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Wu Youfang,Tian Ying,Tan Jun,Zhao Shuai,Zhou Wenzhen,Luo Rui,Guo Jian-Jun 한국응용곤충학회 2021 Journal of Asia-Pacific Entomology Vol.24 No.2
Aspongopus chinensis Dallas, 1851 is an important insect resource with a long utilization history as traditional Chinese medicine and food owing to its various health benefits, including anti-cancer, anti-bacteria, and anticlotting properties. However, the long period of reproductive diapause during the overwintering stage has limited the broad utilization and artificial cultivation of A. chinensis. Diapause is largely regulated by juvenile hormones. Therefore, understanding the relationship between juvenile hormone metabolism and A. chinensis diapause may provide useful insight for developing genetic engineering strategies to regulate diapause. We identified differentially expressed genes in diapause and non-diapause adults of A. chinensis by transcriptome sequencing. A total of 336,230,260 clean reads were assembled into 80,769 unigenes. Overall, 3,524 differen tially expressed genes were identified, including 2,174 down-regulated and 1,350 up-regulated genes in diapause adults. Among these differentially expressed genes, 22 were significantly enriched in the JH III metabolismrelated pathway based on Kyoto Encyclopedia of Genes and Genomes analysis. These results provide insight into the molecular-level mechanism of diapause regulation and highlight new targets for preventing diapause to improve A. chinensis cultivation and productivity.
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Bevacizumab Regulates Cancer Cell Migration by Activation of STAT3
Wu, Huan-Huan,Zhang, Shuai,Bian, Huan,Li, Xiao-Xu,Wang, Lin,Pu, Yin-Fei,Wang, Yi-Xiang,Guo, Chuan-Bin Asian Pacific Journal of Cancer Prevention 2015 Asian Pacific journal of cancer prevention Vol.16 No.15
There are numerous clinical cases indicating that long-term use of bevacizumab may increase the invasiveness of tumors. However, to date, little is known about underlying molecular mechanisms. Therefore, the purpose of our study was to investigate effects of bevacizumab in four cancer cells lines (WSU-HN6, CAL27, Tca83, and HeLa). It was found to promote migration and invasion in the WSU-HN6 and Tca83 cases, while exerting inhibitory effects in CAL27 and HeLa cells. The signal transducer and activator of transcription (STAT) 3 inhibitors niclosamide and S3I-201 inhibited the STAT3 signal pathway, which is activated by bevacizumab. These inhibitors also substantially blocked bevacizumab-induced migration of WSU-HN6 and Tca83 cells. Bevacizumab upregulated interleukin (IL)-6 and phosphorylated (p)-STAT3 expression time-dependently. Therefore, we propose that bevacizumab has differential effects on the migration of different cancer cell lines and promotes migration via the IL-6/STAT3 signaling pathway.
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Haojun Fan,Ke Zeng,Qiao Guo,Shuai Gao,Dimeng Wu,Gang Yang 한국고분자학회 2012 Macromolecular Research Vol.20 No.1
A series of new asymmetric biphenyl dianhydrides, 2-phenoxy(o-methylphenoxy, m-methylphenoxy, and p-methylphenoxy)-4,4,5,5-biphenyltetracarboxylic dianhydrides, was readily synthesized using a five-step route. A new symmetric biphenyl dianhydride, 2,2-di(o-methylphenoxy)-4,4,5,5-biphenyltetracarboxylic dianhydride, was also synthesized using the similar procedure. The polyimides were prepared from such new dianhydrides and commercial diamines by high-temperature one-step polymerization. The asymmetric and symmetric substituent solubility and thermal property relationships of the resulting polyimides were investigated. Interestingly, the thermally reversible sol–gel transitions were observed for the polymer solutions of the polyimides derived from those asymmetric dianhydrides and 1,4-phenylenediamine (p-PDA). Unexpectedly, the polyimides derived from asymmetric dianhydrides did not show better organosolubility than those of the homologous polyimides derived from symmetric dianhydrides. The structures of the substituents (phenoxy, o-methylphenoxy, m-methylphenoxy and p-methylphenoxy)have a significant effect on both the solubility and the thermal properties of these polyimides. The polyimides derived from asymmetric dianhydrides show enhanced thermal properties relative to the symmetric dianhydridesderived polyimides. These results can be attributed to their different degrees of molecular packing revealed by wideangle X-ray diffraction measurements.
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Rui Chen,Mengting Wang,Qiaoling Qi,Yanli Tang,Zhenzhao Guo,Shuai Wu,Qiyan Li 대한치주과학회 2023 Journal of Periodontal & Implant Science Vol.53 No.1
Purpose: Our pilot study showed that a 3-dimensional dual drug delivery scaffold (DDDS) loaded with Chinese herbs significantly increased the regenerated bone volume fraction. This study aimed to confirm the synergistic anti-inflammatory and osteogenic preclinical effects of this system. Methods: The targets and pathways of parthenolide and naringin were predicted. Three cell models were used to assess the anti-inflammatory effects of parthenolide and the osteogenic effects of naringin. First, the distance between the cementoenamel junction and alveolar bone crest (CEJ-ABC) and the bone mineral density (BMD) of surgical defects were measured in a rat model of periodontitis with periodontal fenestration defects. Additionally, the mRNA expression levels of matrix metallopeptidase 9 (MMP9) and alkaline phosphatase (ALP) were measured. Furthermore, the number of inflammatory cells and osteoclasts, as well as the protein expression levels of tumor necrosis factor-alpha (TNF-α) and levels of ALP were determined. Results: Target prediction suggested prostaglandin peroxidase synthase (PTGS2) as a potential target of parthenolide, while cytochrome P450 family 19 subfamily A1 (CYP19A1) and taste 2 receptor member 31 (TAS2R31) were potential targets of naringin. Parthenolide mainly targeted inflammation-related pathways, while naringin participated in steroid hormone synthesis and taste transduction. In vitro experiments revealed significant antiinflammatory effects of parthenolide on RAW264.7 cells, and significant osteogenic effects of naringin on bone marrow mesenchymal stem cells and MC3T3-E1 cells. DDDS loaded with parthenolide and naringin decreased the CEJ-ABC distance and increased BMD and ALP levels in a time-dependent manner. Inflammation was significantly alleviated after 14 days of DDDS treatment. Additionally, after 56 days, the DDDS group exhibited the highest BMD and ALP levels. Conclusions: DDDS loaded with parthenolide and naringin in a rat model achieved significant synergistic anti-inflammatory and osteogenic effects, providing powerful preclinical evidence.
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