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1.
J Mol Model ; 30(6): 175, 2024 May 21.
Article En | MEDLINE | ID: mdl-38771411

CONTEXT: Hydrogen sulfide gas poses significant risks to both human health and the environment, with the potential to induce respiratory and neurological effects, and a heightened fatality risk at elevated concentrations. This article investigates the catalytic decomposition of H2S on a Sc-Ti3C2O2 single-atom catalyst(SAC) using the density functional theory-based first-principles calculation approach. Initially, the adsorption behavior of H2S on Ti3C2O2-MXene was examined, revealing weak physical adsorption between them. Subsequently, the transition metal atom Sc was introduced to the Ti3C2O2 surface, and its stability was studied, demonstrating high stability. Further exploration of H2S adsorption on Sc-Ti3C2O2 revealed direct dissociation of H2S gas molecules into HS* and H*, with HS* binding to Sc and H* binding to O on the Ti3C2O2 surface, resulting in OH groups. Using the transition state search method, the dissociation of H2S molecules on the SAC's surface was investigated, revealing a potential barrier of 2.45 eV for HS* dissociation. This indicates that the H2S molecule can be dissociated into H2 and S with the action of the Sc-Ti3C2O2 SAC. Moreover, the S atom left on the catalyst surface can aggregate to produce elemental S8, desorbing on the catalyst surface, completing the catalytic cycle. Consequently, the Sc-Ti3C2O2 SAC is poised to be an efficient catalyst for the catalytic decomposition of H2S. METHODS: The Dmol3 module in Materials Studio software based on density functional theory is used in this study. The generalized gradient approximation method GGA-PBE is used for the exchange-correlation function. The complete LST/QST and the NEB methods in the Dmol3 module were used to study the minimum energy path of the dissociation of hydrogen sulfide molecules on the catalyst surface.

2.
Nanomaterials (Basel) ; 12(17)2022 Aug 30.
Article En | MEDLINE | ID: mdl-36080038

Recently, developing a cost-effective and high-performance catalyst is regarded as an urgent priority for hydrogen generation technology. In this work, ISOBAM-104 stabilized Co/Fe colloidal catalysts were prepared via a co-reduction method and used for the hydrogen generation from KBH4 hydrolysis. The obtained ISOBAM-104 stabilized Co10Fe90 colloidal catalysts exhibit an outstanding catalytic activity of 37,900 mL-H2 min-1 g-Co-1, which is far higher than that of Fe or Co monometallic nanoparticles (MNPs). The apparent activation energy (Ea) of the as-prepared Co10Fe90 colloidal catalysts is only 14.6 ± 0.7 kJ mol-1, which is much lower than that of previous reported noble metal-based catalysts. The X-ray photoelectron spectroscopy results and density functional theory calculations demonstrate that the electron transfer between Fe and Co atoms is beneficial for the catalytic hydrolysis of KBH4.

3.
Bioresour Technol ; 350: 126880, 2022 Apr.
Article En | MEDLINE | ID: mdl-35202829

Separated hydrolysis and acidification is an effective pretreatment method for anaerobic digestion of lignocellulose. However, excess consumption of soluble substrates remains a problem. Rice straw and pig manure were used as substrates with biogas slurry as the inoculum, combined with aerobic and microaerobic conditions in the 14-day hydrolysis and acidification. Aeration can significantly accelerate volatile solid degradation (38.25%), especially the lignocellulose. Soluble chemical oxygen demand (29157 mg/L) and volatile fatty acids (13219 mg/L) of the group with 4 days aerobic treatment, reached their peaks on day 5, obtaining a balanced insoluble substrate degradation and soluble substrate consumption. Candida, Lactobacillus, Bifidobacterium, and Acetobacter were enriched at the balanced point for positive contribution to the degradation of the insoluble substrate and the generation of soluble substrate. This study not only reveals the balance between degradation and consumption, but also provides new insight into biogas slurry recycling and anaerobic digestion precursor substrate production.


Manure , Oryza , Anaerobiosis , Animals , Biofuels , Hydrogen-Ion Concentration , Hydrolysis , Methane , Swine
4.
Mol Oncol ; 14(4): 829-845, 2020 04.
Article En | MEDLINE | ID: mdl-31951095

Patients with metastatic gastric cancer (GC) have a poor prognosis; however, the molecular mechanism of GC metastasis remains unclear. Here, we employed bioinformatics to systematically screen the metastasis-associated genes and found that the levels of basal cell adhesion molecule (BCAM) were significantly increased in GC tissues from patients with metastasis, as compared to those without metastasis. The upregulation of BCAM was also significantly associated with a shorter survival time. Depletion of BCAM inhibited GC cell migration and invasion. Knockout (KO) of BCAM by the CRISPR/Cas9 system reduced the invasion and metastasis of GC cells. To explore the mechanism of BCAM upregulation, we identified a previously uncharacterized BCAM sense lncRNA that spanned from exon 6 to intron 6 of BCAM, and named it as BCAM-associated long noncoding RNA (BAN). Knockdown of BAN inhibited BCAM expression at both mRNA and protein levels. Knockdown of BAN suppressed GC cell migration and invasion, which was effectively rescued by ectopic expression of BCAM. Further clinical data showed that BAN upregulation was associated with GC metastasis and poor prognosis. Importantly, BAN expression was also significantly associated with that of BCAM in GC tissues. Taken together, these results indicate that increased expression of BCAM and its sense lncRNA BAN promote GC cell invasion and metastasis, and are associated with poor prognosis of GC patients.


Cell Adhesion Molecules/genetics , Lutheran Blood-Group System/genetics , Neoplasm Invasiveness/genetics , RNA, Long Noncoding/genetics , Stomach Neoplasms/genetics , Up-Regulation , Cell Line, Tumor , Cell Movement , Gene Expression Regulation, Neoplastic , Humans , Neoplasm Invasiveness/diagnosis , Prognosis , Stomach Neoplasms/diagnosis
5.
Burns ; 43(4): 877-885, 2017 Jun.
Article En | MEDLINE | ID: mdl-28062082

AIMS AND OBJECTIVES: To observe the effect of a rehabilitation intervention on the comprehensive health status of patients with hand burns. BACKGROUND: Most studies of hand-burn patients have focused on functional recovery. There have been no studies involving a biological-psychological-social rehabilitation model of hand-burn patients. DESIGN: A randomized controlled design was used. METHODS: Patients with hand burns were recruited to the study, and sixty patients participated. Participants were separated into two groups: (1) The rehabilitation intervention model group (n=30) completed the rehabilitation intervention model, which included the following measures: enhanced social support, intensive health education, comprehensive psychological intervention, and graded exercise. (2) The control group (n=30) completed routine treatment. Intervention lasted 5 weeks. Analysis of variance (ANOVA) and Student's t test were conducted. RESULTS: The rehabilitation intervention group had significantly better scores than the control group for comprehensive health, physical function, psychological function, social function, and general health. The differences between the index scores of the two groups were statistically significant. CONCLUSIONS: The rehabilitation intervention improved the comprehensive health status of patients with hand burns and has favorable clinical application. RELEVANCE TO CLINICAL PRACTICE: The comprehensive rehabilitation intervention model used here provides scientific guidance for medical staff aiming to improve the integrated health status of hand-burn patients and accelerate their recovery. What does this paper contribute to the wider global clinical community?


Burns/nursing , Exercise Therapy/methods , Hand Injuries/nursing , Health Status , Patient Education as Topic/methods , Rehabilitation Nursing/methods , Social Support , Adaptation, Psychological , Adult , Burns/psychology , Burns/rehabilitation , China , Female , Hand Injuries/psychology , Hand Injuries/rehabilitation , Humans , Male , Middle Aged , Recovery of Function , Treatment Outcome , Young Adult
6.
Mol Med Rep ; 10(5): 2601-8, 2014 Nov.
Article En | MEDLINE | ID: mdl-25231560

Emerging evidence suggests that altered expression of microRNAs (miRNAs) is involved in cancer progression. However, the role of miR-125a-5p in gastric carcinogenesis remains unknown. Quantitative real-time PCR analysis revealed that the expression of miR-125a-5p was significantly decreased in >80% of gastric cancer tissues compared with their adjacent non-tumor tissues, and was markedly reduced in ~95% of intestinal-type gastric cancer tissues. The downregulated miR-125a-5p was significantly associated with gastric cancer metastasis. Ectopic expression of miR-125a-5p substantially inhibited the proliferation, migration and invasion activities of gastric cancer cells. Furthermore, forced expression of miR-125a-5p repressed the activity of a luciferase reporter carrying the 3'-untranslated (3'-UTR) region of E2F3, which was eliminated by mutation of the predicted miR-125a-binding site, indicating that E2F3 may be a potential target gene of miR-125a-5p. These data suggest that by targeting E2F3, miR-125a-5p may be important as a potential tumor suppressor gene in gastric carcinogenesis.


Carcinogenesis/metabolism , E2F3 Transcription Factor/genetics , MicroRNAs/metabolism , Stomach Neoplasms/metabolism , 3' Untranslated Regions , Aged , Carcinogenesis/genetics , Cell Line, Tumor , Cell Movement , Cell Proliferation , Down-Regulation , E2F3 Transcription Factor/metabolism , Female , Gene Expression , Gene Expression Regulation, Neoplastic , Humans , Lymphatic Metastasis , Male , MicroRNAs/genetics , Middle Aged , RNA Interference , Stomach Neoplasms/genetics , Stomach Neoplasms/pathology
7.
PLoS One ; 9(7): e99516, 2014.
Article En | MEDLINE | ID: mdl-25055044

MicroRNAs (miRNAs) have been reported to play a critical role in cancer invasion and metastasis. Our previous study showed that miR-375 frequently downregulated in gastric cancer suppresses cell proliferation by targeting Janus kinase 2 (JAK2). Here, we further found that the expression level of miR-375 is significantly decreased in metastatic gastric cancer tissues compared with the non-metastasis controls. Ectopic expression of miR-375 inhibits the migration and invasion of gastric cancer cells partially by targeting JAK2. Furthermore, miR-375 expression is negatively regulated by the metastasis associated transcription factor Snail, which directly binds to the putative promoter of miR-375. Moreover, overexpression of Snail can partially reverse the inhibition of gastric cancer cell migration caused by miR-375. Taken together, these data suggest that miR-375 may be negatively regulated by Snail and involved in gastric cancer cell migration and invasion potentially by targeting JAK2.


Cell Movement/genetics , Janus Kinase 2/metabolism , MicroRNAs/metabolism , Neoplasm Invasiveness/genetics , Stomach Neoplasms/genetics , Transcription Factors/metabolism , Cell Line, Tumor , Down-Regulation , Gene Expression Regulation, Neoplastic , Humans , MicroRNAs/genetics , Neoplasm Invasiveness/pathology , Snail Family Transcription Factors , Stomach Neoplasms/pathology , Transcription Factors/genetics , Wound Healing/genetics
8.
Cancer Lett ; 342(1): 27-35, 2014 Jan 01.
Article En | MEDLINE | ID: mdl-23981575

Growing evidence indicates that miRNAs play critical roles in tumorigenesis and cancer progression. Here, we report that miR-215 is significantly up-regulated in gastric cancer tissues from either gastrectomy or gastroscopy. Receiver Operator Characteristic (ROC) curve analysis indicated that miR-215 may be a candidate biomarker for gastric cancer diagnosis. Inhibition of miR-215 significantly suppressed gastric cancer cell proliferation possibly via G1 arrest. Further analyses indicated that miR-215 was able to target retinoblastoma tumor-suppressor gene 1 (RB1) through its 3'-UTR in gastric cancer cells. These data suggest that frequently up-regulated miR-215 in gastric cancer may influence cell proliferation by targeting RB1.


Biomarkers, Tumor/genetics , Cell Proliferation , MicroRNAs/genetics , Retinoblastoma Protein/genetics , Stomach Neoplasms/metabolism , 3' Untranslated Regions , Aged , Area Under Curve , Base Sequence , Binding Sites , Biomarkers, Tumor/metabolism , Cell Cycle , Cell Line, Tumor , Female , Gene Expression Regulation, Neoplastic , Humans , Male , MicroRNAs/metabolism , RNA Interference , ROC Curve , Retinoblastoma Protein/metabolism , Stomach Neoplasms/diagnosis , Stomach Neoplasms/genetics , Transcriptome , Up-Regulation
9.
Mol Biol Rep ; 39(7): 7457-63, 2012 Jul.
Article En | MEDLINE | ID: mdl-22318552

A coordination compound of 5, 7-dihydrox-4'-methoxyisoflavone and selenium was synthesized and its structure was identified by IR, LC-MS and (1)H-NMR. Its biochemical effects were investigated using bovine serum albumin (BSA) as a target protein molecule, in which process three-dimensional (3D) fluorescence spectra, ultraviolet spectra, circular dichroism (CD) spectra and fluorescence probe techniques were employed. The interaction of SEIF and BSA was discussed by fluorescence quenching method and Förster non-radiation energy transfer theory. The thermodynamic parameters ΔH (θ), ΔG (θ), ΔS (θ) at different temperatures were calculated according to Van't Hoff isobaric equation and the results indicated the interaction was an exothermic as well as a spontaneous process. The binding site was explored by fluorescence probe method using warfarin and ibuprofen as markers. Intramolecular forces which are responsible for maintaining the binding were mainly hydrogen bond and van der Waals power. The average distance from the tryptophan residue in domain II of BSA (donor) to SEIF (acceptor) is 3.57 nm at body temperature. The conformation changes of BSA were investigated by 3D fluorescence and CD spectra.


Isoflavones/chemical synthesis , Isoflavones/metabolism , Organoselenium Compounds/chemical synthesis , Serum Albumin, Bovine/metabolism , Albumins/metabolism , Animals , Binding Sites , Cattle , Ibuprofen/metabolism , Isoflavones/chemistry , Organoselenium Compounds/chemistry , Organoselenium Compounds/metabolism , Protein Binding , Selenium Compounds/chemistry , Selenium Compounds/metabolism , Serum Albumin, Bovine/chemistry , Thermodynamics , Warfarin/metabolism
10.
Cell Biochem Funct ; 28(2): 122-5, 2010 Mar.
Article En | MEDLINE | ID: mdl-20087844

Iron deficiency leads to abnormal expression and function of band 3 protein in erythrocytes, but the underlying mechanisms remain elusive. The mRNA of erythroid-specific 5-aminolevulinate synthase (eALAS) contains an iron response element and the eALAS protein is an important mediator of iron utilization by erythrocytes. In this study, we investigated the effect of short hairpin RNA (shRNA) mediated silencing of eALAS on the expression of band 3 protein induced by iron. By real-time RT-PCR and Western blot we showed that at mRNA and protein level iron-induced expression of band 3 protein was lower in eALAS-shRNA transfected K562 cells than in control cells. Of note, the lowest expression was detected in K562 cells cultured in iron deficiency condition (p < 0.01). Thus either iron deficiency or depletion of eALAS could suppress the expression of erythroid band 3 protein. These results demonstrated for the first time that iron and the iron-regulatory system regulate the expression of the erythrocyte membrane proteins.


5-Aminolevulinate Synthetase/metabolism , Anion Exchange Protein 1, Erythrocyte/metabolism , Erythrocytes/enzymology , Iron/pharmacology , 5-Aminolevulinate Synthetase/genetics , Down-Regulation , Humans , K562 Cells , RNA Interference , Up-Regulation
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