281 research outputs found
An overview of IoT architectures, technologies, and existing open-source projects
Financiado para publicación en acceso aberto: Universidade da Coruña/CISUG[Abstract]: Today’s needs for monitoring and control of different devices in organizations require an Internet of Things (IoT) platform that can integrate heterogeneous elements provided by multiple vendors and using different protocols, data formats and communication technologies. This article provides a comprehensive review of all the architectures, technologies, protocols and data formats most commonly used by existing IoT platforms. On this basis, a comparative analysis of the most widely used open source IoT platforms is presented. This exhaustive comparison is based on multiple characteristics that will be essential to select the platform that best suits the needs of each organization.This research/work has been supported by GAIN (Galician Innovation Agency) and the Regional Ministry of Economy, Employment and Industry, Xunta de Galicia under grant COV20/00604 through the ERDF Galicia 2014-2020; and by grant PID2019-104958RB-C42 (ADELE) funded by MCIN/AEI/10.13039/501100011033 . Funding for open access charge: Universidade da Coruña/CISUG.Xunta de Galicia; COV20/0060
Fine Time Measurement for the Internet of Things: A Practical Approach Using ESP32
[Abstract]: In the world of Internet of Things (IoT), obtaining the physical location of devices has always been a task of great interest for developing increasingly complex location-based services (LBS). That is why in recent years wireless communication standards have been incorporating new additions focused on providing localization mechanisms to technologies widely used in the IoT world, such as Wi-Fi or Bluetooth. In particular, the IEEE 802.11-2016 Wi-Fi standard introduced ranging estimation between two devices through the so-called fine time measurement (FTM) protocol, defined by the IEEE 802.11mc. FTM is not yet widespread in the IoT field, but commercial modules capable of offering this functionality at a reasonable price are starting to appear. In early 2021, the most widespread system on a chip (SOC) family among IoT devices, the ESP32-XX series, added support for this Wi-Fi standard, enabling, for the first time, the use of a standard designed for location-based systems. This article analyzes the performance of this FTM implementation by carrying out and studying several measurement campaigns in different indoor and outdoor scenarios. Additionally, this work proposes an alternative real-time implementation for distance estimation inside the ESP32 using an approach based on machine learning. Such an implementation is successfully validated in a scenario totally different than those considered for the training and test sets. Finally, both the measurement sets and the developed software are available to the scientific community
SPROUTY-2 represses the epithelial phenotype of colon carcinoma cells via upregulation of ZEB1 mediated by ETS1 and miR-200/miR-150
SPROUTY-2 (SPRY2) is a modulator of tyrosine kinase receptor signaling with
receptor- and cell type-dependent inhibitory or enhancing effects. Studies on the action
of SPRY2 in major cancers are conflicting and its role remains unclear. Here we have
dissected SPRY2 action in human colon cancer. Global transcriptomic analyses show
that SPRY2 downregulates genes encoding tight junction proteins such as claudin-7 and
occludin and other cell-to-cell and cell-to-matrix adhesion molecules in human SW480-
ADH colon carcinoma cells. Moreover, SPRY2 represses LLGLL2/HUGL2,
PATJ1/INADL and ST14, main regulators of the polarized epithelial phenotype, and
ESRP1, an epithelial-to-mesenchymal transition (EMT) inhibitor. A key action of
SPRY2 is the upregulation of the major EMT inducer ZEB1, as these effects are
reversed by ZEB1 knock-down by means of RNA interference. Consistently, we found
an inverse correlation between the expression level of claudin-7 and those of SPRY2
and ZEB1 in human colon tumors. Mechanistically, ZEB1 upregulation by SPRY2
results from the combined induction of ETS1 transcription factor and the repression of
microRNAs (miR-200 family, miR-150) that target ZEB1 RNA. Moreover, SPRY2
increased AKT activation by epidermal growth factor (EGF) whereas AKT and also Src
inhibition reduced the induction of ZEB1. Altogether, these data suggest that AKT and
Src are implicated in SPRY2 action. Collectively, these results show a tumorigenic role
of SPRY2 in colon cancer that is based on the dysregulation of tight junction and
epithelial polarity master genes via upregulation of ZEB1. The dissection of the
mechanism of action of SPRY2 in colon cancer cells is important to understand the
upregulation of this gene in a subset of patients with this neoplasia that have poor
prognosis.This study was supported by the Ministerio de
Economía y Competitividad of Spain and Fondo Europeo de Desarrollo Regional
(FEDER) (grant SAF2013-43468-R to A.M., SAF2011-29530 to F.X.R.); FEDERInstituto
de Salud Carlos III (RD12/0036/0021 to A.M. and J.M.R., RD12/0036/0034 to
F.X.R., RD12/0036/0016 to M.S., RD12/0036/0012 to H.G.P., RD06/0020/0003,
PS09/00562 and PI13/00703 to J.M.R.); Comunidad de Madrid (S2010/BMD-2344
Colomics2 to A.M.); Fundación Científica de la Asociación Española contra el Cáncer
(to J.M.R.); U.S. Department of Defense (CA093471 and CA110602 to E.H.); National
Institutes of Health/National Cancer Institute (1R01CA155234-01 to E.H.); National
Institutes of Health/National Institute of Arthritis and Musculoskeletal and Skin
Diseases (1R21AR062239-01 to E.H.); and the Melanoma Research Alliance (to E. H.)
Vocabulario de morfoloxía, anatomía e citoloxía veterinaria [galego-español-inglés]
Consellaría do Medio Rural. Xunta de Galici
Sur8, a determinant protein in colorectal cancer tumor progression
Resumen del trabajo presentado en el 43rd Annual Meeting of the SEBBM, celebrado en Barcelona (España) del 19 al 21 de julio de 2021.Colorectal cancer (CRC) has the highest incidence rate in the Spanish population. The most important challenge consists on the discovery of efficient disease treatments, due to high mortality rates in highly developed stages. Sur8 is a scaffold protein that positively modulates ERK signaling pathway, which has a major role in the progression and metastasis in colorectal cancer. The main goals of our research are to determine the role that Sur8 plays in the development and progression of CRC and to analyze its possible therapeutic potential. For this purpose, our group has developed an inducible conditional mouse model msur8f/fVillinCreERT2. In order to determine Sur8 action in the colonic tissue, we have developed organoids from the colon epithelium of healthy mice and have analyzed gene expression pattern by an RNAseq approach. Sur8 KO affects oncogenic CRC transcription factors expression, as well as the modulation of some Wnt pathway regulators. In regard to miRNA data, we have observed deregulation of miRNAs related to CRC in Sur8 KO organoids. To determine the role that Sur8 plays in the development and progression of CRC, we have subjected our inducible conditional mice to chemical carcinogenesis and we have observed that Sur8 KO males display less and smaller tumors and do not present any adenocarcinoma. In addition, we have carried out Sur8 silencing in human CRC cell lines by infection with constitutive shRNA lentiviruses. We have observed that Sur8 silencing produces decreases of cell tumor proliferation, and reduction of p-ERK levels. Finally, we are evaluating the effects of putative therapeutic agents against Sur8 in human CRC cell lines. Concretely, we are testing Celastrol, which has been described that binds and blocks the action of Sur8 in vitro. We have observed that Celastrol treatment diminishes the cell tumor proliferation in this model. Altogether, our results indicate that Sur8 may have a determinant role in CRC progression and that Sur8 could be a potential molecular target for the design of novel strategies against CRC
Detection of very high energy gamma-ray emission from the gravitationally-lensed blazar QSO B0218+357 with the MAGIC telescopes
Context. QSO B0218+357 is a gravitationally lensed blazar located at a
redshift of 0.944. The gravitational lensing splits the emitted radiation into
two components, spatially indistinguishable by gamma-ray instruments, but
separated by a 10-12 day delay. In July 2014, QSO B0218+357 experienced a
violent flare observed by the Fermi-LAT and followed by the MAGIC telescopes.
Aims. The spectral energy distribution of QSO B0218+357 can give information on
the energetics of z ~ 1 very high energy gamma- ray sources. Moreover the
gamma-ray emission can also be used as a probe of the extragalactic background
light at z ~ 1. Methods. MAGIC performed observations of QSO B0218+357 during
the expected arrival time of the delayed component of the emission. The MAGIC
and Fermi-LAT observations were accompanied by quasi-simultaneous optical data
from the KVA telescope and X-ray observations by Swift-XRT. We construct a
multiwavelength spectral energy distribution of QSO B0218+357 and use it to
model the source. The GeV and sub-TeV data, obtained by Fermi-LAT and MAGIC,
are used to set constraints on the extragalactic background light. Results.
Very high energy gamma-ray emission was detected from the direction of QSO
B0218+357 by the MAGIC telescopes during the expected time of arrival of the
trailing component of the flare, making it the farthest very high energy
gamma-ray sources detected to date. The observed emission spans the energy
range from 65 to 175 GeV. The combined MAGIC and Fermi-LAT spectral energy
distribution of QSO B0218+357 is consistent with current extragalactic
background light models. The broad band emission can be modeled in the
framework of a two zone external Compton scenario, where the GeV emission comes
from an emission region in the jet, located outside the broad line region.Comment: 11 pages, 6 figures, accepted for publication in A&
Investigating the peculiar emission from the new VHE gamma-ray source H1722+119
The MAGIC (Major Atmospheric Gamma-ray Imaging Cherenkov) telescopes observed
the BL Lac object H1722+119 (redshift unknown) for six consecutive nights
between 2013 May 17 and 22, for a total of 12.5 h. The observations were
triggered by high activity in the optical band measured by the KVA (Kungliga
Vetenskapsakademien) telescope. The source was for the first time detected in
the very high energy (VHE, GeV) -ray band with a statistical
significance of 5.9 . The integral flux above 150 GeV is estimated to
be per cent of the Crab Nebula flux. We used contemporaneous
high energy (HE, 100 MeV GeV) -ray observations from
Fermi-LAT (Large Area Telescope) to estimate the redshift of the source. Within
the framework of the current extragalactic background light models, we estimate
the redshift to be . Additionally, we used contemporaneous
X-ray to radio data collected by the instruments on board the Swift satellite,
the KVA, and the OVRO (Owens Valley Radio Observatory) telescope to study
multifrequency characteristics of the source. We found no significant temporal
variability of the flux in the HE and VHE bands. The flux in the optical and
radio wavebands, on the other hand, did vary with different patterns. The
spectral energy distribution (SED) of H1722+119 shows surprising behaviour in
the Hz frequency range. It can be modelled
using an inhomogeneous helical jet synchrotron self-Compton model.Comment: 12 pages, 5 figures, 2 table
Limits to dark matter annihilation cross-section from a combined analysis of MAGIC and Fermi-LAT observations of dwarf satellite galaxies
We present the first joint analysis of gamma-ray data from the MAGIC
Cherenkov telescopes and the Fermi Large Area Telescope (LAT) to search for
gamma-ray signals from dark matter annihilation in dwarf satellite galaxies. We
combine 158 hours of Segue 1 observations with MAGIC with 6-year observations
of 15 dwarf satellite galaxies by the Fermi-LAT. We obtain limits on the
annihilation cross-section for dark matter particle masses between 10 GeV and
100 TeV - the widest mass range ever explored by a single gamma-ray analysis.
These limits improve on previously published Fermi-LAT and MAGIC results by up
to a factor of two at certain masses. Our new inclusive analysis approach is
completely generic and can be used to perform a global, sensitivity-optimized
dark matter search by combining data from present and future gamma-ray and
neutrino detectors.Comment: 19 pages, 3 figures. V2: Few typos corrected and references added.
Matches published version JCAP 02 (2016) 03
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