking after shifting phase 90° strategy is proposed accordingly. Finally, the simulation model is established through real time digital system (RTDS) to verify the effectiveness of the improved scheme. The results show that the scheme proposed in this paper can effectively solve the abnormal circulation problem of DC line permanent grounding fault under different working conditions.

BackgroundHER2-low expression breast cancer (BC) accounts for approximately 45%-55% of all BC cases. The purpose of this study was to investigate the prognostic difference between patients with HER2-low expression and HER2-zero BC.MethodsAn electronic search of Pubmed, Embase, Cochrane Library, and Web of Science databases was performed to screen studies that included prognostic comparisons between HER2-zero and HER2-low expression groups. A total of 14 studies involving 52106 patients were included.ResultsOur results indicated that HER2-low expression was associated with a significant benefit in OS among all patients with early BC (HR, 0.83; 95% CI, 0.78–0.88), patients with hormone-receptor positive BC (HR, 0.83; 95% CI, 0.77–0.89), and patients with TNBC (HR, 0.78; 95% CI, 0.70–0.87). HER2-low expression was associated with a significant benefit in DFS among all patients (HR, 0.81; 95% CI, 0.71–0.93), patients with hormone receptor-positive BC (HR, 0.81; 95% CI, 0.72–0.90), but no significant difference in DFS was found in patients with TNBC (HR, 0.87; 95% CI, 0.65–1.17). HER2-low expression was associated with a significant benefit in RFS among all patients (HR, 0.90; 95% CI, 0.85–0.95), patients with hormone receptor-positive BC (HR, 0.90; 95% CI, 0.84–0.96), but no significant difference in RFS was found in patients with TNBC (HR, 0.80; 95% CI, 0.55–1.16).ConclusionsAmong patients with early-stage BC, patients with HER2-low expression BC had better OS in the overall population, hormone receptor-positive and TNBC subgroups. Besides, favorable DFS and RFS were observed in both the overall population and hormone receptor-positive subgroup.Systematic review registrationhttps://www.crd.york.ac.uk/PROSPERO/, identifier (CRD 42022349458).

N6-methyladenosine (m6A), the most prevalent RNA internal modification, is present in most eukaryotic species and prokaryotes. Studies have highlighted an intricate network architecture by which m6A epitranscriptome impacts on immune response and function. However, it was only until recently that the mechanisms underlying the involvement of m6A modification in immune system were uncovered. Here, we systematically review the m6A involvement in the regulation of innate and adaptive immune cells. Further, the interplay between m6A modification and anti-inflammatory, anti-viral and anti-tumour immunity is also comprehensively summarized. Finally, we focus on the future prospects of m6A modification in immune modulation. A better understanding of the crosstalk between m6A modification and immune system is of great significance to reveal new pathogenic pathways and to develop promising therapeutic targets of diseases.

Container technology has become a widely used virtualization technology in cloud platform due to its lightweight virtualization characteristics. However, it shares the kernel with the host, so it has poor security and isolation, and is vulnerable to flood, denial of service, and escape attacks. In order to effectively detect whether the container is attacked or not, an intrusion detection method based on host system call frequency was proposed. This method took advantage of the different frequency of system call between different attack behaviors, collected the system call generated when the container was running, extracted the system call features by combining the sliding window and TF-IDF algorithm, and classified by comparing the feature similarity. The experimental results show that the detection rate of this method can reach 97%, and the false alarm rate is less than 4%.

In recent years, microfluidic bioreactors have become important in chemical production; however, the production cost is high, and it becomes difficult to balance scale, efficiency, and cost. Therefore, a low-cost, efficient, high-delivery-capacity, green-fluid reactor is urgently required. Herein, a cellulose bioreactor with dual-scale directional channels and a porous inner wall is reported for the continuous catalytic conversion of polydatin into resveratrol. The dual-scale directional channel structure endows the reactor with high mass transfer speed and large transport capacity, resulting in fast fluid diffusion rate and more severe "disturbance" inside the reactor. It accelerates the mass transfer state of the whole reaction and further improves the catalytic performance compared to the uniform channel reactor. The reactor can achieve a high conversion rate of 98.58% of resveratrol within 2 h and exhibits excellent stability, owing to which it has broad application prospects in catalytic reactions, and helps derive a new approach for constructing fluid catalysis bioreactors. [ABSTRACT FROM AUTHOR]

This paper explores the variations in cross-correlations among the carbon trading market, geopolitical risk (GPR) and economic policy uncertainty (EPU), focusing on their multifractality and asymmetric properties. Therefore, the study employs the multifractal detrended cross-correlation analysis (MF-DCCA) and multifractal asymmetric detrended cross-correlation analysis (MF-ADCCA) approaches to examine these relationships from a three-dimensional perspective. Also, the study looks into cross-correlations at different phases of carbon trading. Our findings reveal that the multifractal cross-correlations between the carbon trading market and GPR or EPU exhibit anti-persistence and asymmetry. The anti-persistent cross-correlations are notably stronger when GPR experiences a downtrend or when EPU undergoes an uptrend. Furthermore, distinct fluctuation patterns emerge across various trends and scales on Hurst surfaces. In the short term, the carbon trading market exhibits heightened sensitivity to changes in GPR or EPU when they rise or fall. The cross-correlations remain multifractal, anti-persistent and asymmetric across different stages of carbon trading. Notably, the multifractality of cross-correlations is most pronounced for the series pair EUA/GPR in Phase II and for the series pair EUA/UK EPU in Phase III and Phase IV. Except for the series pair EUA/UK EPU in Phase II, the anti-persistent cross-correlations are more pronounced during uptrend than downtrend for the other series pairs. Moreover, the series pair EUA/UK EPU exhibits the highest degree of asymmetry at all stages. [ABSTRACT FROM AUTHOR]

The segmentation of abnormal regions is vital in smart manufacturing. The blurring sauce-packet leakage segmentation task (BSLST) is designed to distinguish the sauce packet and the leakage's foreground and background at the pixel level. However, the existing segmentation system for detecting sauce-packet leakage on intelligent sensors encounters an issue of imaging blurring caused by uneven illumination. This issue adversely affects segmentation performance, thereby hindering the measurements of leakage area and impeding the automated sauce-packet production. To alleviate this issue, we propose the two-stage illumination-aware sauce-packet leakage segmentation (ISLS) method for intelligent sensors. The ISLS comprises two main stages: illumination-aware region enhancement and leakage region segmentation. In the first stage, YOLO-Fastestv2 is employed to capture the Region of Interest (ROI), which reduces redundancy computations. Additionally, we propose image enhancement to relieve the impact of uneven illumination, enhancing the texture details of the ROI. In the second stage, we propose a novel feature extraction network. Specifically, we propose the multi-scale feature fusion module (MFFM) and the Sequential Self-Attention Mechanism (SSAM) to capture discriminative representations of leakage. The multi-level features are fused by the MFFM with a small number of parameters, which capture leakage semantics at different scales. The SSAM realizes the enhancement of valid features and the suppression of invalid features by the adaptive weighting of spatial and channel dimensions. Furthermore, we generate a self-built dataset of sauce packets, including 606 images with various leakage areas. Comprehensive experiments demonstrate that our ISLS method shows better results than several state-of-the-art methods, with additional performance analyses deployed on intelligent sensors to affirm the effectiveness of our proposed method. [ABSTRACT FROM AUTHOR]

The growing preference for incorporating microbial aspartic proteases in industries is due to their high catalytic function and high degree of substrate selectivity. These properties, however, are attributable to molecular alterations in their structure and a variety of other characteristics. Molecular tools, functional genomics, and genome editing technologies coupled with other biotechnological approaches have aided in improving the potential of industrially important microbial proteases by addressing some of their major limitations, such as: low catalytic efficiency, low conversion rates, low thermostability, and less enzyme yield. However, the native folding within their full domain is dependent on a surrounding structure which challenges their functionality in substrate conversion, mainly due to their mutual interactions in the context of complex systems. Hence, manipulating their structure and controlling their expression systems could potentially produce enzymes with high selectivity and catalytic functions. The proteins produced by microbial aspartic proteases are industrially capable and far-reaching in regulating certain harmful distinctive industrial processes and the benefits of being eco-friendly. This review provides: an update on current trends and gaps in microbial protease biotechnology, exploring the relevant recombinant strategies and molecular technologies widely used in expression platforms for engineering microbial aspartic proteases, as well as their potential industrial and biotechnological applications. [ABSTRACT FROM AUTHOR]

Long non-coding RNAs (lncRNAs) are characterized as key layers of the genome in various cancers. TSPEAR-AS2 was highlighted to be a candidate lncRNA potentially involved in gastric cancer (GC) progression. However, the clinical significance and mechanism of TSPEAR-AS2 in GC required clarification. The clinical significance of TSPEAR-AS2 was elucidated through Kaplan-Meier Plotter. The mechanism of TSPEAR-AS2 in GC was clarified in vitro and in vivo using luciferase reporter, chromatin immunoprecipitation, RNA immunoprecipitation assays, and animal models. TSPEAR-AS2 elevation was closely correlated with overall survival of GC patients. A basic transcription element-binding protein 2 (BTEB2)-activated TSPEAR-AS2 model was first explored in this study. TSPEAR-AS2 silencing substantially reduced tumorigenic capacities of GC cells, while TSPEAR-AS2 elevation had the opposite effect. Mechanistically, TSPEAR-AS2 bound with both polycomb repressive complex 2 (PRC2) and argonaute 2 (Ago2). TSPEAR-AS2 knockdown significantly decreased H3K27me3 levels at promoter regions of gap junction protein alpha 1 (GJA1). Ago2 was recruited by TSPEAR-AS2, which was defined to sponge miR-1207-5p, contributing to the repression of claudin 4 (CLDN4) translation. The axis of EZH2/GJA1 and miR-1207-5p/CLDN4 mediated by BTEB2-activated-TSPEAR-AS2 plays an important role in GC progression, suggesting a new therapeutic direction in GC treatment.

Abstract Background Gastric cancer (GC) is the third leading cause of cancer-related mortality globally. Long noncoding RNAs (lncRNAs) are dysregulated in obvious malignancies including GC and exploring the regulatory mechanisms underlying their expression is an attractive research area. However, these molecular mechanisms require further clarification, especially upstream mechanisms. Methods LncRNA MNX1-AS1 expression in GC tissue samples was investigated via microarray analysis and further determined in a cohort of GC tissues via quantitative reverse transcription polymerase chain reaction (qRT-PCR) assays. Cell proliferation and flow cytometry assays were performed to confirm the roles of MNX1-AS1 in GC proliferation, cell cycle regulation, and apoptosis. The influence of MNX1-AS1 on GC cell migration and invasion was explored with Transwell assays. A xenograft tumour model was established to verify the effects of MNX1-AS1 on in vivo tumourigenesis. The TEAD4-involved upstream regulatory mechanism of MNX1-AS1 was explored through ChIP and luciferase reporter assays. The mechanistic model of MNX1-AS1 in regulating gene expression was further detected by subcellular fractionation, FISH, RIP, ChIP and luciferase reporter assays. Results It was found that MNX1-AS1 displayed obvious upregulation in GC tissue samples and cell lines, and ectopic expression of MNX1-AS1 predicted poor clinical outcomes for patients with GC. Overexpressed MNX1-AS1 expression promoted proliferation, migration and invasion of GC cells markedly, whereas decreased MNX1-AS1 expression elicited the opposite effects. Consistent with the in vitro results, MNX1-AS1 depletion effectively inhibited the growth of xenograft tumour in vivo. Mechanistically, TEAD4 directly bound the promoter region of MNX1-AS1 and stimulated the transcription of MNX1-AS1. Furthermore, MNX1-AS1 can sponge miR-6785-5p to upregulate the expression of BCL2 in GC cells. Meanwhile, MNX1-AS1 suppressed the transcription of BTG2 by recruiting polycomb repressive complex 2 to BTG2 promoter regions. Conclusions Our findings demonstrate that MNX1-AS1 may be able to serve as a prognostic indicator in GC patients and that TEAD4-activatd MNX1-AS1 can promote GC progression through EZH2/BTG2 and miR-6785-5p/BCL2 axes, implicating it as a novel and potent target for the treatment of GC.