PLAGL2 increases adriamycin resistance and EMT in breast cancer cells by activating the Wnt pathway

Li Yuxiao,Liu Ruolin,Han Xingzhao,Xu Wei,Liu Yahui 한국유전학회 2023 Genes & Genomics Vol.45 No.1

Background Adriamycin (ADR) is an effective treatment for breast cancer; nevertheless, it is often linked with acquired resistance in breast cancer cells, reducing ADR’s therapeutic efficacy and increasing the risk of recurrence and poor prognosis. It has been revealed that the zinc-finger transcription factor pleomorphic adenoma gene like-2 (PLAGL2) is required for epithelial to mesenchymal transition (EMT) in cancer cells. Recent data indicates that PLAGL2 is also involved in regulating chemotherapeutic drug resistance, albeit the exact mechanism by which this happens remains unknown. Objective This study examines the effect of PLAGL2 on adriamycin resistance and EMT in breast cancer cells. Methods The small interfering RNA (siRNA) targeting PLAGL2 was transfected to breast cancer cells to alter PLAGL2 expression. Cell counting kit-8 (CCK-8) and colony formation assay detected cell growth and proliferation rate. Moreover, wound-healing and transwell assays were conducted to evaluate migration and invasion. Western blot (WB) checked the apoptosis and EMT-associated proteins. Results PLAGL2 expression is associated with breast cancer cells’ acquired resistance to ADR in this investigation. Additionally, deletion of PLAGL2 was associated with enhanced sensitivity to ADR, reduced proliferation, migration, and invasion capabilities, increased E-cadherin levels, and reduced Wnt6, β-catenin, and DVL1 levels in ADR-resistant breast cancer cells (MCF-7/ADR and MDA-MB-231/ADR cells). PLAGL2 could bind to the promoter region of Wnt6 and promote its expression. Additionally, the results of this research established that Wnt signaling is implicated in breast cancer cells’ resistance to ADR since BML-284, a Wnt signaling activator partly restored the sensitivity of MCF-7/ADR and MDA-MB-231/ADR cells to ADR. Conclusion PLAGL2 promotes adriamycin resistance and cell aggressiveness in breast cancer cells via activating the Wnt signaling pathway.

Reconfigurable DDP-type transmitter coil for electric vehicle wireless charging under misaligned conditions

Wen, Feng,Li, Qiang,Li, Rui,Liu, Ling,Wang, Tao,Liu, Li,Wu, Tao,Li, Yuxiao The Korean Institute of Power Electronics 2020 JOURNAL OF POWER ELECTRONICS Vol.20 No.1

This paper presents a new type of a transmitter coil for wireless power transfer (WPT) to assist in the achievement of a constant output power and in the reduction of magnetic field leakage under misaligned electric vehicle (EV) wireless-charging conditions. The proposed DDP coil is an improvement upon the conventional DD coil and can be adaptively reconfigured depending on the misalignment of different sizes or types of receiver coils. The reconfigurable resonant circuit is designed to compensate various coil structures and to maintain a high-energy efficiency. The reconfiguration strategy is presented by studying the characteristics of the magnetic field and mutual inductance of the coils. A precise human anatomic model and a full-scale Tesla EV model are built to evaluate the magnetic field leakage and human exposure to the WPT system. Simulation results show that the power transfer efficiency (PTE) reaches 99.16% and that the maximum electric field induced in humans is -1.11 dBV/m, while the transfer power is 6.6 kW with a 12 cm lateral offset on both the x-axis and y-axis. The effectiveness of the proposed type of transmitter coil is verified through simulation and experimental results.

Glutamic Acid Decarboxylase Autoantibody Detection by Electrochemiluminescence Assay Identifies Latent Autoimmune Diabetes in Adults with Poor Islet Function

Yuxiao Zhu,Li Qian,Qing Liu,Jing Zou,Ying Zhou,Tao Yang,Gan Huang,Zhiguang Zhou,Yu Liu 대한당뇨병학회 2020 Diabetes and Metabolism Journal Vol.44 No.2

Background: The detection of glutamic acid decarboxylase 65 (GAD65) autoantibodies is essential for the prediction and diagnosis of latent autoimmune diabetes in adults (LADA). The aim of the current study was to compare a newly developed electrochemiluminescence (ECL)-GAD65 antibody assay with the established radiobinding assay, and to explore whether the new assay could be used to define LADA more precisely. Methods: Serum samples were harvested from 141 patients with LADA, 95 with type 1 diabetes mellitus, and 99 with type 2 diabetes mellitus, and tested for GAD65 autoantibodies using both the radiobinding assay and ECL assay. A glutamic acid decarboxylase antibodies (GADA) competition assay was also performed to assess antibody affinity. Furthermore, the clinical features of these patients were compared. Results: Eighty-eight out of 141 serum samples (62.4%) from LADA patients were GAD65 antibody-positive by ECL assay. Compared with ECL-GAD65 antibody-negative patients, ECL-GAD65 antibody-positive patients were leaner (P<0.0001), had poorer β-cell function (P<0.05), and were more likely to have other diabetes-associated autoantibodies. The β-cell function of ECLGAD65 antibody-positive patients was similar to that of type 1 diabetes mellitus patients, whereas ECL-GAD65 antibody-negative patients were more similar to type 2 diabetes mellitus patients. Conclusion: Patients with ECL-GAD65 antibody-negative share a similar phenotype with type 2 diabetes mellitus patients, whereas patients with ECL-GAD65 antibody-positive resemble those with type 1 diabetes mellitus. Thus, the detection of GADA using ECL may help to identify the subtype of LADA.

Differential Profile of Plasma Circular RNAs in Type 1 Diabetes Mellitus

Yangyang Li,Ying Zhou,Minghui Zhao,Jing Zou,Yuxiao Zhu,Xuewen Yuan,Qianqi Liu,Hanqing Cai,Cong-Qiu Chu,Yu Liu 대한당뇨병학회 2020 Diabetes and Metabolism Journal Vol.44 No.6

Background No currently available biomarkers or treatment regimens fully meet therapeutic needs of type 1 diabetes mellitus (T1DM). Circular RNA (circRNA) is a recently identified class of stable noncoding RNA that have been documented as potential biomarkers for various diseases. Our objective was to identify and analyze plasma circRNAs altered in T1DM. Methods We used microarray to screen differentially expressed plasma circRNAs in patients with new onset T1DM (n=3) and age-/gender-matched healthy controls (n=3). Then, we selected six candidates with highest fold-change and validated them by quantitative real-time polymerase chain reaction in independent human cohort samples (n=12). Bioinformatic tools were adopted to predict putative microRNAs (miRNAs) sponged by these validated circRNAs and their downstream messenger RNAs (mRNAs). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed to gain further insights into T1DM pathogenesis. Results We identified 68 differentially expressed circRNAs, with 61 and seven being up- and downregulated respectively. Four of the six selected candidates were successfully validated. Curations of their predicted interacting miRNAs revealed critical roles in inflammation and pathogenesis of autoimmune disorders. Functional relations were visualized by a circRNA-miRNA-mRNA network. GO and KEGG analyses identified multiple inflammation-related processes that could be potentially associated with T1DM pathogenesis, including cytokine-cytokine receptor interaction, inflammatory mediator regulation of transient receptor potential channels and leukocyte activation involved in immune response. Conclusion Our study report, for the first time, a profile of differentially expressed plasma circRNAs in new onset T1DM. Further in silico annotations and bioinformatics analyses supported future application of circRNAs as novel biomarkers of T1DM.

Dynamic model-based back-stepping control design for-trajectory tracking of seabed tracked vehicles

Hong Xiong,Yuxiang Chen,Yuxiao Li,Hong Zhu,Chunliang Yu,Jingguo Zhang 대한기계학회 2022 JOURNAL OF MECHANICAL SCIENCE AND TECHNOLOGY Vol.36 No.8

Tracked vehicles are widely used as seabed production tools to ensure a stable motion on soft sediments. However, the slippage resulted from the complex nonlinear trackterrain interaction while trajectory tracking causes problems for precisely predicting the motion. Accordingly, a “proper” motion control method is necessitated. This work proposes a novel dynamic modeling approach and motion control method for seabed tracked vehicles under nonholonomic constraints, with the inclusion of the effects of the bulldozing resistance, compaction resistance, water resistance, and the direction and velocity of the current. The backstepping control based on a model-based proportional-integral-derivative three degrees-offreedom method is applied in the controller, and its stability is proven by Lyapunov theory. The effectiveness and accuracy of the method in controlling seabed tracked vehicles are validated by simulation examples.

Effects of silyl concentration, hydrogen concentration, ion flux, and silyl surface diffusion length on microcrystalline silicon film growth

Jingxiao Lu,Shutang Wen,Liwei Zhang,Yuxiao Li,Zhiyong Du 한국화학공학회 2008 Korean Journal of Chemical Engineering Vol.25 No.6

Two sets of μc-Si : H films as a function of pressure were fabricated by very-high-frequency plasma enhanced chemical vapor deposition (VHF-PECVD). Deposition rate, Raman crystallinity, and photo/dark conductivity were investigated under both low and high power conditions. A plasma fluid model and a surface hydride-dependent precursor diffusion model were constructed to understand the evolution of microcrystalline silicon under low and high power conditions. Silyl, hydrogen, ion flux, silyl surface diffusion length are believed to have much influence on film growth rate, crystallinity and photo electronic properties. But the interesting point is that under a certain condition one or more of these parameters dominate μc-Si : H growth, while other parameters have weak influence. Short-life radicals are found to be the possible major factor on the deterioration of photo sensitivity of μc-Si : H films.

Enhancement of CO2 desorption using ultrasound and vacuum in water scrubbing biogas upgrading system

Fuqiang Jin,Haipeng Xu,Dongliang Hua,Lei Chen,Yan Li,Yuxiao Zhao,Bin Zuo 한국화학공학회 2021 Korean Journal of Chemical Engineering Vol.38 No.1

Ultrasound and vacuum were respectively employed to enhance CO2 desorption in a water scrubbing biogas upgrading system. Results showed that incomplete CO2 desorption could cause a high CO2 content in the water and seriously affect the purity of the product gas. Vacuum had a strong enhancement effect on CO2 desorption. When a vacuum of 0.04MPa was used to enhance CO2 desorption, the amount of the stripping air could be reduced to 1/16- th of that without enhancement, indicating that vacuum could greatly enhance CO2 desorption and significantly decrease the amount of the stripping air, which was expected to reduce a large amount of energy consumption. In contrast, the enhancement effect of ultrasound was not so obvious for CO2 desorption in the desorption column with air stripping, since the solution could be well desorbed by gas stripping, though ultrasound could strongly affect the static CO2 desorption.

Indole-3-propionic acid inhibits gut dysbiosis and endotoxin leakage to attenuate steatohepatitis in rats

Ze-Hua Zhao,Feng-Zhi Xin,Yaqian Xue,Zhimin Hu,Yamei Han,Fengguang Ma,Da Zhou,Xiao-Lin Liu,Aoyuan Cui,Zhengshuai Liu,Yuxiao Liu,Jing Gao,Qin Pan,Yu Li,Jian-Gao Fan 생화학분자생물학회 2019 Experimental and molecular medicine Vol.51 No.-

Microbial metabolites have emerged as critical components that mediate the metabolic effects of the gut microbiota. Here, we show that indole-3-propionic acid (IPA), a tryptophan metabolite produced by gut bacteria, is a potent anti-non-alcoholic steatohepatitis (NASH) microbial metabolite. Here, we demonstrate that administration of IPA modulates the microbiota composition in the gut and inhibits microbial dysbiosis in rats fed a high-fat diet. IPA induces the expression of tight junction proteins, such as ZO-1 and Occludin, and maintains intestinal epithelium homeostasis, leading to a reduction in plasma endotoxin levels. Interestingly, IPA inhibits NF-κB signaling and reduces the levels of proinflammatory cytokines, such as TNFα, IL-1β, and IL-6, in response to endotoxin in macrophages to repress hepatic inflammation and liver injury. Moreover, IPA is sufficient to inhibit the expression of fibrogenic and collagen genes and attenuate diet-induced NASH phenotypes. The beneficial effects of IPA on the liver are likely mediated through inhibiting the production of endotoxin in the gut. These findings suggest a protective role of IPA in the control of metabolism and uncover the gut microbiome and liver cross-talk in regulating the intestinal microenvironment and liver pathology via a novel dietary nutrient metabolite. IPA may provide a new therapeutic strategy for treating NASH.

Ginkgolic Acid Suppresses Nasopharyngeal Carcinoma Growth by Inducing Apoptosis and Inhibiting AKT/NF-κB Signaling

Yu Xiao,Fen Li,Anyuan Zheng,Qibing Chen,Fuhai Chen,Xiang Cheng,Zezhang Tao 한국식품영양과학회 2021 Journal of medicinal food Vol.24 No.8

Even though nasopharyngeal carcinoma (NPC) is not common worldwide, it is a major public health burden in endemic areas. Distant metastasis often leads to a poor prognosis for NPC; therefore, new and effective anticancer strategies are needed. Ginkgolic acid (GA) is small-molecule compound existing in Ginkgo biloba that has various biologically relevant activities, including antitumor properties; however, its effects and mechanism of action in NPC are unknown. The effects of GA on NPC and such underlying mechanisms were investigated using 5–8F and CNE2 cells and NP69 human immortalized nasopharyngeal epithelial cells in this study. Moreover, the xenograft models were built to examine GA's effection in vivo. GA treatment decreased the survival and invasive capacity of 5–8F and CNE2 and induced their apoptosis, which varied with dose; this was accompanied by downregulation of B cell lymphoma (Bcl)2, upregulation of Bcl2-associated X protein, and activation of poly-ADP ribose polymerase, and caspase-9/-3. G0/G1 phase arrest was induced by GA in NPCs. It also reduced the expression of cyclin-dependent kinase 6 and its regulators cyclin D2 and cyclin D3. GA inhibited the activation of protein kinase B/nuclear factor signaling; this effect was potentiated with GA and 5-fluorouracil (5-FU), which also enhanced 5-FU-induced apoptosis. In summary, GA may be effective as an adjuvant to conventional chemotherapy drugs in preventing the progression of NPC.