1.The clinical application of VATS lung volume reduction surgery
Guo LI ; Jianli WANG ; Wu CHEN ; Liuhuan HUANG ; Yutao DANG ; Jiangping GAO
Chinese Journal of Postgraduates of Medicine 2012;(z1):6-7
Objective To evaluate the efficacy of lung volum ereduction surgery(LVRS) on severe chronic obstrutive pulmonary emphysema (COPE).Methods Fifteen patients with COPE with LVRS were retrospectively analyzed.The lung volume was reduced with GIA by a degree of 20%-30%.The activity and the lung function indexes of patients before LVRS,half a year and 1 year after LVRS were analyzed.Results Fifteen patients recovered and were discharged in 8-54 (14.7 ± 8.8) days after LVRS.The forced expiratory volume in one second (FEV1),total lung capacity (TLC),residual volume (RV),and 6-minute walk distance (6MWD) of patients with LVRS were significantly improved after operation (P < 0.05).Conclusion The lung volume reduction surgery provides a quite new and effective treatment for some cases of severe chronic obstructive pulmonary disease.
2.Expression of Cx43 in human lung adenocarcinoma and its significance
Guo LI ; Jianli WANG ; Wu CHEN ; Liuhuan HUANG ; Yutao DANG ; Jiangping GAO
Cancer Research and Clinic 2013;(5):303-305
Objective To investigate the expression of connexin43 (Cx43) protein and mRNA in human adenocarcinoma of lung and its clinical significance.Methods One hundred and forty-eight human adenocarcinoma of lung tissues were detected by immunohistochemistry for Cx43 expression and fluorescence in situ hybridization for mRNA.The relationship between Cx43 expression and clinicopathologcal factors was analyzed.Results The positive rates of Cx43 expression in well/moderately differentiated and poorlydifferemiated/indififerentiated lung cancer tissues were 48.7 % (38/78) and 30.0 % (21/70),respectively (P < 0.05).The positive rates of Cx43 expression in negative lymph node metastasis and positive lymphnode metastasis lung cancer tissues were 56.3 % (18/32) and 34.5 % (40/116),respectively (P < 0.05).The positive rates of Cx43 expression in stage Ⅰ-Ⅱ and Ⅲ-Ⅳ lung cancer tissues were 51.5 % (49/95) and 34.0 %(18/53),respectively (P < 0.05).The positive rates of Cx43 mRNA expression in adenocarcinoma of lung adenocarcinoma and normal lung tissues were 32.4 % (48/148) and 60.0 % (12/20) (P < 0.05).Conclusion The expression of Cx43 is closely related with well differentiation,invasion,status of lymphnode,clinical stage and prognosis of human lung adenocarcinoma.It may participate in the development and progression of human lung adenocarcinoma,and may be used to predict the prognosis of human lung adenocarcinoma.
3.TIM-1 acts a dual-attachment receptor for Ebolavirus by interacting directly with viral GP and the PS on the viral envelope.
Shuai YUAN ; Lei CAO ; Hui LING ; Minghao DANG ; Yao SUN ; Xuyuan ZHANG ; Yutao CHEN ; Liguo ZHANG ; Dan SU ; Xiangxi WANG ; Zihe RAO
Protein & Cell 2015;6(11):814-824
Ebolavirus can cause hemorrhagic fever in humans with a mortality rate of 50%-90%. Currently, no approved vaccines and antiviral therapies are available. Human TIM1 is considered as an attachment factor for EBOV, enhancing viral infection through interaction with PS located on the viral envelope. However, reasons underlying the preferable usage of hTIM-1, but not other PS binding receptors by filovirus, remain unknown. We firstly demonstrated a direct interaction between hTIM-1 and EBOV GP in vitro and determined the crystal structures of the Ig V domains of hTIM-1 and hTIM-4. The binding region in hTIM-1 to EBOV GP was mapped by chimeras and mutation assays, which were designed based on structural analysis. Pseudovirion infection assays performed using hTIM-1 and its homologs as well as point mutants verified the location of the GP binding site and the importance of EBOV GP-hTIM-1 interaction in EBOV cellular entry.
Ebolavirus
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metabolism
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Flow Cytometry
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Glycoproteins
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metabolism
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Hepatitis A Virus Cellular Receptor 1
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Hepatitis A Virus Cellular Receptor 2
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Humans
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Membrane Glycoproteins
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metabolism
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Membrane Proteins
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metabolism
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Protein Binding
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Receptors, Virus
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metabolism
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Surface Plasmon Resonance
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Viral Envelope Proteins
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metabolism
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Viral Proteins
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metabolism