Virtual Platform-Based Design Space Exploration of Power-Efficient Distributed Embedded Applications

Networked embedded systems are essential building blocks of a broad variety of distributed applications ranging from agriculture to industrial automation to healthcare and more. These often require specific energy optimizations to increase the battery lifetime or to operate using energy harvested from the environment. Since a dominant portion of power consumption is determined and managed by software, the software development process must have access to the sophisticated power management mechanisms provided by state-of-the-art hardware platforms to achieve the best tradeoff between system availability and reactivity. Furthermore, internode communications must be considered to properly assess the energy consumption. This article describes a design flow based on a SystemC virtual platform including both accurate power models of the hardware components and a fast abstract model of the wireless network. The platform allows both model-driven design of the application and the exploration of power and network management alternatives. These can be evaluated in different network scenarios, allowing one to exploit power optimization strategies without requiring expensive field trials. The effectiveness of the approach is demonstrated via experiments on a wireless body area network application

Full-scale shake table tests of a reinforced concrete structure equipped with a novel active mass damper

This paper presents the results of an experimental program involving shake table testing of two full-scale reinforced concrete frame buildings. These tests were conducted to investigate the effectiveness and reliability of a newly proposed servo-hydraulic Active Mass Damper (AMD) that can be designed to enhance the target seismic performance of a building at multiple earthquake intensity levels. The two nominally identical case-study buildings were intentionally designed to exhibit a “soft story” mechanism at the first level when subject to ground shaking of sufficient intensity, but one was equipped with the newly proposed AMD, installed on the roof. The two specimens were then subject to the same loading protocol consisting of a ground shaking sequence of varying intensity, with the seismic input consisting of a selected natural ground motion. The experimental results demonstrated that the proposed AMD is extremely effective at enhancing building seismic performance. Specifically, the AMD provided peak displacement reductions in the order of 70% and was shown capable of absorbing more than 60% of the total input energy. As a consequence, the un-retrofitted structure suffered nontrivial structural and non-structural damage, while the AMD-retrofitted building remained virtually undamaged at all shaking intensities considered

VEGF-induced intracellular Ca2+ oscillations are down-regulated and do not stimulate angiogenesis in breast cancer-derived endothelial colony forming cells.

Endothelial colony forming cells (ECFCs) represent a population of truly endothelial precursors that promote the angiogenic switch in solid tumors, such as breast cancer (BC). The intracellular Ca2+ toolkit, which drives the pro-angiogenic response to VEGF, is remodelled in tumor-associated ECFCs such that they are seemingly insensitive to this growth factor. This feature could underlie the relative failure of anti-VEGF therapies in cancer patients. Herein, we investigated whether and how VEGF uses Ca2+ signalling to control angiogenesis in BC-derived ECFCs (BCECFCs). Although VEGFR-2 was normally expressed, VEGF failed to induce proliferation and in vitro tubulogenesis in BC-ECFCs. Likewise, VEGF did not trigger robust Ca2+ oscillations in these cells. Similar to normal cells, VEGF-induced intracellular Ca2+ oscillations were triggered by inositol-1,4,5-trisphosphate-dependent Ca2+ release from the endoplasmic reticulum (ER) and maintained by store-operated Ca2+ entry (SOCE). However, InsP3-dependent Ca2+ release was significantly lower in BC-ECFCs due to the down-regulation of ER Ca2+ levels, while there was no remarkable difference in the amplitude, pharmacological profile and molecular composition of SOCE. Thus, the attenuation of the pro-angiogenic Ca2+ response to VEGF was seemingly due to the reduction in ER Ca2+ concentration, which prevents VEGF from triggering robust intracellular Ca2+ oscillations. However, the pharmacological inhibition of SOCE prevented BC-ECFC proliferation and in vitro tubulogenesis. These findings demonstrate for the first time that BC-ECFCs are insensitive to VEGF, which might explain at cellular and molecular levels the failure of anti-VEGF therapies in BC patients, and hint at SOCE as a novel molecular target for this disease

Psychosocial Issues in Long-Term Survivors of Testicular Cancer

Testicular cancer is the most frequent tumor in young males aged 15–39 years. As cure rates are currently around 90%, the prevalence of survivors is increasing. However, a disease-free condition does not necessarily correspond to a life free of physical and psychosocial health problems. The aim of this review was to explore psychosocial morbidity among testicular cancer survivors. A literature search was conducted in three electronic databases (PubMed, Medline, and Embase). The results of the search on cancer survivors were then combined with those of the search on psychosocial concerns and work performance. Eighty-four publications met the inclusion criteria. Physical, psychological, work-related problems and changing perspectives about work and life in general influenced life and career decisions among testicular cancer survivors. Individual health, sexual relationships and work problems, affect several important aspects of survival and significantly influence the QoL of long-term survivors

Adjuvant High-Dose Chemotherapy with Autologous Hematopoietic Stem Cell Support for High-Risk Primary Breast Cancer: Results from the Italian National Registry

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Residual peripheral blood CD26+leukemic stem cells in chronic myeloid leukemia patients during TKI therapy and during treatment-free remission

Chronic myeloid leukemia (CML) patients in sustained “deep molecular response” may stop TKI treatment without disease recurrence; however, half of them lose molecular response shortly after TKI withdrawing. Well-defined eligibility criteria to predict a safe discontinuation up-front are still missing. Relapse is probably due to residual quiescent TKI-resistant leukemic stem cells (LSCs) supposedly transcriptionally low/silent and not easily detectable by BCR-ABL1 qRT-PCR. Bone marrow Ph+ CML CD34+/CD38− LSCs were found to specifically co-express CD26 (dipeptidylpeptidase-IV). We explored feasibility of detecting and quantifying CD26+ LSCs by flow cytometry in peripheral blood (PB). Over 400 CML patients (at diagnosis and during/after therapy) entered this cross-sectional study in which CD26 expression was evaluated by a standardized multiparametric flow cytometry analysis on PB CD45+/CD34+/CD38− stem cell population. All 120 CP-CML patients at diagnosis showed measurable PB CD26+ LSCs (median 19.20/μL, range 0.27–698.6). PB CD26+ LSCs were also detectable in 169/236 (71.6%) CP-CML patients in first-line TKI treatment (median 0.014 cells/μL; range 0.0012–0.66) and in 74/112 (66%), additional patients studied on treatment-free remission (TFR) (median 0.015/μL; range 0.006–0.76). Notably, no correlation between BCR-ABL/ABLIS ratio and number of residual LSCs was found both in patients on or off TKIs. This is the first evidence that “circulating” CML LSCs persist in the majority of CML patients in molecular response while on TKI treatment and even after TKI discontinuation. Prospective studies evaluating the dynamics of PB CD26+ LSCs during TKI treatment and the role of a “stem cell response” threshold to achieve and maintain TFR are ongoing

Improving SoC Design Flow by means of MDA and UML Profiles ⋆

Abstract. We tackle the problem of improving the SoC (System on a Chip) design flow in order to provide a modeling framework which allows exchange, reuse and integration of IP (Intellectual Property) models. In this paper, exploiting the MDA capabilities of defining modeling languages platform independent and reducible to platform dependent languages, we present a UML profile for the SystemC language. Furthermore, we discuss the advantages of high-level modeling SoC components in the style of UML using the SystemC design primitives, rather than designing at a lower level by means of coding.