Electrically Responsive Photonic Crystals with Enhanced Suspension Stability and Color Saturation for Electrophoretic Displays and Smart Windows.

Electrophoretic displays (EPDs) based on photonic crystals show great potential due to their reduced eye fatigue and low power consumption. However, the current image quality and service life of this system still face great challenges. In this work, we fabricated a new kind of electrically responsive photonic crystal (ERPC) device based on PSMA@SiO2 liquid colloidal crystals (LCCs) for EPDs. By introduction of the PSMA core with lower density and higher refractive index, the suspension stability and color saturation of PSMA@SiO2 LCCs were greatly enhanced compared with those of bare SiO2 LCCs. The PSMA@SiO2 LCCs showed brilliant colors, wide color tuning range (∼200 nm), and good reversibility under low voltages (<4 V). Interestingly, the transparency of PSMA@SiO2 LCCs could also be obviously regulated by an electric field, which was different from the traditional ways that change the thickness of PCs or contrast of refractive index (Δn) between the nanospheres and matrix. This transparency modulation offered a novel idea for the transmittance control of smart windows. As a proof of concept, we fabricated a new type of patterned ERPC device to demonstrate their potential in electrophoretic displays and smart windows with controllable transmittance under an electric field.

Immobilization of Multivalent Titanium Cations on Magnetic Composite Microspheres for Highly Efficient DNA Extraction and Amplification.

Magnetic-assisted DNA testing technology has attracted much attention in genetics, clinical diagnostics, environmental microbiology, and molecular biology. However, achieving satisfying DNA adsorption and desorption efficiency in real samples is still a big challenge. In this paper, a new kind of high-quality magnetic composite microsphere of MM@PGMA-PA-Ti4+ was designed and prepared for DNA extraction and detection based on the strong interaction of Ti4+ and phosphate groups. By taking the advantages of high magnetic susceptibility and high Ti4+ content, the MM@PGMA-PA-Ti4+ microspheres possessed remarkable extraction capacity for mimic biological samples (salmon sperm specimens) with saturated loadings up to 533.0 mg/g. When the DNA feeding amount was 100 µg and the MM@PGMA-PA-Ti4+ dosage was 1 mg, the adsorption and desorption efficiencies were 80 and 90%, respectively. The kinetic and equilibrium extraction data were found to fit well with the pseudo-second-order model and Freundlich isotherm model. Furthermore, the MM@PGMA-PA-Ti4+ microspheres were successfully employed for DNA extraction from mouse epithelial-like fibroblasts. The extraction ability (84 ± 4 µg/mg) and DNA purity were superior to the comparative commercial spin kits, as evaluated by electrophoresis assays and qPCR analysis. The experimental results suggest that the MM@PGMA-PA-Ti4+ microspheres possess great potential as an adsorbent for DNA purification from complex biological samples.

Prevalence, diagnosis, and treatment of chronic obstructive pulmonary disease in a hospitalized lung cancer population: a single center study.

Background: Chronic obstructive pulmonary disease (COPD) often coexists with lung cancer (LC) and has a detrimental effect on the prognosis of LC patients. Presently, there is a lack of adequate assessment regarding the management of COPD in LC patients. This study assessed the screening, prevalence, diagnosis and treatment of COPD in hospitalized LC patients and compared the management practices between two departments at our hospital. Methods: We retrospectively assessed the data of 3,578 patients diagnosed with primary LC in the Department of Respiratory and Critical Care Medicine and the Department of Thoracic Surgery from January 2019 to December 2020. We also compared the rate of spirometry, COPD diagnosis and COPD inhalation treatment between the LC patients from both departments, the proportion of patients aware of their COPD diagnosis and adhered to inhaled therapy, and analyzed factors influencing COPD diagnosis and inhalation treatment. Results: A total of 2,762 (77.2%) LC patients underwent spirometry, and the observed spirometry-defined COPD prevalence was 25.0% (690/2,762). The proportion of spirometry performed in the Department of Thoracic Surgery was significantly higher than in the Department of Respiratory and Critical Care Medicine (90.5% vs. 62.9%; P<0.001). The overall COPD diagnosis rate recorded in the discharge diagnosis in the 690 spirometry-defined COPD patients was 46.5% (321/690), and the COPD treatment rate during hospitalization was 45.2% (312/690). In addition, physicians from the Department of Respiratory and Critical Care Medicine had a higher diagnostic rate than surgeons from the Department of Thoracic Surgery (69.1% vs. 7.5%; P<0.001), as well as a better-standardized COPD treatment rate (60.6% vs. 18.6%; P<0.001). Further, the proportion of COPD inhalation treatment was higher among LC patients with COPD recorded in discharge diagnosis (74.8% vs. 19.5%; P<0.001), and multivariate logistic regression analysis showed that COPD recorded in discharge diagnosis significantly increased the proportion of COPD awareness post-hospitalization (P<0.001). Conclusions: This study showed that COPD could be a frequently undiagnosed and undertreated condition among LC patients, especially those hospitalized in a surgical ward. Additionally, a discharge diagnosis of COPD may increase the rate of inhalation treatment and awareness of the condition in LC patients.

Improved U-net-based leukocyte segmentation method.

Significance: Leukocytes are mainly composed of neutrophils, basophils, eosinophils, monocytes, and lymphocytes. The number and proportion of different types of leukocytes correspond to different diseases, so an accurate segmentation of each type of leukocyte is important for the diagnosis of disease. However, the acquisition of blood cell images can be affected by external environmental factors, which can lead to variable light and darkness, complex backgrounds, and poorly characterized leukocytes. Aim: To address the problem of complex blood cell images collected under different environments and the lack of obvious leukocyte features, a leukocyte segmentation method based on improved U-net is proposed. Approach: First, adaptive histogram equalization-retinex correction was introduced for data enhancement to make the leukocyte features in the blood cell images clearer. Then, to address the problem of similarity between different types of leukocytes, convolutional block attention module is added to the four skip connections of U-net to focus the features from spatial and channel aspects, so that the network can quickly locate the high-value information of features in different channels and spaces. It avoids the problem of large amount of repeated computation of low-value information, prevents overfitting, and improves the training efficiency and generalization ability of the network. Finally, to solve the problem of class imbalance in blood cell images and to better segment the cytoplasm of leukocytes, a loss function combining focal loss and Dice loss is proposed. Results: We use the BCISC public dataset to verify the effectiveness of the proposed method. The segmentation of multiple leukocytes using the method of this paper can achieve 99.53% accuracy and 91.89% mIoU. Conclusions: The experimental results show that the method achieves good segmentation results for lymphocytes, basophils, neutrophils, eosinophils, and monocytes.

Artemin Promotes the Migration and Invasion of Cervical Cancer Cells through AKT/mTORC1 Signaling.

Background: The neurotrophic factor Artemin (ARTN) is involved in tumor proliferation and metastasis. Nonetheless, ARTN's significance in cervical cancer (CC) has not been studied. In our study, we propose to investigate the biological function of ARTN in CC as well as its particular regulatory mechanism. Methods: Immunohistochemistry (IHC) was used to examine the degree of ARTN protein expression in CC patient tissue. Real-time PCR and Western blotting were performed to reveal related genes' levels in CC cells. The CCK-8 test, the colony formation assay, the wound-healing assay, and the transwell assay were utilized to determine the proliferation, migration, and invasion capabilities, respectively. To generate lung metastasis models, stable ARTN-expressing SiHa cells were injected into the caudal tail vein of mice. IHC was used to examine the protein levels in CC mice model tissues. Results: ARTN was overexpressed in CC tissues relative to normal cervical tissues and linked positively with lymph node metastases (P=0.012) and recurrence (P=0.015) in CC patients. In vitro, ARTN overexpression promoted the proliferation, invasion, and migration of CC cells. In contrast, the consequences of depleting endogenous ARTN were the opposite. Moreover, overexpression of ARTN increased lung metastasis of CC cells in vivo and shortened the lifespan of mice models. In addition, ARTN overexpression significantly enhanced AKT phosphorylation on Ser473 and mTOR phosphorylation on Ser2448 and promoted the epithelial-mesenchymal transition (EMT) cascade. In addition, rapamycin, a selective inhibitor of mTORC1, might rescue the EMT phenotype caused by ARTN. Conclusion: Our findings suggested that ARTN may enhance CC metastasis through the AKT/mTORC1 pathway. ARTN is anticipated to be a novel potential therapeutic target for the treatment of CC metastases.

Leukocyte Segmentation Method Based on Adaptive Retinex Correction and U-Net.

To address the issues of uneven illumination and inconspicuous leukocyte properties in the gathered cell pictures, a leukocyte segmentation method based on adaptive retinex correction and U-net was proposed. The procedure begins by processing a peripheral blood image to clearly distinguish leukocytes from other components in the image. The adaptive retinex correction, which is based on multiscale retinex with colour replication (MSRCR), redefines the colour recovery function by introducing Michelson contrast. Then, the image is trained with the U-net convolutional neural network, and the leukocyte segmentation is completed. The innovation is in the manner of processing peripheral blood images, which improves the accuracy of leukocyte segmentation. This study conducts experimental evaluations on the Cellavision, BCCD, and LISC datasets. The experimental results show that the method in this study is better than the current best method, and the segmentation accuracy rate reaches 98.87%.

Robust Large-Sized Photochromic Photonic Crystal Film for Smart Decoration and Anti-Counterfeiting.

Photochromic materials are widely investigated due to their vivid color transformation for many real applications. In this work, a new kind of multiangle photochromic photonic crystal (PC) material with high robustness and long durability for smart phone decoration and anticounterfeiting features is fabricated. After thermal mixing of spiropyran powder and monodisperse core-interlayer-shell (CIS) particles, a large-area and high-quality photochromic PC film has been prepared by the self-designed bending-induced ordering technique (BIOT). The spiropyran powder can be well dispersed in the order-structured PC system, so the perfect synergistic combination of photochromism and angle-dependent structure colors can be achieved. The color-switching test for the as-prepared photochromic PC film proved its excellent reversibility and stability. Because of the excellent flexibility of the photo-cross-linked PC films, they can be designed and cut into various shapes with high robustness and long durability. Interestingly, a temperature-controlled photochromic effect was found in this photochromic PC system. Therefore, the as-prepared photochromic PC films can play a significant role in the fields of smart decoration and anticounterfeiting by their unique color switching effects under different stimuli. More importantly, our work verified the feasibility of this route to prepare a series of large-sized advanced smart PC devices by adding versatile functional materials.

Efficient Synthesis of α-FeOOH from Pickling Wastewater in Falling Film Tower and Its Kinetics.

An efficient way to synthesize α-FeOOH from pickling wastewater in a falling film tower was proposed for the first time. This method overcomes the shortcomings of the traditional air oxidation method, and its production efficiency is increased by 16 times. The purity of α-FeOOH synthesized from pickling wastewater can reach 96.3%, and the iron recovery rate is greater than 90%. At the same time, we have systematically studied its kinetics in the falling film tower. The reaction rate constant k at different temperatures was also determined with the activation energy E a = 32.2497 kJ/mol and the pre-exponential A = 47.4132 s-1. In addition, based on the double-film theory, a corresponding macrokinetic model was established. Also, the Hatta number in the reaction system was obtained, which proved the excellent gas-liquid mass transfer performance in the falling film tower. This work provides a promising method for the efficient production of α-FeOOH and the recycling of pickling wastewater.

MTA1, a Target of Resveratrol, Promotes Epithelial-Mesenchymal Transition of Endometriosis via ZEB2.

Endometriosis is a benign disease that shares some malignant features. Epithelial-mesenchymal transition (EMT) is involved in the pathogenesis of endometriosis. Metastasis-associated protein 1 (MTA1) plays an important role in various cancers by promoting EMT, yet there are no studies on its function in endometriosis. In the present study, we found that MTA1 was highly expressed in the ectopic endometrium of endometriosis patients and that the expression of MTA1 was related to the revised American Fertility Society stage. MTA1 facilitated endometrial stroma cell proliferation, migration, and invasion by inducing EMT, and the promotion function and MTA1 expression were suppressed by resveratrol, a natural polyphenol. Moreover, we revealed that MTA1 induced EMT through interaction with ZEB2. The findings in a mouse endometriosis model further showed that MTA1 and ZEB2 were upregulated in ectopic tissues and that resveratrol inhibited the growth of ectopic lesions and expression of MTA1 and ZEB2. Taken together, we demonstrate that MTA1 is a protein that promotes EMT via interacting with ZEB2 in the pathogenesis of endometriosis, and may be a target of resveratrol.

Metastasis-associated protein 1, modulated by miR-30c, promotes endometrial cancer progression through AKT/mTOR/4E-BP1 pathway.

OBJECTIVE: Though metastasis-associated protein 1 (MTA1) is widely overexpressed in human cancers and is associated with advanced clinicopathological characteristics and survival in related diseases, the association between MTA1 and endometrial cancer (EC) is little known and needs to be studied. METHODS: Western blot and immunohistochemistry were used to analyze protein expression level of cells and tissues, while real-time PCR was used for RNA detection. Bioinformatics tool analysis revealed the relationship between MTA1 and clinicopathological characteristics and survival. CCK-8 assay, colony-formation assay, cell scratch assay, and Transwell assay were performed to determine cell proliferation, migration and invasion abilities, respectively. RESULTS: The expression level of MTA1 was significantly higher in human EC tissues than in normal endometrium. MTA1 expression was correlated positively with lymph nodes metastasis and poor survival rate in EC. Experimentally overexpressed MTA1 could promote cell proliferation, migration and invasion abilities of EC cell lines Ishikawa, HEC-1B, and RL-952, while reduction of MTA1 inhibited these cell biological behaviors. Moreover, MTA1 could also reverse the negative effect of miR-30c, a direct modulator of MTA1, on EC cells. Our research also revealed that overexpression of MTA1 contributed to EC tumor growth, while knockdown of MTA1 resulted in tumor growth inhibition. Additionally, the phosphorylation levels of mTOR (S2448) and 4E-BP1 (T37/46) changed significantly along with AKT (T308) under regulation of MTA1, both in vivo and vitro. CONCLUSION: Our results showed that MTA1, as a downstream target of miR-30c, might promote EC progression via AKT/mTOR/4E-BP1 pathway, which indicated the potential therapy target of MTA1 in EC.