Inhibition of neddylation disturbs zygotic genome activation through histone modification change and leads to early development arrest in mouse embryos.

Post-translational modification and fine-tuned protein turnover are of great importance in mammalian early embryo development. Apart from the classic protein degradation promoting ubiquitination, new forms of ubiquitination-like modification are yet to be fully understood. Here, we demonstrate the function and potential mechanisms of one ubiquitination-like modification, neddylation, in mouse preimplantation embryo development. Treated with specific inhibitors, zygotes showed a dramatically decreased cleavage rate and almost all failed to enter the 4-cell stage. Transcriptional profiling showed genes were differentially expressed in pathways involving cell fate determination and cell differentiation, including several down-regulated zygotic genome activation (ZGA) marker genes. A decreased level of phosphorylated RNA polymerase II was detected, indicating impaired gene transcription inside the embryo cell nucleus. Proteomic data showed that differentially expressed proteins were enriched in histone modifications. We confirmed the lowered in methyltransferase (KMT2D) expression and a decrease in histone H3K4me3. At the same time, acetyltransferase (CBP/p300) reduced, while deacetylase (HDAC6) increased, resulting in an attenuation in histone H3K27ac. Additionally, we observed the up-regulation in YAP1 and RPL13 activities, indicating potential abnormalities in the downstream response of Hippo signaling pathway. In summary, we found that inhibition of neddylation induced epigenetic changes in early embryos and led to abnormalities in related downstream signaling pathways. This study sheds light upon new forms of ubiquitination regulating mammalian embryonic development and may contribute to further investigation of female infertility pathology.

Differential alternative splicing landscape identifies potentially functional RNA binding proteins in early embryonic development in mammals.

Alternative splicing (AS) as one of the important post-transcriptional regulatory mechanisms has been poorly studied during embryogenesis. In this study, we comprehensively collected and analyzed the transcriptome data of early embryos from human and mouse. We found that AS plays an important role in this process and predicted candidate RNA binding protein (RBP) regulators that are associated with reproductive development. The predicted RBPs such as EIF4A3, MAK16, SRSF2, and UTP23 were found to be associated with reproductive disorders. By Smart-seq2 sequencing analysis, we identified 5445 aberrant alternative splicing events in Eif4a3-knockdown embryos. These events were preferentially associated with RNA processing. In conclusion, our work on the landscape and potential function of alternative splicing events will boost further investigation of detailed mechanisms and key factors regulating mammalian early embryo development and promote the inspiration of pharmaceutical approaches for disorders in this crucial biology process.

Identification of cuproptosis-related gene clusters and immune cell infiltration in major burns based on machine learning models and experimental validation.

Introduction: Burns are a global public health problem. Major burns can stimulate the body to enter a stress state, thereby increasing the risk of infection and adversely affecting the patient's prognosis. Recently, it has been discovered that cuproptosis, a form of cell death, is associated with various diseases. Our research aims to explore the molecular clusters associated with cuproptosis in major burns and construct predictive models. Methods: We analyzed the expression and immune infiltration characteristics of cuproptosis-related factors in major burn based on the GSE37069 dataset. Using 553 samples from major burn patients, we explored the molecular clusters based on cuproptosis-related genes and their associated immune cell infiltrates. The WGCNA was utilized to identify cluster-specific genes. Subsequently, the performance of different machine learning models was compared to select the optimal model. The effectiveness of the predictive model was validated using Nomogram, calibration curves, decision curves, and an external dataset. Finally, five core genes related to cuproptosis and major burn have been was validated using RT-qPCR. Results: In both major burn and normal samples, we determined the cuproptosis-related genes associated with major burns through WGCNA analysis. Through immune infiltrate profiling analysis, we found significant immune differences between different clusters. When K=2, the clustering number is the most stable. GSVA analysis shows that specific genes in cluster 2 are closely associated with various functions. After identifying the cross-core genes, machine learning models indicate that generalized linear models have better accuracy. Ultimately, a generalized linear model for five highly correlated genes was constructed, and validation with an external dataset showed an AUC of 0.982. The accuracy of the model was further verified through calibration curves, decision curves, and modal graphs. Further analysis of clinical relevance revealed that these correlated genes were closely related to time of injury. Conclusion: This study has revealed the intricate relationship between cuproptosis and major burns. Research has identified 15 cuproptosis-related genes that are associated with major burn. Through a machine learning model, five core genes related to cuproptosis and major burn have been selected and validated.

Gut Microbiota and Respiratory Infections: Insights from Mendelian Randomization.

The role of the gut microbiota in modulating the risk of respiratory infections has garnered increasing attention. However, conventional clinical trials have faced challenges in establishing the precise relationship between the two. In this study, we conducted a Mendelian randomization analysis with single nucleotide polymorphisms employed as instrumental variables to assess the causal links between the gut microbiota and respiratory infections. Two categories of bacteria, family Lactobacillaceae and genus Family XIII AD3011, were causally associated with the occurrence of upper respiratory tract infections (URTIs). Four categories of gut microbiota existed that were causally associated with lower respiratory tract infections (LRTIs), with order Bacillales and genus Paraprevotella showing a positive association and genus Alistipes and genus Ruminococcaceae UCG009 showing a negative association. The metabolites and metabolic pathways only played a role in the development of LRTIs, with the metabolite deoxycholine acting negatively and menaquinol 8 biosynthesis acting positively. The identification of specific bacterial populations, metabolites, and pathways may provide new clues for mechanism research concerning therapeutic interventions for respiratory infections. Future research should focus on elucidating the potential mechanisms regulating the gut microbiota and developing effective strategies to reduce the incidence of respiratory infections. These findings have the potential to significantly improve global respiratory health.

Impact of Digital Globalization on Health Behavior Through Integration of Ideological and Political Education in Schools Leading to the Spirit for Fighting Against (COVID)-19.

Objectives: In this study, we examined the impact of digital globalization on health behavior among students in Chinese schools, particularly in relation to the fight against COVID-19. Despite China's well-established system and positive health behavior towards the pandemic, students' health behavior is lacking. The study focuses on the role of ideological and political education in addressing this issue. Methods: Data were collected from Chinese schools with the help of a survey questionnaire by using area cluster sampling. Data analysis was carried out by employing Smart PLS. Results: We found that digital globalization has a positive effect on health behavior. Digital globalization also has a positive effect on global knowledge about COVID-19 and ideological and political education leading to health behavior. Conclusion: We identified that the influential role of digital globalization can change health behavior. Digital globalization led to global knowledge about the COVID-19 and further caused an influence health behavior among schools that led to improved health behavior of students. The outcomes of the study have valuable importance for the management of schools to decrease the effect of COVID-19 by developing positive health behavior.

Upregulation of circ_0080968 in diabetic foot ulcer inhibits wound healing via repressing the migration and promoting proliferation of keratinocytes.

BACKGROUND: Diabetic foot ulcer (DFU) is a serious chronic complication of diabetes mellitus whose pathogenesis remains unclear. Circular RNA (circRNA) refers to a group of covalently closed non-coding RNAs that are reported to be dysregulated in patients with DFU. However, the mechanism whereby dysregulation in circRNAs contributes to DFU remains unclear. In this study, we investigated the role of dysregulated circRNAs in DFU. MATERIALS AND METHODS: A gene expression dataset was downloaded from the Gene Expression Omnibus portal and analyzed by the limma package of R. The levels of 24 upregulated circRNAs were detected in two independent cohorts by RT-qPCR. Interactions between miRNAs and circRNAs were predicted through bioinformatics and confirmed using a dual luciferase assay. The circularity and subcellular localization of circRNA-080968 was examined by northern blotting after digestion with RNase-R and in situ hybridization. Cell migration and proliferation were examined using Transwell and MTT assays. The apoptotic cells were detected by flow cytometry. RESULTS: The level of circRNA-080968 was upregulated in DFU tissues compared to that of non-DFU samples and normal human wounds. CircRNA-080968 was mainly localized in the cytoplasm and its overexpression inhibited the migration and promoted the proliferation of keratinocytes. MiR-326 and miR-766-3p were identified to interact with and be negatively correlated with circRNA-080968 levels. Increased glucose upregulated circRNA-080968, and its overexpression accelerated the degradation of both miR-326 and miR-766-3p. Reduced levels of miR-326 and miR-766-3p upregulated the expression of several genes controlling cell adhesion and proliferation which are related to the pathogenesis of DFU. CONCLUSIONS: The upregulation of circRNA-080968 in DFU induced the degradation of miR-326 and miR-766-3p, which further repressed the migration and increased the proliferation of keratinocytes.

Niobium- and cobalt-modified dual-source-derived porous carbon with a honeycomb-like stable structure for supercapacitor and hydrogen evolution reaction.

Designing porous carbon materials with tailored architecture and appropriate compositions is essential for supercapacitor (SC) and hydrogen evolution reaction (HER). Herein, Nb/Co-modified dual-source porous carbon (Nb/Co-DSPC) with a honeycomb structure was obtained by introducing a secondary carbon source (Co/Zn-ZIF) and transition metal Nb into activated Typha carbon (ATC). The addition of a secondary carbon source and Nb resulted in superior specific surface area (1272.38 m2/g), excellent hydrophilicity (34.73°) and abundant bimetallic active sites (Nb/Co-Nx) in Nb/Co-DSPC, providing excellent charge storage capacity and electrocatalytic activity. The Nb/Co-DSPC electrode displayed an outstanding capacitance of 337 F/g at 0.5 A/g and showed excellent stability after 15,000 charge-discharge cycles. In addition, Nb/Co-DSPC shows an overpotential of 114 mV at 10 mA cm-2, better than those of Co-DSPC (139 mV) and ATC (162 mV) alone. This study offers a reliable strategy for advanced multifunctional porous carbon electrode materials preparations.

Designing nitrogen-enriched heterogeneous NiS@CoNi2S4 embedded in nitrogen-doped carbon with hierarchical 2D/3D nanocage structure for efficient alkaline hydrogen evolution and triiodide reduction.

Fabrication of efficient non-precious electrocatalysts with hierarchical nanostructures and the desired compositions is highly desirable to enhance the catalytic activity and stability for hydrogen evolution reaction (HER) and triiodide reduction reaction (IRR). This work proposes a zeolitic imidazolate framework (ZIF) template-based strategy to generate sulfide embedded in nitrogen-doped carbon with a hierarchical 2D/3D nanocage structure. ZIF-67, as a sacrificial template, is first etched to form 2D/3D NiCo layered double hydroxide/2-Methylimidazole (NiCo LDH/MeIm) and then converted to CoNi2S4 nanoparticles embedded in nitrogen-doped carbon (CoNi2S4/NC) through one-step sulfurization and pyrolysis. When a core-shell ZIF-8@ZIF-67 is designed as a template for the generation of Ni@NiCo LDH/MeIm, the obtained NiS@CoNi2S4/NC not only retains the unique 2D/3D nanostructure but also has a high N content, abundant active sites, larger specific surface area, and hierarchical pore distribution. NiS@CoNi2S4/NC mediates an overpotential of 126 mV at 10 mA cm-2 and a Tafel slope of 47.2 mV dec-1 in the alkaline HER. The solar cell equipped with NiS@CoNi2S4/NC as the IRR catalyst achieves a high cell efficiency of 7.96 %. NiS@CoNi2S4/NC shows durably high HER and IRR activity. This controllable synthetic strategy provides a valuable support for developing efficient catalysts in electrocatalytic energy conversion systems.

Long-term exposure to nano-TiO2 interferes with microbial metabolism and electron behavior to influence wastewater nitrogen removal and associated N2O emission.

The extensive use of nano-TiO2 has caused concerns regarding their potential environmental risks. However, the stress responses and self-recovery potential of nitrogen removal and greenhouse gas N2O emissions after long-term nano-TiO2 exposure have seldom been addressed yet. This study explored the long-term effects of nano-TiO2 on biological nitrogen transformations in a sequencing batch reactor at four levels (1, 10, 25, and 50 mg/L), and the reactor's self-recovery potential was assessed. The results showed that nano-TiO2 exhibited a dose-dependent inhibitory effect on the removal efficiencies of ammonia nitrogen and total nitrogen, whereas N2O emissions unexpectedly increased. The promoted N2O emissions were probably due to the inhibition of denitrification processes, including the reduction of the denitrifying-related N2O reductase activity and the abundance of the denitrifying bacteria Flavobacterium. The inhibition of carbon source metabolism, the inefficient electron transfer efficiency, and the electronic competition between the denitrifying enzymes would be in charge of the deterioration of denitrification performance. After the withdrawal of nano-TiO2 from the influent, the nitrogen transformation efficiencies and the N2O emissions of activated sludge recovered entirely within 30 days, possibly attributed to the insensitive bacteria survival and the microbial community diversity. Overall, this study will promote the current understanding of the stress responses and the self-recovery potential of BNR systems to nanoparticle exposure.

Neddylation Inhibition Causes Impaired Mouse Embryo Quality and Blastocyst Hatching Failure Through Elevated Oxidative Stress and Reduced IL-1ß.

Mammalian blastocyst hatching is an essential prerequisite for successful embryo implantation. As the rate-limiting step of current assisted reproductive technology, understanding the key factors regulating blastocyst hatching would be significantly helpful to improve the performance of the assisted reproductive practice. In early embryo development, the fine-tuned elimination of maternal materials and the balanced protein turnover are inevitable for the competent to hatch and implant into endometrium. Neddylation, a ubiquitination-like protein modification, has been shown to be involved in oocyte maturation and early embryo development. In this study, aiming to discover an unknown role of neddylation in the blastocyst hatching process, we provided functional evidence of neddylation in mammalian embryo quality and blastocyst hatching. Treatment with MLN4924, a specific neddylation inhibitor, lowered the embryo quality and dramatically reduced the hatching rate in mouse blastocysts. The transcriptional profile showed the upregulation of oxidative stress-related genes and aberrant expression of immune-related genes. The elevated oxidative stress was validated by qPCR and markers of apoptosis, DNA damage, reactive oxygen species, and cytoskeleton. Moreover, we found the secreted IL-1ß level was reduced in an NF-κB-independent manner, leading to the final poor embryo quality and blastocyst hatching failure. This is the first report of neddylation being of great importance in the mammalian blastocyst hatching process. Further investigations uncovering more detailed molecular mechanisms of neddylation regulation in blastocyst hatching would greatly promote not only the understanding of this crucial biological process but also the clinical application in reproductive centers.

Promotion and mechanisms of Bdellovibrio sp. Y38 on membrane fouling alleviation in membrane bioreactor.

Membrane fouling is a major bottleneck limiting the widespread application of membrane bioreactors (MBR). In this study, Bdellovibrio sp. Y38, an obligate bacteriophage bacterium of Bdellovibrio-and-like organisms (BALOs), was enriched into highly concentrated culture medium (106-107 PFU/mL), and daily dosed into the MBR to investigate its effects on membrane fouling mitigation. The strain Y38 prolonged the membrane fouling cycle from 73 days to 90 days, indicating its membrane fouling alleviation potentials. The concentration of BALOs was increased 625 times higher than the control group after the whole operation, resulting in the concentration of chemical oxygen demand and nucleic acids in the liquid phase of the MBR system being significantly increased by 169.8 ± 1.5% and 126.7 ± 2.2%, respectively. The biomass growth rate was reduced by 27.2 ± 0.7% from day 0 to day 54. These results indicated the predation potential of Bdellovibrio sp. Y38 on the microorganisms in the sludge. The improvement of homogenized sludge and filtration and settling performance by the strain Y38 alleviated the membrane fouling. Compared with the control group, the macromolecular proteins in SMP and EPS were partially declined, and the polysaccharide in EPS decreased by 14.0 ± 3.9%, and the ratios of protein content to polysaccharide content (PN/PS) in SMP and EPS significantly increased by 35.6 ± 16.8% and 57.8 ± 6.1% at the middle stage, respectively, indicating the strain Y38 could alleviate membrane fouling by reducing and modifying SMP and EPS. Furthermore, the relative abundance of γ-proteobacteria decreased from 13.2% to 5.1% at the pre-middle stage, and Planctomycetes decreased from 1.5% to 0.8% at the end-stage, which were probably responsible for the membrane fouling mitigation. In addition, the strain Y38 had few impacts on the water treatment performance of MBR. There findings provide a promising strategy for in situ membrane pollution mitigation via exogenous additions of BALOs.

Pluripotency of endogenous AHL-mediated quorum sensing in adaptation and recovery of biological nitrogen removal system under ZnO nanoparticle long-term exposure.

The impacts of quorum sensing (QS) on nanoparticle (NP)-stressed biological nitrogen removal (BNR) system have seldom been addressed yet. In this study, the contributions of endogenous N-acyl-homoserine lactone (AHL)-based QS regulation to the BNR system's adaptation to the zinc oxide (ZnO) NP stress and its recovery potential were systematically investigated. Although 1 mg/L ZnO NPs exerted little impact on the BNR system, chronic exposure to 10 mg/L ones depressed the system's BNR performance which irreversibly impaired the nitrification process even when the system entered the recovery period with no NP added anymore. Meanwhile, ZnO NPs exhibited hormesis effects on the production of AHLs and extracellular polymeric substance (EPS), and activities of superoxide dismutase and catalase. During the ZnO NP exposure period, C4-HSL, C6-HSL, and C10-HSL were discovered to be positively associated with nitrogen removal efficiency, tightly-bound EPS production, and antioxidase activities. Besides, the shifts of Nitrospira, Dechloromonas, Aeromonas, Acinetobacter, Delftia, and Bosea were expected to determine the AHL's dynamic distribution. During the system's recovery stage, Dechloromonas replaced Candidatus_Competibacter as the dominant denitrification-related genus. Dechloromonas abundance elevated with the increased contents of C4-HSL in the aqueous and EPS phases and C10-HSL in EPS and sludge phases, and were expected to promote the activities of BNR-related and antioxidant enzymes, and the EPS production to assist in the recovery of the impaired system's BNR performance. The QS-related BNR genera exhibited higher resilience to ZnO NPs than quorum quenching-related ones, indicating their critical role in nitrogen removal in the restored system. This work provided an insight into the potential pluripotency of AHL-based QS regulation on the ZnO NP-stressed BNR system's adaptation and recovery.

Target-Sequencing of Female Infertility Pathogenic Gene Panel and a Novel TUBB8 Loss-of-Function Mutation.

Genetic screening is an important approach for etiology determination and helps to optimize administration protocols in reproductive centers. After the first pathogenic gene of female infertility was reported in 2016, more and more new pathogenic genes were discovered, and we sought to develop an efficient and cost-effective method for genetic screening in patients. In this study, we designed a target-sequencing panel with 22 female infertility-related genes, namely, TUBB8, PATL2, WEE2, and PANX1 and sequenced 68 primary infertility (PI) and recurrent pregnancy loss (RPL) patients. We sequenced 68 samples reaching an average depth of 1559× and detected 3,134 variants. Among them, 62.2% were synonymous single-nucleotide variants (SNVs) and 36.3% were non-synonymous SNVs. The remaining 1.5% are indels (insertions and deletions) and stop-gains. DNAH11 and TUBB8 are the two genes that mutated most frequently. We also found a novel TUBB8 variant (c.898_900del; p.300_300del), proved its loss-of-function mechanism, and profiled the interactome of the wild-type (WT) and mutant TUBB8 proteins. Overall, this target-sequencing method provides an efficient and cost-effective approach for screening in IVF clinics and will support researchers for the discovery of new pathogenic variants.

Effects of nicotinamide on follicular development and the quality of oocytes.

BACKGROUND: Nicotinamide (NAM) is an important antioxidant, which is closely related to female fertility, but its role has not been clearly elucidated. The purpose of the present study was to investigate the effects of NAM on follicular development at different stages and the quality of oocytes. METHODS: The concentration of NAM in follicular fluid (FF) of 236 women undergoing in vitro fertilization (IVF) was ascertained by enzyme-linked immunosorbent assay (ELISA), and the correlation between NAM and clinical indexes was analyzed. During the in vitro maturation (IVM) of mice cumulus-oocyte complexes (COCs), different concentrations of NAM were added to check the maturation rate and fertilization rate. The reactive oxygen species (ROS) levels in the oocytes treated with different hydrogen peroxide (H2O2) and NAM were assessed. Immunofluorescence staining was performed to measure the proportion of abnormal spindles. RESULTS: The level of NAM in large follicles was significantly higher than that in small follicles. In mature FF, the NAM concentration was positively correlated with the rates of oocyte maturation and fertilization. Five mM NAM treatment during IVM increased maturation rate and fertilization rate in the oxidative stress model, and significantly reduced the increase of ROS levels induced by H2O2 in mice oocytes. CONCLUSIONS: Higher levels of NAM in FF are associated with larger follicle development. The supplement of 5 mM NAM during IVM may improve mice oocyte quality, reducing damage caused by oxidative stress.

Soluble CD83 suppresses experimental food allergy via regulating aberrant T helper 2 responses.

Aberrant T helper-2 (Th2) responses play a critical role in the pathogenesis of allergic diseases. The underlying mechanism is to be further investigated. It is reported that soluble CD83 (sCD83) has immune-regulatory effects. This study aims to investigate the role of sCD83 in the regulation of Th2 polarization. Blood samples were collected from pediatric patients with food allergy (FA). The Th2 response was analyzed by pertinent immunological approaches. An FA murine model was developed to test the role of sCD83 in the regulation of FA response. We found that the serum sCD83 levels were lower in FA patients. A negative correlation was detected between serum sCD83 levels and serum Th2 cytokine levels. The presence of sCD83 suppressed Th2 cell differentiation and antigen-specific Th2 cell activation. sCD83 upregulated the T-bet expression and suppressed the GATA3 expression in CD4+ T cells. Administration of sCD83 suppressed experimental FA. Pediatric FA patients have low serum sCD83 levels. Administration of sCD83 can alleviate experimental FA via suppression of aberrant Th2 polarization.

Rapid Cold Hardening Confers a Transient Increase in Low Temperature Survival in Diapausing Chilo suppressalis Larvae.

The striped stem borer, Chilo suppressalis (Walker), overwinters as a diapausing larva. The diapausing larvae were tested for a rapid cold hardening (RCH) response and its role in the insect’s survival of sub-zero temperatures. When laboratory-reared diapausing larvae were transferred directly from the rearing temperature of 25 °C to −14 °C and maintained there for 2 h, 21% survived. Acclimation of diapausing larvae for 4 h at 5 °C before their exposure for 2 h to −14 °C increased survival to approximately 41%, indicating an RCH response. Durability of RCH effects on low temperature survival was less than 1 h. Although transient in the test, the increased survival acquired through rapid cold hardening may play a role in preparing the diapausing larvae for abrupt temperature drops in the field that would otherwise be lethal.

Disturbance of the let-7/LIN28 double-negative feedback loop is associated with radio- and chemo-resistance in non-small cell lung cancer.

Radio- and chemo-resistance represent major obstacles in the therapy of non-small-cell lung cancer (NSCLC) and the underlying molecular mechanisms are not known. In the present study, during induction of radio- or chemo-resistance in NSCLC cells, dynamic analyses revealed that decreased expression of let-7 induced by irradiation or cisplatin resulted in increased expression of its target gene LIN28, and increased expression of LIN28 then contributed to further decreased expression of let-7 by inhibiting its maturation and biogenesis. Moreover, we showed that down-regulation of let-7 and up-regulation of LIN28 expression promoted resistance to irradiation or cisplatin by regulating the single-cell proliferative capability of NSCLC cells. Consequently, in NSCLC cells, let-7 and LIN28 can form a double-negative feedback loop through mutual inhibition, and disturbance of the let-7/LIN28 double-negative feedback loop induced by irradiation or chemotherapeutic drugs can result in radio- and chemo-resistance. In addition, low expression of let-7 and high expression of LIN28 in NSCLC patients was associated significantly with resistance to radiotherapy or chemotherapy. Therefore, our study demonstrated that disturbance of the let-7/LIN28 double-negative feedback loop is involved in the regulation of radio- and chemo-resistance, and that let-7 and LIN28 could be employed as predictive biomarkers of response to radiotherapy or chemotherapy in NSCLC patients.

The regulatory and predictive functions of miR-17 and miR-92 families on cisplatin resistance of non-small cell lung cancer.

BACKGROUND: Chemotherapy is an important therapeutic approach for non-small cell lung cancer (NSCLC). However, a successful long-term treatment can be prevented by the occurring of chemotherapy resistance frequently, and the molecular mechanisms of chemotherapy resistance in NSCLC remain unclear. In this study, abnormal expressions of miR-17 and miR-92 families are observed in cisplatin-resistant cells, suggesting that miR-17 and miR-92 families are involved in the regulation of cisplatin resistance in NSCLC. METHODS: miRNA microarray shows that miR-17 and miR-92 families are all down-regulated in cisplatin-resistant A549/DDP cells compared with cisplatin-sensitive A549 cells. The aim of this study is to investigate the regulatory functions of miR-17 and miR-92 families on the formation of cisplatin resistance and the predictive functions of them as biomarkers of platinum-based chemotherapy resistance in NSCLC. RESULTS: The low expressions of miR-17 and miR-92 families can maintain cisplatin resistance through the regulation of CDKN1A and RAD21. As a result of high expressions of CDKN1A and RAD21, the inhibition of DNA synthesis and the repair of DNA damage are achieved and these may be two major contributing factors to cisplatin resistance. Moreover, we demonstrate that the expressions of miR-17 and miR-92 families in NSCLC tissues are significantly associated with platinum-based chemotherapy response. CONCLUSION: Our study indicates that miR-17 and miR-92 families play important roles in cisplatin resistance and can be used as potential biomarkers for better predicting the clinical response to platinum-based chemotherapy in NSCLC.

[Modification of activated carbon fiber for electro-Fenton degradation of phenol].

Microwave-modified activated carbon fiber (ACF-1), nitric acid-modified activated carbon fiber (ACF-2), phosphoric acid-modified activated carbon fiber (ACF-3) and ammonia-modified activated carbon fiber (ACF-4) were successfully fabricated. The electro-Fenton catalytic activities of modified activated carbon fiber were evaluated using phenol as a model pollutant. H2O2 formation, COD removal efficiency and phenol removal efficiency were investigated compared with the unmodified activated carbon fiber (ACF-0). Results indicated that ACF-1 showed the best adsorption and electrocatalytic activity. Modification was in favor of the formation of H2O2. The performance of different systems on phenol degradation and COD removal were ACF-1 > ACF-3 > ACF-4 > ACF-2 > ACF-0 and ACF-1 > ACF-4 > ACF-3 > ACF-2 > ACF-0, respectively, which confirmed that electrocatalytic activities of modified activated carbon fiber were better than the unmodified. In addition, phenol intermediates were not the same while using different modified activated carbon fibers.