Sigma pole position and errors of a once and twice subtracted dispersive analysis of pi-pi scattering data

We show how the new precise data on kaon decays together with forward dispersion relations, sum rules and once- and twice-subtracted Roy's equations allow for a precise determination of the sigma meson pole position. We present a comparison and a study of the different sources of uncertainties when using either once- or twice-subtracted Roy's equations to analyze the data. Finally we present a preliminary determination of the sigma pole from the constrained dispersive data analysis.Comment: 4 pages, 6 figures. Contribution to the proceedings of the QCD08 14th International QCD Conference. 7-12th July 2008 Montpellier (France); one reference removed, changed errors in Eqs (4), (5) and (7

New dispersion relations in the description of ππ\pi\pi scattering amplitudes

We present a set of once subtracted dispersion relations which implement crossing symmetry conditions for the $\pi\pi$ scattering amplitudes below 1 GeV. We compare and discuss the results obtained for the once and twice subtracted dispersion relations, known as Roy's equations, for three $\pi\pi$ partial JI waves, S0, P and S2. We also show that once subtracted dispersion relations provide a stringent test of crossing and analyticity for $\pi\pi$ partial wave amplitudes, remarkably precise in the 400 to 1.1 GeV region, where the resulting uncertainties are significantly smaller than those coming from standard Roy's equations, given the same input.Comment: 8 pages, 2 figures, to appear in the Proceedings of the Meson 2008 conference, June 6-10, 2008, Cracow, Polan

Histological and mutational profile of diffuse gastric cancer: current knowledge and future challenges

Gastric cancer (GC) pathogenesis is complex and heterogeneous, reflecting morphological, molecular and genetic diversity. Diffuse gastric cancer (DGC) and intestinal gastric cancer (IGC) are the major histological types. GC may be sporadic or hereditary; sporadic GC is related to environmental and genetic low-risk factors and hereditary GC is caused by inherited high-risk mutations, so far identified only for the diffuse histotype. DGC phenotypic heterogeneity challenges the current understanding of molecular mechanisms underlying carcinogenesis. The definition of a DGC-specific mutational profile remains controversial, possibly reflecting the heterogeneity of DGC-related histological subtypes [signet-ring cell carcinoma (SRCC) and poorly cohesive carcinoma not otherwise specified (PCC-NOS)]. Indeed, DGC and DGC-related subtypes may present specific mutational profiles underlying the particularly aggressive behaviour and dismal prognosis of DGC vs IGC and PCC-NOS vs SRCC. In this systematic review, we revised the histological presentations, molecular classifications and approved therapies for gastric cancer, with a focus on DGC. We then analysed results from the most relevant studies, reporting mutational analysis data specifying mutational frequencies, and their relationship with DGC and IGC histological types, and with specific DGC subtypes (SRCC and PCC-NOS). We aimed at identifying histology-associated mutational profiles with an emphasis in DGC and its subtypes (DGC vs IGC; sporadic vs hereditary DGC; and SRCC vs PCC-NOS). We further used these mutational profiles to identify the most commonly affected molecular pathways and biological functions, and explored the clinical trials directed specifically to patients with DGC. This systematic analysis is expected to expose a DGC-specific molecular profile and shed light into potential targets for therapeutic intervention, which are currently missing.The authors acknowledge the support of the National Infrastructure ‘GenomePT’ – National Laboratory for Genome Sequencing and Analysis (POCI-01-0145-FEDER-022184). J.G-P acknowledges the support of Faculty of Medicine from University of Porto, specifically by the Doctoral Programme in Biomedicine and the Solve-RD Project (H2020-SC1-2017-Single-Stage-RTD) for his PhD fellowship. R.B-M. acknowledges the support of Institute of Biomedical Sciences Abel Salazar from University of Porto, specifically by the Doctoral Programme BiotechHealth and the FCT – Fundação para a Ciência e a Tecnologia for her PhD fellowship (ref. SFRH/BD/145132/2019). This research and its authors were funded by FEDER – Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020 – Operacional Programme for Competitiveness and Internationalization (POCI), Portugal 2020, and by Portuguese funds through FCT – Fundação para a Ciência e a Tecnologia/Ministério da Ciência, Tecnologia e Inovação in the framework of the project ‘Institute for Research and Innovation in Health Sciences’ (POCI-01-0145-FEDER-007274). This work was also financed by the projects NORTE-01-0145-FEDER-000003 (DOCnet) and NORTE-01-0145-FEDER-000029 (CANCER) – supported by Norte Portugal Regional Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF) – project POCI-01-0145-FEDER-016390 (CancelStem) and PTDC/BTM-TEC/30164/2017 (3DChroMe), funded by ERDF, POCI and FCT

Study of a possible S=+1 dynamically generated baryonic resonance

Starting from the lowest order chiral Lagrangian for the interaction of the baryon decuplet with the octet of pseudoscalar mesons we find an attractive interaction in the $\Delta K$ channel with L=0 and I=1, while the interaction is repulsive for I=2. The attractive interaction leads to a pole in the second Riemann sheet of the complex plane and manifests itself in a large strength of the $\Delta K$ scattering amplitude close to the $\Delta K$ threshold, which is not the case for I=2. However, we also make a study of uncertainties in the model and conclude that the existence of this pole depends sensitively upon the input used and can disappear within reasonable variations of the input parameters. We take advantage to study the stability of the other poles obtained for the ${3/2}^-$ dynamically generated resonances of the model and conclude that they are stable and not contingent to reasonable changes in the input of the theory

Bosonic Quartic Couplings at LHC

We analyze the potential of the CERN Large Hadron Collider (LHC) to study anomalous quartic vector-boson interactions Z Z gamma gamma, Z Z Z gamma, W+ W- gamma gamma, and W+ W- Z gamma through the weak boson fusion processes q q -> q q gamma gamma and q q -> q q gamma Z(-> l+ l-) with l = electron or muon. After a careful study of the backgrounds and how to extract them from the data, we show that the process p p -> j j gamma l+ l- is potentially the most sensitive to deviations from the Standard Model, improving the sensitivity to anomalous couplings by up to a factor 10^4 (10^2) with respect to the present direct (indirect) limits.Comment: 18 pages, 2 figures, revised versio