11 research outputs found

    Knockdown of a novel lincRNA AATBC suppresses proliferation and induces apoptosis in bladder cancer

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    Long intergenic noncoding RNAs (lincRNAs) play important roles in regulating various biological processes in cancer, including proliferation and apoptosis. However, the roles of lincRNAs in bladder cancer remain elusive. In this study, we identified a novel lincRNA, which we termed AATBC. We found that AATBC was overexpressed in bladder cancer patient tissues and positively correlated with tumor grade and pT stage. We also found that inhibition of AATBC resulted in cell proliferation arrest through G1 cell cycle mediated by cyclin D1, CDK4, p18 and phosphorylated Rb. In addition, inhibition of AATBC induced cell apoptosis through the intrinsic apoptosis signaling pathway, as evidenced by the activation of caspase-9 and caspase-3. The investigation for the signaling pathway revealed that the apoptosis following AATBC knockdown was mediated by activation of phosphorylated JNK and suppression of NRF2. Furthermore, JNK inhibitor SP600125 could attenuate the apoptotic effect achieved by AATBC knockdown, confirming the involvement of JNK signaling in the induced apoptosis. Moreover, mouse xenograft model revealed that knockdown of AATBC led to suppress tumorigenesis in vivo. Taken together, our study indicated that AATBC might play a critical role in pro-proliferation and anti-apoptosis in bladder cancer by regulating cell cycle, intrinsic apoptosis signaling, JNK signaling and NRF2. AATBC could be a potential therapeutic target and molecular biomarker for bladder cancer

    Functional Supramolecular Gels Based on the Hierarchical Assembly of Porphyrins and Phthalocyanines

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    Supramolecular gels containing porphyrins and phthalocyanines motifs are attracting increased interests in a wide range of research areas. Based on the supramolecular gels systems, porphyrin or phthalocyanines can form assemblies with plentiful nanostructures, dynamic, and stimuli-responsive properties. And these π-conjugated molecular building blocks also afford supramolecular gels with many new features, depending on their photochemical and electrochemical characteristics. As one of the most characteristic models, the supramolecular chirality of these soft matters was investigated. Notably, the application of supramolecular gels containing porphyrins and phthalocyanines has been developed in the field of catalysis, molecular sensing, biological imaging, drug delivery and photodynamic therapy. And some photoelectric devices were also fabricated depending on the gelation of porphyrins or phthalocyanines. This paper presents an overview of the progress achieved in this issue along with some perspectives for further advances

    A Coarse-to-Fine Contour Optimization Network for Extracting Building Instances from High-Resolution Remote Sensing Imagery

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    Building instances extraction is an essential task for surveying and mapping. Challenges still exist in extracting building instances from high-resolution remote sensing imagery mainly because of complex structures, variety of scales, and interconnected buildings. This study proposes a coarse-to-fine contour optimization network to improve the performance of building instance extraction. Specifically, the network contains two special sub-networks: attention-based feature pyramid sub-network (AFPN) and coarse-to-fine contour sub-network. The former sub-network introduces channel attention into each layer of the original feature pyramid network (FPN) to improve the identification of small buildings, and the latter is designed to accurately extract building contours via two cascaded contour optimization learning. Furthermore, the whole network is jointly optimized by multiple losses, that is, a contour loss, a classification loss, a box regression loss and a general mask loss. Experimental results on three challenging building extraction datasets demonstrated that the proposed method outperformed the state-of-the-art methods’ accuracy and quality of building contours
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