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Background Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies worldwide because of rapid progression and high incidence of metastasis or recurrence. Accumulating evidence shows that CD73-expressing tumor cell is implicated in development of several types of cancer. However, the role of CD73 in HCC cell has not been systematically investigated and its underlying mechanism remains elusive. Methods CD73 expression in HCC cell was determined by RT-PCR, Western blot, and immunohistochemistry staining. Clinical significance of CD73 was evaluated by Cox regression analysis. Cell counting kit-8 and colony formation assays were used for proliferation evaluation. Transwell assays were used for motility evaluations. Co-immunoprecipitation, cytosolic and plasma membrane fractionation separation, and ELISA were applied for evaluating membrane localization of P110β and its catalytic activity. NOD/SCID/γc(null) (NOG) mice model was used to investigate the in vivo functions of CD73. Results In the present study, we demonstrate that CD73 was crucial for epithelial-mesenchymal transition (EMT), progression and metastasis in HCC. CD73 expression is increased in HCC cells and correlated with aggressive clinicopathological characteristics. Clinically, CD73 is identified as an independent poor prognostic indicator for both time to recurrence and overall survival. CD73 knockdown dramatically inhibits HCC cells proliferation, migration, invasion, and EMT in vitro and hinders tumor growth and metastasis in vivo. Opposite results could be observed when CD73 is overexpressed. Mechanistically, adenosine produced by CD73 binds to adenosine A2A receptor (A2AR) and activates Rap1, which recruits P110β to the plasma membrane and triggers PIP3 production, thereby promoting AKT phosphorylation in HCC cells. Notably, a combination of anti-CD73 and anti-A2AR achieves synergistic depression effects on HCC growth and metastasis than single agent alone. Conclusions CD73 promotes progression and metastasis through activating PI3K/AKT signaling, indicating a novel prognostic biomarker for HCC. Our data demonstrate the importance of CD73 in HCC in addition to its immunosuppressive functions and revealed that co-targeting CD73 and A2AR strategy may be a promising novel therapeutic strategy for future HCC management.

Background Drought stress limits significantly the crop productivity. However, plants have evolved various strategies to cope with the drought conditions by adopting complex molecular, biochemical, and physiological mechanisms. Members of the nuclear factor Y (NF-Y) transcription factor (TF) family constitute one of the largest TF classes and are involved in plant responses to abiotic stresses. Results TaNF-YB2 , a NY-YB subfamily gene in T. aestivum , was characterized in this study focusing on its role in mediating plant adaptation to drought stress. Yeast two-hybrid (Y-2 H), biomolecular fluoresence complementation (BiFC), and Co-immunoprecipitation (Co-IP) assays indicated that TaNF-YB2 interacts with the NF-YA member TaNF-YA7 and NF-YC family member TaNF-YC7, which constitutes a heterotrimer TaNF-YB2/TaNF-YA7/TaNF-YC7. The TaNF-YB2 transcripts are induced in roots and aerial tissues upon drought signaling; GUS histochemical staining analysis demonstrated the roles of cis -regulatory elements ABRE and MYB situated in TaNF-YB2 promoter to contribute to target gene response to drought. Transgene analysis on TaNF-YB2 confirmed its functions in regulating drought adaptation via modulating stomata movement, osmolyte biosynthesis, and reactive oxygen species (ROS) homeostasis. TaNF-YB2 possessed the abilities in transcriptionally activating TaP5CS2 , the P5CS family gene involving proline biosynthesis and TaSOD1 , TaCAT5 , and TaPOD5 , the genes encoding antioxidant enzymes. Positive correlations were found between yield and the TaNF-YB2 transcripts in a core panel constituting 45 wheat cultivars under drought condition, in which two types of major haplotypes including TaNF-YB2-Hap1 and -Hap2 were included, with the former conferring more TaNF-YB2 transcripts and stronger plant drought tolerance. Conclusions TaNF-YB2 is transcriptional response to drought stress. It is an essential regulator in mediating plant drought adaptation by modulating the physiological processes associated with stomatal movement, osmolyte biosynthesis, and reactive oxygen species (ROS) homeostasis, depending on its role in transcriptionally regulating stress response genes. Our research deepens the understanding of plant drought stress underlying NF-Y TF family and provides gene resource in efforts for molecular breeding the drought-tolerant cultivars in T. aestivum .

Accumulating evidence indicates that hepatocellular carcinoma (HCC) tumorigenesis, recurrence, metastasis, and therapeutic resistance are strongly associated with liver cancer stem cells (CSCs), a rare subpopulation of highly tumorigenic cells with self-renewal capacity and differentiation potential. Previous studies identified B cell leukemia/lymphoma-11b (BCL11B) as a novel tumor suppressor with impressive capacity to restrain CSC traits. However, the implications of BCL11B in HCC remain unclear. In this study, we found that low BCL11B expression was an independent indicator for shorter overall survival (OS) and time to recurrence (TTR) for HCC patients with surgical resection. In vitro and in vivo experiments confirmed BCL11B as a tumor suppressor in HCC with inhibitory effects on proliferation, cell cycle progression, apoptosis, and mobility. Furthermore, BCL11B could suppress CSC traits, as evidenced by dramatically decreased tumor spheroid formation, self-renewal potential and drug resistance. A Cignal Finder Array and dual-luciferase activity reporter assays revealed that BCL11B could activate the transcription of P73 via an E2F1-dependent manner. Thus, we concluded that BCL11B is a strong suppressor of retaining CSC traits in HCC. Ectopic expression of BCL11B might be a promising strategy for anti-HCC treatment with the potential to cure HBV-related HCC regardless of P53 mutation status.

There is a significant interest in developing environmentally responsive or stimuli-responsive smart materials. The purpose of this study was to investigate multi-function responsive cotton fabrics with surface modification on the nanoscale. Three technologies including electrospinning technology, interpenetrating polymer network technology, and cross-linking technology were applied to prepare the multi-function sericin/poly(N-isopropylacrylamide)/Poly(ethylene oxide) nanofibers, which were then grafted onto the surfaces of cotton textiles to endow the cotton textiles with outstanding stimuli-responsive functionalities. The multi-function responsive properties were evaluated via SEM, DSC, the pH-responsive swelling behavior test and contact angle measurements. The results demonstrate that with this method, multi-function responsive, including thermo- and pH-responsiveness, cotton fabrics were fast formed, and the stimuli-responsiveness of the materials was well controlled. In addition, the antimicrobial testing reveals efficient activity of cotton fabrics with the sericin/PNIPAM/PEO nanofiber treatments against Gram-positive bacteria and Gram-negative bacteria such as Staphylococcus aureus and Escherichia coli. The research shows that the presented strategy demonstrated the great potential of multi-function responsive cotton fabrics fabricated using our method.

Heat fusion method and hot-press method were applied to immobilize hydroxyapatite (HAp) particles onto the surface of PET filter fabric separately. The effects of treating temperature, treating time and HAp amount on immobilization rate of HAp and pore size of filter fabric were discussed. The high immobilization rate of HAp could be obtained and pore size could be maintained. FTIR, SEM and XRD were used to characterize the structure of filter fabric embedded with HAp particles. Good adsorption property of Cd2+ onto HAp immobilized filter fabric was achieved.

In this paper, the basalt fiber/polylactic acid composites were prepared by laying-up hot-pressing process, using PLA sheet as the matrix material and basalt fiber fabrics as the reinforced material, besides, the mechanical properties were studied and the parameters of hot-pressing were optimized. PLA mass fraction, heat pressing temperature, heat pressing pressure and heat pressing time were selected as the four main influence factors and tensile strength and bending strength were taken as the test indexes, the best processing conditions: PLA mass fraction 63%, Heat pressing temperature 195 °C, Heat pressing pressure 7MPa, Heat pressing time 10min were optimized through orthogonal experiment and range analysis. The significance of the study was providing theoretical guidance for the further development of high-performance basalt fiber composites.

In this paper, flame-retardant fiberboard was prepared by blend mastication and hot-pressing method, using abandoned glass fiber and polypropylene as raw materials and magnesium hydroxide as flame-retardant reagent. The optimized processing conditions were concluded through orthogonal experiment and the range analysis: magnesium hydroxide mass fraction 25% , polypropylene mass fraction 70% , hot-pressing temperature 180, hot-pressing pressure 10 Mpa. Under these conditions, properties of fiberboard were as follow: tensile strength 20.55 Mpa , bending strength 30.98 Mpa , impact strength 3.65 Mpa , limiting oxygen index 28.2%.

Background Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies worldwide because of rapid progression and high incidence of metastasis or recurrence. Accumulating evidence shows that CD73-expressing tumor cell is implicated in development of several types of cancer. However, the role of CD73 in HCC cell has not been systematically investigated and its underlying mechanism remains elusive. Methods CD73 expression in HCC cell was determined by RT-PCR, Western blot, and immunohistochemistry staining. Clinical significance of CD73 was evaluated by Cox regression analysis. Cell counting kit-8 and colony formation assays were used for proliferation evaluation. Transwell assays were used for motility evaluations. Co-immunoprecipitation, cytosolic and plasma membrane fractionation separation, and ELISA were applied for evaluating membrane localization of P110[beta] and its catalytic activity. NOD/SCID/[gamma]c(null) (NOG) mice model was used to investigate the in vivo functions of CD73. Results In the present study, we demonstrate that CD73 was crucial for epithelial-mesenchymal transition (EMT), progression and metastasis in HCC. CD73 expression is increased in HCC cells and correlated with aggressive clinicopathological characteristics. Clinically, CD73 is identified as an independent poor prognostic indicator for both time to recurrence and overall survival. CD73 knockdown dramatically inhibits HCC cells proliferation, migration, invasion, and EMT in vitro and hinders tumor growth and metastasis in vivo. Opposite results could be observed when CD73 is overexpressed. Mechanistically, adenosine produced by CD73 binds to adenosine A2A receptor (A2AR) and activates Rap1, which recruits P110[beta] to the plasma membrane and triggers PIP3 production, thereby promoting AKT phosphorylation in HCC cells. Notably, a combination of anti-CD73 and anti-A2AR achieves synergistic depression effects on HCC growth and metastasis than single agent alone. Conclusions CD73 promotes progression and metastasis through activating PI3K/AKT signaling, indicating a novel prognostic biomarker for HCC. Our data demonstrate the importance of CD73 in HCC in addition to its immunosuppressive functions and revealed that co-targeting CD73 and A2AR strategy may be a promising novel therapeutic strategy for future HCC management. Keywords: Hepatocellular carcinoma, CD73, Epithelial-mesenchymal-transition, Prognosis, PI3K/AKT

Selecting rubber powders, which is divided into 80 mesh and 150 mesh, as the research object, to understand the influence of high performance of lower clinker concrete mechanical properties of rubber powder with different varieties and volume. Taking the compressive strength, flexural strength and ratio of flexural strength to compressive strength as an indicator, the thesis explores the influence of the high performance concrete with low clinker, which rubber powder are mixed into as fine aggregate, on the compressive strength bending strength and ductility.

Aim： To investigate the possible association of the CYP2D6 gene C100T polymorphism and the CYP1A2 gene C163A polymorphism with tardive dyskinesia （TD） in Chinese patients with schizophrenia. Methods： The recruited schizophrenic patients were assessed with the Abnormal Involuntary Movement Scale （AIMS）, and divided into groups with TD （n=91） and without TD （n=91） according to the AIMS score. Polymorphisms of the CYP2D6 and CYP1A2 genes were determined by polymerase chain reaction （PCR）-restriction fragment length polymorphism （RFLP）, Results： No allele frequencies deviated from Hardy-Weinberg equilibrium. No significant differences in genotypes frequencies of the CYP2D6 C100T polymorphism were observed between patients with TD and without TD （x^2=4.078, P〉0.05）, but patients with TD had a significant excess of the T allele compared with those without TD （x^2=4.28, P〈0.05）. Moreover, the frequency of the CYP1A2 C allele in patients with TD was significantly higher than that in those without TD （x^2=6.38, P〈0.05）. An association between TD and the CYP2D6 100T and CYP1A2 163C alleles was observed. Additionally, there were no differences in the mean AIMS scores among different genotypes in TD patients as a group or in smokers. The results of logistic regression analysis demonstrated that mean age and duration of illness were risk factors for TD, but not sex, cumulative exposure to neuroleptic drugs in years, CYP2D6 or CYP1A2 genotype. Conclusion： The C100T polymorphism of the CYP2D6 gene and the C163A polymorphism of the CYP1A2 gene may be associated with neuroleptic drug-induced tardive dyskinesia in Chinese patients with schizophrenia. However, genetic factors have a weaker association with susceptibility to TD compared with mean age and duration of illness.