Chen,S

Phys Rev Lett. 2012 Apr 13;108 (15):152001 22587245

Observation of a New χ_{b} State in Radiative Transitions to Υ(1S) and Υ(2S) at ATLAS.

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Fakultät für Mathematik und Physik, Albert-Ludwigs-Universität, Freiburg i.Br., Germany.

The χ_{b}(nP) quarkonium states are produced in proton-proton collisions at the Large Hadron Collider at sqrt[s]=7 TeV and recorded by the ATLAS detector. Using a data sample corresponding to an integrated luminosity of 4.4 fb^{-1}, these states are reconstructed through their radiative decays to Υ(1S,2S) with Υ→μ^{+}μ^{-}. In addition to the mass peaks corresponding to the decay modes χ_{b}(1P,2P)→Υ(1S)γ, a new structure centered at a mass of 10.530±0.005(stat)±0.009(syst) GeV is also observed, in both the Υ(1S)γ and Υ(2S)γ decay modes. This structure is interpreted as the χ_{b}(3P) system.

IEEE Trans Inf Technol Biomed. 2012 May 9;: 22581142

A Feasibility Study of Enhancing Independent Task Performance for People with Cognitive Impairments Through Use of a Handheld Location-Based Prompting System.

Y Chang, S Chen, L Chou

An autonomous task-prompting system is presented to increase workplace and life independence for people with cognitive impairments such as traumatic brain injury, intellectual disability, schizophrenia, and Down syndrome. This paper describes an approach to providing distributed cognition support of work engagement for persons with cognitive disabilities. In the pilot study, a prototype was built and tested in a community-based rehabilitation program involving pre-service food preparation training of 8 participants with cognitive impairments. The results show improvement in helping with task engagement is statistically significant compared to the oral-instruction method. A follow-up comparative study with 2 participants evaluated the shadow-team approach against the proposed system. Although the number of participants was few, the participants were studied in depth and the findings were very promising. The results in the autonomous task prompting without staff intervention indicate that the performance is statistically as good as the shadow-team approach. Our findings suggest that acquisition of job skills may be facilitated by the proposed system in conjunction with operant conditioning strategies.

Oncogene. 2012 Apr 30;: 22543582

Glucocorticoids and histone deacetylase inhibitors cooperate to block the invasiveness of basal-like breast cancer cells through novel mechanisms.

M E Law, P E Corsino, S C Jahn, B J Davis, S Chen, B Patel, K Pham, J Lu, B Sheppard, P Nørgaard, J Hong, P Higgins, J-S Kim, H Luesch, B K Law

1] Department of Pharmacology and Therapeutics, University of Florida, Gainesville, FL, USA [2] The UF and Shands Cancer Center, University of Florida, Gainesville, FL, USA.

Aggressive cancers often express E-cadherin in cytoplasmic vesicles rather than on the plasma membrane and this may contribute to the invasive phenotype of these tumors. Therapeutic strategies are not currently available that restore the anti-invasive function of E-cadherin in cancers. MDA-MB-231 cells are a frequently used model of invasive triple-negative breast cancer, and these cells express low levels of E-cadherin that is mislocalized to cytoplasmic vesicles. MDA-MB-231 cell lines stably expressing wild-type E-cadherin or E-cadherin fused to glutathione S-transferase or green fluorescent protein were used as experimental systems to probe the mechanisms responsible for cytoplasmic E-cadherin localization in invasive cancers. Although E-cadherin expression partly reduced cell invasion in vitro, E-cadherin was largely localized to the cytoplasm and did not block the invasiveness of the corresponding orthotopic xenograft tumors. Further studies indicated that the glucocorticoid dexamethasone and the highly potent class I histone deacetylase (HDAC) inhibitor largazole cooperated to induce E-cadherin localization to the plasma membrane in triple-negative breast cancers, and to suppress cellular invasion in vitro. Dexamethasone blocked the production of the cleaved form of the CDCP1 (that is, CUB domain-containing protein 1) protein (cCDCP1) previously implicated in the pro-invasive activities of CDCP1 by upregulating the serine protease inhibitor plasminogen activator inhibitor-1. E-cadherin preferentially associated with cCDCP1 compared with the full-length form. In contrast, largazole did not influence CDCP1 cleavage, but increased the association of E-cadherin with γ-catenin. This effect on E-cadherin/γ-catenin complexes was shared with the nonisoform selective HDAC inhibitors trichostatin A (TSA) and vorinostat (suberoylanilide hydroxamic acid, SAHA), although largazole upregulated endogenous E-cadherin levels more strongly than TSA. These results demonstrate that glucocorticoids and HDAC inhibitors, both of which are currently in clinical use, cooperate to suppress the invasiveness of breast cancer cells through novel, complementary mechanisms that converge on E-cadherin.Oncogene advance online publication, 30 April 2012; doi:10.1038/onc.2012.138.

Phys Rev Lett. 2012 Mar 16;108 (11):111803 22540463

Search for the Standard Model Higgs Boson in the Diphoton Decay Channel with 4.9 fb^{-1} of pp Collision Data at sqrt[s]=7 TeV with ATLAS.

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Fakultät für Mathematik und Physik, Albert-Ludwigs-Universität, Freiburg i.Br., Germany.

A search for the standard model Higgs boson is performed in the diphoton decay channel. The data used correspond to an integrated luminosity of 4.9 fb^{-1} collected with the ATLAS detector at the Large Hadron Collider in proton-proton collisions at a center-of-mass energy of sqrt[s]=7 TeV. In the diphoton mass range 110-150 GeV, the largest excess with respect to the background-only hypothesis is observed at 126.5 GeV, with a local significance of 2.8 standard deviations. Taking the look-elsewhere effect into account in the range 110-150 GeV, this significance becomes 1.5 standard deviations. The standard model Higgs boson is excluded at 95% confidence level in the mass ranges of 113-115 GeV and 134.5-136 GeV.

Phys Rev Lett. 2012 Mar 16;108 (11):111802 22540462

Search for the Higgs Boson in the H→WW^{(*)}→l^{+}νl^{-}ν[over ¯] Decay Channel in pp Collisions at sqrt[s]=7 TeV with the ATLAS Detector.

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Zerwas, G Zevi Della Porta, Z Zhan, D Zhang, H Zhang, J Zhang, X Zhang, Z Zhang, L Zhao, T Zhao, Z Zhao, A Zhemchugov, S Zheng, J Zhong, B Zhou, N Zhou, Y Zhou, C G Zhu, H Zhu, J Zhu, Y Zhu, X Zhuang, V Zhuravlov, D Zieminska, R Zimmermann, S Zimmermann, M Ziolkowski, R Zitoun, L Zivković, V V Zmouchko, G Zobernig, A Zoccoli, Y Zolnierowski, A Zsenei, M Zur Nedden, V Zutshi, L Zwalinski

Fakultät für Mathematik und Physik, Albert-Ludwigs-Universität, Freiburg im Breisgau, Germany.

A search for the Higgs boson has been performed in the H→WW^{(*)}→ℓ^{+}νℓ^{-}ν[over ¯] channel (ℓ=e/μ) with an integrated luminosity of 2.05 fb^{-1} of pp collisions at sqrt[s]=7 TeV collected with the ATLAS detector at the Large Hadron Collider. No significant excess of events over the expected background is observed and limits on the Higgs boson production cross section are derived for a Higgs boson mass in the range 110 GeV<m_{H}<300 GeV. The observations exclude the presence of a standard model Higgs boson with a mass 145<m_{H}<206 GeV at 95% confidence level.

Life Sci. 2012 Apr 13;: 22525377

Renal, retinal and cardiac changes in type 2 diabetes are attenuated by macitentan, a dual endothelin receptor antagonist.

S Sen, S Chen, B Feng, M Iglarz, S Chakrabarti

Dept. of Pathology, University of Western Ontario, Canada.

AIMS: Diabetes is known to cause alteration of the endothelin (ET) system. We have previously demonstrated that ETs regulate augmented production of extracellular matrix proteins causing structural alterations in type 1 diabetes. Here we investigated the effects of macitentan, an orally-active, tissue-targeting dual ET receptor antagonist on chronic complications in type 2 diabetes. MAIN METHODS: db/db mice and their age- and sex-matched controls were examined after 2 and 4months of diabetes. Groups of diabetic animals were treated with oral macitentan (25mg/kg/day). The animals were monitored with respect to body weight and blood glucose. Urine analyses were performed for albumin. Cardiac hemodynamic studies were carried out. Renal, cardiac and retinal tissues were analyzed for ET-1, transforming growth factor-β1 (TGF-β1), vascular endothelial growth factor (VEGF), fibronectin (FN), extradomain B containing FN (EDB(+)FN) and collagen α-I (IV) mRNA. Cardiac atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) were measured. Protein expressions were measured by ELISA and Western blot. Microscopic analyses were performed in the kidneys. KEY FINDINGS: Diabetic animals showed hyperglycemia, increased urinary albumin and augmented serum creatinine levels. Diabetes caused increased renal, cardiac and retinal ET-1, TGF-β1, VEGF, FN, EDB(+)FN, collagen α-I(IV) mRNA expression along with increased FN and collagen protein and NF-κB activation. Diabetic mice also demonstrated mesangial expansion, cardiac dysfunction and increased expression of ANP and BNP. Treatment with macitentan attenuated such abnormalities. SIGNIFICANCE: These experiments confirmed that ET system plays a significant role in the pathogenesis of chronic complications in type 2 diabetes. Such diabetes induced changes can be reduced macitentan therapy.

Poult Sci. 2012 May ;91 (5):1276 22499889

Erratum to "Histopathology, immunohistochemistry, in situ apoptosis, and ultrastructure characterization of the digestive and lymphoid organs of new type gosling viral enteritis virus experimentally infected gosling"(Poult. Sci. 89(4):668-680).

S Chen, A C Cheng, M S Wang, D K Zhu, R Y Jia, Q H Luo, H M Cui, Y Zhou, Y Wang, Z W Xu, Z L Chen, X Y Chen, X Y Wang

Cytopathology. 2012 Apr 11;: 22489965

Fine needle aspiration cytology of a clear cell (lipid-rich) pancreatic neuroendocrine tumour in a patient without von Hippel-Lindau disease.

S Chen, H H Wu, H Cramer

Department of Pathology and Laboratory Medicine, Indiana University, Indianapolis, IN, USA.

Br J Cancer. 2012 Apr 3;: 22472879

Dynamic equilibrium between cancer stem cells and non-stem cancer cells in human SW620 and MCF-7 cancer cell populations.

G Yang, Y Quan, W Wang, Q Fu, J Wu, T Mei, J Li, Y Tang, C Luo, Q Ouyang, S Chen, L Wu, T K Hei, Y Wang

State Key Laboratory of Nuclear Physics and Technology, School of Physics, Peking University, Beijing 100871, People's Republic of China.

Background:Cancer stem cells (CSCs) paradigm suggests that CSCs might have important clinical implications in cancer therapy. Previously, we reported that accumulation efficiency of CSCs is different post low- and high-LET irradiation in 48 h.Methods:Cancer stem cells and non-stem cancer cells (NSCCs) were sorted and functionally identified through a variety of assays such as antigen profiles and sphere formation. Inter-conversion between CSCs and NSCCs were in situ visualised. Cancer stem cells proportions were assayed over multiple generations under normal and irradiation surroundings. Supplement and inhibition of TGF-β1, as well as immunofluorescence assay of E-cadherin and Vimentin, were performed.Results:Surface antigen markers of CSCs and NSCCs exist in an intrinsic homoeostasis state with spontaneous and in situ visualisable inter-conversions, irrespective of prior radiations. Supplement with TGF-β1 accelerates the equilibrium, whereas inhibition of TGF-β signalling disturbs the equilibrium and significantly decreases CSC proportion. Epithelial mesenchymal transition (EMT) might be activated during the process.Conclusion:Our results indicate that the intrinsic inter-conversion and dynamic equilibrium between CSCs and NSCCs exist under normal and irradiation surroundings, and TGF-β might have important roles in the equilibrium through activating EMT.British Journal of Cancer advance online publication, 3 April 2012; doi:10.1038/bjc.2012.126 www.bjcancer.com.

Insect Mol Biol. 2012 Mar 27;: 22458842

Next-generation small RNA sequencing for microRNAs profiling in Apis mellifera: comparison between nurses and foragers.

F Liu, W Peng, Z Li, W Li, L Li, J Pan, S Zhang, Y Miao, S Chen, S Su

College of Animal Sciences, Zhejiang University, Hangzhou, China Key Laboratory of Pollinating Insect Biology of the Ministry of Agriculture, Institute of Apicultural Research, Chinese Academy of Agricultural Science, Xiangshan, Beijing, China ARC Centre of Excellence in Vision Science, Research School of Biology, College of Medicine, Biology and Environment, The Australian National University, Canberra, Australia.

MicroRNAs (miRNAs) are endogenous small non-coding RNAs regulating gene expression in animals and plants. To find some differentially expressed miRNAs that may be associated with age-dependent behavioural changes in honey bees (Apis mellifera), we applied next-generation high-throughput sequencing technology to detect small RNAs in nurses and foragers. Our results showed that both nurses and foragers had a complicated small RNA population, and the length of small RNAs varied, 22 nucleotides being the predominant length. Combining deep sequencing and bioinformatic analysis, we discovered that nine known miRNAs were significantly different between nurses and foragers (P < 0.01; absolute value of fold-change ≥1). Some of their target genes were related to neural function. Moreover, 67 novel miRNAs were identified in nurses and foragers. Ame-miR-31a and ame-miR-13b were further validated using quantitative reverse-transcription PCR assays. The present study provides new information on the miRNA abundance of honey bees, and enhances our understanding of miRNA function in the regulation of honey bee development.

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