Single spin asymmetries in QCD

Measurements of single transverse spin asymmetries in high energy inclusive processes have always shown unexpected and challenging results. Several cases are considered and discussed within a QCD approach which couples perturbative dynamics to new non perturbative partonic information; the aim is that of developing a consistent phenomenological description of these unusual single spin phenomena, based on a generalized QCD factorization scheme.Comment: 14 pages, lectures delivered at School on "Symmetries and Spin", Praha-SPIN-2001, Prague, July 15 - July 28, 200

Investigating the origins of transverse spin asymmetries at RHIC

We discuss possible origins of transverse spin asymmetries in hadron-hadron collisions and propose an explanation in terms of a chiral-odd T-odd distribution function with intrinsic transverse momentum dependence, which would signal a correlation between the transverse spin and the transverse momentum of quarks inside an unpolarized hadron. We will argue that despite its conceptual problems, it can account for single spin asymmetries, for example in p + p(transversely polarized) -> pion + X, and at the same time for the large cos(2 phi) asymmetry in the unpolarized Drell-Yan cross section, which still lacks understanding. We use the latter asymmetry to arrive at a crude model for this function and show explicitly how it relates unpolarized and polarized observables in the Drell-Yan process, as could be measured with the proton-proton collisions at RHIC. Moreover, it would provide an alternative method of accessing the transversity distribution function h_1. For future reference we also list the complete set of azimuthal asymmetries in the unpolarized and polarized Drell-Yan process at leading order involving T-odd distribution functions with intrinsic transverse momentum dependence.Comment: 14 pages, Revtex, 4 Postscript figures, uses aps.sty, epsf.sty, Minor mistakes in cross sections corrected, Conclusions are unaffecte

Azimuthal asymmetries in lepton-pair production at a fixed-target experiment using the LHC beams (AFTER)

A multi-purpose fixed-target experiment using the proton and lead-ion beams of the LHC was recently proposed by Brodsky, Fleuret, Hadjidakis and Lansberg, and here we concentrate our study on some issues related to the spin physics part of this project (referred to as AFTER). We study the nucleon spin structure through $pp$ and $pd$ processes with a fixed-target experiment using the LHC proton beams, for the kinematical region with 7 TeV proton beams at the energy in center-of-mass frame of two nucleons $\sqrt{s}=115$ GeV. We calculate and estimate the $\cos2\phi$ azimuthal asymmetries of unpolarized $pp$ and $pd$ dilepton production processes in the Drell--Yan continuum region and at the $Z$-pole. We also calculate the $\sin(2\phi-\phi_S)$, $\sin(2\phi+\phi_S)$ and $\sin2\phi$ azimuthal asymmetries of $pp$ and $pd$ dilepton production processes with the target proton and deuteron longitudinally or transversally polarized in the Drell--Yan continuum region and around $Z$ resonances region. We conclude that it is feasible to measure these azimuthal asymmetries, consequently the three-dimensional or transverse momentum dependent parton distribution functions (3dPDFs or TMDs), at this new AFTER facility.Comment: 15 pages, 40 figures. Version accepted for publication in EPJ

Lambda polarization from unpolarized quark fragmentation

The longstanding problem of explaining the observed polarization of Lambda hyperons inclusively produced in the high energy collisions of unpolarized hadrons is tackled by considering spin and k_T dependent quark fragmentation functions. The data on Lambda's and Lambda-bar's produced in p-N processes are used to determine simple phenomenological expressions for these new "polarizing fragmentation functions", which describe the experiments remarkably well.Comment: LaTeX, 21+1 pages, 6 eps figures, uses epsfig.st

Gene expression profiling of mucinous ovarian tumors and comparison with upper and lower gastrointestinal tumors identifies markers associated with adverse outcomes.

PURPOSE: Advanced-stage mucinous ovarian carcinoma (MOC) has poor chemotherapy response and prognosis and lacks biomarkers to aid stage I adjuvant treatment. Differentiating primary MOC from gastrointestinal (GI) metastases to the ovary is also challenging due to phenotypic similarities. Clinicopathologic and gene-expression data were analyzed to identify prognostic and diagnostic features. EXPERIMENTAL DESIGN: Discovery analyses selected 19 genes with prognostic/diagnostic potential. Validation was performed through the Ovarian Tumor Tissue Analysis consortium and GI cancer biobanks comprising 604 patients with MOC (n = 333), mucinous borderline ovarian tumors (MBOT, n = 151), and upper GI (n = 65) and lower GI tumors (n = 55). RESULTS: Infiltrative pattern of invasion was associated with decreased overall survival (OS) within 2 years from diagnosis, compared with expansile pattern in stage I MOC [hazard ratio (HR), 2.77; 95% confidence interval (CI), 1.04–7.41, P = 0.042]. Increased expression of THBS2 and TAGLN was associated with shorter OS in MOC patients (HR, 1.25; 95% CI, 1.04–1.51, P = 0.016) and (HR, 1.21; 95% CI, 1.01–1.45, P = 0.043), respectively. ERBB2 (HER2) amplification or high mRNA expression was evident in 64 of 243 (26%) of MOCs, but only 8 of 243 (3%) were also infiltrative (4/39, 10%) or stage III/IV (4/31, 13%). CONCLUSIONS: An infiltrative growth pattern infers poor prognosis within 2 years from diagnosis and may help select stage I patients for adjuvant therapy. High expression of THBS2 and TAGLN in MOC confers an adverse prognosis and is upregulated in the infiltrative subtype, which warrants further investigation. Anti-HER2 therapy should be investigated in a subset of patients. MOC samples clustered with upper GI, yet markers to differentiate these entities remain elusive, suggesting similar underlying biology and shared treatment strategies

The effect of chronic ingestion of ethanol on modulation of granulomatous inflammation in experimental schistosomiasis in mice Efeito da ingestão crônica de etanol na modulação da resposta inflamatória granulomatosa no fígado de camundongos infectados por Schistosoma mansoni

We studied the role of ethanol on the modulation of liver granulomata around Schistosoma mansoni eggs in mice. Albino mice, receiving 7% ethanol as the sole drinking liquid, at 60 and 90 days post-infection, presented smaller granulomata than controls did, when sacrificed at 120 days post-infection. No differences in diameters could be observed, when ethanol was given 4 months before up to 120 days after infection. The results suggested that modulation of schistosome granulomata by ethanol ingestion varies with time and duration of drug consumption.<br>Estudamos a modulação da resposta inflamatória granulomatosa em torno de ovos de S. mansoni no fígado de camundongos albinos (Mus musculus), que receberam 7% de etanol como única fonte de líquido. Os animais que receberam etanol aos 60 e 90 dias após a infecção apresentaram granulomas menores do que os controles, quando sacrificados aos 120 dias após a infecção. Não houve diferença no diâmetro dos granulomas quando a ingestão de etanol foi iniciada 4 meses antes e prolongada até 120 dias após a infecção. Nossos resultados indicam que a modulação da inflamação granulomatosa varia de acordo com o tempo e a duração da ingestão do etanol