Endowing cationic surfactant micellar solution with pH, light and temperature triple-response characteristics by introducing 4- (phenylazo)-benzoic acid

Jing Li,Qi Liu,Ruixin Jin,Bolin Yin,Xilian Wei,Dongmei Lv 한국공업화학회 2022 Journal of Industrial and Engineering Chemistry Vol.109 No.-

A practical and smart micelle system with pH, light and temperature responses, prepared using the cationicsurfactant 3-hexadecyloxy-2-hydroxypropyl trimethyl ammonium bromide and 4-(phenylazo)-benzoic acid (ACA) (in its salt form), was developed as a highly promising fluid for applications in differentfields. With increasing the trans-ACA concentration, g0 of the solution increases first and decreasessubsequently, and the maximum was at 17 mM, the micellar structure transform from spherical towormlike micelles, and then to rod morphology. The solution viscosity could be reversibly regulated atpH 4–12 due to the transition of aggregate morphology of self-assembling structure. UV/vis irradiationresulted in a trans to cis photoisomerization of the ACA molecule, and induced the conversion of correspondingwormlike structures into the rodlike micelles. With temperature increase the g0 of solutionpeaks at 28.6 C and it doesn’t follow an Arrhenius law, micellar contour length profile also variesbetween wormlike and rodlike. The regulatory mechanism of the micellar solution under the three stimuliis discussed based on the obtained data. This novel smart system may provide a new theoretical basisfor future applications, opening a new avenue for synthesizing multifunctional aggregates to adapt tovarious environmental changes.

Upregulation of long non-coding RNA XIST has anticancer effects on epithelial ovarian cancer cells through inverse downregulation of hsa-miR-214-3p

Changhong Wang,Shan Qi,Cheng Xie,Chunfu Li,Pu Wang,Dongmei Liu 대한부인종양학회 2018 Journal of Gynecologic Oncology Vol.29 No.6

Objective: The present study is to evaluate the biological functions of long non-coding RNA (lncRNA), X-inactive specific transcript, X-inactive specific transcript (XIST) in human epithelial ovarian cancer (EOC). Methods: XIST was upregulated in EOC cell lines, CAOV3 and OVCAR3 cells by lentiviral transduction. The effects of XIST overexpression on cancer cell proliferation, invasion, chemosensitivity and in vivo tumor growth were investigated, respectively. Possible sponging interaction between XIST and human microRNA hsa-miR-214-3p was further evaluated. Furthermore, hsa-miR-214-3p was overexpressed in XIST-upregulated CAOV3 and OVCAR3 cells to evaluate its effect on XIST-mediated EOC regulation. Results: Lentivirus-mediated XIST upregulation had significant anticancer effects in CAOV3 and OVCAR3 cells by suppressing cancer cell proliferation, invasion, increasing cisplatin chemosensitivity and inhibiting in vivo tumor growth. Hsa-miR-214-3p was confirmed to directly bind XIST, and inversely downregulated in XIST-upregulated EOC cells. In EOC cells with XIST upregulation, secondary lentiviral transduction successfully upregulated hsa-miR-214-3p expression. Subsequently, hsa-miR-214-3p upregulation functionally reversed the anticancer effects of XIST-upregulation in EOC. Conclusion: Upregulation of lncRNA XIST may suppress EOC development, possibly through sponging effect to induce hsa-miR-214-3p downregulation.

Silencing the PIK3CA Gene Enhances the Sensitivity of Childhood Leukemia Cells to Chemotherapy Drugs by Suppressing the Phosphorylation of Akt

Mingde Ding,Xiuling Liang,Xianfang Xin,Dongmei Qi,Chengyan Fu 연세대학교의과대학 2019 Yonsei medical journal Vol.60 No.2

Purpose: This study aimed to investigate the effects of PIK3CA on the sensitivity of acute B lymphocytic leukemia cells (Nalm-6cells) to chemotherapy drugs. Materials and Methods: Children’s normal B lymphocytes and Nalm-6 cells were cultured. Nalm-6 cells were transfected withPIK3CA siRNA (siPIK3CA group) or its negative control (PIK3CA-Control group). Normal Nalm-6 cells were named Mock group. Nalm-6 cells transfected by PIK3CA siRNA were treated with Akt inhibitor (siPIK3CA+Akti-1/2 group). mRNA and protein expressionwas detected by qRT-PCR and Western blot. Proliferation and sensitivity to chemotherapeutic drugs was detected by MTTassay. Cell cycle and apoptosis was explored by low cytometry. Transwell assay was performed to test invasion. Results: PIK3CA mRNA (p=0.008) and protein (p=0.006) expression was higher in Nalm-6 cells than that in normal B lymphocytes. Compared with the Mock group and PIK3CA-Control group, Nalm-6 cells of the siPIK3CA group had lower OD495 values (allp<0.05) and invasion cell numbers (p=0.03 and p=0.025), as well as a higher proportion of G0/G1 phase cells (p=0.020 and p=0.022), percentage of apoptosis (p=0.016 and p=0.022), and inhibition rate (all p<0.05). pAkt expression in the siPIK3CA group (p=0.026 and p=0.031) and siPIK3CA+Akti-1/2 group (p=0.019 and p=0.023) was lower than that in the Mock group. Conclusion: PIK3CA silencing inhibited Nalm-6 cell proliferation and invasion, and promoted their apoptosis and sensitivity tochemotherapeutic drugs, potentially through regulation of the PI3K/AKT signaling pathway.

Ginseng polysaccharides: A potential neuroprotective agent

Na Wang,Xianlei Wang,Mengjiao He,Wenxiu Zheng,Dongmei Qi,Yongqing Zhang,Chun-chao Han 고려인삼학회 2021 Journal of Ginseng Research Vol.45 No.2

The treatments of nervous system diseases (NSDs) have long been difficult issues for researchers because of their complexity of pathogenesis. With the advent of aging society, searching for effective treatments of NSDs has become a hot topic. Ginseng polysaccharides (GP), as the main biologically active substance in ginseng, has various biological properties in immune-regulation, anti-oxidant, anti-inflammation and etc. Considering the association between the effects of GP and the pathogenesis of neurological disorders, many related experiments have been conducted in recent years. In this paper, we reviewed previous studies about the effects and mechanisms of GP on diseases related to nervous system. We found GP play an ameliorative role on NSDs through the regulation of immune system, inflammatory response, oxidative damage and signaling pathway. Structure-activity relationship was also discussed and summarized. In addition, we provided new insights into GP as promising neuroprotective agent for its further development and utilization.

NMAAP1 Expressed in BCG-Activated Macrophage Promotes M1 Macrophage Polarization

Liu, Qihui,Tian, Yuan,Zhao, Xiangfeng,Jing, Haifeng,Xie, Qi,Li, Peng,Li, Dong,Yan, Dongmei,Zhu, Xun Korean Society for Molecular and Cellular Biology 2015 Molecules and cells Vol.38 No.10

Macrophages are divided into two subpopulations: classically activated macrophages (M1) and alternatively activated macrophages (M2). BCG (Bacilli Calmette-$Gu{\acute{e}}rin$) activates disabled $na{\ddot{i}}ve$ macrophages to M1 macrophages, which act as inflammatory, microbicidal and tumoricidal cells through cell-cell contact and/or the release of soluble factors. Various transcription factors and signaling pathways are involved in the regulation of macrophage activation and polarization. We discovered that BCG-activated macrophages (BAM) expressed a new molecule, and we named it Novel Macrophage Activated Associated Protein 1 (NMAAP1). 1 The current study found that the overexpression of NMAAP1 in macrophages results in M1 polarization with increased expression levels of M1 genes, such as inducible nitric oxide synthase (iNOS), tumor necrosis factor alpha (TNF-${\alpha}$), Interleukin 6 (IL-6), Interleukin 12 (IL-12), Monocyte chemoattractant protein-1 (MCP-1) and Interleukin-1 beta (IL-$1{\beta}$), and decreased expression of some M2 genes, such as Kruppel-like factor 4 (KLF4) and suppressor of cytokine signaling 1 (SOCS1), but not other M2 genes, including arginase-1 (Arg-1), Interleukin (IL-10), transforming growth factor beta (TGF-${\beta}$) and found in inflammatory zone 1 (Fizz1). Moreover, NMAAP1 overexpression in the RAW264.7 cell line increased cytotoxicity against MCA207 tumor cells, which depends on increased inflammatory cytokines rather than cell-cell contact. NMAAP1 also substantially enhanced the phagocytic ability of macrophages, which implies that NMAAP1 promoted macrophage adhesive and clearance activities. Our results indicate that NMAAP1 is an essential molecule that modulates macrophages phenotype and plays an important role in macrophage tumoricidal functions.

NMAAP1 Expressed in BCG-Activated Macrophage Promotes M1 Macrophage Polarization

Qihui Liu,Xun Zhu,Yuan Tian,Xiangfeng Zhao,Haifeng Jing,Qi Xie,Peng Li,Dong Li,Dongmei Yan 한국분자세포생물학회 2015 Molecules and cells Vol.38 No.10

Macrophages are divided into two subpopulations: classically activated macrophages (M1) and alternatively activated macrophages (M2). BCG (Bacilli Calmette-Guérin) activates disabled naïve macrophages to M1 macrophages, which act as inflammatory, microbicidal and tumoricidal cells through cell-cell contact and/or the release of soluble factors. Various transcription factors and signaling pathways are involved in the regulation of macrophage activation and polarization. We discovered that BCG-activated macrophages (BAM) expressed a new molecule, and we named it Novel Macrophage Activated Associated Protein 1 (NMAAP1). 1 The current study found that the overexpression of NMAAP1 in macrophages results in M1 polarization with increased expression levels of M1 genes, such as inducible nitric oxide synthase (iNOS), tumor necrosis factor alpha (TNF-α), Interleukin 6 (IL-6), Interleukin 12 (IL-12), Monocyte chemoattractant protein-1 (MCP-1) and Interleukin-1 beta (IL-1β), and decreased expression of some M2 genes, such as Kruppel-like factor 4 (KLF4) and suppressor of cytokine signaling 1 (SOCS1), but not other M2 genes, including arginase-1 (Arg-1), Interleukin (IL-10), transforming growth factor beta (TGF-β) and found in inflammatory zone 1 (Fizz1). Moreover, NMAAP1 overexpression in the RAW264.7 cell line increased cytotoxicity against MCA207 tumor cells, which depends on increased inflammatory cytokines rather than cell-cell contact. NMAAP1 also substantially enhanced the phagocytic ability of macrophages, which implies that NMAAP1 promoted macrophage adhesive and clearance activities. Our results indicate that NMAAP1 is an essential molecule that modulates macrophages phenotype and plays an important role in macrophage tumoricidal functions.