411 research outputs found

    Co-creating “smart” sustainable food futures with urban food growers

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    The futuristic visions, infrastructures, and developments of smart cities continue to gather pace, with municipal authorities and businesses in the UK investing increasing amounts of resources into their manifestation. At the same time local communities continue to be hard hit by austerity, with more local services being affected by government cuts, with the North-East of England being particularly affected. In this paper we report on a case study that aimed to explore how the top-down, technocentric, and corporate visions of smart cities stand in contrast to the reality of grassroots communities who are dealing with the consequences of austerity. Our case study focuses on a community of urban food growers. We describe our speculative and participatory approach that we devised for co-designing “smart” urban food-growing futures from the bottom-up with local residents in a deprived neighbourhood of Newcastle upon Tyne, and reflect on how they elicited realities and future visions that stand as a counterpoint to the corporate visions of future cities

    Community Justice and Public Safety: Assessing Criminal Justice Policy Through the Lens of the Social Contract

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    A reconceptualization of the idea of “community justice” is framed in the logic of the social contract and emphasizes the responsibility of the justice system for the provision of public safety. First, we illustrate the ways in which the criminal justice system has hindered the efforts of community residents to participate in the production of public safety by disrupting informal social networks. Then we turn to an examination of the compositional dynamics of California prison populations over time to demonstrate that the American justice system has failed to meet their obligations to provide public safety by incapacitating dangerous offenders. We argue that these policy failures represent a breach of the social contract and advocate for more effective collaboration between communities and the formal criminal justice system so that all parties can fulfill their obligations under the contract

    Holocene-scale fire dynamics of central European temperate sprucebeech forests

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    This study investigated the long-term role and drivers of fire in the central European temperate sprucebeech forests from Pråƥilské Jezero, Czech Republic. The results illustrate the complex relationship between broad-scale climate, vegetation composition, and local human activities on fire throughout the Holocene. Biomass burning was the highest (average 3 fires/1000 years) and most severe during the early Holocene when fire resistant taxa (Pinus, Corylus and Betula) dominated. Using a Generalized Additive Model to assess the response of dominant canopy taxa to changes in biomass burning and fire severity, response curves demonstrate a positive relationship (p < 0.01) between fire resistant taxa and increases in biomass burning. Norway spruce (Picea abies) established ~10,000 cal yr BP and expanded during peak biomass burning. Response curves show a slight negative relationship with Picea and increasing biomass burning, and a positive relationship with increasing fire severity. This suggests that central European spruce forests may not be significantly impacted by fire. Regional biomass burning dramatically decreased with the expansion of fire sensitive taxa (e.g. Fagus sylvatica) ~6500 cal yr BP, yet no dramatic reduction in local fire frequency occurred. This suggests either human activities or rare fire-promoting climatic events were important in shaping local fire regimes. Fire activity peaked (6 fires/1000 years) ~2500 cal yr BP and paralleled increases in anthropogenic pollen indicators. Fagus response curves illustrates a negative (p < 0.01) relationship with increasing biomass burning and fire severity suggesting that natural Fagus forests may be increasingly vulnerable to projected increases in wildfire occurrence

    Adipocytes disrupt the translational programme of acute lymphoblastic leukaemia to favour tumour survival and persistence

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    The specific niche adaptations that facilitate primary disease and Acute Lymphoblastic Leukaemia (ALL) survival after induction chemotherapy remain unclear. Here, we show that Bone Marrow (BM) adipocytes dynamically evolve during ALL pathogenesis and therapy, transitioning from cellular depletion in the primary leukaemia niche to a fully reconstituted state upon remission induction. Functionally, adipocyte niches elicit a fate switch in ALL cells towards slow-proliferation and cellular quiescence, highlighting the critical contribution of the adipocyte dynamic to disease establishment and chemotherapy resistance. Mechanistically, adipocyte niche interaction targets posttranscriptional networks and suppresses protein biosynthesis in ALL cells. Treatment with general control nonderepressible 2 inhibitor (GCN2ib) alleviates adipocyte-mediated translational repression and rescues ALL cell quiescence thereby significantly reducing the cytoprotective effect of adipocytes against chemotherapy and other extrinsic stressors. These data establish how adipocyte driven restrictions of the ALL proteome benefit ALL tumours, preventing their elimination, and suggest ways to manipulate adipocyte-mediated ALL resistance

    Understanding the UK hospital supply chain in an era of patient choice

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    Author Posting © Westburn Publishers Ltd, 2011. This is a post-peer-review, pre-copy-edit version of an article which has been published in its definitive form in the Journal of Marketing Management, and has been posted by permission of Westburn Publishers Ltd for personal use, not for redistribution. The article was published in Journal of Marketing Management, 27(3-4), 401 - 423, doi:10.1080/0267257X.2011.547084 http://dx.doi.org/10.1080/0267257X.2011.547084The purpose of this paper is to investigate the UK hospital supply chain in light of recent government policy reform where patients will have, inter alia, greater choice of hospital for elective surgery. Subsequently, the hospital system should become far more competitive with supply chains having to react to these changes as patient demand becomes less predictable. Using a qualitative case study methodology, hospital managers are interviewed on a range of issues. Views on the development of the hospital supply chain in different phases are derived, and are used to develop a map of the current hospital chain. The findings show hospital managers anticipating some significant changes to the hospital supply chain and its workings as Patient Choice expands. The research also maps the various aspects of the hospital supply chain as it moves through different operational phases and highlights underlying challenges and complexities. The hospital supply chain, as discussed and mapped in this research, is original work given there are no examples in the literature that provide holistic representations of hospital activity. At the end, specific recommendations are provided that will be of interest to service to managers, researchers, and policymakers

    Co-activation of NF-ÎșB and MYC renders cancer cells addicted to IL6 for survival and phenotypic stability

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    NF-ÎșB and MYC are found co-deregulated in human B and plasma-cell cancers. In physiology, NF-ÎșB is necessary for terminal B-to-plasma cell differentiation, whereas MYC repression is required. It is thus unclear if NF-ÎșB/MYC co-deregulation is developmentally compatible in carcinogenesis and/or impacts cancer cell differentiation state, possibly uncovering unique sensitivities. Using a mouse system to trace cell lineage and oncogene activation we found that NF-ÎșB/MYC co-deregulation originated cancers with a plasmablast-like phenotype, alike human plasmablastic-lymphoma and was linked to t(8;14)[MYC-IGH] multiple myeloma. Notably, in contrast to NF-ÎșB or MYC activation alone, co-deregulation rendered cells addicted to IL6 for survival and phenotypic stability. We propose that conflicting oncogene-driven differentiation pressures can be accommodated at a cost in poorly-differentiated cancers. SIGNIFICANCE: Our studies improve the understanding of cancer pathogenesis by demonstrating that co-deregulation of NF-ÎșB and MYC synergize in forming a cancer with a poorly-differentiated state. The cancers in the mouse system share features with human Plasmablastic lymphoma that has a dismal prognosis and no standard of care, and with t(8;14)[MYC-IGH] Multiple myeloma, which is in overall resistant to standard therapy. Notably, we found that NF-ÎșB and MYC co-deregulation uniquely render cells sensitive to IL6 deprivation, providing a road-map for patient selection. Because of the similarity of the cancers arising in the compound mutant mouse model with that of human Plasmablastic lymphoma and t(8;14)[MYC-IGH] Multiple myeloma, this model could serve in preclinical testing to investigate novel therapies for these hard-to-treat diseases

    Genomic profiling reveals spatial intra-tumor heterogeneity in follicular lymphoma

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    We are indebted to the patients for donating tumor specimens as part of this study. The authors thank the Centre de Ressources Biologiques (CRB)-SantĂ© of Rennes (BB-0033-00056) for patient samples, Queen Mary University of London Genome Centre for Illumina Miseq sequencing, and the support by the National Institute for Health Research (NIHR) Biomedical Research Centre at Guy’s and St Thomas’ NHS Foundation Trust and King’s College London for Illumina Hiseq sequencing. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR, or the Department of Health. This work was supported by grants from the Kay Kendall Leukaemia Fund (KKL 757 awarded to J.O.), Cancer Research UK (22742 awarded to J.O., 15968 awarded to J.F., Clinical Research Fellowship awarded to S.A.), Bloodwise through funding of the Precision Medicine for Aggressive Lymphoma (PMAL) consortium, Centre for Genomic Health, Queen Mary University of London, Carte d’IdentitĂ© des Tumeurs (CIT), Ligue National contre le Cancer, PĂŽle de biologie hospital universitaire de Rennes, CRB-SantĂ© of Rennes (BB-0033-00056), and CeVi/Carnot program

    Additively Homomorphic IBE from Higher Residuosity

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    We present an identity-Based encryption (IBE) scheme that is group homomorphic for addition modulo a ``large\u27\u27 (i.e. superpolynomial) integer, the first such group homomorphic IBE. Our first result is the construction of an IBE scheme supporting homomorphic addition modulo a poly-sized prime ee. Our construction builds upon the IBE scheme of Boneh, LaVigne and Sabin (BLS). BLS relies on a hash function that maps identities to ee-th residues. However there is no known way to securely instantiate such a function. Our construction extends BLS so that it can use a hash function that can be securely instantiated. We prove our scheme IND-ID-CPA secure under the (slightly modified) ee-th residuosity assumption in the random oracle model and show that it supports a (modular) additive homomorphism. By using multiple instances of the scheme with distinct primes and leveraging the Chinese Remainder Theorem, we can support homomorphic addition modulo a ``large\u27\u27 (i.e. superpolynomial) integer. We also show that our scheme for e>2e > 2 is anonymous by additionally assuming the hardness of deciding solvability of a special system of multivariate polynomial equations. We provide a justification for this assumption by considering known attacks
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