Influence of Anatomical Variation in the Nasal Cavity on Inflammation of the Paranasal Sinuses

We investigated the correlation between the incidence of anatomical variations in the nasal cavity and mucosal inflammation in the paranasal sinuses, using computed tomography (CT). In total, 239 patients (478 sides; 138 men and 101 women; age range, 8-89 years) underwent coronal plane CT for screening from November 2001 to October 2006. Patients with facial trauma, paranasal sinus carcinoma, inverted papilloma, or previous sinus surgery were excluded from this study. We evaluated the incidence of agger nasi air cells, Haller\u27s cells, middle and superior turbinate pneumatization, paradoxically curved uncinate processes, paradoxically curved middle turbinates, and septal deviation. The mucosal condition and ostiomeatal complex were evaluated by the Lund-Mackay staging system, and correlations between groups were analyzed using Mann-Whitney\u27s U tests. The incidence of nasal septal deviation was 14.6% and the incidences of agger nasi air cells, concha bullosa (pneumatization of the middle nasal turbinate) and Haller\u27s cells were 47.7%, 22.4% and 10.7%, respectively. Paranasal CT showed partial or total opacification of the sinuses in approximately 40% of the anterior and posterior ethmoid and maxillary sinuses. Concha bullosa increased the CT opacification of the paranasal sinuses, except for the sphenoid sinus. There was no significant association between the occurrence of concha bullosa and nasal septal deviation. Our results suggest anatomical variations in the nasal cavity induce mucosal inflammation in the paranasal sinuses

Identification of anti-cancer chemical compounds using Xenopus embryos

Cancer tissues have biological characteristics similar to those observed in embryos during development. Many types of cancer cells acquire pro-invasive ability through epithelial-mesenchymal transition (EMT). Similar processes (gastrulation and migration of cranial neural crest cells [CNCC]) are observed in the early stages of embryonic development in Xenopus during which cells that originate from epithelial sheets through EMT migrate to their final destinations. The present study examined Xenopus embryonic tissues to identify anti-cancer compounds that prevent cancer invasion. From the initial test of known anti-cancer drugs, AMD3100 (an inhibitor of CXCR4) and paclitaxel (a cytoskeletal drug targeting microtubules) effectively prevented migration during gastrulation or CNCC development. Blind-screening of 100 synthesized chemical compounds was performed, and nine candidates that inhibited migration of these embryonic tissues without embryonic lethality were selected. Of these, C-157 (an analog of podophyllotoxin) and D-572 (which is an indole alkaroid) prevented cancer cell invasion through disruption of interphase microtubules. In addition, these compounds affected progression of mitotic phase and induced apoptosis of SAS oral cancer cells. SAS tumors were reduced in size after intratumoral injection of C-157, and peritoneal dissemination of melanoma cells and intracranial invasion of glioma cells were inhibited by C-157 and D-572. When the other analogues of these chemicals were compared, those with subtle effect on embryos were not tumor suppressive. These results suggest that a novel chemical-screening approach based on Xenopus embryos is an effective method for isolating anti-cancer drugs and, in particular, targeting cancer cell invasion and proliferation

Expression of asporin reprograms cancer cells to acquire resistance to oxidative stress

Asporin (ASPN), a small leucine-rich proteoglycan expressed predominantly by cancer associated fibroblasts (CAFs), plays a pivotal role in tumor progression. ASPN is also expressed by some cancer cells, but its biological significance is unclear. Here, we investigated the effects of ASPN expression in gastric cancer cells. Overexpression of ASPN in 2 gastric cancer cell lines, HSC-43 and 44As3, led to increased migration and invasion capacity, accompanied by induction of CD44 expression and activation of Rac1 and MMP9. ASPN expression increased resistance of HSC-43 cells to oxidative stress by reducing the amount of mitochondrial reactive oxygen species. ASPN induced expression of the transcription factor HIF1 alpha and upregulated lactate dehydrogenase A (LDHA) and PDH-E1 alpha, suggesting that ASPN reprograms HSC-43 cells to undergo anaerobic glycolysis and suppresses ROS generation in mitochondria, which has been observed in another cell line HSC-44PE. By contrast, 44As3 cells expressed high levels of HIF1 alpha in response to oxidant stress and escaped apoptosis regardless of ASPN expression. Examination of xenografts in the gastric wall of ASPN(-/-) mice revealed that growth of HSC-43 tumors with increased micro blood vessel density was significantly accelerated by ASPN; however, ASPN increased the invasion depth of both HSC-43 and 44As3 tumors. These results suggest that ASPN has 2 distinct effects on cancer cells: HIF1 alpha-mediated resistance to oxidative stress via reprogramming of glucose metabolism, and activation of CD44-Rac1 and MMP9 to promote cell migration and invasion. Therefore, ASPN may be a new therapeutic target in tumor fibroblasts and cancer cells in some gastric carcinomas

Search for the h_c meson in B^+- ->h_c K^+-

We report a search for the $h_c$ meson via the decay chain $B^{\pm}\to h_c K^{\pm}$, \etac \gamma with $\eta_c \to K_S^0 K^{\pm} \pi^{\mp}$ and $p\bar{p}$. No significant signals are observed. We obtain upper limits on the branching fractions for $B^{\pm} \to \eta_c\gamma K^{\pm}$ in bins of the $\eta_c\gamma$ invariant mass. The results are based on an analysis of 253 fb$^{-1}$ of data collected by the Belle detector at the KEKB $e^+e^-$ collider.Comment: 12 pages, 6 figures, submitted to Phys. Rev.

Status of the GEO600 gravitational wave detector

The GEO600 laser interferometric gravitational wave detector is approaching the end of its commissioning phase which started in 1995.During a test run in January 2002 the detector was operated for 15 days in a power-recycled michelson configuration. The detector and environmental data which were acquired during this test run were used to test the data analysis code. This paper describes the subsystems of GEO600, the status of the detector by August 2002 and the plans towards the first science run

Evidence of the Purely Leptonic Decay B- --> tau- nu_tau-bar

We present the first evidence of the decay B- --> tau- nu_tau-bar using 414 fb^-1 of data collected at the Upsilon(4S) resonance with the Belle detector at the KEKB asymmetric-energy e+e- collider. Events are tagged by fully reconstructing one of the B mesons in hadronic modes. We detect the signal with a significance of 3.5 standard deviations including systematics, and measure the branching fraction to be Br(B- --> tau- nu_tau-bar) = (1.79 +0.56-0.49(stat) +0.46-0.51(syst))*10^-4. This implies that f_B = 0.229 +0.036-0.031(stat) +0.034-0.037(syst) GeV and is the first direct measurement of this quantity.Comment: 6 pages, 3 figures, to appear in Physical Review Letter

Moments of the Hadronic Invariant Mass Spectrum in B --> X_c l nu Decays at Belle

We present a measurement of the hadronic invariant mass squared (M^2_X) spectrum in charmed semileptonic B meson decays B --> X_c l nu based on 140 fb^-1 of Belle data collected near the Y(4S) resonance. We determine the first, the second central and the second non-central moments of this spectrum for lepton energy thresholds ranging between 0.7 and 1.9 GeV. Full correlations between these measurements are evaluated.Comment: published version of the paper (one figure added, minor changes in the text); 16 pages, 3 figures, 10 table

Study of J/psi to p pbar, Lambda Lambdabar and observation of eta_c to Lambda Lambdabar at Belle

We study the baryonic charmonium decays of B mesons, B+ to etac K+ and B+ to J/psi K+, where the etac and J/psi subsequently decay into a p pbar or Lambda Lambdabar pair. We measure the J/psi to p pbar, Lambda Lambdabar anisotropy parameters, alpha_B = -0.60 +- 0.13 +-0.14 (p pbar), -0.44 +- 0.51 +- 0.31 (Lambda Lambdabar) and compare to results from e+e- to J/psi formation experiments. We also report the first observation of etac to Lambda Lambdabar. The measured branching fraction is B(etac to Lambda Lambdabar) = (0.87 +0.24 -0.21(stat) +0.09 -0.14(syst) +- 0.27 (PDG)) x 10^-3. This study is based on a 357 fb^-1 data sample recorded on the Upsilon(4S) resonance with the Belle detector at the KEKB asymmetric-energy e+e- collider.Comment: 8 pages, two figures (4 figure files), an update of hep-ex/0509020 for journal submissio

Observation of Two Resonant Structures in e+e- to pi+ pi- psi(2S) via Initial State Radiation at Belle

The cross section for e+e- to pi+ pi- psi(2S) between threshold and \sqrt{s}=5.5 GeV is measured using 673 fb^{-1} of data on and off the \Upsilon(4S) resonance collected with the Belle detector at KEKB. Two resonant structures are observed in the pi+ pi- psi(2S) invariant mass distribution, one at 4361\pm 9\pm 9 MeV/c2 with a width of 74\pm 15\pm 10 MeV/c2, and another at 4664\pm 11\pm 5 MeV/c2 with a width of 48\pm 15\pm 3 MeV/c2, if the mass spectrum is parameterized with the coherent sum of two Breit-Wigner functions. These values do not match those of any of the known charmonium states.Comment: 10 pages, 5 figures, 2 tables, version to appear in Phys. Rev. Let