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1.
Cell Biol Int ; 47(1): 260-272, 2023 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-36200528

RESUMO

The incidence rate of renal cell carcinoma (RCC) is about 3% of all adult cancers. Of these, the Kidney clear cell renal cell carcinoma (KIRC) is the most common type, accounting for about 70%-75% of RCC. KIRC is difficult to be detected in time clinically. KIRC still has no effective treatment at this stage. We combined high-throughput bioinformatics analysis to obtained the structural sequence transcriptome data, relevant clinical information, and m6 A gene map of KIRC patients from genomics TCGA database. Pearson's correlation analysis was used to explore m6 A related gene long noncoding RNAs (lncRNAs), and then univariate Cox regression analysis was performed to screen the prognostic role of KIRC patients. Lasso-Cox regression was performed to establish the lncRNAs risk model associated with m6 A.LINC02154 and AC016773.2, Z98200.2, AL161782.1, EMX2OS, AC021483.2, CD27-AS1, AC006213.3 were iidentif. Compared with the low-risk group, the overall survival of patients in the high-risk group was significantly worse. Analyzing whether there are differences in immune cells between high-risk and low-risk subgroups. There were CD4 memory resting, Monocytes, Macrophages M1, Dendritic cells activated, Mast cells resting, which had higher infiltrations in the low-risk group. We performed Go enrichment analysis, Kyoto Encyclopedia of Genes and Genomes enrichment analysis and gene set enrichment analysis enrichment analysis. Overall, our results suggest that the component of m6A-related lncRNAs in the prognostic signal may be a key mediator in the immune microenvironment of KIRC, which represents a promising therapeutic effect.


Assuntos
Carcinoma de Células Renais , RNA Longo não Codificante , Adulto , Humanos , Carcinoma de Células Renais/diagnóstico , Carcinoma de Células Renais/genética , Biologia Computacional/métodos , Rim , Neoplasias Renais/diagnóstico , Neoplasias Renais/genética , RNA Longo não Codificante/genética , Microambiente Tumoral , Prognóstico , Biomarcadores Tumorais/análise , Análise de Regressão
2.
Inflamm Res ; 70(4): 407-428, 2021 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-33640999

RESUMO

BACKGROUND: The aim of this review is to explore whether patients with autoimmune diseases (AIDs) were at high risk of infection during the COVID-19 epidemic and how severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic affected immune system. METHODS: A systematic literature search was performed using the foreign databases (NCBI, web of science, EBSCO, ELSEVIER ScienceDirect) and Chinese databases (WanFang, CNKI (China National Knowledge Infrastructure), VIP, CBM) to locate all relevant publications (up to January 10, 2021). The search strategies used Medical Search Headings (MeSH) headings and keywords for "COVID-19" or "SARS-CoV-2" or "coronavirus" and "autoimmune disease". RESULTS: This review evaluates the effect of SARS-CoV-2 on the immune system through ACE-2 receptor binding as the main pathway for cell attachment and invasion. It is speculated that SARS-COV-2 infection can activate lymphocytes and inflammatory response, which may play a role in the clinical onset of AIDs and also patients were treated with immunomodulatory drugs during COVID-19 outbreak. Preliminary studies suggested that the risk of developing severe forms of COVID-19 in patients with AIDs treated with immunomodulators or biologics might not increase. A large number of samples are needed for further verification, leading to an excessive immune response to external stimuli. CONCLUSION: The relationship between autoimmune diseases and SARS-CoV-2 infection is complex. During the COVID-19 epidemic, individualized interventions for AIDs should be provided such as Internet-based service.


Assuntos
Doenças Autoimunes/complicações , Doenças Autoimunes/epidemiologia , COVID-19/complicações , COVID-19/epidemiologia , Monofosfato de Adenosina/análogos & derivados , Monofosfato de Adenosina/uso terapêutico , Alanina/análogos & derivados , Alanina/uso terapêutico , Enzima de Conversão de Angiotensina 2/metabolismo , Artrite Reumatoide/imunologia , Doenças Autoimunes/imunologia , Azetidinas/uso terapêutico , COVID-19/terapia , Células Dendríticas/virologia , Humanos , Sistema Imunitário , Imunidade Inata , Imunização Passiva/tendências , Doenças Inflamatórias Intestinais/imunologia , Células Matadoras Naturais/virologia , Lúpus Eritematoso Sistêmico/imunologia , Monócitos/virologia , Esclerose Múltipla/imunologia , Purinas/uso terapêutico , Pirazóis/uso terapêutico , Sulfonamidas/uso terapêutico , Tratamento Farmacológico da COVID-19 , Soroterapia para COVID-19
3.
Sci Total Environ ; 703: 135491, 2020 Feb 10.
Artigo em Inglês | MEDLINE | ID: mdl-31740063

RESUMO

BACKGROUND: Brucellosis has always been one of the major public health problems in China. Investigating the influencing factors of brucellosis is conducive to its prevention and control. The incidence trend of brucellosis shows an obvious seasonality, suggesting that there may be a correlation between brucellosis and meteorological factors, but related studies were few. We aimed to use the autoregressive integrated moving average (ARIMA) model to analyze the relationship between meteorological factors and brucellosis. METHODS: The data of monthly incidence of brucellosis and meteorological factors in Hebei province from January 2004 to December 2015 were collected from the Chinese Public Health Science Data Center and Chinese meteorological data website. An ARIMA model incorporated with covariables was conducted to estimate the effects of meteorological variables on brucellosis. RESULTS: There was a highest peak from May to July every year and an upward trend during the study period. Atmospheric pressure, wind speed, mean temperature, and relative humidity had significant effects on brucellosis. The ARIMA(1,0,0)(1,1,0)12 model with the covariates of atmospheric pressure, wind speed and mean temperature was the optimal model. The results showed that the atmospheric pressure with a 2-month lag (ß = -0.004, p = 0.037), the wind speed with a 1-month lag (ß = 0.030, p = 0.035), and the mean temperature with a 2-month lag (ß = -0.003, p = 0.034) were significant predictors. CONCLUSION: Our study suggests that atmospheric pressure, wind speed, mean temperature, and relative humidity have a significant impact on brucellosis. Further understanding of its mechanism would help facilitate the monitoring and early warning of brucellosis.


Assuntos
Brucelose/epidemiologia , Exposição Ambiental/estatística & dados numéricos , Conceitos Meteorológicos , Pressão Atmosférica , China/epidemiologia , Humanos , Umidade , Incidência , Saúde Pública , Estações do Ano , Temperatura , Vento
4.
Autoimmunity ; 53(1): 1-7, 2020 02.
Artigo em Inglês | MEDLINE | ID: mdl-31646913

RESUMO

Fibrosis is characterised by excessive deposition of the extracellular matrix (ECM) and develops because of fibroblast differentiation during the process of inflammation. There are few effective treatment options for this diseases due to the aetiology of fibrosis is not completely clarified. Long non-coding RNAs (lncRNAs), a type of ncRNA with a length of greater than 200 nucleotides without evident protein coding function, are important regulators of most biological and pathological processes, including participation, regulation or mediation of disease development. Among them, H19 is recently discovered as a class of lncRNAs which is related to fibrotic disease and inflammation. These observations implied a potential role for H19 as a promising therapeutic targets for treatment of fibrotic diseases. In this review, we will describe the characteristics of H19 and summarise recent advances in the mechanisms of H19 in the process of fibrosis. Finally, we will succinctly discuss the recent progress of the involvement of H19 in the development and pathogenesis of fibrosis diseases.


Assuntos
Suscetibilidade a Doenças , Fibrose/genética , Fibrose/metabolismo , RNA Longo não Codificante/genética , Animais , Biomarcadores , Diferenciação Celular/genética , Matriz Extracelular , Fibroblastos/citologia , Fibroblastos/metabolismo , Fibrose/patologia , Fibrose/terapia , Regulação da Expressão Gênica , Predisposição Genética para Doença , Humanos , Terapia de Alvo Molecular , Especificidade de Órgãos/genética , Interferência de RNA , RNA Longo não Codificante/química , Regeneração , Transdução de Sinais
5.
Arch Med Res ; 50(6): 368-376, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-31678895

RESUMO

BACKGROUND: This study aims to evaluate whether the Vitamin D receptor (VDR) gene polymorphisms were associated with systemic sclerosis (SSc) in a Chinese Han population. METHODS: Using a hospital-based case-control study including 100 SSc patients and 100 healthy controls. Single nucleotide polymorphisms (SNPs) in the VDR region were genotyped by the improved multiplex ligase detection reaction (i MLDR) method. Haplotypes were also constructed after linkage disequilibrium (LD) analysis. RESULTS: Eight SNPs (rs731236 (TaqI), rs2228570 (FokI), rs7975232 (ApaI), rs1544410 (BsmI), rs11574010 (Cdx2), rs739837 (BglI), rs757343 (Tru9I) and rs11168267) were included. There were significant differences between SSc patients and healthy individuals in ApaI and BglI genotype (both adjusted p = 0.008). Through the genotyping, significantly association of SSc were found for: dominant model of ApaI and BglI (both OR (95% CI) = 1.80 (1.03,3.16), p = 0.040). Furthermore, the elevation of erythrocyte sedimentation rate (ESR) had a higher percentage of BglI GT genotype frequency (p = 0.034) and dominant model of ApaI (p = 0.016) in SSc. There was high linkage disequilibrium was detected in BglI and ApaI polymorphisms (r2 = 1.0, D' = 1.0), Tru9I and rs11168267 (r2 = 0.926, D' = 0.969), respectively. No significant difference were found in these four haplotypes (all p >0.05). The correlation between VD levels and VDR gene polymorphisms was not statistically significant. CONCLUSIONS: Our preliminary study indicates the ApaI and BglI genotype may possibly have a role in the pathogenesis of SSc patients. Dominant model of ApaI and BglI GT genotype frequency may be associated with the increased risk of ESR.


Assuntos
Predisposição Genética para Doença/genética , Receptores de Calcitriol/genética , Escleroderma Sistêmico/genética , Alelos , Povo Asiático/genética , Estudos de Casos e Controles , Feminino , Genótipo , Haplótipos/genética , Humanos , Desequilíbrio de Ligação/genética , Masculino , Pessoa de Meia-Idade , Polimorfismo de Nucleotídeo Único/genética
6.
Nanoscale ; 10(11): 5246-5253, 2018 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-29498387

RESUMO

Vanadium nitride and graphene have been widely used as pseudo-capacitive and electric double-layer capacitor electrode materials for electrochemical capacitors, respectively. However, the poor cycling stability of vanadium nitride and the low capacitance of graphene impeded their practical applications. Herein, we demonstrated an in situ self-sacrificed template method for the synthesis of vanadium nitride/nitrogen-doped graphene (VN/NGr) nanocomposites by the pyrolysis of a mixture of dicyandiamide, glucose, and NH4VO3. Vanadium nitride nanoparticles of the size in the range of 2 to 7 nm were uniformly embedded into the nitrogen-doped graphene skeleton. Furthermore, the VN/NGr nanocomposites with a high specific surface area and pore volume showed a high specific capacitance of 255 F g-1 at 10 mV s-1, and an excellent cycling stability (94% capacitance retention after 2000 cycles). The excellent capacitive properties were ascribed to the excellent conductivity of nitrogen-doped graphene, high surface area, high pore volume, and the synergistic effect between vanadium nitride and nitrogen-doped graphene.

7.
Zhonghua Fu Chan Ke Za Zhi ; 44(11): 841-5, 2009 Nov.
Artigo em Chinês | MEDLINE | ID: mdl-20079037

RESUMO

OBJECTIVE: To study the effect of intrauterine hyperglycemia on leptin level and offspring development in rats. METHODS: Female and male adult Wistar rats were mated, streptozotocin (STZ, 50 mg/kg) was administered intraperitoneally on 5th day of gestation to induce diabetic model, diabetic pups (DP) were exposed to intrauterine hyperglycemia; control pups (CP) were exposed to controls, which was injected with citrate buffer, 8 pups were choosed from each group. Weight gain between 3 - 10 weeks were recorded. Plasma leptin was detected by enzyme-linked immunosorbent assay (ELISA) when the rats were 11 weeks old, and the expression of leptin receptor in hypothalamus was measured at protein level by histomorphology and mRNA level measured by realtime PCR [expressed with integral absorbance (IA)] in 11 weeks in order to discuss the relation of leptin and offspring development. RESULTS: The fasting blood glucose level was significantly higher in diabetic mother compared with the controls [(28.3 +/- 5.1) mmol/L vs. (6.3 +/- 1.4) mmol/L, P < 0.05]. However, there was no difference between the fasting blood glucose level in DP group and CP group [(5.1 +/- 0.8) mmol/L vs. (5.3 +/- 0.6) mmol/L, P > 0.05]. The growth rate between 3-10 weeks was significantly higher in DP group 649.7% than CP group 479.2%, P < 0.05. The base insulin level was lower in DP group [(0.76 +/- 0.37) microg/L vs. (1.06 +/- 0.14) microg/L, P < 0.05]; while there was no difference in plasma leptin and the expression of leptin receptor in hypothalamus [(113 +/- 37) microg/L vs. (128 +/- 40) microg/L, P > 0.05]. The growth rate was not associated with plasma leptin in DP group (r = -0.501, P = 0.311) but associated in CP group (r = -0.553, P = 0.001). The protein level of DP group (4125 +/- 414) did not significantly differ from that of CP group (4244 +/- 511). The median of mRNA of leptin receptor in hypothalamus in DP group did not altered significantly compared with that of CP group (1.25 vs 1.80, P > 0.05). CONCLUSIONS: Intrauterine hyperglycemia accelerated growth rate of offsprings between 3 and 10 weeks, however, plasma leptin was not discreased, which indicated leptin resistance. Intrauterine hyperglycemia did not influence the expression of leptin receptor in hypopthalamus in offsprings, this suggested the leptin resistance may be not caused by the quantity of leptin receptors.


Assuntos
Insulina , Leptina , Animais , Hiperglicemia/metabolismo , Insulina/sangue , Leptina/sangue , Ratos Wistar , Estreptozocina
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