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1.
Biomed Pharmacother ; 179: 117302, 2024 Aug 19.
Artigo em Inglês | MEDLINE | ID: mdl-39163678

RESUMO

Inflammatory bowel disease (IBD), including Crohn's disease and ulcerative colitis, is a complex disorder with an unknown cause. However, the dysbiosis of the gut microbiome has been found to play a role in IBD etiology, including exacerbated immune responses and defective intestinal barrier integrity. The gut microbiome can also be a potential biomarker for several diseases, including IBD. Currently, conventional treatments targeting pro-inflammatory cytokines and pathways in IBD-associated dysbiosis do not yield effective results. Other therapies that directly target the dysbiotic microbiome for effective outcomes are emerging. We review the role of the gut microbiome in health and IBD and its potential as a diagnostic, prognostic, and therapeutic target for IBD. This review also explores emerging therapeutic advancements that target gut microbiome-associated alterations in IBD, such as nanoparticle or encapsulation delivery, fecal microbiota transplantation, nutritional therapies, microbiome/probiotic engineering, phage therapy, mesenchymal stem cells (MSCs), gut proteins, and herbal formulas.

2.
Theranostics ; 14(2): 640-661, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38169587

RESUMO

Regulated cell death (RCD) is considered a critical pathway in cancer therapy, contributing to eliminating cancer cells and influencing treatment outcomes. The application of RCD in cancer treatment is marked by its potential in targeted therapy and immunotherapy. As a type of RCD, PANoptosis has emerged as a unique form of programmed cell death (PCD) characterized by features of pyroptosis, apoptosis, and necroptosis but cannot be fully explained by any of these pathways alone. It is regulated by a multi-protein complex called the PANoptosome. As a relatively new concept first described in 2019, PANoptosis has been shown to play a role in many diseases, including cancer, infection, and inflammation. This study reviews the application of PCD in cancer, particularly the emergence and implication of PANoptosis in developing therapeutic strategies for cancer. Studies have shown that the characterization of PANoptosis patterns in cancer can predict survival and response to immunotherapy and chemotherapy, highlighting the potential for PANoptosis to be used as a therapeutic target in cancer treatment. It also plays a role in limiting the spread of cancer cells. PANoptosis allows for the elimination of cancer cells by multiple cell death pathways and has the potential to address various challenges in cancer treatment, including drug resistance and immune evasion. Moreover, active investigation of the mechanisms and potential therapeutic agents that can induce PANoptosis in cancer cells is likely to yield effective cancer treatments and improve patient outcomes. Research on PANoptosis is still ongoing, but it is a rapidly evolving field with the potential to lead to new treatments for various diseases, including cancer.


Assuntos
Neoplasias , Morte Celular Regulada , Humanos , Imunoterapia , Neoplasias/tratamento farmacológico , Apoptose , Morte Celular
3.
ISA Trans ; 105: 210-220, 2020 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-32466844

RESUMO

In order to detect the incipient faults of nonlinear industrial processes effectively, this paper proposes an enhanced kernel principal component analysis (KPCA) method, called multi-block probability related KPCA method (DMPRKPCA). First of all, one probability related nonlinear statistical monitoring framework is constructed by combining KPCA with Kullback Leibler divergence (KLD), which measures the probability distribution changes caused by small shifts. Second, in view of the problem that the traditional KLD ignores the dynamic characteristic of process data, the dynamic KLD component is designed by applying the exponentially weighted moving average approach, which highlights the temporal data changes in the moving window. Third, considering that the holistic KLD component may submerge the local statistical changes, a multi-block modeling strategy is designed by dividing the whole KLD components into two sub-blocks corresponding to the mean and variance information, respectively. Case studies on one numerical system and the simulated chemical reactor demonstrate the superiority of the DMPRKPCA method over the conventional KPCA method.

4.
Med Sci Monit ; 23: 6033-6041, 2017 Dec 21.
Artigo em Inglês | MEDLINE | ID: mdl-29263314

RESUMO

BACKGROUND High expression of the RNA-binding motif protein 3 (RBM3) has previously been described as a favorable clinicopathological factor in several cancers, including ovarian cancer, colorectal cancer, prostate cancer, and breast cancer. The aim of this study was to examine the prognostic implications of RBM3 expression in gastric cancer. MATERIAL AND METHODS Immunohistochemical analysis of RBM3 expression from 123 patients showed that upregulated RBM3 was mainly found in intestinal-type (n=78, case=59) cancer compared to diffuse-type (n=15, case=8) and mixed-type (n=30, case=17). There were no significant differences in RBM3 expression in subgroups of clinicopathological parameters. RBM3 expression was strongly associated with p53 but not with Ki-67. Cox univariate analysis revealed that high RBM3 expression was closely associated with prolonged overall survival time (HR 0.504, 95% CI: 0.300-0.845, P=0.009). Multivariate analysis remained supporting these associations when adjusted for age, sex, tumor size, differentiation grade, TNM stage, lymphatic invasion, and Ki-67 and p53 expression (HR 0.541, 95% CI: 0.308-0.952, P=0.033), where Lauren grade was not included. Lauren grade was the only factor with independent prognostic significance in a model adjusted for all factors. These results were confirmed by Kaplan-Meier analysis. RESULTS Therefore, together with the upregulated RBM3 expression observed in intestinal-type of Lauren grade, we suggest that upregulation of RBM3 is partially responsible for the favorable overall survival in cases with intestinal Lauren grade, which is demonstrated by the box diagram and Kaplan-Meier analysis. Our results showed that high RBM3 expression in gastric cancer is mainly found in intestinal-type of Lauren grade and is associated with longer overall survival time. CONCLUSIONS We found that RBM3 is a potential biomarker of good prognosis and deserves further validation.


Assuntos
Proteínas de Ligação a RNA/biossíntese , Neoplasias Gástricas/metabolismo , Adulto , Idoso , Idoso de 80 Anos ou mais , Biomarcadores Tumorais/biossíntese , Biomarcadores Tumorais/genética , Biomarcadores Tumorais/metabolismo , Intervalo Livre de Doença , Feminino , Humanos , Imuno-Histoquímica , Intestinos/patologia , Estimativa de Kaplan-Meier , Masculino , Pessoa de Meia-Idade , Inclusão em Parafina , Prognóstico , Proteínas de Ligação a RNA/genética , Proteínas de Ligação a RNA/metabolismo , Fatores de Risco , Neoplasias Gástricas/genética , Neoplasias Gástricas/mortalidade , Neoplasias Gástricas/patologia , Análise Serial de Tecidos , Regulação para Cima
5.
Chin Med J (Engl) ; 126(6): 1159-65, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23506598

RESUMO

BACKGROUND: Wheat-dependent exercise-induced anaphylaxis (WDEIA) is a complex disease resulting from interaction of environmental and genetic factors. The aim of this study was to investigate the association of three single nucleotide polymorphisms (SNPs) (IL-4-C590T, IL-4RA A1727G and IL-10-A627C) with WDEIA. METHODS: SNP genotyping was conducted among the case subset composing 51 patients with WDEIA and four control subsets by sequencing DNA yielded from polymerase chain reaction (PCR). Statistical analysis of genotype/allele's frequencies between cases and controls were carried out through Fisher's exact test with the software of SPSS16.0. RESULTS: For IL-4-C590T, there were statistically significant differences of genotype frequencies in case-control 1 (P = 0.03) and case-control 4 (P = 0.001) and statistically significant differences of allele frequencies in three case-control models (case-control 1: OR = 4.27 (95%CI = 1.40 - 13.07), P = 0.009; case-control 3: OR = 1.99 (95%CI = 1.13 - 3.50), P = 0.02; case-control 4: OR = 2.39 (95%CI = 1.49 - 3.84), P = 0.001). All other association studies showed no statistically significant (P > 0.05). CONCLUSIONS: IL-4-C590T may be related to the susceptibility of WDEIA, and the minor allele C might be a potential risk factor accounting for WDEIA. IL-4RA A1727G and IL-10-A627C might not be involved in the occurrence of WDEIA.


Assuntos
Anafilaxia/genética , Exercício Físico/fisiologia , Polimorfismo de Nucleotídeo Único/genética , Triticum/imunologia , Adolescente , Adulto , Idoso , Povo Asiático/genética , Criança , Pré-Escolar , Feminino , Frequência do Gene/genética , Genótipo , Gliadina/imunologia , Glutens/imunologia , Humanos , Imunoglobulina E , Masculino , Pessoa de Meia-Idade , Adulto Jovem
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