Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 6 de 6
Filtrar
Más filtros

Banco de datos
País/Región como asunto
Tipo del documento
Asunto de la revista
País de afiliación
Intervalo de año de publicación
1.
Biochim Biophys Acta ; 1840(6): 2004-13, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24534329

RESUMEN

BACKGROUND: Ubiquitin-proteasome pathway (UPP) plays a very important role in the degradation of proteins. Finding novel UPP inhibitors is a promising strategy for treating multiple myeloma (MM). METHODS: Ub-YFP reporter assays were used as cellular UPP models. MM cell growth, apoptosis and overall death were evaluated with the MTS assay, Annexin V/PI dual-staining flow cytometry, poly (ADP-ribose) polymerase (PARP) cleavage, and PI uptake, respectively. The mechanism of UPP inhibition was analyzed by western blotting for ubiquitin, in vitro and cellular proteasomal and deubiquitinases (DUBs) activity assays. Cellular reactive oxygen species (ROS) were measured with H2DCFDA. RESULTS: Curcusone D, identified as a novel UPP inhibitor, causes cell growth inhibition and apoptosis in MM cells. Curcusone D induced the accumulation of poly-ubiquitin-conjugated proteins but could not inhibit proteasomal activity in vitro or in cells. Interestingly, the mono-ubiquitin level and the total cellular DUB activity were significantly downregulated following curcusone D treatment. Furthermore, curcusone D could induce ROS, which were closely correlated with DUB inhibition that could be nearly completely reversed by NAC. Finally, curcusone D and the proteasomal inhibitor bortezomib showed a strong synergistic effect against MM cells. CONCLUSIONS: Curcusone D is novel UPP inhibitor that acts via the ROS-induced inhibition of DUBs to produce strong growth inhibition and apoptosis of MM cells and synergize with bortezomib. GENERAL SIGNIFICANCE: The anti-MM molecular mechanism study of curcusone D will promote combination therapies with different UPP inhibitors against MM and further support the concept of oxidative stress regulating the activity of DUBs.


Asunto(s)
Ácidos Borónicos/uso terapéutico , Diterpenos/farmacología , Jatropha/química , Mieloma Múltiple/tratamiento farmacológico , Inhibidores de Proteasoma/farmacología , Pirazinas/uso terapéutico , Especies Reactivas de Oxígeno/metabolismo , Proteasas Ubiquitina-Específicas/antagonistas & inhibidores , Apoptosis/efectos de los fármacos , Bortezomib , Línea Celular Tumoral , Humanos , Mieloma Múltiple/patología
2.
Parasitol Int ; 103: 102933, 2024 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-39048024

RESUMEN

Tick saliva contains a range of critical biological molecules which could inhibit host defenses and guarantee their food supply. Hq023, a novel cDNA sequence, was cloned from a cDNA library constructed from salivary glands of partially-engorged Haemaphysalis qinghaiensis. Hq023 has an open reading frame (ORF) of 408 bp coding a protein containing 135 amino acid residues with a molecular mass of 15 kDa. Database homology showed that Hq023 protein was structurally similar to a natural toxin U33-theraphotoxin-Cg1c from the Chinese tarantula Chilobrachys guangxiensis. A recombinant protein was expressed with the novel cDNA in a prokaryotic system and its analgesic effect was evaluated in mice model. Both tail immersion and hot-plate tests uncovered an antinociceptive activity, while in the acetic acid-induced writhing test this effect was not observed. These results indicated that the novel recombinant protein Hq023 (rHq023) probably possessed a central antinociceptive activity. Finding of the novel protein might pave a new avenue for the development of tick-derived analgesics.


Asunto(s)
Analgésicos , Clonación Molecular , Ixodidae , Proteínas Recombinantes , Animales , Ratones , Analgésicos/farmacología , Ixodidae/efectos de los fármacos , Ixodidae/genética , Proteínas Recombinantes/administración & dosificación , Secuencia de Aminoácidos , Proteínas de Artrópodos/genética , Masculino , ADN Complementario , Femenino , Secuencia de Bases , Dolor/tratamiento farmacológico , Saliva , Glándulas Salivales
3.
J Biol Chem ; 287(45): 37973-85, 2012 Nov 02.
Artículo en Inglés | MEDLINE | ID: mdl-22969086

RESUMEN

Liver X receptors (LXRs) are nuclear receptors that function to modulate lipid metabolism as well as immune and inflammatory responses. Upon activation by their ligands, LXRs up-regulate a spectrum of gene transcription programs involved in cholesterol and fatty acid homeostasis. However, the mechanisms by which LXR-mediated transcriptional activation is regulated remain incompletely understood. Here, we show that PIAS1, a member of the protein inhibitor of the activated STAT family of proteins with small ubiquitin-like modifier (SUMO) E3 ligase activity, acts to suppress LXR ligand-dependent transcriptional activation of the lipogenic program in hepatocytes. We found that liver mRNA expression levels of Pias1 and Pias3 were inversely associated with those of genes involved in lipogenesis in mouse models with diet-induced or genetic obesity. Overexpression of PIAS1 in primary hepatocytes resulted in a reduction of LXR ligand-induced fatty acid synthesis and suppression of the expression of lipogenic genes, including Srebp1c and Fas. Moreover, PIAS1 was able to interact with LXRß and repress its transcriptional activity upon ligand stimulation, which did not require PIAS1-promoted SUMO modification of LXRß. In addition, PIAS1 could also interact with PGC-1ß and attenuate its association with LXRß, blunting the ability of PGC-1ß to co-activate LXRß. Importantly, PIAS1 impaired LXRß binding to its target DNA sequence. Taken together, our results suggest that PIAS1 may serve as a lipogenic regulator by negatively modulating LXRs in a SUMOylation-independent manner.


Asunto(s)
Lipogénesis/genética , Receptores Nucleares Huérfanos/genética , Proteínas Inhibidoras de STAT Activados/genética , Activación Transcripcional/genética , Animales , Western Blotting , Células Cultivadas , Ácidos Grasos/biosíntesis , Células HEK293 , Hepatocitos/citología , Hepatocitos/metabolismo , Humanos , Hidrocarburos Fluorados/farmacología , Ligandos , Hígado/citología , Hígado/metabolismo , Receptores X del Hígado , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Obesos , Obesidad/etiología , Obesidad/genética , Obesidad/metabolismo , Receptores Nucleares Huérfanos/agonistas , Receptores Nucleares Huérfanos/metabolismo , Coactivador 1-alfa del Receptor Activado por Proliferadores de Peroxisomas gamma , Unión Proteica/efectos de los fármacos , Proteínas Inhibidoras de STAT Activados/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Sulfonamidas/farmacología , Sumoilación , Transactivadores/genética , Transactivadores/metabolismo , Factores de Transcripción , Activación Transcripcional/efectos de los fármacos
4.
World J Microbiol Biotechnol ; 28(10): 3039-52, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-22806743

RESUMEN

The diversity and distribution of bacterial and archaeal communities in four different water flooding oil reservoirs with different geological properties were investigated using 16S rDNA clone library construction method. Canonical correspondence analysis was used to analyze microbial community clustering and the correlation with environmental factors. The results indicated that the diversity and abundance in the bacterial communities were significantly higher than the archaeal communities, while both of them had high similarity within the communities respectively. Phylogenetic analysis showed that of compositions of bacterial communities were distinctly different both at phylum and genus level. Proteobacteria dominated in each bacterial community, ranging from 61.35 to 75.83 %, in which α-proteobacteria and γ-proteobacteria were the main groups. In comparison to bacterial communities, the compositions of archaeal communities were similar at phylum level, while varied at genus level, and the dominant population was Methanomicrobia, ranging from 65.91 to 92.74 % in the single oil reservoir. The factor that most significantly influenced the microbial communities in these reservoirs was found to be temperature. Other environmental factors also influenced the microbial communities but not significantly. It is therefore assumed that microbial communities are formed by an accumulated effect of several factors. These results are essential for understanding ecological environment of the water flooding oil reservoirs and providing scientific guidance to the performance of MEOR technology.


Asunto(s)
Biodiversidad , ADN Bacteriano/aislamiento & purificación , Inundaciones , Yacimiento de Petróleo y Gas/microbiología , Microbiología del Agua , Alphaproteobacteria/clasificación , Alphaproteobacteria/genética , Archaea/clasificación , Archaea/genética , Fenómenos Químicos , China , Clonación Molecular , ADN Bacteriano/genética , Euryarchaeota/clasificación , Euryarchaeota/genética , Gammaproteobacteria/clasificación , Gammaproteobacteria/genética , Biblioteca de Genes , Filogenia , ARN Ribosómico 16S/genética , Análisis de Secuencia de ADN
5.
Ann Clin Lab Sci ; 51(2): 262-266, 2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-33941568

RESUMEN

BRAF and NRAS are oncogenes in the RAS/RAF/MEK/MAP-kinase signaling pathway. Coexistent mutations of BRAF and NRAS in a single colorectal cancer patient have always been considered mutually exclusive or at least rare. The clinical outcome of these patients remains undetermined. Herein we report a 53-year-old man harboring an NRAS Q61L mutation in his primary rectal carcinoma, who presented with a concomitant mutation of BRAF V600E in his liver metastasis biopsy 55 months after the primary CRC surgical resection. Our findings suggest that a BRAF and NRAS developed co-mutation may lead to a distinct clinicopathological progression. BRAF-mutated CRCwill not benefit from anti-RAS targeted therapy.


Asunto(s)
GTP Fosfohidrolasas/genética , Proteínas de la Membrana/genética , Proteínas Proto-Oncogénicas B-raf/genética , Neoplasias del Recto/genética , Análisis Mutacional de ADN , GTP Fosfohidrolasas/metabolismo , Humanos , Masculino , Proteínas de la Membrana/metabolismo , Persona de Mediana Edad , Mutación/genética , Proteínas Proto-Oncogénicas B-raf/metabolismo , Transducción de Señal
6.
Huan Jing Ke Xue ; 33(2): 625-32, 2012 Feb.
Artículo en Zh | MEDLINE | ID: mdl-22509607

RESUMEN

Denaturing gradient gel electrophoresis (DGGE) method and principal component analysis (PCA) method were used to analyze the structures of microorganism population in injection wells and production wells of a post-polymer-flooding oil reservoir in Daqing oil field. The results showed that the dominant species in injection wellhead were aerobic bacteria Pseudomonas and Acinenobacter. Facultative anaerobic bacteria Enterbacter was the dominant bacteria in near area of injection wells. Bacteria detected in production wells included Thauera, Clostridia, Pseudomonas, Petrobacter and some uncultured bacteria. Methanosaeta turned out to be the only archaea detected in injection wells, which was an aceticlastic methane-producing archaeon. Archaea detected in production wells consisted of Methanomicrobium, Methanospirillum and Methanobacterium. In general, aerobic bacteria, facultative anaerobe, and strictly anaerobic bacteria distributed successively from injection wells to production wells in this block. The dominant populations of archaea were different between injection wells and production wells, while were influenced by different environments and microbial metabolism products.


Asunto(s)
Archaea/clasificación , Bacterias/clasificación , Yacimiento de Petróleo y Gas/microbiología , Petróleo/microbiología , Acinetobacter/aislamiento & purificación , Archaea/crecimiento & desarrollo , Archaea/aislamiento & purificación , Bacterias/crecimiento & desarrollo , Bacterias/aislamiento & purificación , China , ADN Bacteriano/genética , Electroforesis en Gel de Gradiente Desnaturalizante/métodos , Filogenia , Polímeros , Análisis de Componente Principal , Pseudomonas/aislamiento & purificación , ARN Ribosómico 16S/genética , Pozos de Agua/microbiología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA