The a0(980)a_0(980) in the single Cabibbo-suppressed process Λc→π0ηp\Lambda_c \to \pi^0\eta p

In this work, we have investigated the Cabibbo-suppressed process $\Lambda_c \to \pi^0\eta p$, by taking into account the intermediate scalar state $a_0(980)$, which could be dynamically generated from the $S$-wave pseudoscalar-pseudoscalar interaction within the chiral unitary approach. We have calculated the $\pi^0\eta$ invariant mass distribution, and found that there is a significant structure associated to the $a_0(980)$. We have also roughly estimated the branching fraction $\mathcal{B}(\Lambda_c \to \pi^0\eta p) \approx 10^{-4}$. We encourage our experimental colleagues to measure the process $\Lambda_c \to \pi^0\eta p$ for searching for the state $a_0(980)$ signal in this reaction.Comment: 8 pages, 5 figure

A mutation in the interferon regulatory element of HBV may influence the response of interferon treatment in chronic hepatitis B patients

<p>Abstract</p> <p>Background</p> <p>A functional interferon regulatory element (IRE) has been found in the EnhI/X promoter region of hepatitis B virus (HBV) genome. The purpose of this study is to compare the gene order of responder and non-responder to interferon therapy in patients with chronic hepatitis B (CHB), so as to evaluate the relationship between IRE mutation and the response to interferon treatment for CHB patients.</p> <p>Results</p> <p>Synthetic therapeutic effect is divided into complete response (CR), partial response (PR) and non-response (NR). Among the 62 cases included in this study, 40 cases (64.5%) were in the response group (CR and PR) and 22 (35.5%) cases were in the NR group. Wild type sequence of HBV IRE TTTCACTTTC were found in 35 cases (56.5%), and five different IRE gene sequences. included TTTtACTTTC, TTTCAtTTTC, TTTtAtTTTC, TTTtACTTTt and cTTtACcTTC, were found in 22 cases (35.5%), 1 case (1.6%), 1 case (1.6%), 2 cases (3.2%) and 1 case (1.6%) respectively. There were 41.9%cases (26/62) with forth base C→T mutation, consisted of 32.5% (13/40) cases in response group and 59.1% (13/22) cases in NR group. Among the 35 cases with IRE sequences, there were 67.5% (27/40) cases in response group and 36.4% (8/22) in NR group, and the difference in IRE sequences between two groups was statistic significantly (P = 0.027). The result suggested that there is likely relationship between the forth base mutation (C→T) of IRE region and the response of HBV to Interferon therapy, and this mutation may partially decrease the inhibition effect of interferon on HBV.</p> <p>Conclusion</p> <p>The forth base C→T mutation in IRE element of HBV may partially influence the response of Interferon treatment in CHB patients.</p

Near Real-Time Gravitational Wave Data Analysis of the Massive Black Hole Binary with TianQin

Space-borne gravitational wave detectors can detect sources like the merger of massive black holes. The rapid identification and localization of the source would play a crucial role in multi-messenger observation. The geocentric orbit of the space-borne gravitational wave detector, TianQin, makes it possible to conduct real-time data transmission. In this manuscript, we develop a search and localization pipeline for massive black hole binaries with TianQin, under both regular and real-time data transmission modes. We demonstrate that with real-time data transmission, it is possible to accurately localize the massive black hole binaries on-the-fly. With the approaching of the merger, the localization rapidly shrinks, and the data analysis can be finished at a speed comparable to the data downlink speed

Connexin 43 recruits E-cadherin expression and inhibits the malignant behaviour of lung cancer cells.

The interaction of connexin 43 and E-cadherin may play an important role in carcinogenesis and malignant behaviour of tumours. In this study, we examined the relationship between connexin 43 and E-cadherin in human non-small cell lung cancers (NSCLC). Expression levels of connexin 43 and E-cadherin were examined in 107 NSCLC specimens by immunohistochemistry. The connexin 43 gene was transfected into lung cancer LH7 cells. The protein localizations and levels of connexin 43 and E-cadherin were detected using immunofluorescence staining and western blot. Cell cycle and proliferation of lung cancer cells were examined using flow cytometry and MTT. We found that reduced expression of both connexin 43 and E-cadherin significantly correlated to poor differentiation, advanced TNM stage, and lymph note metastasis of NSCLCs. Connexin 43 and E-cadherin expression significantly correlated with each other. Over-expression of connexin 43 significantly induced E-cadherin expression. Moreover, connexin 43-transfected LH7 cells showed significantly decreased cell proliferation. The percentage of cells in G1 phase increased, while the number of cells in S and G2 phases significantly decreased. We concluded that concurrent reduction of connexin 43 and E-cadherin may contribute to the development of lung cancer. Connexin 43 may induce E-cadherin expression and inhibit cell proliferation and progression of lung cancer

Expression changes and roles of matrix metalloproteinases in a rat model of traumatic deep vein thrombosis

AbstractObjectiveTo study the expression changes of matrix metalloproteinases (MMPs) in traumatic deep vein thrombosis (TDVT) in a rat model with the aid of gene chip technology and to explore the roles of MMPs in TDVT.MethodsTotally 150 Sprague Dawley rats were randomly divided into control group (n=10) and model group (n=140). Rat models of TDVT were established by clamping the femoral vein and fixing the bilateral hind limbs. Then fixation of the hip spica with plaster bandage was conducted. According to the observation phases and/or biological situations of the femoral vein thrombosis, the model rats were further divided into 7 groups. Vascular tissues were obtained from each group through noninvasive incision into the femoral vein at corresponding time points. We adopted the Trizol one-step method for total RNA extraction, Affymetrix RAT 230 2.0 array for detection of RNA expressions and fold change (FC) analysis for changes of differential expressions of MMPs in each group. The main outcome parameters measured included expressions of MMP-2, MMP-3, MMP-7, MMP-8, MMP-9, MMP-10, MMP-11, MMP-12, MMP-13, MMP-14, MMP-16, MMP-23 and MMP-24. Gene array data of these MMPs were analyzed by the Affymetrix Microarray Analysis software (Version 5.0).ResultsFC analysis showed differential expressions of MMPs in each group during the course of TDVT. At the initial period of thrombosis, MMP-2, MMP-3, MMP-7, MMP-8, MMP-9, MMP-10, MMP-11, and MMP-24 had significantly high expression, while MMP-12, MMP-13, MMP-14, MMP-16 and MMP-23 had relatively low expression. MMPs were all highly expressed at the peak time of thrombosis. In the process of thrombus resolution, MMP-2, MMP-10, MMP-16 and MMP-24 have relatively low expression, while MMP-12, MMP-13, MMP-14, MMP-16 and MMP-23 have significantly high expression.ConclusionMMPs may affect the process of TDVT through transcription regulation of the fibrinolysis-anti-fibrinolytic system during the course of thrombosis and thrombus resolution