2,730 research outputs found

    Silencing E3 Ubiqutin ligase ITCH as a potential therapy to enhance chemotherapy efficacy in p53 mutant neuroblastoma cells

    Get PDF
    P53 mutations are responsible for drug-resistance of tumour cells which impacts on the efficacy of treatment. Alternative tumour suppressor pathways need to be explored to treat p53- deficient tumours. The E3 ubiquitin ligase, ITCH, negatively regulates the tumour suppressor protein TP73, providing a therapeutic target to enhance the sensitivity of the tumour cells to the treatment. In the present study, two p53-mutant neuroblastoma cell lines were used as in vitro models. Using immunostaining, western blot and qPCR methods, we firstly identified that ITCH was expressed on p53-mutant neuroblastoma cell lines. Transfection of these cell lines with ITCH siRNA could effectively silence the ITCH expression, and result in the stabilization of TP73 protein, which mediated the apoptosis of the neuroblastoma cells upon irradiation treatment. Finally, in vivo delivery of the ITCH siRNA using nanoparticles to the neuroblastoma xenograft mouse model showed around 15–20% ITCH silencing 48 hours after transfection. Our data suggest that ITCH could be silenced both in vitro and in vivo using nanoparticles, and silencing of ITCH sensitizes the tumour cells to irradiation treatment. This strategy could be further explored to combine the chemotherapy/radiotherapy treatment to enhance the therapeutic effects on p53-deficient neuroblastoma

    Physiological response to groundwater depth varies among species and with river flow regulation

    Get PDF
    We investigated the physiological response of two native riparian tree species (Populus fremontii and Salix gooddingii) and one exotic species (Tamarix chinensis) to groundwater availability along gradients of depth to groundwater at two rivers in Arizona. Depth to groundwater (DGW) at the dam-regulated Bill Williams River (BWR) was relatively constant and shallow (,4 m). Populus fremontii at BWR did not experience reduced water availability at deeper groundwater depths, as evidenced by high predawn water potential. However, leaf gas exchange of P. fremontii was sensitive to high vapor pressure deficit where surface flow was ephemeral at BWR. Lower predawn water potentials of S. gooddingii at BWR suggested reduced water availability at deeper groundwater depths, but these reductions did not adversely affect net photosynthetic rate. Along the range of depth to groundwater at BWR, all three species suffered little canopy dieback, and dieback was not related to depth to groundwater. Depth to groundwater at the free-flowing Hassayampa River (HRP) was much greater and declined more rapidly in the ephemeral reaches than at BWR. Both P. fremontii and S. gooddingii experienced reduced water availability at deeper groundwater depths at HRP, as evidenced by lower predawn water potential. Both species also experienced reduced leaf gas exchange at deeper groundwater depths. Canopy dieback of all species was higher at HRP than at BWR and increased with increasing DGW, especially when DGW fell below 3 m. There was evidence to support branch sacrifice in these three riparian tree species as a means of improving water status in the surviving shoot. However, branch sacrifice was insufficient to prevent mortality in some of the native trees where DGW fell below 3 m at HRP. In contrast to the native species, T. chinensis showed no change in water availability, leaf gas exchange, or canopy dieback with increasing DGW at either river. Leaf gas exchange was lower and dieback was greater for T. chinensis at HRP where depth to groundwater was greater than at BWR, but there was no mortality at either river. Our results show that deep groundwater is more detrimental to the physiological condition of P. fremontii and S. gooddingii than it is to T. chinensis. Also, the pronounced differences in DGW and tree physiological performance between BWR and HRP suggest that dam regulation can increase water availability to mature trees in some desert riparian ecosystems. Finally, our study also provides estimates of the range of DGW that can maintain healthy, mature P. fremontii and S. gooddingii trees

    Liposomal delivery of hydrophobic RAMBAs provides good bioavailability and significant enhancement of retinoic acid signalling in neuroblastoma tumour cells

    Get PDF
    Retinoid treatment is employed during residual disease treatment in neuroblastoma, where the aim is to induce neural differentiation or death in tumour cells. However, although therapeutically effective, retinoids have only modest benefits and suffer from poor pharmacokinetic properties. In vivo, retinoids induce CYP26 enzyme production in the liver, enhancing their own rapid metabolic clearance, while retinoid resistance in tumour cells themselves is considered to be due in part to increased CYP26 production. Retinoic acid metabolism blocking agents (RAMBAs), which inhibit CYP26 enzymes, can improve retinoic acid pharmacokinetics in pre-clinical neuroblastoma models. Here we demonstrate that in cultured neuroblastoma tumour cells, RAMBAs enhance retinoic acid action as seen by morphological differentiation, AKT signalling and suppression of MYCN protein. Although active as retinoid enhancers, these RAMBAs are highly hydrophobic and their effective delivery in humans will be very challenging. Here we demonstrate that such RAMBAs can be loaded efficiently into cationic liposomal particles, where the RAMBAs achieve good bioavailability and activity in cultured tumour cells. This demonstrates the efficacy of RAMBAs in enhancing retinoid signaling in neuroblastoma cells and shows for the first time that liposomal delivery of hydrophobic RAMBAs is a viable approach, providing novel opportunities for their delivery and application in humans

    Minicircle DNA provide enhanced and prolonged transgene expression following airway gene transfer

    Get PDF
    Gene therapy for cystic fibrosis using non-viral, plasmid-based formulations has been the subject of intensive research for over two decades but a clinically viable product has yet to materialise in large part due to inefficient transgene expression. Minicircle DNA give enhanced and more persistent transgene expression compared to plasmid DNA in a number of organ systems but has not been assessed in the lung. In this study we compared minicircle DNA with plasmid DNA in transfections of airway epithelial cells. In vitro, luciferase gene expression from minicircles was 5-10-fold higher than with plasmid DNA. In eGFP transfections in vitro both the mean fluorescence intensity and percentage of cells transfected was 2-4-fold higher with minicircle DNA. Administration of equimolar amounts of DNA to mouse lungs resulted in a reduced inflammatory response and more persistent transgene expression, with luciferase activity persisting for 2 weeks from minicircle DNA compared to plasmid formulations. Transfection of equal mass amounts of DNA in mouse lungs resulted in a 6-fold increase in transgene expression in addition to more persistent transgene expression. Our findings have clear implications for gene therapy of airway disorders where plasmid DNA transfections have so far proven inefficient in clinical trials

    Development of targeted siRNA nanocomplexes to prevent fibrosis in experimental glaucoma filtration surgery

    Get PDF
    RNA interference induced by double-stranded, small interfering RNA (siRNA) molecules has attracted great attention as a naturally-occurring approach to silence gene expression with high specificity. The Myocardin-Related Transcription Factor/Serum Response Factor (MRTF/SRF) pathway is a master regulator of cytoskeletal gene expression and thus represents a promising target to prevent fibrosis. A major hurdle to implementing siRNA therapies is the method of delivery and we have thus optimised lipid-peptide-siRNA (LPR) nanoparticles containing MRTF-B siRNAs as a targeted approach to prevent conjunctival fibrosis. We tested fifteen LPR nanoparticle formulations with different lipid compositions, surface charges and targeting or non-targeting peptides in human conjunctival fibroblasts. In vitro, the LPR formulation of DOTMA/DOPE lipid with the targeting peptide Y (LYR) was the most efficient in MRTF-B gene silencing and non-cytotoxic compared to the non-targeting formulation. In vivo, subconjunctival administration of LYR nanoparticles containing MRTF-B siRNAs doubled bleb survival in a pre-clinical rabbit model of glaucoma filtration surgery. Furthermore, MRTF-B LYR nanoparticles reduced the MRTF-B mRNA by 29.6% in rabbit conjunctival tissues, which led to significantly decreased conjunctival scarring with no adverse side effects. LYR-mediated delivery of siRNA shows promising results to increase bleb survival and to prevent conjunctival fibrosis after glaucoma filtration surgery

    The Algorithm Theoretical Basis Document for the GLAS Atmospheric Data Products

    Get PDF
    The purpose of this document is to present a detailed description of the algorithm theoretical basis for each of the GLAS data products. This will be the final version of this document. The algorithms were initially designed and written based on the authors prior experience with high altitude lidar data on systems such as the Cloud and Aerosol Lidar System (CALS) and the Cloud Physics Lidar (CPL), both of which fly on the NASA ER-2 high altitude aircraft. These lidar systems have been employed in many field experiments around the world and algorithms have been developed to analyze these data for a number of atmospheric parameters. CALS data have been analyzed for cloud top height, thin cloud optical depth, cirrus cloud emittance (Spinhirne and Hart, 1990) and boundary layer depth (Palm and Spinhirne, 1987, 1998). The successor to CALS, the CPL, has also been extensively deployed in field missions since 2000 including the validation of GLAS and CALIPSO. The CALS and early CPL data sets also served as the basis for the construction of simulated GLAS data sets which were then used to develop and test the GLAS analysis algorithms
    • …
    corecore