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Resveratrol, a phytochemical found in various plants and Chinese herbs, is associated with multiple tumor-suppressing activities, has been tested in clinical trials. However, the molecular mechanisms involved in resveratrol-mediated tumor suppressing activities are not yet completely defined. Here, we showed that treatment with resveratrol inhibited cell mobility through induction of the mesenchymal-epithelial transition (MET) in lung cancer cells. We also found that downregulation of FOXC2 (forkhead box C2) is critical for resveratrol-mediated suppression of tumor metastasis in an in vitro and in vivo models. We also identified a signal cascade, namely, resveratrol-∣miRNA-520h-∣PP2A/C-∣Akt → NF-κB → FOXC2, in which resveratrol inhibited the expression of FOXC2 through regulation of miRNA-520h-mediated signal cascade. This study identified a new miRNA-520h-related signal cascade involved in resveratrol-mediated tumor suppression activity and provide the clinical significances of miR-520h, PP2A/C and FOXC2 in lung cancer patients. Our results indicated a functional link between resveratrol-mediated miRNA-520h regulation and tumor suppressing ability, and provide a new insight into the role of resveratrol-induced molecular and epigenetic regulations in tumor suppression.

Einfach mal blau machen: Die Photolumineszenz in Suspensionen von Graphenoxid (GO) lässt sich von roter zu blauer Emission durchstimmen (siehe Bild), indem man die Anteile von sp2‐ und sp3‐C‐Atomen durch Reduktion der Oxidgruppen auf der Oberfläche schrittweise verändert. Eine Elektron‐Loch‐Rekombination aus zwei Typen angeregter Zustände kann die GO‐Lumineszenz bei unterschiedlichen Reduktionsgraden erklären.

Metrics & MoreArticle Recommendations * sı Supporting Information ABSTRACT: "Spin" has been recently reported as an important degree of electronic freedom to improve the performance of electrocatalysts and photocatalysts. This work demonstrates the manipulations of spin-polarized electrons in CsPbBr 3 halide perovskite nanoplates (NPLs) to boost the photocatalytic CO 2 reduction reaction (CO 2 RR) efficiencies by doping manganese cations (Mn 2+ ) and applying an external magnetic field. Mn-doped CsPbBr 3 (Mn-CsPbBr 3 ) NPLs exhibit an outstanding photocatalytic CO 2 RR compared to pristine CsPbBr 3 NPLs due to creating spinpolarized electrons after Mn doping. Notably, the photocatalytic CO 2 RR of Mn-CsPbBr 3 NPLs is significantly enhanced by applying an external magnetic field. Mn-CsPbBr 3 NPLs exhibit 5.7 times improved performance of photocatalytic CO 2 RR under a magnetic field of 300 mT with a permanent magnet compared to pristine CsPbBr 3 NPLs. The corresponding mechanism is systematically investigated by magnetic circular dichroism spectroscopy, ultrafast transient absorption spectroscopy, and density functional theory simulation. The origin of enhanced photocatalytic CO 2 RR efficiencies of Mn-CsPbBr 3 NPLs is due to the increased number of spin-polarized photoexcited carriers by synergistic doping of the magnetic elements and applying a magnetic field, resulting in prolonged carrier lifetime and suppressed charge recombination. Our result shows that manipulating spin-polarized electrons in photocatalytic semiconductors provides an effective strategy to boost photocatalytic CO 2 RR efficiencies.

We fabricated the defect passivation of perovskite solar cells using CdSe/ZnS quantum dots. The efficient defect passivation of reduces the trap charge density and elongates the charge carrier life time.

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Supporting information for this article, including preparation of FeS 2 nanocrystal ink, fabrication of DSCCs, characterizations, and first-principles calculations on the charge transfer and adsorption energy between I 3 À and the FeS 2 NC surface, is available on the WWW under http://dx.

MicroRNAs (miRNAs) are small RNAs that suppress gene expression by their interaction with 3'untranslated region of specific target mRNAs. Although the dysregulation of miRNAs has been identified in human cancer, only a few of these miRNAs have been functionally documented in breast cancer. Thus, defining the important miRNA and functional target involved in chemoresistance is an urgent need for human breast cancer treatment. In this study, we, for the first time, identified a key role of miRNA 520h (miR-520h) in drug resistance. Through protecting cells from paclitaxel-induced apoptosis, expression of miR-520h promoted the drug resistance of human breast cancer cells. Bioinformatics prediction, compensatory mutation and functional validation further confirmed the essential role of miR-520h-suppressed Death-associated protein kinase 2 (DAPK2) expression, as restoring DAPK2 abolished miR-520h-promoted drug resistance, and knockdown of DAPK2 mitigated cell death caused by the depletion of miR-520h. Furthermore, we observed that higher level of miR-520h is associated with poor prognosis and lymph node metastasis in human breast cancer patients. These results show that miR-520h is not only an independent prognostic factor, but is also a potential functional target for future applications in cancer therapeutics.