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1.
Mol Cancer ; 23(1): 72, 2024 Apr 05.
Artigo em Inglês | MEDLINE | ID: mdl-38581001

RESUMO

For decades, great strides have been made in the field of immunometabolism. A plethora of evidence ranging from basic mechanisms to clinical transformation has gradually embarked on immunometabolism to the center stage of innate and adaptive immunomodulation. Given this, we focus on changes in immunometabolism, a converging series of biochemical events that alters immune cell function, propose the immune roles played by diversified metabolic derivatives and enzymes, emphasize the key metabolism-related checkpoints in distinct immune cell types, and discuss the ongoing and upcoming realities of clinical treatment. It is expected that future research will reduce the current limitations of immunotherapy and provide a positive hand in immune responses to exert a broader therapeutic role.


Assuntos
Imunidade , Neoplasias , Humanos , Imunoterapia , Imunomodulação , Neoplasias/terapia
2.
Opt Lett ; 48(8): 2034-2037, 2023 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-37058635

RESUMO

There is an increasing demand for high-precision gas absorption spectroscopy in basic research and industrial applications, such as gas tracking and leak warning. In this Letter, a novel, to the best of our knowledge, high-precision and real-time gas detection method is proposed. A femtosecond optical frequency comb is used as the light source, and a broadening pulse containing a range of oscillation frequencies is formed after passing through a dispersive element and a Mach-Zehnder interferometer. Four absorption lines of H13C14N gas cells are measured at five different concentrations within a single pulse period. A single scan detection time of only 5 ns is obtained along with a coherence averaging accuracy of 0.0055 nm. High-precision and ultrafast detection of the gas absorption spectrum is accomplished while overcoming complexities related to the acquisition system and light source that are encountered in existing methods.

3.
Phys Rev Lett ; 130(7): 078101, 2023 Feb 17.
Artigo em Inglês | MEDLINE | ID: mdl-36867811

RESUMO

Topological defects usually emerge and vary during the phase transition of ordered systems. Their roles in thermodynamic order evolution keep being the frontier of modern condensed matter physics. Here, we study the generations of topological defects and their guidance on the order evolution during the phase transition of liquid crystals (LCs). With a given preset photopatterned alignment, two different types of topological defects are achieved depending on the thermodynamic process. Because of the memory effect of LC director field across the Nematic-Smectic (N-S) phase transition, a stable array of toric focal conic domains (TFCDs) and a frustrated one are generated in S phase, respectively. The frustrated one transfers to a metastable TFCD array with a smaller lattice constant, and further changes to a crossed-walls type N state due to the inheritance of orientational order. A free energy on temperature diagram and corresponding textures vividly describe the phase transition process and the roles of topological defects in the order evolution across the N-S phase transition. This Letter reveals the behaviors and mechanisms of topological defects on order evolution during phase transitions. It paves a way for investigating topological defect guided order evolution which is ubiquitous in soft matter and other ordered systems.

4.
Mar Drugs ; 21(2)2023 Jan 31.
Artigo em Inglês | MEDLINE | ID: mdl-36827144

RESUMO

Based on the structures of natural products streptochlorin and pimprinine derived from marine or soil microorganisms, a series of streptochlorin derivatives containing the nitrile group were designed and synthesized through acylation and oxidative annulation. Evaluation for antifungal activity showed that compound 3a could be regarded as the most promising candidate-it demonstrated over 85% growth inhibition against Botrytis cinerea, Gibberella zeae, and Colletotrichum lagenarium, as well as a broad antifungal spectrum in primary screening at the concentration of 50 µg/mL. The SAR study revealed that non-substituent or alkyl substituent at the 2-position of oxazole ring were favorable for antifungal activity, while aryl and monosubstituted aryl were detrimental to activity. Molecular docking models indicated that 3a formed hydrogen bonds and hydrophobic interactions with Leucyl-tRNA Synthetase, offering a perspective for the possible mechanism of action for antifungal activity of the target compounds.


Assuntos
Antifúngicos , Fungicidas Industriais , Antifúngicos/farmacologia , Estrutura Molecular , Relação Estrutura-Atividade , Simulação de Acoplamento Molecular , Oxazóis/química , Fungicidas Industriais/farmacologia
5.
Phys Chem Chem Phys ; 24(45): 27660-27669, 2022 Nov 23.
Artigo em Inglês | MEDLINE | ID: mdl-36367080

RESUMO

In view of the potential importance of 3-hydroxychromone derivatives, in this work, we mainly focused on exploring the solvent-polarity-dependent photoinduced behaviors of 2-(benzimidazol-2-yl)-3-hydroxychromone (BI3HC). Distinguished from previous work, we first checked the coexisting three conformations (i.e., BI3HC-A, BI3HC-B, and BI3HC-C) and the presence of a coexistence mechanism between BI3HC-A and BI3HC-C. Most importantly, BI3HC-A is the main component in non-polar solvents, while BI3HC-C is the main one in polar solvents. Through combined analysis of the infrared (IR) vibrational spectra and geometrical variations as well as predicted hydrogen bonding energy via the bond critical point (BCP) between S0 and S1 states, we present a hydrogen bonding strengthening phenomenon that facilitates the excited-state intramolecular proton-transfer (ESIPT) behavior for BI3HC-A and BI3HC-C. To qualitatively investigate photoinduced behaviors based on frontier molecular orbitals (MOs), we found that photoinduced intramolecular charge transfer (ICT) and charge redistribution promoted an ESIPT tendency. By comparing the barriers of the potential energy curves (PECs) between twisting dihedral angles and ESIPT paths, we could rule out mutual transformations in the S1 state and also propose a solvent-polarity-regulated ESIPT behavior for BI3HC-A and BI3HC-C. Furthermore, via searching the transition state (TS) and performing intrinsic reaction coordinate (IRC) simulations, we further checked the ESIPT mechanism. Through gaining insights in spectral variations in solvents, we uncovered the solvent-polarity-dependent spectral behaviors. We sincerely hope this work will not only help clarify the solvent-polarity-regulated dynamical behaviors of BI3HC but also pave the way for further explorations and applications of other 3-hydroxychromone derivatives.


Assuntos
Prótons , Solventes/química , Modelos Moleculares , Conformação Molecular
6.
J Nanobiotechnology ; 20(1): 304, 2022 Jun 27.
Artigo em Inglês | MEDLINE | ID: mdl-35761332

RESUMO

Muscle atrophy is a frequently observed complication, characterized by the loss of muscle mass and strength, which diminishes the quality of life and survival. No effective therapy except exercise is currently available. In our previous study, repressing miR-29b has been shown to reduce muscle atrophy. In our current study, we have constructed artificially engineered extracellular vesicles for the delivery of CRISPR/Cas9 to target miR-29b (EVs-Cas9-29b). EVs-Cas9-29b has shown a favorable functional effect with respect to miR-29b repression in a specific and rapid manner by gene editing. In in vitro conditions, EVs-Cas9-29b could protect against muscle atrophy induced by dexamethasone (Dex), angiotensin II (AngII), and tumor necrosis factor-alpha (TNF-α). And EVs-Cas9-29b introduced in vivo preserved muscle function in the well-established immobilization and denervation-induced muscle atrophy mice model. Our work demonstrates an engineered extracellular vesicles delivery of the miR-29b editing system, which could be potentially used for muscle atrophy therapy.


Assuntos
Vesículas Extracelulares , MicroRNAs , Atrofia Muscular , Animais , Sistemas CRISPR-Cas , Camundongos , MicroRNAs/genética , Atrofia Muscular/genética , Atrofia Muscular/terapia , Fator de Necrose Tumoral alfa
7.
Gynecol Endocrinol ; 38(6): 516-522, 2022 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-35426338

RESUMO

OBJECTIVE: This study aims to investigate the expressions of matrix metalloproteinase-9 (MMP-9), estrogen receptor (ER), and progesterone receptor (PR) in thin endometrium. METHODS: Patients who received treatment in our hospital between January 2018 and September 2020 were enrolled. Endometrial thickness was measured using transvaginal ultrasound; in patients with a midluteal phase endometrial thickness of <7 mm, a sample of endometrial tissue was obtained using a hysteroscope, and the MMP-9, ER, and PR expressions were detected using immunohistochemistry. In addition, the number of endometrial glands was calculated in a complete field of view under a low-power (100×) microscope, and the serum estrogen and progesterone levels were determined. Following hormone therapy, the midluteal phase endometrial thickness was measured again using transvaginal ultrasound, and the patients were divided into two groups: the thin endometrium group and the normal endometrium group (n = 50, each). Patients in the thin endometrium group had an endometrial thickness of <7 mm, while patients in the normal endometrium group had an endometrial thickness of 7-10 mm. RESULTS: The number of endometrial glands as well as the ER and MMP-9 expressions were lower in the thin endometrium group than in the normal endometrium group; the differences were statistically significant (p < .05). The receiver operator characteristic curve revealed that ER and MMP-9 had a high prediction accuracy in patients with refractory thin endometrium, while the number of endometrial glands was moderately predictive. CONCLUSION: Compared with other patients with thin endometrium, patients with refractory thin endometrium had a reduced the number of endometrial glands and significantly lower ER and MMP-9 expressions.


Assuntos
Receptores de Estrogênio , Receptores de Progesterona , Endométrio/diagnóstico por imagem , Endométrio/metabolismo , Feminino , Humanos , Imuno-Histoquímica , Metaloproteinase 9 da Matriz/metabolismo , Receptores de Estrogênio/metabolismo , Receptores de Progesterona/metabolismo
8.
Bioorg Med Chem ; 35: 116073, 2021 04 01.
Artigo em Inglês | MEDLINE | ID: mdl-33610010

RESUMO

Streptochlorin is a small molecule of indole alkaloid isolated from marine Streptomyces sp., it is a promising lead compound due to its potent bioactivity in preventing many phytopathogens in our previous study, but further structural modifications are required to improve its antifungal activity. Our work in this paper focused on the replacement of oxazole ring in streptochlorin with the imidazole ring, to discover novel analogues. Based on this design strategy, three series of streptochlorin analogues were efficiently synthesized through sequential Vilsmeier-Haack reaction, Van Leusen imidazole synthesis and halogenation reaction. Some of the analogues displayed excellent activity in the primary assays, and this is highlighted by compounds 4g and 4i, the growth inhibition against Alternaria Leaf Spot and Rhizoctorzia solani under 50 µg/mL are 97.5% and 90.3%, respectively, even more active than those of streptochlorin, pimprinine and Osthole. Molecular docking models indicated that streptochlorin binds with Thermus thermophiles Leucyl-tRNA Synthetase in a similar mode to AN2690, offering a perspective on the mode of action study for antifungal activities of streptochlorin derivatives. Further study is still ongoing with the aim of discovering synthetic analogues, with improved antifungal activity and clear mode of action.


Assuntos
Alternaria/efeitos dos fármacos , Antifúngicos/farmacologia , Desenho de Fármacos , Indóis/farmacologia , Simulação de Acoplamento Molecular , Oxazóis/farmacologia , Rhizoctonia/efeitos dos fármacos , Antifúngicos/síntese química , Antifúngicos/química , Relação Dose-Resposta a Droga , Indóis/síntese química , Indóis/química , Testes de Sensibilidade Microbiana , Estrutura Molecular , Oxazóis/síntese química , Oxazóis/química , Relação Estrutura-Atividade
9.
Ecotoxicol Environ Saf ; 224: 112643, 2021 Aug 16.
Artigo em Inglês | MEDLINE | ID: mdl-34411817

RESUMO

The positive roles of earthworms on soil functionality has been extensively documented. The capacity of the earthworm gut microbiota on decomposition and nutrient cycling under long-term fertilization in field conditions has rarely been studied. Here, we report the structural, taxonomic, and functional responses of Eisenia foetida and Pheretima guillelmi gut microbiota to different fertilization regimes and durations using 16S rRNA gene-based Illumina sequencing and high-throughput quantitative PCR techniques. Our results revealed that the core gut microbiota, especially the fermentative bacteria were mainly sourced from the soil, but strongly stimulated with species-specificity, potential benefits for the host and soil health. The functional compositions of gut microbiota were altered by fertilization with fertilization duration being more influential than fertilization regimes. Moreover, the combination of organic and inorganic fertilization with the longer duration resulted in a higher richness and connectivity in the gut microbiota, and also their functional potential related to carbon (C), nitrogen, and phosphorus cycling, particularly the labile C decomposition, denitrification, and phosphate mobilization. We also found that long-term inorganic fertilization increased the abundance of pathogenic bacteria in the P. guillelmi gut. This study demonstrates that understanding earthworm gut microbiota can provide insights into how agricultural practices can potentially alter soil ecosystem functions through the interactions between soil and earthworm gut microbiotas.

10.
J Phys Chem A ; 124(15): 2951-2960, 2020 Apr 16.
Artigo em Inglês | MEDLINE | ID: mdl-32223135

RESUMO

A thorough investigation of the initial decomposition pathways of triazoles and their nitro-substituted derivatives has been conducted using the MP2 method for optimization and DLPNO-CCSD(T) method for energy. Different initial thermolysis mechanisms are proposed for 1,2,4-triazole and 1,2,3-triazole, the two kinds of triazoles. The higher energy barrier of the primary decomposition path of 1,2,4-triazole (H-transfer path, ∼52 kcal/mol) compared with that of 1,2,3-triazole (ring-open path, ∼45 kcal/mol) shows that 1,2,4-triazole is more stable, consistent with experimental observations. For nitro-substituted triazoles, more dissociation channels associated with the nitro group have been obtained and found to be competitive with the primary decomposition paths of the triazole skeleton in some cases. Besides, the effect of the nitro group on the decomposition pattern of the triazole skeleton has been explored, and it has been found that the electron-withdrawing nitro group has an opposite effect on the primary dissociation channels of 1,2,4-triazole derivatives and 1,2,3-triazole derivatives.

11.
J Cell Physiol ; 233(9): 7164-7172, 2018 09.
Artigo em Inglês | MEDLINE | ID: mdl-29630731

RESUMO

Long non-coding RNAs (lncRNAs) have been validated to play important role in multiple cancers, including non-small cell lung cancer (NSCLC). In present study, our team investigate the biologic role of SNHG15 in the NSCLC tumorigenesis. LncRNA SNHG15 was significantly upregulated in NSCLC tissue samples and cells, and its overexpression was associated with poor prognosis of NSCLC patients. In vitro, loss-of-functional cellular experiments showed that SNHG15 silencing significantly inhibited the proliferation, promoted the apoptosis, and induced the cycle arrest at G0//G1 phase. In vivo, xenograft assay showed that SNHG15 silencing suppressed tumor growth of NSCLC cells. Besides, SNHG15 silencing decreased CDK14 protein expression both in vivo and vitro. Bioinformatics tools and luciferase reporter assay confirmed that miR-486 both targeted the 3'-UTR of SNHG15 and CDK14 and was negatively correlated with their expression levels. In summary, our study conclude that the ectopic overexpression of SNHG15 contribute to the NSCLC tumorigenesis by regulating CDK14 protein via sponging miR-486, providing a novel insight for NSCLC pathogenesis and potential therapeutic strategy for NSCLC patients.


Assuntos
Carcinoma Pulmonar de Células não Pequenas/genética , Quinases Ciclina-Dependentes/genética , Progressão da Doença , Regulação Neoplásica da Expressão Gênica , Neoplasias Pulmonares/genética , MicroRNAs/metabolismo , RNA Longo não Codificante/metabolismo , Animais , Apoptose/genética , Sequência de Bases , Carcinoma Pulmonar de Células não Pequenas/patologia , Pontos de Checagem do Ciclo Celular/genética , Linhagem Celular Tumoral , Proliferação de Células/genética , Quinases Ciclina-Dependentes/metabolismo , Feminino , Inativação Gênica , Humanos , Neoplasias Pulmonares/patologia , Masculino , Camundongos Endogâmicos BALB C , Camundongos Nus , MicroRNAs/genética , Pessoa de Meia-Idade , Metástase Neoplásica , Prognóstico , RNA Longo não Codificante/genética , Regulação para Cima/genética
12.
Anal Chem ; 90(24): 14230-14238, 2018 12 18.
Artigo em Inglês | MEDLINE | ID: mdl-30398847

RESUMO

Recent outbreaks of Ebola-virus infections in several countries demand a rapid point-of-care (POC)-detection strategy. This paper reports on an innovative pathway founded on electronic-resonance-frequency modulation to detect Ebola glycoprotein (GP), on the basis of a carrier-injection-trapping-release-transfer mechanism and the standard antibody-antigen-interaction principle within a dielectric-gated reduced graphene oxide (rGO) field-effect transistor (GFET). The sensitivity of Ebola detection can be significantly enhanced by monitoring the device's electronic-resonance frequency, such as its inflection frequency ( fi), where the phase angle reaches a maximum (θmax). In addition to excellent selectivity, a sensitivity of ∼36-160% and ∼17-40% for 0.001-3.401 mg/L Ebola GP can be achieved at high and low inflection-resonance frequencies, respectively, which are several orders of magnitude higher than the sensitivity from other electronic parameters (e.g., resistance-based sensitivity). Using equivalent circuit modeling for contributions from channel and contact, analytical equations for resonance shifts have been generalized. When matching with the incoming ac-measurement signal, electronic resonance from the phase-angle spectrum evolves from various relaxation processes (e.g., trap and release of injected charges at surface-trap sites of the channel-gate oxide and channel-source or drain interfaces) that are associated with a characteristic emission frequency. Using charge-relaxation dynamics, a high-performance bio-FET sensing platform for healthcare and bioelectronic applications is realized through resonance shifting.


Assuntos
Ebolavirus/metabolismo , Grafite/química , Sistemas Automatizados de Assistência Junto ao Leito , Transistores Eletrônicos , Proteínas Virais/imunologia , Anticorpos Imobilizados/química , Anticorpos Imobilizados/imunologia , Anticorpos Antivirais/química , Anticorpos Antivirais/imunologia , Reações Antígeno-Anticorpo , Ouro/química , Doença pelo Vírus Ebola/diagnóstico , Humanos , Nanopartículas Metálicas/química , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/imunologia , Proteínas Recombinantes/isolamento & purificação , Ressonância de Plasmônio de Superfície , Proteínas Virais/genética , Proteínas Virais/metabolismo
13.
Analyst ; 143(22): 5583-5588, 2018 Nov 05.
Artigo em Inglês | MEDLINE | ID: mdl-30318531

RESUMO

The development of fluorescent probes to selectively and sensitively detect more than one target analyte under a given condition is a challenging task due to the lack of designing strategies. In this paper, we report the utilisation of the solvatochromic properties of a coumarin-pyridine based probe L1 to detect Mg2+ and PPi, respectively, by using different solvents such as acetonitrile, DMF and DMF-HEPES buffered solutions. When acetonitrile was used as the solvent, L1 was weakly fluorescent and showed a selective and sensitive fluorescence "turn on" response towards Mg2+ with a detection limit of 86 nM, while in DMF and DMF-HEPES buffered solutions, L1 was brightly fluorescent and was able to form a non-fluorescent L1-Fe3+ complex. The obtained L1-Fe3+ complex was further determined to be a selective and sensitive fluorescent "turn on" probe for PPi with a detection limit of 94 nM.

14.
J Oral Maxillofac Surg ; 76(8): 1786-1793, 2018 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-29544754

RESUMO

PURPOSE: The aims of this study are to review our surgical experience in maxillary and midface reconstruction using free vascularized tissue and to compare the postoperative outcomes based on superficial temporal versus cervical recipient vessels. MATERIALS AND METHODS: We performed a retrospective review of patients who underwent maxillary and midface reconstruction with free vascularized tissue from March 2001 to July 2014. Two groups were analyzed: those in whom superficial temporal vessels were used as the recipient vessels and those in whom cervical vessels were used as the recipient vessels. Patient gender and age, cause and classification of the defect, flap choice for reconstruction, recipient vessels, postoperative course, and complications also were recorded and analyzed. A 2-tailed Fisher exact test was used to compare outcomes between the 2 groups. RESULTS: On the basis of the different recipient vessels, 94 patients were divided into 2 groups: those with superficial temporal recipient vessels (n = 44) and those with cervical recipient vessels (n = 50). The overall flap survival rate was 99.0%. The overall complication rate for vascular anastomoses was 5.3%. The complication rate in patients with cervical recipient vessels was higher than the complication rate in those with superficial temporal recipient vessels (8.0% vs 2.27%, P = .37). In addition, in patients in the group with superficial temporal recipient vessels, the postoperative scar in the pre-tragal region was rated as more satisfactory than the postsurgical scar in those in the cervical recipient vessel group. CONCLUSIONS: We recommend that the superficial temporal vessels be the first option for recipient vessels in free vascularized tissue maxillary and midface reconstruction because of proximity, superficial positioning, and suitability for anastomosis and monitoring and because these vessels are rarely compromised by prior operations or radiotherapy.


Assuntos
Face/irrigação sanguínea , Face/cirurgia , Retalhos de Tecido Biológico/irrigação sanguínea , Doenças Maxilares/cirurgia , Procedimentos de Cirurgia Plástica/métodos , Artérias Temporais/cirurgia , Adolescente , Adulto , Idoso , Criança , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Complicações Pós-Operatórias , Estudos Retrospectivos , Resultado do Tratamento , Veias/cirurgia
15.
Artigo em Inglês | MEDLINE | ID: mdl-28712867

RESUMO

This article has been withdrawn at the request of the author(s) and/or editor. The Publisher apologizes for any inconvenience this may cause. The full Elsevier Policy on Article Withdrawal can be found at https://www.elsevier.com/about/our-business/policies/article-withdrawal.

16.
J Chem Phys ; 147(12): 124303, 2017 Sep 28.
Artigo em Inglês | MEDLINE | ID: mdl-28964035

RESUMO

The ground state bending levels of 11BH2 have been studied experimentally using a combination of low-resolution emission spectroscopy and high-resolution stimulated emission pumping (SEP) measurements. The data encompass the energy range below, through, and above the calculated position of the barrier to linearity. For the bending levels (0,3,0) and above, the data show substantial K-reordering, with the Ka″ = 1 levels falling well below those with Ka″ = 0. A comparison of the high-resolution rotationally resolved SEP data to our own very high level ab initio calculations of the rovibronic energy levels shows agreement approaching near-spectroscopic accuracy (a few cm-1). The data reported in this work provide very stringent tests for future theoretical treatments of this prototypical seven-electron free radical.

17.
Hepatology ; 62(1): 118-28, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25802187

RESUMO

UNLABELLED: Hepatitis B virus affects more than 2 billion people worldwide, 350 million of which have developed chronic hepatitis B (CHB). The genetic factors that confer CHB risk are still largely unknown. We sought to identify genetic variants for CHB susceptibility in the Chinese population. We undertook a genome-wide association study (GWAS) in 2,514 CHB cases and 1,130 normal controls from eastern China. We replicated 33 of the most promising signals and eight previously reported CHB risk loci through a two-stage validation totaling 6,600 CHB cases and 8,127 controls in four independent populations, of which two populations were recruited from eastern China, one from northern China and one from southern China. The joint analyses of 9,114 CHB cases and 9,257 controls revealed significant association of CHB risk with five novel loci. Four loci are located in the human leukocyte antigen (HLA) region at 6p21.3, including two nonsynonymous variants (rs12614 [R32W] in complement factor B [CFB], Pmeta =1.28 × 10(-34) ; and rs422951 [T320A] in NOTCH4, Pmeta = 5.33 × 10(-16) ); one synonymous variant (rs378352 in HLA-DOA corresponding to HLA-DOA*010101, Pmeta = 1.04 × 10(-23) ); and one noncoding variant (rs2853953 near HLA-C, Pmeta = 5.06 × 10(-20) ). Another locus is located at 20q13.1 (rs1883832 in the Kozak sequence of CD40, Pmeta = 2.95 × 10(-15) ). Additionally, we validated seven of eight previously reported CHB susceptibility loci (rs3130542 at HLA-C, rs1419881 at TCF19, rs652888 at EHMT2, rs2856718 at HLA-DQB1, rs7453920 at HLA-DQB2, rs3077 at HLA-DPA1, and rs9277535 at HLA-DPA2, which are all located in the HLA region, 9.84 × 10(-71) ≤ Pmeta ≤ 9.92 × 10(-7) ). CONCLUSION: Our GWAS identified five novel susceptibility loci for CHB. These findings improve the understanding of CHB etiology and may provide new targets for prevention and treatment of this disease.


Assuntos
Antígenos CD40/genética , Fator B do Complemento/genética , Antígenos HLA-C/genética , Hepatite B Crônica/genética , Antígenos CD40/sangue , Fator B do Complemento/metabolismo , Feminino , Predisposição Genética para Doença , Estudo de Associação Genômica Ampla , Humanos , Desequilíbrio de Ligação , Masculino , Pessoa de Meia-Idade
18.
Anticancer Drugs ; 27(1): 1-8, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26426520

RESUMO

Temozolomide (TMZ) combination with whole-brain radiotherapy (WBRT) has been tested by many randomized controlled trials in the treatment of brain metastases (BMs) in China and other countries. We performed an up-to-date meta-analysis to determine (i) the log odds ratios (LORs) of objective response (ORR) and adverse effects (AEs) for all-grade, and (ii) the T value of mean overall survival in patients with BMs treated with WBRT combined with TMZ versus WBRT alone. PubMed, Chinese National Knowledge Infrastructure, and WanFang Data were searched for articles published up to 28 January 2015. Eligible studies were selected according to the PRISMA statement. ORR, AEs, and 95% confidence intervals were calculated using random-effects models. Eighteen studies were included in our analysis. A total of 1028 participants were enrolled. Summary LORs of ORR were 1.0239 (P<0.0001) on comparing WBRT plus TMZ with WBRT ORR (n=17). The overall mean difference of mean overall survival (n=17) between TMZ plus WBRT and WBRT was 2.2505 weeks (P=0.02185). There was a significant difference between WBRT plus TMZ and WBRT alone with a LOR of AEs for all-grade of (i) 0.923 for gastrointestinal toxicity and (ii) 0.7978 for myelosuppression. Sensitivity analysis and subgroup analysis were also performed. The 18 eligible randomized controlled trials demonstrated that the combination of WBRT and TMZ significantly improves the ORR and is statistically insignificant in prolonging the survival of patients with BMs. In addition, an increase in the incidence of gastrointestinal toxicity and myelosuppression was significant for all-grade.


Assuntos
Antineoplásicos Alquilantes/uso terapêutico , Neoplasias Encefálicas/tratamento farmacológico , Neoplasias Encefálicas/radioterapia , Dacarbazina/análogos & derivados , Neoplasias Encefálicas/secundário , Terapia Combinada , Dacarbazina/uso terapêutico , Humanos , Ensaios Clínicos Controlados Aleatórios como Assunto , Temozolomida
19.
Biochim Biophys Acta ; 1843(7): 1365-72, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-24721172

RESUMO

Stringent negative regulation of the transcription factor NF-κB is essential for maintaining cellular stress responses and homeostasis. However, the tight regulation mechanisms of IKKß are still not clear. Here, we reported that nemo-like kinase (NLK) is a suppressor of tumor necrosis factor (TNFα)-induced NF-κB signaling by inhibiting the phosphorylation of IKKß. Overexpression of NLK largely blocked TNFα-induced NF-κB activation, p65 nuclear localization and IκBα degradation; whereas genetic inactivation of NLK showed opposing results. Mechanistically, we identified that NLK interacted with IκB kinase (IKK)-associated complex, which in turn inhibited the assembly of the TAK1/IKKß and thereby, diminished the IκB kinase phosphorylation. Our results indicate that NLK functions as a pivotal negative regulator in TNFα-induced activation of NF-κB via disrupting the interaction of TAK1 with IKKß.


Assuntos
Quinase I-kappa B/metabolismo , Peptídeos e Proteínas de Sinalização Intracelular/metabolismo , MAP Quinase Quinase Quinases/metabolismo , NF-kappa B/metabolismo , Proteínas Serina-Treonina Quinases/metabolismo , Núcleo Celular/efeitos dos fármacos , Núcleo Celular/metabolismo , Regulação da Expressão Gênica , Células HCT116 , Células HEK293 , Humanos , Quinase I-kappa B/genética , Peptídeos e Proteínas de Sinalização Intracelular/antagonistas & inibidores , Peptídeos e Proteínas de Sinalização Intracelular/genética , MAP Quinase Quinase Quinases/genética , NF-kappa B/genética , Fosforilação/efeitos dos fármacos , Ligação Proteica , Proteínas Serina-Treonina Quinases/antagonistas & inibidores , Proteínas Serina-Treonina Quinases/genética , Proteólise , RNA Interferente Pequeno/genética , RNA Interferente Pequeno/metabolismo , Transdução de Sinais , Fator de Necrose Tumoral alfa/farmacologia
20.
J Chem Phys ; 142(12): 124301, 2015 Mar 28.
Artigo em Inglês | MEDLINE | ID: mdl-25833573

RESUMO

In this and previous work [D. J. Clouthier, J. Chem. Phys. 141, 244309 (2014)], the spectroscopic signatures of the X2BY (X = H, halogen, Y = O, S) free radicals have been predicted using high level ab initio theory. The theoretical results have been used to calculate the electronic absorption and single vibronic level (SVL) emission spectra of the radicals under typical jet-cooled conditions. Using these diagnostic predictions, the previously unknown F2BS and Cl2BS free radicals have been identified and characterized. The radicals were prepared in a free jet expansion by subjecting precursor mixtures of BF3 or BCl3 and CS2 vapor to an electric discharge at the exit of a pulsed molecular beam valve. The B̃(2)A1-X̃(2)B2 laser-induced fluorescence spectra were found within 150 cm(-1) of their theoretically predicted positions with vibronic structure consistent with our Franck-Condon simulations. The B̃(2)A1 state emits down to the ground state and to the low-lying Ã(2)B1 excited state and the correspondence between the observed and theoretically derived SVL emission Franck-Condon profiles was used to positively identify the radicals and make assignments. Excited state Coriolis coupling effects complicate the emission spectra of both radicals. In addition, a forbidden component of the electronically allowed B̃-X̃ band system of Cl2BS is evident, as signaled by the activity in the b2 modes in the spectrum. Symmetry arguments indicate that this component gains intensity due to a vibronic interaction of the B̃(2)A1 state with a nearby electronic state of (2)B2 symmetry.

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