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The wave energy harvesting efficiency (EHE) and electrical energy storage efficiency (ESE) significantly impact ocean power at the front-end and back-end stages, respectively. In this work, to maximize the overall energy conversion affected by these two factors, a clip-like structured pendulum coupled nanogenerator (CP-CNG) integrated with a dual-track circuit (DTC) is elaborately designed to address poor energy conversion of the TENGs for marine monitoring. The optimized EHE was realized through coupling one freestanding triboelectric nanogenerator (FR-TENG) unit and two electromagnetic generator (EMG) units into two contact-separation triboelectric nanogenerator (CS-TENG) units. The space utilization rate of CP-CNG can be as high as 91.9%. Meanwhile, increased ESE is achieved by integrating DTC as voltage regulators, which perform backend energy management for CS-TENG and EMG, respectively. It is worth noting that for a 1 mF capacitor, the stored energy via the cooperation of CP-CNG and DTC can reach 60.7 mJ in 110 s, which is about 164 times that of CS-TENG (0.37 mJ) coupling with FR-TENG and EMG and 1.6 times that of CS-TENG (36.8 mJ) with buck circuit, demonstrating excellent synergistic effects. Owing to the synergistic effect, one CP-CNG can continuously drive four thermohygrometers under simulated water wave conditions. In additional, a hazard alarm system, including an immersion sensor, Bluetooth and gateway support, can also be powered by one CP-CNG successfully. This work develops a state-of-the-art concept for maximum energy conversion of TENGs, which should have a profound impact on the design of high-performance TENGs in the future. [Display omitted] • Space utilization of 91.9% through highly-coupled different generators. • Introduce a dual-track energy managed circuit instead of single one. • Synergistically enhanced output through space utilization and management circuit. [ABSTRACT FROM AUTHOR]

Polarimetric radars make it possible to retrieve information on hydrometeors types, sizes and concentrations. Additional information on cloud electrification can be obtained from Lightning Mapping Arrays (LMAs). To study the development time and height of the hydrometeors and electrification require tracking their evolution within the lifecycle of convective cells. A new methodology for multi-cell identification and tracking (MCIT) is presented in this study. The algorithm in this study is different from traditional tracking methods; this new algorithm is applied to time series of radar volume scans. It tracks local maxima of vertically integrated liquid (VIL) water by identifying the two cells in consecutive radar scans that have maximum common VIL. The vertical profile of the polarimetric variables is used for constructing the time-height cross section of the cells' microphysical properties around the peak reflectivity as a function of height. The LMA sources that occur within the cell area are integrated as a function of height as well for each time step, as determined by the radar volume scans. The result of the tracking can provide insights on the evolution of storms, hydrometer types, precipitation initiation and cloud electrification under different thermodynamic and aerosol conditions. The details of the MCIT algorithm, its products and their performance for different type of storms are described in this paper. • Development of a novel cloud cell tracking algorithm. • Tracking cloud types include: convective and stratiform, isolated and clustered. • Tracking cloud cells through maturation into stratiform storm elements. • Use a synergy of polarimetric radar, satellite, lightning detection and model data. • Algorithm has flexible output options and possibilities for further studies. [ABSTRACT FROM AUTHOR]

Graphical abstract Highlights • NiO, a new cataluminescence sensing material, was synthesized by a simple template-free hydrothermal method. • Camellia-like NiO with high specific surface area showed excellent sensing performance towards H 2 S. • The sensing mechanism was studied which proved the main emission peak is from SO 2 *. Abstract In this work, three different microstructures of NiO nanomaterials including tremella, camellia and hexagonal nanosheets were successfully synthesized by a simple template-free hydrothermal method. Among them, camellia-like NiO was reported and applied to cataluminescence (CTL) for the first time. SEM, TEM, XRD, XPS, BET and BJH were employed to characterize the as-prepared samples. As sensing materials, these NiO with various morphologies showed different CTL capabilities to detect H 2 S, and the camellia-like NiO exhibited the best catalytic performance with high sensitivity and selectivity, which may be attributed to the synergistic effect of its high specific surface area, porous nanostructure, as well as the surface adsorption oxygen. After optimization, a good linear relationship was obtained in the range of 0.8–30.8 ppm and the detection limit (S/N = 3, LOD) was 0.3 ppm. Sixteen common volatile organic compounds (VOCs), such as carbon disulfide, ethyl mercaptan and formaldehyde, were discussed as possible interferent components, and the sensing mechanism of the CTL sensing towards H 2 S was discussed in detail. Camellia-like NiO could be used as a new sensing material for H 2 S monitoring. [ABSTRACT FROM AUTHOR]

In order to analyze the brain shift situation accurately, we need to register the medical image and analyze its deformation. In this paper, we introduce a framework with volume-preserving registration for brain shift analysis. First, a volume-preserving mapping is introduced for general manifolds supported by a rigorous continuous theory. The registration is then performed on the spherical tetrahedron mesh with MRI gray values. The registration can retain the equality of local volume elements while registering the manifold to a template at the same time. We use simulated brain shift data to test our method. The results show that our method can efficiently register the brain while preserving the volume of each vertex. [ABSTRACT FROM AUTHOR]

We report that gastric cancer patients exhibiting high levels of heparanase 2 (Hpa2) survive longer. Similarly, mice administrated with gastric carcinoma cells engineered to overexpress Hpa2 produced smaller tumors and survived longer than mice administrated with control cells. These beneficial effects were found to associate with increased phosphorylation of AMP-activated protein kinase (AMPK) that play an instrumental role in cell metabolism and is situated at the center of a tumor suppressor network. We also found that MG132, an inhibitor of the proteasome that results in proteotoxic stress, prominently enhances Hpa2 expression. Notably, Hpa2 induction by MG132 appeared to be mediated by AMPK, thus establishing a loop that feeds itself where Hpa2 enhances AMPK phosphorylation that, in turn, induces Hpa2 expression, possibly leading to attenuation of gastric tumorigenesis. Heparanase is highly implicated in tumor metastasis due to its capacity to cleave heparan sulfate and, consequently, remodel the extracellular matrix underlying epithelial and endothelial cells. In striking contrast, only little attention was given to its close homolog, heparanase 2 (Hpa2), possibly because it lacks heparan sulfate-degrading activity typical of heparanase. We subjected sections of gastric carcinoma to immunostaining and correlated Hpa2 immunoreactivity with clinical records, including tumor grade, stage and patients' status. We over-expressed Hpa2 in gastric carcinoma cell lines and examined their tumorigenic properties in vitro and in vivo. We also evaluated the expression of Hpa2 by gastric carcinoma cells following inhibition of the proteasome, leading to proteotoxic stress, and the resulting signaling responsible for Hpa2 gene regulation. Here, we report that gastric cancer patients exhibiting high levels of Hpa2 survive longer. Similarly, mice administrated with gastric carcinoma cells engineered to over-express Hpa2 produced smaller tumors and survived longer than mice administrated with control cells. This was associated with increased phosphorylation of AMP-activated protein kinase (AMPK), a kinase that is situated at the center of a tumor suppressor network. We also found that MG132, an inhibitor of the proteasome that results in proteotoxic stress, prominently enhances Hpa2 expression. Notably, Hpa2 induction by MG132 appeared to be mediated by AMPK, and AMPK was found to induce the expression of Hpa2, thus establishing a loop that feeds itself where Hpa2 enhances AMPK phosphorylation that, in turn, induces Hpa2 expression, leading to attenuation of gastric tumorigenesis. These results indicate that high levels of Hpa2 in some tumors are due to stress conditions that tumors often experience due to their high rates of cell proliferation and high metabolic demands. This increase in Hpa2 levels by the stressed tumors appears critically important for patient outcomes. [ABSTRACT FROM AUTHOR]

• Protective autophagy induced by DDP decreases chemosensitivity in GC cells. • MGMT inhibited ATG4B to repress autophagy. • Inhibition of autophagy enhanced the chemosensitivity to DDP in GC xenograft model. • High MGMT expression and low ATG4B expression are significantly correlated with survival of GC. Cisplatin (DDP) is the first-line drug for the treatment of gastric cancer (GC). However, DDP resistance is common. Autophagy, which is closely related to chemoresistance, is a process of resolving and recycling proteins and damaged cellular organs. Additionally, O-6-methylguanine-DNA methyltransferase (MGMT) is responsible for alkylating drug resistance. However, the relationship between autophagy and MGMT in response to DDP in GC is still unknown. In the present study, we determined that autophagy induced by DDP decreases chemosensitivity in GC cell lines. DDP may have induced autophagy in GC by inhibiting MGMT to increase autophagy-related gene (ATG) 4B. Inhibition of MGMT-mediated ATG4B suppression resulted in autophagy induction and DDP resistance. In vivo , combined DDP and autophagy inhibitor chloroquine (CQ) enhanced the anti-tumor effect of DDP; additionally, the negative correlation of MGMT and ATG4B was confirmed. High expression of MGMT and low expression of ATG4B were significantly correlated with favorable five-year survival rate (P < 0.05) in 66 clinicopathologically characterized GC cases. Our study demonstrate that DDP inhibits MGMT-mediated autophagy suppression to decrease chemosensitivity in GC, which provides a novel therapeutic strategy to promote DDP chemosensitivity in GC. [ABSTRACT FROM AUTHOR]

The acrolein derived cyclic 1,N 2 -propanodeoxyguanosine adduct (Acr-dG), formed primarily from ω-3 polyunsaturated fatty acids such as docosahexaenoic acid (DHA) under oxidative conditions, while proven to be mutagenic, is potentially involved in DHA-induced apoptosis. The latter may contribute to the chemopreventive effects of DHA. Previous studies have shown that the levels of Acr-dG are correlated with apoptosis induction in HT29 cells treated with DHA. Because Acr-dG is shown to be repaired by the nucleotide excision repair (NER) pathway, to further investigate the role of Acr-dG in apoptosis, in this study, NER-deficient XPA and its isogenic NER-proficient XAN1 cells were treated with DHA. The Acr-dG levels and apoptosis were sharply increased in XPA cells, but not in XAN1 cells when treated with 125 μM of DHA. Because DHA can induce formation of various DNA damage, to specifically investigate the role of Acr-dG in apoptosis induction, we treated XPA knockdown HCT116 + ch3 cells with acrolein. The levels of both Acr-dG and apoptosis induction increased significantly in the XPA knockdown cells. These results clearly demonstrate that NER deficiency induces higher levels of Acr-dG in cells treated with DHA or acrolein and sensitizes cells to undergo apoptosis in a correlative manner. Collectively, these results support that Acr-dG, a ubiquitously formed mutagenic oxidative DNA adduct, plays a role in DHA-induced apoptosis and suggest that it could serve as a biomarker for the cancer preventive effects of DHA. [ABSTRACT FROM AUTHOR]