N-Myc Downstream-Regulated Gene 2 (NDRG2) as a Novel Tumor Suppressor in Multiple Human Cancers

N-myc downstream-regulated gene 2 (NDRG2) was identified as a novel tumor suppressor gene in regulating the proliferation, differentiation, apoptosis and metastasis of multiple cancer types. Consistent with this finding, we and other groups observed the decreased NDRG2 expression in multiple human cancer cell lines and tumors, including breast cancer, colorectal cancer, and cervical cancer. We identified NDRG2 as a stress sensor for hypoxia, DNA damage stimuli and endoplasmic reticulum stress (ERS). Our recent data showed that NDRG2 could promote the differentiation of colorectal cancer cells. Interestingly, we found that reduced NDRG2 expression was a powerful and independent predictor of poor prognosis of colorectal cancer patients. Furthermore, NDRG2 can inhibit epithelial-mesenchymal transition (EMT) by positively regulating E-cadherin expression. Moreover, NDRG2-deficient mice show spontaneous development of various tumor types, including T-cell lymphomas, providing in vivo evidence that NDRG2 functions as a tumor suppressor gene. We believe that NDRG2 is a novel tumor suppressor and might be a therapeutic target for cancer treatment

Dual encoding for abstractive text summarization

Recurrent Neural Network (RNN) based sequence-to-sequence attentional models have proven effective in abstractive text summarization. In this paper, we model abstractive text summarization using a dual encoding model. Different from the previous works only using a single encoder, the proposed method employs a dual encoder including the primary and the secondary encoders. Specifically, the primary encoder conducts coarse encoding in a regular way, while the secondary encoder models the importance of words and generates more fine encoding based on the input raw text and the previously generated output text summarization. The two level encodings are combined and fed into the decoder to generate more diverse summary that can decrease repetition phenomenon for long sequence generation. The experimental results on two challenging datasets (i.e., CNN/DailyMail and DUC 2004) demonstrate that our dual encoding model performs against existing methods

Preparation and Photocatalytic Performance of Ti 3

Ti3C2/TiO2/CuO nanocomposites were synthesized via the decomposition of a mixture of Ti3C2 (a novel two-dimensional carbide) and cupric nitrate under an argon atmosphere. The morphology and structures of the obtained samples were characterized. X-ray diffraction and energy dispersive spectrometer analysis indicate that the sample is composed of Ti3C2, anatase-TiO2, and CuO. Scanning electron microscopy images show that CuO and TiO2 nanoparticles were evenly distributed on the surface of Ti3C2. The particles size increased with an increase in the cupric nitrate content. Photocatalytic degradation of methyl orange shows that the Ti3C2/TiO2/CuO nanocomposite has good photocatalytic degradation efficiency. A possible photocatalytic mechanism of the Ti3C2/TiO2/CuO nanocomposites was proposed. The data indicated that CuO and Ti3C2 effectively promote the separation of photoelectrons from vacancies

The enhancement of electrochemical capacitance of biomass-carbon by pyrolysis of extracted nanofibers

Biomass-derived carbons have been extensively researched as electrode material for energy storage and conversion recently. However, most of the previous works convert crude biomass directly into carbon and the electrochemical capacitances for the resultant carbons are quite often underestimated as well as large variations in capacitances exist in literatures due to the complex nature of biomass, which practically hinder their applications. In this work, polysaccharide nanofibers were extracted from an inexpensive natural fungus using a hydrothermal method and were converted to porous carbon nanofibers (CNFs) by potassium hydroxide activation. The porous carbons were assembled into symmetric supercapacitors using both potassium hydroxide and an ionic liquid (IL) as electrolytes. Solid state nuclear magnetic resonance characterization showed that the micropores of the as-prepared carbons are accessible to the IL electrolyte when uncharged and thus high capacitance is expected. It is found in both electrolytes the electrochemical capacitances of CNFs are significantly higher than those of the porous carbon derived directly from the crude fungus. Furthermore, the CNFs delivered an extraordinary energy density of 92.3 Wh kg−1 in the IL electrolyte, making it a promising candidate for electrode materials for supercapacitors.<br/

Overexpression of N-Myc Downstream-Regulated Gene 2 (NDRG2) Regulates the Proliferation and Invasion of Bladder Cancer Cells In Vitro and In Vivo

N-Myc downstream-regulated gene 2 (NDRG2) is a candidate tumor suppressor gene, which plays an important role in controlling tumor growth. The aim of this study was to investigate the expression of NDRG2 gene in bladder cancer (BC) tissues and several bladder cancer cell lines, and to seek its clinical and pathological significance. Ninety-seven bladder carcinoma and 15 normal bladder tissue sections were analyzed retrospectively with immunohistochemistry. The human bladder cancer cell line T24 was infected with LEN-NDRG2 or LEN-LacZ. The effects of NDRG2 overexpression on T24 cells and T24 nude mouse xenografts were measured via cell growth curves, tumor growth curves, flow cytometric analysis, western blot and Transwell assay. NDRG2 was highly expressed in normal bladder tissue, but absent or rarely expressed in cacinomatous tissues (χ2=8.761, p < 0.01). The NDRG2 level was negatively correlated with tumor grade and pathologic stage(r=-0.248, p < 0.05), as well as increased c-myc level (r=-0.454, p< 0.001). The expression of NDRG2 was low in the three BC cell lines. T24 cells infected with LEN-NDRG2 showed inhibition of proliferation both in vitro and in vivo, and NDRG2 overexpression can inhibit tumor growth and invasion in vitro

Ndrg2 regulates vertebral specification in differentiating somites

AbstractIt is generally thought that vertebral patterning and identity are globally determined prior to somite formation. Relatively little is known about the regulators of vertebral specification after somite segmentation. Here, we demonstrated that Ndrg2, a tumor suppressor gene, was dynamically expressed in the presomitic mesoderm (PSM) and at early stage of differentiating somites. Loss of Ndrg2 in mice resulted in vertebral homeotic transformations in thoracic/lumbar and lumbar/sacral transitional regions in a dose-dependent manner. Interestingly, the inactivation of Ndrg2 in osteoblasts or chondrocytes caused defects resembling those observed in Ndrg2−/− mice, with a lower penetrance. In addition, forced overexpression of Ndrg2 in osteoblasts or chondrocytes also conferred vertebral defects, which were distinct from those in Ndrg2−/− mice. These genetic analyses revealed that Ndrg2 modulates vertebral identity in segmented somites rather than in the PSM. At the molecular level, combinatory alterations of the amount of Hoxc8-11 gene transcripts were detected in the differentiating somites of Ndrg2−/− embryos, which may partially account for the vertebral defects in Ndrg2 mutants. Nevertheless, Bmp/Smad signaling activity was elevated in the differentiating somites of Ndrg2−/− embryos. Collectively, our findings unveiled Ndrg2 as a novel regulator of vertebral specification in differentiating somites

Potential-Mediated Recycling of Copper From Brackish Water by an Electrochemical Copper Pump.

Copper ions (Cu2+ ) disposed to the environment at massive scale pose severe threat to human health and waste of resource. Electrochemical deionization (EDI) which captures ions by electrical field is a promising technique for water purification. However, the removal capacity and selectivity toward Cu2+ are unsatisfying, yet the recycling of the captured copper in EDI systems is yet to be explored. Herein, an efficient electrochemical copper pump (ECP) that can deliver Cu2+ from dilute brackish water into much more concentrated solutions is constructed using carbon nanosheets for the first time, which works based on reversible electrosorption and electrodeposition. The trade-off between the removal capacity and reversibility is mediated by the operation voltage. The ECP exhibits a removal capacity of 702.5 mg g-1 toward Cu2+ and a high selectivity coefficient of 64 for Cu2+ /Na+ in the presence of multiple cations; both are the highest reported to date. The energy consumption of 1.79 Wh g-1 is among the lowest for EDI of copper. More importantly, the Cu species captured can be released into a 20-fold higher concentrated solution. Such a high performance is attributed to the optimal potential distribution between the two electrodes that allows reversible electrodeposition and efficient electrosorption

NDRG2 Ameliorates Hepatic Fibrosis by Inhibiting the TGF-β1/Smad Pathway and Altering the MMP2/TIMP2 Ratio in Rats

Liver fibrosis is a worldwide clinical issue. It has been well established that activated hepatic stellate cells (HSCs) are responsible for excessive extracellular matrix (ECM) deposition in chronically damaged livers. The identification of key elements that control HSCs activation will help to further our understanding of liver fibrosis and improve the outcome of clinical treatment. This study demonstrates that N-Myc downstream-regulated gene 2 (NDRG2) is a potential regulator of liver fibrosis as NDRG2 mRNA and protein levels were reduced during HSCs activation. In addition, enhanced NDRG2 expression reduced Smad3 transcription and phosphorylation, which inhibited HSCs activation by blocking the TGF-β1 signal. Moreover, NDRG2 contributed to an increase in the ratio of matrix metalloproteinase 2 (MMP2) to tissue inhibitor of matrix metalloproteinase 2 (TIMP2), which may facilitate the degradation of the ECM. In dimethylnitrosamine (DMN)-induced fibrotic rat livers, adenovirus-mediated NDRG2 overexpression resulted in decreased ECM deposition and improved liver function compared with controls. In conclusion, the present findings indicate that the modulation of NDRG2 is a promising strategy for the treatment of liver fibrosis