1.Immunogenicity and safety of Sabin IPV vaccine in Banna mini pigs
Yina CUN ; Wei CAI ; Shaohui SONG ; Jian ZHOU ; Shengjie OUYANG ; Wenzhu HU ; Weidong LI ; Guoyang LIAO ; Lei MA
Acta Laboratorium Animalis Scientia Sinica 2018;26(3):331-334
		                        		
		                        			
		                        			Objective To evaluate the immunogenicity and safety of inactivated poliovirus vaccine derived from Sabin strain (sIPV) in Banna mini pigs, and to provide experimental evidence for the new animal model. Methods sIPV vaccines which are listed at Institute of Medical Biology at Chinese Academy of Medical Sciences were used in this study. The groups of intramuscular sIPV and the wild strain IPV injections (IPV derived from wild strain, wIPV) were designed, and the saline group was used as a negative control group. The Banna mini pigs in various groups were immunized at 0, 1 and 2 months. Blood samples were collected before immunization and on days 30 after each immunization. Levels of neutralizing antibodies were tested for evaluating immunogenicity. The safety was evaluated by observation of the status and weight of mini pigs. Results After the three dose immunization schedules in the Banna mini pigs, the seroconversion rates of type Ⅰ,Ⅱ and Ⅲ sIPV experimental groups and wIPV group were all up to 100%. The neutralizing antibody levels in all the three types were much higher than the protective titer 1: 8. The weight of mini pigs increased after vaccination. Conclusions The sIPV vaccine has good immunogenicity and safety in Banna mini pigs. Banna mini pigs could be a new animal model for evaluation of sIPV vaccine.
		                        		
		                        		
		                        		
		                        	
2.Participation of CCL1 in Snail-Positive Fibroblasts in Colorectal Cancer Contribute to 5-Fluorouracil/Paclitaxel Chemoresistance.
Ziqian LI ; Kaying CHAN ; Yifei QI ; Linlin LU ; Fen NING ; Mengling WU ; Haifang WANG ; Yuan WANG ; Shaohui CAI ; Jun DU
Cancer Research and Treatment 2018;50(3):894-907
		                        		
		                        			
		                        			PURPOSE: Cancer-associated fibroblasts (CAFs) activated by cancer cells has a central role in development and malignant biological behavior in colorectal cancer (CRC). Adult fibroblasts do not express Snail, but Snail-positive fibroblasts are discovered in the stroma of malignant CRC and reported to be the key role to chemoresistance. However, the reciprocal effect of CAFs expressed Snail to chemoresistance on CRC cells and the underlying molecular mechanisms are not fully characterized. MATERIALS AND METHODS: Snail-overexpressed 3T3 stable cell lines were generated by lipidosome and CT26 mixed with 3T3-Snail subcutaneous transplanted CRC models were established by subcutaneous injection. Cell Counting Kit-8, flow cytometry and western blotting assays were performed, and immunohistochemistry staining was studied. The cytokines participated in chemoresistance was validated with reverse transcriptase-polymerase chain reaction and heatmap. RESULTS: Snail-expression fibroblasts are discovered in human and mouse spontaneous CRCs. Overexpression of Snail induces 3T3 fibroblasts transdifferentiation to CAFs. CT26 co-cultured with 3T3-Snail resisted the impairment from 5-fluorouracil and paclitaxel in vitro. The subcutaneous transplanted tumor models included 3T3-Snail cells develop without restrictions even after treating with 5-fluorouracil or paclitaxel. Moreover, these chemoresistant processes may be mediated by CCL1 secreted by Snail-expression fibroblasts via transforming growth factor β/nuclear factor-κB signaling pathways. CONCLUSION: Taken together, Snail-expressing 3T3 fibroblasts display CAFs properties that support 5-fluorouracil and paclitaxel chemoresistance in CRC via participation of CCL1 and suggest that inhibition of the Snail-expression fibroblasts in tumor may be a useful strategy to limit chemoresistance.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Blotting, Western
		                        			;
		                        		
		                        			Cell Count
		                        			;
		                        		
		                        			Cell Line
		                        			;
		                        		
		                        			Colorectal Neoplasms*
		                        			;
		                        		
		                        			Cytokines
		                        			;
		                        		
		                        			Drug Resistance, Multiple
		                        			;
		                        		
		                        			Fibroblasts*
		                        			;
		                        		
		                        			Flow Cytometry
		                        			;
		                        		
		                        			Fluorouracil
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Immunohistochemistry
		                        			;
		                        		
		                        			In Vitro Techniques
		                        			;
		                        		
		                        			Injections, Subcutaneous
		                        			;
		                        		
		                        			Mice
		                        			;
		                        		
		                        			Paclitaxel
		                        			;
		                        		
		                        			Snails
		                        			;
		                        		
		                        			Transforming Growth Factors
		                        			
		                        		
		                        	
3.Quantification analysis of the leaflet anatomy in aortic regurgitation patients using real-time three-dimensional echocardiography
Xin FU ; Mingchen XIONG ; Shaohui QU ; Zheng WEI ; Shengguo CAI ; Weixian YIN ; Jiawei TIAN
Chinese Journal of Ultrasonography 2014;23(4):277-280
		                        		
		                        			
		                        			Objective To quantitatively analysis the aortic valve leaf anatomical characteristics in aortic regurgitation(AR) patients by real-time three-dimensional transesophageal echocardiography (RT-3D-TEE),and screening the parameters which significantly affect AR to further reveal the mechanism of AR.Methods 32 patients with AR were enrolled as AR group and 20 cases of non-AR people were involved as control group.RT-3D-TEE was using to collect images in two groups and offline analysis was performed.4 sets of parameters of the aortic valves(left coronary valve,right coronary valve,and non-coronary valve):leaflet edge length(LL,RL,NL),leaflet height (LH,RH,N H),leaflet length/height ratio (LRa,RRa,NRa),leaflet tip plane distance(LTH,RTH,NTH) were acquired.Parameters of two groups were compared,and the parameters were incorporated into the logistic regression model,then the ROC curves were obtained.Results ①Compared with the control group,LL,RL,NL,RH,LRa,NRa,RRa in AR group increased (P < 0.05),while the rest parameters had no statistical differences (P >0.05).②Multivariable logistic regression model gradually screening of the significant factors influencing the reflux,and as a result RL and RTH had significant influence on AR,P values were 0.001,0.011.③The ROC curve analysis showed that the area of RL or RTH curve were both greater than 0.5,which were 0.811 and 0.605 respectively.Conclusions The free edge length and free edge length/height ratio have changed unbalanced.Furthermore,right coronary valve parameters changed significantly,and this might be one of the possible mechanism of AR.
		                        		
		                        		
		                        		
		                        	
4.Hyperproliferation of human colon cancer cells in co-cultures of rat regenerating hepatocytes
Bo XU ; Wensong CAI ; Guanghui ZHU ; Shaohui TANG ; Jiefeng WENG ; Weixian SU
International Journal of Surgery 2009;36(4):223-226
		                        		
		                        			
		                        			Objective To investigate the stimulated proliferation of colon cancer cells in co-cultures of regenerating hepatocytes. Methods Regenerating hepatocytes(24 hours after partial hepatectomy)were obtained by collagenase perfusion of models of rats undergoing 70% liver resection. To determine whether the ratio of human colon cell line SW480 cells to hepatocytes in co-cultures has influence on their interaction,these cells were cultured in ratios of 1: 101:1, or 10: 1. Proliferation capacity was assessed by the percentage of 3 H-TdR incorporation. Expression of epidermal growth factor receptor(EGFR), insulin-like growth factor1 receptor(IGF-1R)and hepatocyte growth factor receptor(c-met) were analyzed by western blot. Results For co-cultured SW480 and hepatocytes in the ratios of 1: 1 and 1: 10, an increase of disintegrations per minute(dpm) occurred after 72 hours' culture, and lasted at 120 hours' culture(P < 0.05). No difference was found between the group with ratio of 10:1 and control group. Protein levels of EGFR and IGF-1R, but not c-met, were significantly increased between culture of 24 hours and 120 hours; however, no change of these receptors was found in the ratio of 10: 1. Conclusions These results imply that co-culturing human colon cancer cells with regenerating hepatocytes leads to increased expression of EGFR and IGF-1R. We conclude that this effect is probably dependent on paracrine stimulation, by which numerous signals from the hepatocytes contribute to the hyperproliferative state of colon cancer cells via up-regulating the responding receptors.
		                        		
		                        		
		                        		
		                        	
5.Construction of intrakine mutant SDF-1alpha/54/KDEL and its inhibiting effects upon CXCR4 expression on cell membrane.
Hongyuan CHEN ; Yi TAN ; Zhigang GUO ; Weifeng MA ; Shaoxi CAI ; Jun DU ; Jun HUANG ; Houwen HU ; Shaohui CAI
Journal of Biomedical Engineering 2008;25(3):647-677
		                        		
		                        			
		                        			To investigate the impact of phenotypic knockout of CXCR4 on Molt-4 cells via intrakine technology,the C-terminal alpha-helix gene SDF-1alpha/54/KDEL of human stromal cell-derived Faceor-1 deletion is fused to a retention signal 4-peptide -KDEL that retains the newly synthesized receptor within the Molt-4 cells endoplasimc reticulum. Subsequently, PCR is used to amplify the target gene SDF-1alpha/54/ KDEL from the constructed plasmid SDF-WT-Gly x 4-Dec/PET-30a(+) at its C-terminal and subclone it into eukaryotic expression vectors pEGFP-C3 for generating recombinant vector cells by lipEGFP-C3/SDF-1alpha/54/KDEL, and then have it sequenced. After the transfection of recombinant plasmids into COS-7 posome, SDF-1alpha/54/KDEL protein is confirmed with Western blot. The recombinant plasmids pEGFP-C3/SDF-1alpha/54/KDEL are isolated and transiently transfected in Molt-4 cells by electroporation. Flow cytometric analysis shows a dramatic reduction of CXCR4 expression on Molt-4 cells. The conclusion is that SDF-1alpha/54/KDEL could assume a role in the phenotypic knockout of CXCR4, and the findings suggest that the inhibiting effect of SDF-1alpha/54 against CXCR4 is not influenced by the deletion of SDF-1alpha helix at the C terminal.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			COS Cells
		                        			;
		                        		
		                        			Cell Membrane
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Cercopithecus aethiops
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		                        			Chemokine CXCL12
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		                        			genetics
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		                        			Cloning, Molecular
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		                        			Electroporation
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		                        			Gene Knockout Techniques
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		                        			Genetic Vectors
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		                        			genetics
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		                        			Humans
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		                        			Mutation
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		                        			Receptors, CXCR4
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
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		                        			Recombinant Proteins
		                        			;
		                        		
		                        			genetics
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		                        			Stromal Cells
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Transfection
		                        			
		                        		
		                        	
6.The action of decorin in anti-fibrosis and anti-cancer.
Weifeng MA ; Yi TAN ; Shaohui CAI ; Hongyuan CHEN ; Jun DU ; Shaoxi CAI
Journal of Biomedical Engineering 2007;24(1):222-225
		                        		
		                        			
		                        			Decorin (DCN) is a member of the small leucine-rich proteoglycan gene family. Many studies indicated that DCN inhibited fibrosis and scar-formation by neutralization of TGF-P and interfering the binding of TGF-beta with its receptor, which induced ectopic deposition of extracellular matrix. Additionally, DCN can prevent the proliferation and metastasis of tumor cells by activating EGFR/MAPK/p21 signal pathway and inhibiting the cell proliferation pathway mediated by EGF-EGFR. It is suggested that the recombinant DCN had potential pharmaceutical potency in treatment of chronic fibrosis and neoplasm for its critical biological activities and low immunogenicity.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Antineoplastic Agents
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			Decorin
		                        			;
		                        		
		                        			Extracellular Matrix Proteins
		                        			;
		                        		
		                        			chemistry
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			Fibrosis
		                        			;
		                        		
		                        			prevention & control
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Proteoglycans
		                        			;
		                        		
		                        			chemistry
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		                        			pharmacology
		                        			;
		                        		
		                        			Receptor, Epidermal Growth Factor
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		                        			antagonists & inhibitors
		                        			;
		                        		
		                        			Recombinant Proteins
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			Transforming Growth Factor beta1
		                        			;
		                        		
		                        			antagonists & inhibitors
		                        			
		                        		
		                        	
7.The role of SDF-1 and its receptor CXCR4 in tumor metastasis.
Hongyuan CHEN ; Yi TAN ; Shaohui CAI ; Weifeng MA ; Zhigang GUO ; Jun DU ; Shaoxi CAI
Journal of Biomedical Engineering 2007;24(5):1180-1183
		                        		
		                        			
		                        			The chemokine SDF-1 (CXCL12) and its receptor, CXCR4, have been implicated in organ-specific metastases of several malignancies. CXCR4 expression has recently been characterized in many cancer cell types and is thought to play a pivotal role in directing the migration of metastasizing tumor cells to SDF-1-rich tissues. SDF-1, which is highly expressed in the organs where breast cancers preferentially metastasize, has been shown to promote cancer cell migration. The tumor cells use chemotaxis which occurred between CXCR4 and its ligand SDF-1 to direct migration from their primary sites via the circulation to the preferential sites of metastases, and further studies on the mechanism involved in a variety of cellular signaling pathways are beneficial to tumor therapy.
		                        		
		                        		
		                        		
		                        			Breast Neoplasms
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Chemokine CXCL12
		                        			;
		                        		
		                        			physiology
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Multiple Myeloma
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Neoplasm Metastasis
		                        			;
		                        		
		                        			Receptors, CXCR4
		                        			;
		                        		
		                        			physiology
		                        			;
		                        		
		                        			Signal Transduction
		                        			;
		                        		
		                        			physiology
		                        			
		                        		
		                        	
8.Status Quo of Pharmacist Training in Hong Kong and Its Enlightenment on Pharmaceutical Education Reform of Mainland College
Sha LI ; Peishan LIAO ; Peiting LIU ; Jintang ZHENG ; Shaohui CAI ; Weimin CHEN ; Jie JIANG
China Pharmacy 2007;0(29):-
		                        		
		                        			
		                        			OBJECTIVE: To investigate the status quo of pharmacists training in Hong Kong,and to provide reference for pharmaceutical education reform of college in mainland.METHODS: The status quo,role,license examination and culture system of licensed pharmacist in Hong Kong were analyzed.Based on the practice of our university,the difference in culture system of pharmacentical talents and curriculum setting of pharmaceutical education were compared between Hong Kong and mainland.RESULTS & CONCLUSION: On the basis of education reform practice of our university for Hong Kong students,it is suggested to match the pharmacy curriculum setting and training program used in Hong Kong,to improve the clinical practice,to explore "4+2" culture model,and to enhance English training of pharmaceutical education.
		                        		
		                        		
		                        		
		                        	
9.The cell micro-encapsulation techniques and its advancement in the field of gene therapy.
Journal of Biomedical Engineering 2006;23(6):1355-1358
		                        		
		                        			
		                        			It is no doubt that the gene therapy using recombinant engineering cells provides a novel approach to many refractory diseases. However, the transplant rejection from the host's immune system against heterogeneous cells has been the main handicap of its clinical application. The modern cell micro-encapsulation technique with good immune isolation makes it possible to overcome this problem and has shown potential application foreground in clinical therapies for a lot of diseases such as Parkinson's disease and Hemophiliac disease. This article reviews mainly the relative materials and techniques in processing micro-encapsulation, the host cells used to construct the recombinant genetic engineering cells and application of cell micro-encapsulation technique in the field of gene therapy.
		                        		
		                        		
		                        		
		                        			Biomedical Engineering
		                        			;
		                        		
		                        			methods
		                        			;
		                        		
		                        			trends
		                        			;
		                        		
		                        			Cell Transplantation
		                        			;
		                        		
		                        			methods
		                        			;
		                        		
		                        			trends
		                        			;
		                        		
		                        			Genetic Therapy
		                        			;
		                        		
		                        			trends
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Miniaturization
		                        			;
		                        		
		                        			Tissue Engineering
		                        			;
		                        		
		                        			methods
		                        			;
		                        		
		                        			trends
		                        			
		                        		
		                        	
10.Primary exploration on application of virtual classroom in general education programs
Shaoxian CAI ; Weiying CHEN ; Jingyan CHEN ; Mianhua YANG ; Danian QIN ; Shaohui LIU
Chinese Journal of Medical Education Research 2006;0(08):-
		                        		
		                        			
		                        			In order to strengthen the education for university students’all-round devel-opment,and to improve the quality of teaching,Shantou University,by making good use of higher education resources,built a digital campus consisting of virtual classrooms based on advantage of computer and Internet network environment,and plenty of general education programs were carried out.The teaching practice showed that virtual classroom,as a network platform,played an important role in general education programs.
		                        		
		                        		
		                        		
		                        	
            
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