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FUS-mediated alternative splicing and METTL3-regulated RNA methylation play crucial roles in RNA processing. The purpose of this study was to investigate the interactive roles of FUS and METTL3 in gastric cancer (GC) progression. RNA sequencing data were obtained from the TCGA-STAD dataset. Differentially expressed genes (DEGs) were analyzed across groups stratified by the medians of FUS, METTL3, and NEAT1, respectively. Endoplasmic reticulum (ER) stress markers PERK, IRE1, pIRE1, Bip, and CHOP, as well as related apoptosis stress markers PARP, cleaved-PARP, (Cleaved) Caspase 7, and (Cleaved) Caspase 3, were assessed through western blotting. Alternative splicing and N6-methyladenosine (m(6)A) methylation of specific genes were detected with MeRIP-PCR. Finally, in vivo experiments were conducted using nude mice bearing sh-FUS-transfected HGC27 xenograft tumors. FUS and METTL3 expression levels were elevated in GC tissues. A significant overlap of DEGs was observed between the FUS- and METTL3-stratified groups. These overlapping DEGs were predominantly enriched in mRNA processing and protein processing in the ER. ER stress and apoptosis were induced by sh-FUS or sh-METTL3, which was further enhanced by ER stress inducer tunicamycin in both MKN45 and HGC27 cells. Similarly, DEGs for NEAT1 high- and low-expressed groups were enriched in protein processing in the ER and spliceosome. To a lesser extent, ER stress was also induced by sh-NEAT1 and enhanced by tunicamycin in HGC27 cells. Furthermore, sh-FUS or sh-METTL3 influenced alternative splicing and methylation of specific mRNAs, including FUS, NEAT1, PCNA, MCM2, and BIRC5. Tumor progression was inhibited by sh-FUS in mice, and ER stress and apoptosis were induced, which were further enhanced by tunicamycin. FUS and METTL3 collaborate to facilitate RNA maturation. Inhibiting FUS or METTL3 promoted ER stress and apoptosis and inhibited progression in GC. Aberrant levels of FUS and METTL3 can evoke endoplasmic reticulum (ER) stress and apoptosis by generating splicing and methylation variants of mRNAs in gastric cancer, supporting the therapeutic potential of inducing ER stress [ABSTRACT FROM AUTHOR]

Perovskite solar cells have emerged as a promising technology for renewable energy generation. However, the successful integration of perovskite solar cells with energy storage devices to establish high‐efficiency and long‐term stable photorechargeable systems remains a persistent challenge. Issues such as electrical mismatch and restricted integration levels contribute to elevated internal resistance, leading to suboptimal overall efficiency (ηoverall) within photorechargeable systems. Additionally, the compatibility of perovskite solar cells with electrolytes from energy storage devices poses another significant concern regarding their stability. To address these limitations, we demonstrate a highly integrated photorechargeable system that combines perovskite solar cells with a solid‐state zinc‐ion hybrid capacitor using a streamlined process. Our study employs a novel ultraviolet‐cured ionogel electrolyte to prevent moisture‐induced degradation of the perovskite layer in integrated photorechargeable system, enabling perovskite solar cells to achieve maximum power conversion efficiencies and facilitating the monolithic design of the system with minimal energy loss. By precisely matching voltages between the two modules and leveraging the superior energy storage efficiency, our integrated photorechargeable system achieves a remarkable ηoverall of 10.01% while maintaining excellent cycling stability. This innovative design and the comprehensive investigations of the dynamic photocharging process in monolithic systems, not only offer a reliable and enduring power source but also provide guidelines for future development of self‐power off‐grid electronics. [ABSTRACT FROM AUTHOR]

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In order to improve the poor engineering characteristics of the expansive soil, such as cracking resulting from dry–wet swelling and shrinkage. In this study, coal gangue and cement were used as improving materials to improve the expansive soil. The research focuses on testing the efficacy of various coal gangue additions in enhancing the soil properties through compaction, liquid–plastic limit, expansion rate, unconfined strength, direct shear tests, as well as the dry–wet cycle stability of cement–coal gangue composite improved the samples. The findings suggest that as the coal gangue content raise, there is a corresponding decrease observed in both the maximum dry density and the expansion rate of the expansive soil. Simultaneously, the unconfined compressive strength (UCS) an increment from 0.07 MPa for the untreated soil to 0.6 MPa. Additionally, the inclusion of cement as a compound improvement agent substantially improves the UCS of the composite soil samples, with the highest recorded value reaching 3.14 MPa. The UCS of the composite improved soil is observed through three distinct stages: small increase, followed by a rapid decline, and ultimately reaching a state of gradual stabilization. Following 15 cycles of dry–wet cycles, the strength of the enhanced soil undergoes a reduction ranging from 26% to 57%. Scanning electron microscopy (SEM) analysis of the internal structure of the improved soil sample reveals that the cementitious material generated by cement hydration encapsulates the expansive soil particles and establishes connections with the coal gangue particles. However, fine cracks are observed in the cement hydration products near the surface of the coal gangue particles. [ABSTRACT FROM AUTHOR]

Metal oxide charge transport materials are preferable for realizing long‐term stable and potentially low‐cost perovskite solar cells (PSCs). However, due to some technical difficulties (e.g., intricate fabrication protocols, high‐temperature heating process, incompatible solvents, etc.), it is still challenging to achieve efficient and reliable all‐metal‐oxide‐based devices. Here, we developed efficient inverted PSCs (IPSCs) based on solution‐processed nickel oxide (NiOx) and tin oxide (SnO2) nanoparticles, working as hole and electron transport materials respectively, enabling a fast and balanced charge transfer for photogenerated charge carriers. Through further understanding and optimizing the perovskite/metal oxide interfaces, we have realized an outstanding power conversion efficiency (PCE) of 23.5% (the bandgap of the perovskite is 1.62 eV), which is the highest efficiency among IPSCs based on all‐metal‐oxide charge transport materials. Thanks to these stable metal oxides and improved interface properties, ambient stability (retaining 95% of initial PCE after 1 month), thermal stability (retaining 80% of initial PCE after 2 weeks) and light stability (retaining 90% of initial PCE after 1000 hours aging) of resultant devices are enhanced significantly. In addition, owing to the low‐temperature fabrication procedures of the entire device, we have obtained a PCE of over 21% for flexible IPSCs with enhanced operational stability. [ABSTRACT FROM AUTHOR]