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| 1 | Intracellular HMGB1 as a novel tumor suppressor of pancreatic cancer显示文摘尽管有最近的进展, oncogenic K 地岬驾驶的胰腺的 ductal 腺癌(PDAC ) 在最致命的人的癌症之中留在现代医学。PDAC 的致病对内在的染色体不稳定性和外来的发炎激活部分可归因。然而,在在胰腺的 tumorigenesis 的这二个事件之间的分子的连接充分还没被建立了。这里,我们证明(HMGB1 ) 细胞内部的高活动性组盒子 1 显著地压制 oncogenic 由禁止染色体的 K-Ras-driven 胰腺的 tumorigenesis 调停不稳定性的支持 inflammatory nucleosome 版本。任何一个单身者的有条件的基因脱离或在胰的 HMGB1 的两等位基因在出生使老鼠变为极其敏感到先锋损害的 oncogenic K-Ras-driven 开始,包括胰腺的 intraepithelial 瘤, intraductal 乳突的 mucinous 瘤,和 mucinous 膀胱的瘤。在胰的 HMGB1 的损失与染色体重新整理和 telomere 畸形描绘的氧化 DNA 损坏和 chromosomal 不稳定性被联系。这些导致煽动性的 nucleosome 版本并且宣传 K-Ras-driven 胰腺的 tumorigenesis。细胞外的 nucleosomes 支持 interleukin 6 (IL-6 ) 由渗入 macrophages/neutrophils 的分泌物并且提高在胰腺的损害表明激活的 oncogenic K 地岬。到 IL-6 或 histone H3 或为先进 glycation 的受体的大美人的抵销的抗体结束产品都限制表明激活的 K 地岬,阻止癌症开发和转移 / 侵略,并且延长在 Pdx1-Cre 的动物幸存; K 地岬 G12D/+;Hmgb1/ 鼠标。由 glycyrrhizin 的 HMGB1 损失的药理学抑制在煽动性的条件下面在老鼠限制 oncogenic K-Ras-driven tumorigenesis。减少在 PDAC 病人的 HMGB1 的原子、全部的细胞的表示与差的全面幸存相关,在 PDAC 与预示、治疗学的关联作为新奇肿瘤 suppressor 支持细胞内部的 HMGB1。 | Rui Kang Yangchun Xie Qiuhong Zhang Wen Hou Qingping Jiang Shan Zhu Jinbao Liu Dexing Zeng Haichao Wang David L Bartlet Timothy R Billiar Herbert J Zeh III Michael T Lotze Daolin Tang | 2017 | Cell Research2017，27，7： | 22 |
| 2 | Nuclear Aurora kinase A switches m^(6)A reader YTHDC1 to enhance an oncogenic RNA splicing of tumor suppressor RBM4显示文摘Aberrant RNA splicing produces alternative isoforms of genes to facilitate tumor progression,yet how this process is regulated by oncogenic signal remains largely unknown.Here,we unveil that non-canonical activation of nuclear AURKA promotes an oncogenic RNA splicing of tumor suppressor RBM4 directed by m^(6)A reader YTHDC1 in lung cancer.Nuclear translocation of AURKA is a prerequisite for RNA aberrant splicing,specifically triggering RBM4 splicing from the full isoform(RBM4-FL)to the short isoform(RBM4-S)in a kinase-independent manner. | SiSi Li YangFan Qi JiaChuan Yu YuChao Hao Bin He MengJuan Zhang ZhenWei Dai TongHui Jiang SuYi Li Fang Huang Ning Chen Jing Wang MengYing Yang DaPeng Liang Fan An JinYao Zhao WenJun Fan YuJia Pan ZiQian Deng YuanYuan Luo Tao Guo Fei Peng ZhiJie Hou ChunLi Wang FeiMeng Zheng LingZhi Xu Jie Xu QingPing Wen BiLian Jin Yang Wang Quentin Liu | 2022 | Signal Transduction and Targeted Therapy2022，7，5： | 4 |
| 3 | Protection of exendin-4 analogue in early experimental diabetic retinopathy显示文摘 | Yu Zhang Qingping Wang Jingfa Zhang Xia Lei Guo-Tong Xu Wen Ye | 2009 | Graefe’s Archive for Clinical and Experimental Ophthalmology2009，，5： | 1 |
| 4 | Large Curvature Folding Strategies of Butterfly Proboscis显示文摘Due to its real-time control,high folding ratio,and structure self-locking,flexible large curvature self-folding devices have broad application prospects,such as foldable human implants,flexible electronics,and flexible robots.Driven by this background,flexible large curvature folding butterfly(Polyura eudamippus)proboscises were studied in this work.The folding ratio of the proboscises was about 15.The curvature of coiled proboscises ranged from about 150 m_1 to 880 m The external and internal structures of the proboscises were studied by different methods.Three main strategies for large-curvature folding of proboscises were identified:a gradual decrease in thickness,a lower elastic modulus,and(most importantly)large numbers of regular corrugated cracks arranged on the surface.These corrugated cracks can effectively accommodate the coiled strain and provide space for the large curvature folding of proboscises.Finally,a 4D printed coiled sample with corrugated cracks was fabricated to mimic the proboscises stretching process.Large-curvature folding strategies,based on these proboscises,provide insights for the biomimetic design of artificial highly folded components. | Daobing Chen Honglie Song Qingping Liu Jie Gan Yang Liu Keyu Che' Chong Wang Shifeng Wen Yan Zhou Chunze Yan Junqiu Zhang Yusheng Shi Zhiwu Han | 2020 | Journal of Bionic Engineering2020，17，6： | 1 |
| 5 | Protection of exendin-4 analogue in early experimental diabetic retinopathy显示文摘 | Yu Zhang Qingping Wang Jingfa Zhang Xia Lei Guo-Tong Xu Wen Ye | 2009 | Graefe’s Archive for Clinical and Experimental Ophthalmology2009，，5： | 1 |
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