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Background Cerebral-cardiac syndrome (CCS) is a severe cardiac complication following acute ischemic stroke, often associated with adverse outcomes. This study developed and validated a machine learning (ML) model to predict CCS using clinical, laboratory, and pre-extracted imaging features. A retrospective cohort of 511 post-stroke patients was analyzed. Data on demographics, laboratory results, imaging findings, and medications were collected. CCS diagnosis was based on cardiac dysfunction occurring after stroke, excluding pre-existing cardiac diseases. Five machine learning models, including Logistic Regression, Random Forest, Support Vector Machine (SVM), XGBoost, and Deep Neural Network, were trained on 80% of the data and tested on the remaining 20%. Discrimination was assessed by AUC (95% CI), calibration by Hosmer–Lemeshow test and Brier score, and thresholds by Youden’s index. Model interpretability was evaluated using SHAP. On the test set, XGBoost achieved the highest discrimination (AUC 0.879; 95% CI 0.807–0.942), accuracy 0.825, precision 0.844, recall 0.675, and F1 score 0.750. Random forest followed closely (AUC 0.866; accuracy 0.845; precision 0.962; recall 0.625; F1 0.758). SVM and logistic regression yielded AUCs of 0.853 and 0.818, respectively. Calibration was optimal for SVM (HL p  > 0.05; Brier 0.126) and random forest (HL p  > 0.05; Brier 0.131). SHAP analysis identified D-dimer, ACEI/ARB use, HbA1c, C-reactive protein, and prothrombin time as top predictors. ML-based models accurately predict early CCS in ischemic stroke patients. XGBoost offers superior discrimination, while SVM and random forest demonstrate better calibration. Incorporation of these models into clinical workflows may enhance risk stratification and guide targeted preventive strategies.

This study aimed to investigate risk factors associated with oxaliplatin hypersensitivity reactions in cancer patients through a meta-analysis. A comprehensive retrieve of Chinese databases China National Knowledge Infrastructure, Wanfang Data, VIP Database and English databases PubMed, ScienceDirect, Embase and Cochrane library was conducted. The studies that meet the requirements for meta-analysis according to inclusion and exclusion criteria were screened and assessed for eligibility. Odds ratio (OR) / Weighted mean difference (WMD) and 95% confidence intervals (95% CIs) or calculable dichotomous and continuous raw data were extracted to perform meta-analysis using random effect model or fixed effect model on the basis of heterogeneity between studies through Review Manager 5.4 software. A total of 14 cross-sectional studies and 3367 cancer patients were included. Meta-analysis results showed that platinum exposure history (OR value 3.13, 95% CI 2.19–4.48, heterogeneity P = 0.26), allergy history (OR value 1.76, 95% CI 1.09–2.85, heterogeneity P = 0.61), platinum free interval (OR value 3.75, 95% CI 2.00–7.06, heterogeneity P = 0.83), dexamethasone premedication dose (OR value 0.28, 95% CI 0.13–0.58, heterogeneity P = 0.21) were significantly correlated to oxaliplatin hypersensitivity reactions. Gender, age, metastasis, combination with bevacizumab, XELOX regimen and cancer types were detected to have no statistically significant effect on oxaliplatin hypersensitivity reactions. Platinum exposure history, allergy history and long platinum-free interval are risk factors of oxaliplatin hypersensitivity reactions. High dexamethasone premedication dose is a protective factor of oxaliplatin hypersensitivity reactions.

Hepatocellular carcinoma is one of the most common malignant tumors, and radiotherapy plays a pivotal role in its therapeutic regimen. However, radiotherapy resistance is the main cause of therapeutic failure in patients. Our previous study revealed that Adiponectin Receptor 1 (AdipoR1) is involved in regulating radiation resistance in liver cancer patients treated with stereotactic body radiotherapy. To explore the mechanism, we performed high-throughput transcriptome sequencing of hepatocellular carcinoma cells with stable knockdown of AdipoR1. KEGG enrichment analysis indicated that the cell cycle and ubiquitination degradation pathways may be involved in the regulation of radiation resistance by AdipoR1.The knockdown of AdipoR1 can attenuate the radiation-induced G2/M phase arrest through cyclin B1.By the ubiquitination IP assay and a rescue experiment, we confirmed that CCNB1IP1 regulated the ubiquitination and degradation of cyclin B1. Combined with information from transcription factor database and AdipoR1 transcriptome sequencing, these results showed that estrogen receptor 1 (ESR1) may be a transcription factor of CCNB1IP1. We found that AdipoR1 promoted the translocation of ESR1 from the cytoplasm to the nucleus, and ESR1 inhibited the transcription of CCNB1IP1.Therefore, we propose that AdipoR1 regulates the ubiquitination level, cell cycle progression, and radiation resistance of HCC cells through the “AdipoR1 /ESR1/CCNB1IP1/cyclin B1” axis. This study will promote the development of novel targeted radiosensitizing drugs.

Mechanotransduction channels are widely expressed in both vertebrates and invertebrates, mediating various physiological processes such as touch, hearing and blood-pressure sensing. While previously known mechanotransduction channels in metazoans are primarily cation-selective, we identified Anoctamin-1 (ANOH-1), the C. elegans homolog of mammalian calcium-activated chloride channel ANO1/TMEM16A, as an essential component of a mechanosensory channel complex that contributes to the nose touch mechanosensation in C. elegans . Ectopic expression of either C. elegans or human Anoctamin-1 confers mechanosensitivity to touch-insensitive neurons, suggesting a cell-autonomous role of ANOH-1/ANO1 in mechanotransduction. Additionally, we demonstrated that the mechanosensory function of ANOH-1/ANO1 relies on CIB (calcium- and integrin- binding) proteins. Thus, our results reveal an evolutionarily conserved chloride channel involved in mechanosensory transduction in metazoans, highlighting the importance of anion channels in mechanosensory processes. Mechanotransduction channels play key roles in various sensory processes. Here, the authors identify the chloride channel ANOH-1/ANO1 as a core component of a mechanosensory channel complex, highlighting its evolutionary conservation.

Calcium channelopathies have been strongly linked to cardiovascular, muscular, neurological and psychiatric disorders. The voltage-gated calcium channels (VGCC) are vital transducers of membrane potential changes to facilitate the dynamics of calcium ions and release of neurotransmitter. Whether these channels function in the glial cell to mediate calcium variations and regulate behavioral outputs, is poorly understood. Our results showed that odorant and mechanical stimuli evoked robust calcium increases in the amphid sheath (AMsh) glia from C. elegans , which were largely dependent on the L-Type VGCC EGL-19. Moreover, EGL-19 modulates the morphologies of both ASH sensory neurons and AMsh glia. Tissue-specific knock-down of EGL-19 in AMsh glia regulated sensory adaptability of ASH neurons and promoted olfactory adaptation. Our results reveal a novel role of glial L-Type VGCC EGL-19 on olfaction, lead to improved understanding of the functions of VGCCs in sensory transduction.

Poly(acrylic acid- co -acrylamide) (P(AA- co -AM) superabsorbent resin was prepared by solution polymerization of acrylic acid (AA) and acrylamide (AM) using ammonium persulfate (APS) as an initiator and N,N ′-methylenebisacrylamide (MBA) as a cross linker. P(AA- co -AM) was used for the removal methyl orange (MO) from aqueous solutions. Factors influencing the adsorption capacity, such as adsorption time, initial concentration of MO, dosage of the superabsorbent resin, pH value and ionic strength, were investigated in detail. It was found that P(AA- co -AM) was effective to remove MO from its aqueous solutions. The equilibrium adsorption capacity was 394.6 mg/g at room temperature as the initial concentration of MO was 3000 mg/L. The mechanism of the adsorption process was also speculated. Study on the equilibrium adsorption isotherms showed that the adsorption was in accordance with both Langmuir and Freundlich model. Further study of the adsorption kinetics showed that the adsorption process was consistent with the Pseudo second-order kinetic model.

Skeletal muscle plays an essential role in maintaining body energy homeostasis and body flexibility. Loss of muscle mass leads to slower wound healing and recovery from illness, physical disability, poor quality of life, and higher health care costs. So, it is critical for us to understand the mechanism of skeletal muscle myogenic differentiation for maintaining optimal health throughout life. miR-501-3p is a novel muscle-specific miRNA, and its regulation mechanism on myoblast myogenic differentiation is still not clear. We demonstrated that FOS was a direct target gene of miR-501-3p, and MyoD regulated miR-501-3p host gene Clcn5 through bioinformatics prediction. Our previous laboratory experiment found that MDFI overexpression promoted C2C12 myogenic differentiation and MyoD expression. The database also showed there is an FOS binding site in the MDFI promoter region. Therefore, we hypothesize that miR-501-3p formed a feedback loop with FOS, MDFI, and MyoD to regulate myoblast differentiation. To validate our hypothesis, we demonstrated miR-501-3p function in the proliferation and differentiation period of C2C12 cells by transfecting cells with miR-501-3p mimic and inhibitor. Then, we confirmed there is a direct regulatory relationship between miR-501-3p and FOS, MyoD and miR-501-3p, FOS and MDFI through QPCR, dual-luciferase reporter system, and ChIP experiments. Our results not only expand our understanding of the muscle myogenic development mechanism in which miRNA and genes participate in controlling skeletal muscle development, but also provide treatment strategies for skeletal muscle or metabolic-related diseases in the future.

Organo-montmorillonite /poly (acrylic acid) superabsorbent composite was prepared by intercalation polymerization of acrylic acid (AA) and organo-montmorillonite (OMMT). The composite was characterized by means of Fourier-transform spectroscopy (FTIR), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). Maximum absorbency of OMMT/PAA in distilled water and 0.9% NaCl was 1439 and 97 g/g, respectively. Water retention of the composite was also tested. The composite was used for removal of heavy metal ions from aqueous solutions. The maximum adsorption capacities for Pb 2+ , Cu 2+ and Ni 2+ were 1006.97, 280.56 and 165.67 mg/g, respectively, and the adsorption was consistent with the Freundlich model. It was found that the superabsorbent composite showed good re-use performance in wastewater treatment.

A new superabsorbent composite based on the natural material sodium alginate (SA) was synthesized by intercalation graft polymerization of SA, acrylic acid (AA), 2-acrylamido-2-methyl-1-propane sulfonic acid (AMPS) and organo-montmorillonite (OMMT) using ammonium persulfate (APS) as an initiator and N,N'-methylenebisacrylamide (MBA) as a cross linker. The composite was characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA), and was used to remove heavy metal ions such as Pb 2+ , Ni 2+ and Cu 2+ from aqueous solutions. Maximum adsorption capacities for Pb 2+ , Ni 2+ and Cu 2+ were 1485, 303 and 294 mg/g respectively. It was found that the adsorption of Pb 2+ was consistent with both the Langmuir and the Freundlich model, while that of Ni 2+ and Cu 2+ was in accordance with the Langmuir model. Mechanisms for the adsorption process were speculated upon. It revealed that chelation was dominant for the adsorption of Pb 2+ , while ion-exchange played an important role for adsorption of Ni 2+ and Cu 2+ . The superabsorbent composite had good reuse performance in wastewater treatment.

The large carbon footprint of plastic production and the detrimental environment impact of plastic waste demand sustainable substitutes for current non-degradable, fossil-based polymeric materials. Transition-metal catalyzed carbonylative polymerization (COP) offers a methodology to introduce organic carbonyl functional groups to the backbone of polymers in a potentially sustainable way. The organic carbonyl groups bring about degradability under various conditions that are met on the surface of earth. Utilizing carbon monoxide as a cost-effective, low-carbon footprint starting material is key to this process.Carbonylative polymerizations of olefins catalyzed by Pd catalysts have been well-studied since the 1960s. This dissertation studies the development of Ni catalysts for carbonylative polymerizations of olefins. A particular emphasis will be catalyst development to incorporate “defects” in the backbone of alternating CO-ethylene copolymer to improve processibility and mechanical properties of the polymer products. An overview of transition-metal catalyzed carbonylative polymerization will be provided in Chapter I. Chapter II will discuss our zwitterionic Ni catalysts for alternating copolymerization of CO and ethylene. Chater III will explore new catalyst designs to achieve the non-alternating copolymerization of CO and ethylene. Chapter IV will discuss a novel family of Ni catalysts that are capable of catalyzing the terpolymerization of CO, ethylene and propylene.