MicroRNA-133b suppresses bladder cancer malignancy by targeting TAGLN2-mediated cell cycle.

MicroRNAs (miRNAs), a group of small noncoding RNAs, are widely involved in the regulation of gene expression via binding to complementary sequences at 3'-untranslated regions (3'-UTRs) of target messenger RNAs. Recently, downregulation of miR-133b has been detected in various human malignancies. Here, the potential biological role of miR-133b in bladder cancer (BC) was investigated. In this study, we found the expression of miR-133b was markedly downregulated in BC tissues and cell lines (5637 and T24), and was correlated with poor overall survival. Notably, transgelin 2 (TAGLN2) was found to be widely upregulated in BC, and overexpression of TAGLN2 also significantly increased risks of advanced TMN stage. We further identified that upregulation of miR-133b inhibited glucose uptake, invasion, angiogenesis, colony formation and enhances gemcitabine chemosensitivity in BC cell lines by targeting TAGLN2. Additionally, we showed that miR-133b promoted the proliferation of BC cells, at least partially through a TAGLN2-mediated cell cycle pathway. Our results suggest a novel miR-133b/TAGLN2/cell cycle pathway axis controlling BC progression; a molecular mechanism which may offer a potential therapeutic target.

Natural Dissociation Ratio of Carboxyl Group Controlled Highly Dispersed Silver Nanoparticles on PSA Microspheres and Their Catalytic Performance.

The highly dispersed silver nanoparticle-loaded poly(styrene-co-acrylic acid) nanocomposites (nAg@PSA) were prepared and characterized by transmission electron microscopy and thermogravimetry. The amount and distribution of colloidal silver per particle were related to the dissociation ratio of carboxyl groups in the PSA sphere. The amount of carboxyl groups was evaluated by a conductivity titration curve. However, the dissociation of carboxyl groups on PSA is difficult to determine accurately via existing methods because the dissociation ratio will increase with increasing impurity ions during titration. We developed a technique to determine the dissociation ratio of PSA without impurity ions. This employs a novel distance-variable parallel electrode system. Thus, the relationship between nano silver distribution and natural dissociation of carboxyl groups on the surface of the PSA spheres was investigated for the first time. Accurately measuring and controlling the dissociation facilitated the production of PSA spheres containing highly dispersed silver nanoparticles. The catalytic performance of as-prepared nAg@PSA catalysts was studied by reduction of 4-nitrophenol. By controlling the amount of natural dissociation ratio of carboxyl group on PSA sphere, dispersion of silver nanoparticles can be designed and attained controllably. They offer easy synthesis, high catalytic performance, and good recyclability.

Preparation and Structural Analysis of Nano-Silver Loaded Poly(styrene-co-acrylic acid) Core-Shell Nanospheres with Defined Shape and Composition.

A systematic study for the preparation and structural analysis of poly(styrene-co-acrylic acid) composite nanospheres (PSA) and silver nanoparticles loaded poly(styrene-co-acrylic acid) composite nanospheres (nAg@PSA) is reported. Poly(styrene-co-acrylic acid) nanospheres were synthesized by soap-free emulsion polymerization of styrene (St) and acrylic acid (AA) in water. Ag nanoparticles (Ag-NPs) were well-dispersed on the surfaces of poly(styrene-co-acrylic acid) composite nanospheres by in situ chemical reduction of AgNO3 using NaBH4 as a reducing agent in water. The particle size of PSA nanospheres was uniform. The surfaces of PSA nanospheres were distributed by highly uniform half-sphere arrays. Those half-sphere protruded more with the increase of the feeding amount of AA or the feed ratios of AA and St. The carboxyl groups content of nanospheres was directly proportional to the nanosphere surface area. This relationship and X-ray photoelectron spectroscopy and transmission electron microscopy images of the PSA nanospheres indicate that the acrylic acid was mainly distributed on the surface of the polystyrene spheres with unnegligible thickness. The number of Ag-NPs depends on immobilized carboxyl groups on the surface of PSA, according to thermogravimetry, ultraviolet-visible, X-ray diffraction and transmission electron microscopy results.

Preparation and antibacterial properties of gelatin grafted with an epoxy silicone quaternary ammonium salt.

Gelatin (GE) was modified with epoxy silicone quaternary ammonium salt (EPSiQA) under alkaline conditions (pH 10-11). Silyl and quaternary ammonium groups were linked to gelatin skeleton simultaneously. It was illustrated by XRD and DSC that the short-range order of GE is destroyed and the glass transition temperature (Tg) of GE drops 10 °C after modification. The measured contact angles and surface free energy calculated by Owens-Wendt equation showed that the surface energy of modified gelatin EPSiQA-GE is mainly contributed by the dispersive component of non-polarity silicone groups, the hydrophobility of EPSiQA-GE increases with the increase of grafted silicone units in gelatin. The results of minimum inhibitory concentration indicated that EPSiQA-GE has bactericidal property against Gram-positive bacteria, Gram-negative bacteria and has no antibacterial effect on mold.