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Bo Yan,
Qing Ouyang,
Zhining Zhao,
Feng Cao,
Tao Wang,
Xiaofei Jia,
Yanling Meng,
Shuai Jiang,
Jiayun Liu,
Rui Chen,
Lintao Jia,
Rui Zhang,
Weihong Wen,
Boquan Jin,
Siyi Chen,
Jing Zhao,
Angang Yang
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ABSTRACT: Targeted therapy is needed for hepatitis B virus (HBV)-mediated hepatocellular carcinoma (HCC) which shows overexpression of HBV surface antigen (HBsAg). We previously developed scFv15, a human single-chain antibody against HBsAg. Here we tested the strategic feasibility of scFv15-mediated delivery of apoptotic effectors for HBsAg-targeted HCC therapy and application of HA2 motif of influenza hemagglutinin to enhance endosome escape and antitumor effect. A class of HBsAg-targeted immunoproapoptotic molecule was generated by sequentially fusing scFv15, the furin-cleavable motif from diphtheria toxin (Fdt), HA2 and a truncated apoptotic protein Bid (tBid). The resulting scFv15-Fdt-HA2-tBid was prokaryotically expressed and functionally characterized for HBsAg-binding capacity, endosome escape activity and antitumor effect as compared with scFv15-Fdt-tBid. Both scFv15-Fdt-HA2-tBid and scFv15-Fdt-tBid retained affinity and specificity for HBsAg, and bound and selectively killed HBsAg-positive HCC cells via apoptosis. Notably, the IC50 of scFv15-Fdt-HA2-tBid in HBsAg-positive PLC/PRF/5 cells was 10 times lower than that of scFv15-Fdt-tBid. In vivo imaging of antitumor activity demonstrated 95% growth inhibition of orthotopic HCC by scFv15-Fdt-HA2-tBid compared with 75% suppression by scFv15-Fdt-tBid. This study represents an extended application of the immunoproapoptotic strategy in the treatment of HBsAg-positive HCC and shows significant potential of HA2 as a functional enhancer for endosome-encapsulated antibody-conjugates.
Biomaterials 04/2013; · 7.40 Impact Factor
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ABSTRACT: Objective To establish an intrahepatic xenograft tumor model in nude mice and dynamically monitor the tumor growth by in vivo fluorescence imaging system. Methods We first transfected the recombinant plasmid pcDNA3.1-Luc to constructe the PLC/PRF/5 cell line which stably expressed luciferase, and then injected the cell line into the liver of nude mice. Tumor growth was monitored dynamically using in vivo fluorescence imaging system. The fluorescence-positive mouse was dissected to observe the tumor. Immunofluoresence histochemistry was used to detect the expression of HBsAg in Xenografe. Results In the nude mouse model bearing intrahepatic xenograft tumor, robust fluorescence was detected where the PLC/PRF/5 cells were injected. Xenograft was observed in the liver by dissecting the fluorescence-positive mouse. The expression of HBsAg in xenograft tissues was confirmed.Conclusion Intrahepatic xenograft tumor model in nude mice has been established successfully, which offers a tool for therapeutic development and evaluation of anti-hepatocelluar carcinoma drugs.
Xi bao yu fen zi mian yi xue za zhi = Chinese journal of cellular and molecular immunology 04/2013; 29(3):426-9.
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Jiu-Xu Bai, Bo Yan,
Zhi-Ning Zhao,
Xiao Xiao,
Wei-Wei Qin,
Rui Zhang,
Lin-Tao Jia,
Yan-Ling Meng,
Bo-Quan Jin,
Dai-Ming Fan,
Tao Wang,
An-Gang Yang
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ABSTRACT: Although tamoxifen (TAM), a selective estrogen receptor modulator, has been widely used in the treatment of hormone-responsive breast cancer, its estrogen-like effect increases the risk of endometrial cancer. However, the molecular mechanisms of TAM-induced endometrial carcinoma still remain unclear. In this report, we explored the role of microRNAs (miRNAs) in TAM-induced epithelial-mesenchymal transition (EMT) in ECC-1 and Ishikawa endometrial cancer cell lines and found miR-200 is involved in this process via the regulation of c-Myc. When treated with TAM, ECC-1 and Ishikawa cells were characterized by higher invasiveness and motility and underwent EMT. miR-200, a miRNA family with tumor suppressive functions in a wide range of cancers, was found reduced in response to TAM treatment. Consistent with zinc finger E-box binding homeobox 2, which was confirmed as a direct target of miR-200b in endometrial cancer cell lines, some other key factors of EMT such as Snail and N-cadherin increased, whereas E-cadherin decreased in the TAM-treated cells, contributing to TAM-induced EMT in these endometrial cancer cells. In addition, we showed that c-Myc directly binds to and represses the promoter of miR-200 miRNAs, and its up-regulation in TAM-treated endometrial cancer cells leads to the down-regulation of miR-200 and eventually to EMT. Collectively, our data suggest that TAM can repress the miR-200 family and induce EMT via the up-regulation of c-Myc in endometrial cancer cells. These findings describe a possible mechanism of TAM-induced EMT in endometrial cancer and provide a potential new therapeutic strategy for it.
Endocrinology 01/2013; · 4.46 Impact Factor
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ABSTRACT: A group of vaccinia virus (VACV) proteins, including A11, L2, and A6, are required for biogenesis of the primary envelope of VACV, specifically, for the acquisition of viral membrane precursors. However, the interconnection among these proteins is unknown and, with the exception of L2, the connection of these proteins with membranes is also unknown. In this study, prompted by the findings that A6 coprecipitated A11 and that the cellular distribution of A11 was dramatically altered by repression of A6 expression, we studied the localization of A11 in cells by using immunofluorescence and cell fractionation analysis. A11 was found to associate with membranes and colocalize with virion membrane proteins in viral replication factories during normal VACV replication. A11 partitioned almost equally between the detergent and aqueous phases upon Triton X-114 phase separation, demonstrating an intrinsic affinity with lipids. However, in the absence of infection or VACV late protein synthesis, A11 did not associate with cellular membranes. Furthermore, when A6 expression was repressed, A11 did not colocalize with any viral membrane proteins or associate with membranes. In contrast, when virion envelope formation was blocked at a later step by repression of A14 expression or by rifampin treatment, A11 colocalized with virion membrane proteins in the factories. Altogether, our data showed that A11 associates with viral membranes during VACV replication, and this association requires A6 expression. This study provides a physical connection between A11 and viral membranes and suggests that A6 regulates A11 membrane association.
Journal of Virology 08/2012; 86(20):11276-86. · 5.40 Impact Factor
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ABSTRACT: In order to enhance the soil water-retaining capacity of slope farmland and reduce its soil and water loss, a field study was conducted in 2007-2010 to examine the effects of strip planting and fallow rotation on the soil water regime, soil and water loss characteristics, and water use efficiency of a 10 degrees-15 degrees slope farmland in the arid area of southern Ningxia, Northwest China. Compared with the traditional no-strip planting, strip planting and fallow rotation increased the soil water content in 0-200 cm layer significantly, with an increment of 4.9% -7.0%. Strip planting and fallow rotation pattern could also effectively conserve the soil water in rain season, and obviously improve the soil water regime at crops early growth stages. As compared to no-strip planting, strip planting and fallow rotation increased the soil water content in 0-200 cm layer by 5.4%-8.5%, decreased the surface runoff by 0.7-3.2 m3 x hm(-2), sediment runoff by 0.2-1.9 t x hm(-2), and soil total N loss by 42.1% -73.3%, while improved the crop water use efficiency by 6.1% -24.9% and the precipitation use efficiency by 6.3% -15.3%.
Ying yong sheng tai xue bao = The journal of applied ecology / Zhongguo sheng tai xue xue hui, Zhongguo ke xue yuan Shenyang ying yong sheng tai yan jiu suo zhu ban 08/2012; 23(8):2191-8.
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Jian-Yong Sun,
Yi Huang,
Ji-Peng Li,
Xiang Zhang,
Lei Wang,
Yan-Ling Meng, Bo Yan,
Yong-Qian Bian,
Jing Zhao,
Wei-Zhong Wang,
An-Gang Yang,
Rui Zhang
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ABSTRACT: Recent profile studies of microRNA (miRNA) expression have documented a deregulation of miRNA (miR-320a) in human colorectal carcinoma. However, its expression pattern and underlying mechanisms in the development and progression of colorectal carcinoma has not been elucidated clearly. Here, we performed real-time PCR to examine the expression levels of miR-320a in colon cancer cell lines and tumor tissues. And then, we investigated its biological functions in colon cancer cells by a gain of functional strategy. Further more, by the combinational approaches of bioinformatics and experimental validation, we confirmed target associations of miR-320a in colorectal carcinoma. Our results showed that miR-320a was frequently downregulated in cancer cell lines and colon cancer tissues. And we demonstrated that miR-320a restoration inhibited colon cancer cell proliferation and β-catenin, a functionally oncogenic molecule was a direct target gene of miR-320a. Finally, the data of real-time PCR showed the reciprocal relationship between miR-320a and β-catenin's downstream genes in colon cancer tissues. These findings indicate that miR-320a suppresses the growth of colon cancer cells by directly targeting β-catenin, suggesting its application in prognosis prediction and cancer treatment.
Biochemical and Biophysical Research Communications 03/2012; 420(4):787-92. · 2.48 Impact Factor
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ABSTRACT: Poxvirus acquires its primary envelope through a process that is distinct from those of other enveloped viruses. The molecular mechanism of this process is poorly understood, but several poxvirus proteins essential for the process have been identified in studies of vaccinia virus (VACV), the prototypical poxvirus. Previously, we identified VACV A6 as an essential factor for virion morphogenesis by studying a temperature-sensitive mutant with a lesion in A6. Here, we further studied A6 by constructing and characterizing an inducible virus (iA6) that could more stringently repress A6 expression. When A6 expression was induced by the inducer isopropyl-β-D-thiogalactoside (IPTG), iA6 replicated normally, and membrane proteins of mature virions (MVs) predominantly localized in viral factories where virions were assembled. However, when A6 expression was repressed, electron microscopy of infected cells showed the accumulation of large viroplasm inclusions containing virion core proteins but no viral membranes. Immunofluorescence and cell fractionation studies showed that the major MV membrane proteins A13, A14, D8, and H3 did not localize to viral factories but instead accumulated in the secretory compartments, including the endoplasmic reticulum. Overall, our results show that A6 is an additional VACV protein that participates in an early step of virion membrane biogenesis. Furthermore, A6 is required for MV membrane protein localization to sites of virion assembly, suggesting that MV membrane proteins or precursors of MV membranes are trafficked to sites of virion assembly through an active, virus-mediated process that requires A6.
Journal of Virology 03/2012; 86(10):5603-13. · 5.40 Impact Factor
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ABSTRACT: Lung cancer is characterized by a widely ranging incidence variation; it is the most common cancer in China. In this study we will assess the association of low-molecular-mass protease 2 (LMP2) gene codon 60 polymorphism with the risk of lung cancer. Genomic DNA of peripheral blood mononuclear cells was isolated from 207 patients with lung cancer and 264 healthy controls. DNA direct sequencing and polymerase chain reaction-restriction fragment length polymorphism were performed to scrutinize LMP2 gene codon 60 polymorphism. The risk of LMP2 gene polymorphism in lung cancer was assessed using an unconditional logistic regression model adjusted by the confounding factors. As a result of DNA direct sequencing, the LMP2 codon 60 polymorphic substitution of the nucleotide was CGC → TGC in Chinese individuals, not CGC → CAC as reported in other ethnic populations. In histology-specific analysis and TNM stages, there was no apparent association between this LMP2 gene polymorphism and any of the histologic types or TNM stages of lung cancer using the Arg/Arg genotypes as the reference group (all p values > 0.05). These results suggest that the polymorphic site is unique in the Chinese population of Han nationality at the LMP2 codon 60 loci (Arg60Cys), but a lack of association with lung cancer exists.
Human immunology 01/2012; 73(5):580-4. · 2.55 Impact Factor
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ABSTRACT: It is unknown whether white matter abnormalities exist in childhood absence epilepsy (CAE), a syndrome of idiopathic epilepsy (IGE). Diffusion tensor imaging (DTI) can noninvasively quantify white matter integrity. This study used DTI to investigate abnormal changes in white matter of untreated CAE patients.
Subjects included nine patients with untreated CAE and nine age-and sex-matched healthy controls. Diffusion tensor imaging parameters were voxel based and statistically compared between patients and controls. The correlations between DTI parameters in regions of interest (ROIs) and age of seizure onset or duration of epilepsy were analyzed.
Untreated CAE patients had a significantly higher fractional anisotropy (FA) value in the bilateral thalamus, anterior corpus callosum and upper brainstem, while also displaying a lower FA value in prefrontal white matter, anterior cingulate, and bilateral posterior limbs of the internal capsule compared to control subjects. An increase in mean diffusivity (MD) value was observed in parietal lobe white matter, prefrontal white matter, and posterior cerebellar hemispheres, in addition to subcortical structures including bilateral putamen and posterior limb of internal capsule. MD significant correlations between ROI diffusion parameters and the duration of the disease or the age of onset.
The results showed white matter integrity impairment in the basal ganglia-thalamocortical circuit of drug-naïve CAE patients. These abnormalities in white matter may be related to increased cortical excitability and cause cognitive, linguistic, and behavioral/emotional deficits both during and between seizures.
Epilepsy research 01/2012; 99(3):267-73. · 2.48 Impact Factor
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ABSTRACT: Fixation of heavy metals in the slag produced during incineration of sewage sludge will reduce emission of the metals to the atmosphere and make the incineration process more environmentally friendly. The effects of incineration conditions (incineration temperature 500-1100°C, furnace residence time 0-60min, mass fraction of water in the sludge 0-75%) on the fixation rates and species partitioning of Cd, Pb, Cr, Cu, Zn, Mn and Ni in slag were investigated. When the incineration temperature was increased from 500 to 1100°C, the fixation rate of Cd decreased from 87% to 49%, while the fixation rates of Cu and Mn were stable. The maximum fixation rates for Pb and Zn and for Ni and Cr were reached at 900 and 1100°C, respectively. The fixation rates of Cu, Ni, Cd, Cr and Zn decreased as the residence time increased. With a 20min residence time, the fixation rates of Pb and Mn were low. The maximum fixation rates of Ni, Mn, Zn, Cu and Cr were achieved when the mass fraction of water in the sludge was 55%. The fixation rate of Cd decreased as the water mass fraction increased, while the fixation rate of Pb increased. Partitioning analysis of the metals contained in the slag showed that increasing the incineration temperature and residence time promoted complete oxidation of the metals. This reduced the non-residual fractions of the metals, which would lower the bioavailability of the metals. The mass fraction of water in the sludge had little effect on the partitioning of the metals. Correlation analysis indicated that the fixation rates of heavy metals in the sludge and the forms of heavy metals in the incinerator slag could be controlled by optimization of the incineration conditions. These results show how the bioavailability of the metals can be reduced for environmentally friendly disposal of the incinerator slag.
Waste Management 01/2012; 32(5):957-64. · 2.43 Impact Factor
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Zhi-Ning Zhao,
Jiu-Xu Bai,
Qiang Zhou, Bo Yan,
Wei-Wei Qin,
Lin-Tao Jia,
Yan-Ling Meng,
Bo-Quan Jin,
Li-Bo Yao,
Tao Wang,
An-Gang Yang
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ABSTRACT: Histone deacetylase (HDAC) inhibitors are emerging as a novel class of anti-tumor agents and have manifested the ability to decrease proliferation and increase apoptosis in different cancer cells. A significant number of genes have been identified as potential effectors responsible for the anti-tumor function of HDAC inhibitor. However, the molecular mechanisms of these HDAC inhibitors in this process remain largely undefined. In the current study, we searched for microRNAs (miRs) that were affected by HDAC inhibitor trichostatin (TSA) and investigated their effects in endometrial cancer (EMC) cells. Our data showed that TSA significantly inhibited the growth of EMC cells and induced their apoptosis. Among the miRNAs that altered in the presence of TSA, the miR-106b-93-25 cluster, together with its host gene MCM7, were obviously down-regulated in EMC cells. p21 and BIM, which were identified as target genes of miR-106b-93-25 cluster, increased in TSA treated tumor cells and were responsible for cell cycle arrest and apoptosis. We further identified MYC as a regulator of miR-106b-93-25 cluster and demonstrated its down-regulation in the presence of TSA resulted in the reduction of miR-106b-93-25 cluster and up-regulation of p21 and BIM. More important, we found miR-106b-93-25 cluster was up-regulated in clinical EMC samples in association with the overexpression of MCM7 and MYC and the down-regulation of p21 and BIM. Thus our studies strongly indicated TSA inhibited EMC cell growth and induced cell apoptosis and cell cycle arrest at least partially through the down-regulation of the miR-106b-93-25 cluster and up-regulation of it's target genes p21 and BIM via MYC.
PLoS ONE 01/2012; 7(9):e45133. · 4.09 Impact Factor
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ABSTRACT: Nanoparticle Cluster Arrays (NCAs) are a class of electromagnetic materials that comprise chemically defined nanoparticles assembled into clusters of defined size in an extended deterministic arrangement. NCAs are fabricated through integration of chemically synthesized building blocks into predefined patterns using a hybrid top-down/bottom-up fabrication approach that overcomes some of the limitations of conventional top-down fabrication methods with regard to minimum available feature size and structural complexity. NCAs can sustain near-field interactions between nanoparticles within individual clusters as well as between entire neighboring clusters. The availability of near-field interactions on multiple length scales - together with the ability to further enhance the coupled plasmon modes through photonic modes in carefully designed array morphologies - leads to a multiscale cascade electromagnetic field enhancement throughout the array. This feature article introduces the design and fabrication fundamentals of NCAs and characterizes the electromagnetic coupling mechanisms in the arrays. Furthermore, it reviews how the optical properties of NCAs can be tuned through the size and shape of the nanoparticle building blocks and the geometry, size, and separation of the assembled clusters. NCAs have potential applications in many different areas; this feature article focuses on plasmon enhanced biosensing and surface enhanced Raman spectroscopy (SERS), in particular.
The Journal of Physical Chemistry C 12/2011; 115(50):24437-24453. · 4.80 Impact Factor
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ABSTRACT: To construct recombinant plasmid and adenovirus harboring MDA-7 gene, and to investigate its biological function on the proliferation of human hepatocellular carcinoma cells.
The MDA-7 fragments from the T vectors were inserted into pCDNA-3 vector to construct expression plasmids named pCDNA3-MDA-7. To determine its effects on the proliferation of HCC cells, transfected the expression vector into cells and tested the ability of colony formation in cancer cells. Simultaneously, constructed recombinant adenovirus expressing MDA-7, and detected its effect on the proliferation of HCC cells by using MTT assay.
Successfully constructed plasmid- and adenovirus-based system to express MDA-7. The data of colony formation assay and M'T test showed that MDA-7 can obviously suppress cell growth in HCC cells.
MDA-7 may function as tumor suppressor in HCC cells, and the adenovirus-mediated MDA-7 can be a novel strategy for the anti-HCC therapy. Our study established the foundation for future research on the effect of MDA-7 in HCC.
Xi bao yu fen zi mian yi xue za zhi = Chinese journal of cellular and molecular immunology 12/2011; 27(12):1277-9.
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ABSTRACT: In 2007-2010, a field experiment was conducted to study the effects of different rotational tillage practices during summer follow on the soil water regime and grain yield in a winter wheat field in Southern Ningxia arid area. Three treatments were installed, i.e., T1 (no-tillage in first year, subsoiling in second year, and no-tillage in third year), T2 (subsoiling in first year, notillage in second year, and subsoiling in third year), and CT (conventional tillage in the 3 years). Through the three years of the tillage practices, the soil water storage efficiency in treatments T1 and T2 was increased averagely by 15.2% and 26.5%, respectively, as compared to CT. In treatments T1 and T2, the potential rainfall use rate was higher, being 37.8% and 38.5%, respectively, and the rainfall use efficiency was increased averagely by 9.9% and 10.7%, respectively, as compared to CT. Rotational tillage during summer fallow could decrease the soil ineffective evaporation significantly, and save the soil water effectively in wheat growth season. At early growth stage, the water storage in 0-200 cm soil layer in treatments T1 and T2 was increased averagely by 6.8% and 9. 4%, as compared to CT; at jointing, heading, and filling stages, the water storage in 0-200 cm soil layer in treatments T1 and T2 had a significant increase, giving greater contribution to the wheat yield than the control. Different rotational tillage practices increased the water consumption by wheat, but in the meantime, increased the grain yield and water use efficiency. In treatments T1 and T2, the water consumption by wheat through the three years was increased averagely by 5.2% and 6.1%, whereas the grain yield and the water use efficiency were increased averagely by 9.9% and 10.6%, and by 4.5% and 4.3%, respectively, as compared to CT. Correlation analysis showed that in Southern Ningxia arid area, the soil water storage at sowing, jointing, heading, and filling stages, especially at heading stage, could have significant effects on the winter wheat grain yield.
Ying yong sheng tai xue bao = The journal of applied ecology / Zhongguo sheng tai xue xue hui, Zhongguo ke xue yuan Shenyang ying yong sheng tai yan jiu suo zhu ban 10/2011; 22(10):2524-32.
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Gui-Rong Yu,
Wei-Wei Qin,
Ji-Peng Li,
Wei Hua,
Yan-Ling Meng,
Rui Chen, Bo Yan,
Lei Wang,
Xiang Zhang,
Lin-Tao Jia,
Jing Zhao,
Rui Zhang,
An-Gang Yang
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ABSTRACT: Accumulating evidence has demonstrated that FHIT (fragile histidine triad) is a bona fide tumour suppressor gene in a large fraction of human tumours, including hepatocellular cancer. A virus-based delivery system has been developed to transfer the FHIT gene into many types of cancer cells to inhibit growth or even induce apoptosis. However, a protein-based replacement strategy for FHIT has not been performed in cancer cells. Here, we used HIV-TAT (transactivator of transcription)-derived peptide to transfer the purified FHIT protein into HCC (hepatocellular carcinoma) cells and determine the biological effect of this fusion protein in inducing apoptosis. Affinity chromatography was used to purify TAT peptide-fused human FHIT (TAT-FHIT) protein from BL21 Escherichia coli. Immunofluorescence staining and Western blot analysis were performed to identify the expression and internalization of TAT-FHIT in HCC cells compared with the purified FHIT protein. Our study showed that TAT-FHIT protein can translocate into cancer cells in 1 h after incubation at 37°C. Furthermore, the results of MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide] assay, Annexin-V staining and Western blotting demonstrated that TAT-FHIT can robustly inhibit growth and induce apoptosis of HCC cells in vitro. In addition, a mechanistic study showed that both exogenous and intrinsic apoptotic pathways were involved in TAT-FHIT-mediated apoptosis and this effect could be attenuated partially by a mitochondrial protector TAT-BH4, indicating that mitochondrion plays a critical role in TAT-FHIT-mediated pro-apoptotic effect in cancer cells. Taken together, our study suggests that TAT-FHIT is a potential pro-apoptotic molecule in HCC cells and strengthen the hypothesis of its therapeutic application against HCC.
Bioscience Reports 06/2011; 32(3):271-9. · 2.38 Impact Factor
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ABSTRACT: The cascade of caspase processing and activation is the core of apoptotic cell signaling. Initiator caspases are activated by adaptor-mediated clustering, which allows the intermolecular autoprocessing of the zymogens in close proximity. Caspase-8, the prototypical initiator critically involved in apoptosis induced by varied extrinsic stimuli, is physiologically recruited via a classical FasL/Fas/FADD pathway. Meanwhile, artificial models of caspase-8 activation have been proposed via inducible dimerization of a heterologous domain fused to the zymogen. Here, we describe the generation of a chimeric protein of caspase-8 and the ligand-binding domain (LBD) of estrogen receptor α (ERα), which dimerizes and undergoes autocleavage upon engagement by the ligand, estradiol. Breast cancer cells expressing this fusion protein exhibit apoptotic cell death in vitro and suppressed tumor growth in xenograft nude mice models in response to the administration of estrogen. Thus, the suicidal caspase-8/ERα-LBD protein, which reverses the mitogenic effects of estrogens, has potential to provide novel approaches to treating estrogen-dependent and -independent breast cancers.
Cancer biology & therapy 05/2011; 11(9):816-25. · 2.64 Impact Factor
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ABSTRACT: Both embedding in the global value chain and integrating into supply chain are crucial for industrial cluster to obtain competitive advantages which generally remain high-value-added and core strategic segments of value chain, and thus ultimately resulting in industrial cluster upgrading. This paper describes the current situation of toy industries in China, analyzes some problems existing in the toy industrial cluster, as well as introduces global value chain, industrial clusters and cluster supply chain theory. This paper illustrates global value chain and cluster supply chain integration through the case of Guanyao town toy industrial cluster in Guangdong province. Through the study of industrial upgrading based on global value chain and cluster supply chain integration to enhance the competitive power of toy manufacture industrial cluster.
Information Engineering and Electronic Commerce, International Symposium on. 05/2009;
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ABSTRACT: Supply chain and industrial cluster are the results of competition economy. The distinguish and relation of them were discussed in order to put forward that supply chain and industrial cluster could be introjected. This paper illustrates the clusters theory, supply chain management theory and the linkages between supply chain management and Porterpsilas clusters theory. Clusterspsila characteristics enable more efficient supply chain management practices, and supply chain management improves clusters competitive advantage. Taking Guangdong automobile clusters for example, analyzing the present situation of Guangzhou automobile industrial cluster, the paper considers that the establishment of the cluster should take the improvement to fits supply chain as the base and the key factors that determine the development of Guangzhou automobile industrial supply chain and the industrial cluster are enterprise core competitiveness, maturity structure of automobile industrial supply chain, clusters and automobile industrial clusters system based on supply chain management. This is the theory base for application of the supply chain management methods in the industrial cluster construction and obtaining the competition advantage of industrial cluster based on global supply chains.
Business and Information Management, 2008. ISBIM '08. International Seminar on; 01/2009
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ABSTRACT: An accurate small-signal modeling approach applied to GaAs-based pHEMT devices is presented. The procedure for extracting
equivalent-circuit model parameters is illustrated in detail. A genetic algorithm (GA) program is developed to optimize the
model parameters in order to improve the modeling accuracy. The validity of modeling approach is verified by comparing the
simulated and measured result of two pHEMTs and a fabricated ka-band power amplifier. The conclusion can be drawn that the
proposed modeling method is rather accurate and efficient.
International Journal of Infrared and Millimeter Waves 11/2007; 28(12):1133-1141. · 0.58 Impact Factor
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ABSTRACT: C/SiC composites were prepared by polycarbosilane infiltration pyrolysis and ablated by oxyacetylene flame at 1800 °C for 180 s. Morphology and microstructure of C/SiC have been studied by scanning electron microscopy/energy dispersive spectroscopy, and X-ray diffraction analysis. Two concentric ring regions appeared on the surface of the ablated C/SiC. In the centre region of the ablated C/SiC was composed of irregular SiC particles with a lot of pores. The pores were resulted from (i) gas expansion in closed pores during ablation, and (ii) from the release of SiO gas produced by the oxidation of SiC with sufficiently low oxygen partial pressure. The results indicated the ablation was due to a combination of oxidation, mechanical erosion and recrystallization of the surface SiC.
Journal of Materials Processing Technology.
