The Bcl-2/xL inhibitor ABT-263 increases the stability of Mcl-1 mRNA and protein in hepatocellular carcinoma cells

Background Hepatocellular carcinoma (HCC) is one of the major causes of mortality. ABT-263 is a newly synthesized, orally available Bcl-2/xL inhibitor that shows promising efficacy in HCC therapy. ABT-263 inhibits the anti-apoptotic activity of Bcl-2 and Bcl-xL, but not Mcl-1. Previous reports have shown that ABT-263 upregulates Mcl-1 in various cancer cells, which contributes to ABT-263 resistance in cancer therapy. However, the associated mechanisms are not well known. Methods Western blot, RNAi and CCK-8 assays were used to investigate the relationship between Mcl-1 upregulation and ABT-263 sensitivity in HCC cells. Real-time PCR and Western blot were used to detect Mcl-1 mRNA and protein levels. Luciferase reporter assay and RNA synthesis inhibition assay were adopted to analyze the mechanism of Mcl-1 mRNA upregulation. Western blot and the inhibition assays for protein synthesis and proteasome were used to explore the mechanisms of ABT-263-enhanced Mcl-1 protein stability. Trypan blue exclusion assay and flow cytometry were used to examine cell death and apoptosis. Results ABT-263 upregulated Mcl-1 mRNA and protein levels in HCC cells, which contributes to ABT-263 resistance. ABT-263 increased the mRNA level of Mcl-1 in HCC cells by enhancing the mRNA stability without influencing its transcription. Furthermore, ABT-263 increased the protein stability of Mcl-1 through promoting ERK- and JNK-induced phosphorylation of Mcl-1Thr163 and increasing the Akt-mediated inactivation of GSK-3β. Additionally, the inhibitors of ERK, JNK or Akt sensitized ABT-263-induced apoptosis in HCC cells. Conclusions ABT-263 increases Mcl-1 stability at both mRNA and protein levels in HCC cells. Inhibition of ERK, JNK or Akt activity sensitizes ABT-263-induced apoptosis. This study may provide novel insights into the Bcl-2-targeted cancer therapeutics.This study was supported in part by Chongqing Natural Science Foundation (cstc2011BB5030 and 2013jjB10015), the National Natural Science Foundation of China (31201068, 81273226 and 81228005) and the Scientific Funds of Third Military Medical University (2011XHG02 and 2012XZH01)

The novel BH-3 mimetic apogossypolone induces Beclin-1- and ROS-mediated autophagy in human hepatocellular carcinoma cells

Apogossypolone (ApoG2), a novel derivative of gossypol, exhibits superior antitumor activity in Bcl-2 transgenic mice, and induces autophagy in several cancer cells. However, the detailed mechanisms are not well known. In the present study, we showed that ApoG2 induced autophagy through Beclin-1- and reactive oxygen species (ROS)-dependent manners in human hepatocellular carcinoma (HCC) cells. Incubating the HCC cell with ApoG2 abrogated the interaction of Beclin-1 and Bcl-2/xL, stimulated ROS generation, increased phosphorylation of ERK and JNK, and HMGB1 translocation from the nucleus to cytoplasm while suppressing mTOR. Moreover, inhibition of the ROS-mediated autophagy by antioxidant N-acetyl-cysteine (NAC) potentiates ApoG2-induced apoptosis and cell killing. Our results show that ApoG2 induced protective autophagy in HCC cells, partly due to ROS generation, suggesting that antioxidant may serve as a potential chemosensitizer to enhance cancer cell death through blocking ApoG2-stimulated autophagy. Our novel insights may facilitate the rational design of clinical trials for Bcl-2-targeted cancer therapy.Grant support: This study was supported in part by Chongqing Natural Science Foundation (CSTC, 2011BB5030), and by the Scientific Funds of Third Military Medical University (2011XHG02)

Simulation of Electrochemical Impedance Spectra of Solid Oxide Fuel Cells Using Transient Physical Models

A general electrochemical impedance spectroscopy ͑EIS͒ modeling approach by directly solving a one-dimensional transient model based on physical conservation laws was applied for simulating EIS spectra of an anode-supported solid oxide fuel cell ͑SOFC͒ button cell consisting of Ni-yttria-stabilized zirconia ͉Ni-scandia-stabilized zirconia ͑ScSZ͉͒ScSZ͉lanthanum strontium manganate ͑LSM͒-ScSZ multiple layers. The transient SOFC model has been solved for imposed sinusoidal voltage perturbations at different frequencies. The results have then been transformed into EIS spectra. Six parameters had to be tuned ͑three for the cathode and three for the anode͒ and have been estimated using data from a symmetric cathode cell and from a button cell. The experimental and simulated EIS spectra were in good agreement for a range of temperatures ͑750-850°C͒, of feed compositions ͑mixture of H 2 /H 2 O/N 2 ͒, and of oxidants ͑air and oxygen͒. This approach can help in interpreting EIS spectra, as illustrated by identifying the contribution of transport limitation. Fuel cell electrochemical systems are usually complex and are governed by coupled physicochemical processes such as chemical and electrochemical reactions, charge transport, and mass transport. 1,2 Because polarization curves can only provide a general description of the cell performance, electrochemical impedance spectroscopy ͑EIS͒ has become widely used in fuel cell research and development because it involves a relatively simple electrical measurement that gives detailed information about the fuel cell system, from mass-transport properties, chemical reaction rates, and dielectric properties to defects, microstructure, compositional influences, etc. 3 In this dynamic technique, usually a voltage perturbation is applied to a system and the amplitude and phase shift of the resulting current response are measured. Measurements can be conducted over a wide range of frequencies, resulting in the construction of impedance spectra. 5 Although the approach is useful and quite powerful, it often has limitations such as: 1. The approach can lead to ambiguities in data interpretations because the equivalent circuits are seldom unique except for only the simplest circuits. An equivalent circuit involving several circuit elements could often be rearranged in various configurations while still yielding the same impedance. 2. Detailed physical and chemical processes in the system cannot be predicted by equivalent-circuit models. For instance, the effects of current distributions and concentration distributions cannot be taken into account when interpreting data from equivalent-circuit models. 3. The measured system could only be approximated by circuit elements when assuming linear response of the system. The impedance is supposed to be independent of the amplitude of the applied signals. However, the electrochemical system could be highly nonlinear, especially for sinusoidal perturbations with high amplitudes. It was suggested that nonlinear EIS ͑NLEIS͒ measurements have several potential advantages. To investigate solid oxide fuel cell ͑SOFC͒ electrode reaction kinetics, Miterdorfer and Gauckler 7-9 used a state-space model ͑SSM͒, which is widely used in control theory for solving complex differential equations. Bieberle and Gauckler 5 studied in depth elementary electrochemical reactions in SOFC anode by both experimental and SSM approaches. To simulate the electrochemical impedance spectra, the models were solved directly through the SSM approach. Bessler 10 presented a computational method for simulating EIS spectra based on transient numerical simulations of the reaction system. The impedance was then calculated in the time domain from the simulated periodic response of the system, maintaining its full nonlinear response. This method has been further validated by detailed modeling studies on SOFC EIS spectra achieved from gas-transport processes. 11 Gewies et al. 12 also applied this method on Ni/yttria-stabilized zirconia ͑YSZ͒ cermet anodes. Zhu and Kee 13 developed a time-accurate model to analyze EIS spectra in anode-supported button cells with internal methane reforming. This model represented significant advantages regarding physical conservation laws, porous media transport within the electrode, and heterogeneous chemistry reactions mechanisms, all of those being solved in the time domain. However, the spatial variations of ion and electron transport throughout the electrode structures were not considered. In this paper, a general approach for EIS spectra simulation is applied by solving a comprehensive set of coupled transient models based on physical conservation laws. This simulation approach is illustrated by considering a transient model of an anode-supported SOFC button cell consisting of Ni-YSZ͉Ni-scandia-stabilized zirconia ͑ScSZ͉͒ScSZ͉LSM-ScSZ multiple layers. The simulation results of the EIS spectra were then compared to the measured EIS spectra under various conditions to prove the validity of both the transient model and the EIS simulation approach. Experimental Testing cell.-The anode-supported SOFC button cell used in this study consisted of a Ni/YSZ anode support layer ͑680 m͒, a Ni/ScSZ anode active interlayer ͑15 m͒, a ScSZ thin-film electrolyte layer ͑20 m͒, and a lanthanum strontium manganate ͑LSM͒/ ScSZ cathode layer ͑15 m͒. 14,1

Multiomics integration reveals the effect of Orexin A on glioblastoma

Objectives: This study involved a multi-omics analysis of glioblastoma (GBM) samples to elaborate the potential mechanism of drug treatment.Methods: The GBM cells treated with or without orexin A were acquired from sequencing analysis. Differentially expressed genes/proteins/metabolites (DEGs/ DEPs/ DEMs) were screened. Next, combination analyses were conducted to investigate the common pathways and correlations between the two groups. Lastly, transcriptome-proteome-metabolome association analysis was carried out to determine the common pathways, and the genes in these pathways were analyzed through Kaplan-Meier (K-M) survival analysis in public databases. Cell and animal experiments were performed to investigate the anti-glioma activity of orexin A.Results: A total of 1,527 DEGs, 52 DEPs, and 153 DEMs were found. Moreover, the combination analyses revealed that 6, 4, and 1 common pathways were present in the transcriptome-proteome, proteome-metabolome, and transcriptome-metabolome, respectively. Certain correlations were observed between the two data sets. Finally, 11 common pathways were discovered in association analysis, and 138 common genes were screened out in these common pathways. Six genes showed significant differences in terms of survival in both TCGA and CGGA. In addition, orexin A inhibited the proliferation, migration, and invasion of glioma in vitro and in vivo.Conclusion: Eleven common KEGG pathways with six common genes were found among different omics participations, revealing the underlying mechanisms in different omics and providing theoretical basis and reference for multi-omics research on drug treatment

Depth map recovery from videos

The depth map of a video is a very important piece of information. Recovering the depth map of a video expands a 2D video into its 3rd dimension, and creates new possibilities, such as, object insertion, conversion to 3D, shallow depth of field simulation. In this work, we introduce our approach of recovering depth maps from a video sequence with a moving camera and moving objects. Our approach isolates moving objects of each frame and estimates the depth of the scene and the moving objects separately. It takes advantage of the fact that the surfaces that belong to the same object share similar optical flow angles, and have smooth optical flow angle gradients, that can be exploited to recover object boundaries, thereby isolating moving objects from the static part of the scene. \\ It recovers the relative depth of the static part of the scene by calculating the likelihood of a pixel belonging to the farthest background using the magnitude of the optical flow and recovered 3D points. It then estimates the depth of moving objects by finding a statistically most likely actual size of the object and converting the actual size to its actual depth. Finally, we reinsert the estimated depth moving object into the estimated depth of the rest of the scene

Synthesis of Bis (2,2,6,6-tetramethyl-4-piperidinyl) Maleate

Abstract: Bis (2,2,6,6-tetramethyl-4-piperidinyl) maleate is a key intermediate for the synthesis of new types of hindered amine light stabilizers (HALS), so new synthetic routes to this compound are desirable. Through an orthogonal design and follow-up single factor experiments optimal reaction conditions were determined for synthesizing bis (2,2,6,6-tetramethyl-4-piperidiny) maleate using dimethyl maleate, 2,2,6,6-tetramethyl-4-piperidinol and zeolite supported tetraisopropyl titanate as catalyst. Under the selected conditions, the reaction rate and the yield are high, the selectivity is good, the catalyst can be recycled, and there are fewer wastes. The product was characterized and quantitatively analyzed by elemental analysis, mass spectrometry, infrared spectroscopy, nuclear magnetic resonance spectroscopy and ion suppression chromatography