The role of chromatin modulator DPY30 in glucose metabolism of colorectal cancer cells.

Background: Colorectal cancer (CRC) is the third most common cancer worldwide and the second leading cause of cancer-related death. This study investigated the role of DPY30 in the development and progression of CRC cells, especially in the area of cellular glycolysis.

Methods: HT29 control cells and DPY30 knockdown cells were collected for tandem mass tag (TMT) labeling quantitative proteomics analysis of cellular total proteins (n=3).

Degradable FeO-based nanocomposite for cascade reaction-enhanced anti-tumor therapy.

Cascade catalytic therapy has been recognized as a promising cancer treatment strategy, which is due in part to the induced tumor apoptosis when converting intratumoral hydrogen peroxide (HO) into highly toxic hydroxyl radicals (˙OH) based on the Fenton or Fenton-like reactions. Moreover this is driven by the efficient catalysis of glucose oxidization associated with starving therapy. The natural glucose oxidase (GO ), recognized as a "star" enzyme catalyst involved in cancer treatment, can specially and efficiently catalyze the glucose oxidization into gluconic acid and HO.

A novel peptide specifically targeting ovarian cancer identified by in vivo phage display.

Discovery of peptide ligands that can target human ovarian cancer and deliver chemotherapeutics offers new opportunity for cancer therapy. The advent of phage-displayed peptide library facilitated the screening of such peptides. In vivo screening that set in a microanatomic and functional context was applied in our study, and a novel peptide WSGPGVWGASVK targeting ovarian cancer was isolated.

A specific cell-penetrating peptide induces apoptosis in SKOV3 cells by down-regulation of Bcl-2.

Peptides are emerging as pharmaceutical agents in cancer therapy. The peptide, TLSGAFELSRDK (TLS) is a targeting ligand that can specifically triggers cellular uptake by binding to SKOV3 cells. Cell surface proteins and the C-terminal basic residues of the TLS are required for effective cell penetration, and the uptake process is energy-dependent.

Cellular compatibility of biomineralized ZnO nanoparticles based on prokaryotic and eukaryotic systems.

Zinc oxide nanoparticles (NPs) with the size of ∼100 nm were prepared via a facile biomineralization process in the template of silk fibroin (SF) peptide at room temperature. These ZnO NPs have shown the remarkable behavior of low toxicity to gram-positive bacteria (Staphylococcus aureus, Staphylococcus agalactiae), gram-negative bacteria (Escherichia coli), and eukaryotic cells (mouse L929 fibroblasts). Bacteriological testing indicated that ZnO NPs presented a 50% inhibitory effect on Streptococcus agalactiae at the concentrations of >100 mM, whereas at the same concentrations, the growth of Staphylococcus aureus and Escherichia coli were hardly inhibited.

Preparation, characterization, in vitro bioactivity, and osteoblast adhesion of multi-level porous titania layer on titanium by two-step anodization treatment.

To combine the advantages of different electrolytes in anodic oxidation, pure titanium samples were anodized in CH(3) COOH electrolyte according to a novel anodizing treatment regime and then in H(2) SO(4) electrolyte in potentialstatic mode. The in vitro bioactivity of the as-prepared titanium samples was evaluated by simulated body fluid (SBF) test. In addition, MG63 osteoblast-like cells were cultured on surfaces of the as-prepared titanium samples to evaluate osteoblast adhesion ability.

In vitro screening of ovarian tumor specific peptides from a phage display peptide library.

To develop more biomarkers for diagnosis and therapy of ovarian cancer, a 12-mer phage display library was used to isolate peptides that bound specifically to the human ovarian tumor cell line SK-OV-3. After five rounds of in vitro screening, the recovery rate of phages showed a 69-fold increase over the first round of washings and a group of phage clones capable of binding to SK-OV-3 cells were obtained. A phage clone named Z1 with high affinity and specificity to SK-OV-3 cells was identified in vitro.

Structure, morphology and fibroblasts adhesion of surface-porous titanium via anodic oxidation.

Surface-porous titanium samples were prepared by anodic oxidation in H(2)SO(4), H(3)PO(4) and CH(3)COOH electrolytes under various electrochemical conditions. X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX) were employed to characterize the structure, morphology and chemical composition of the surface layer, respectively. Closer analysis on the effect of the electrochemical conditions on pore configuration was involved.

Biomineralization of uniform gallium oxide rods with cellular compatibility.

Monodispersed single crystalline alpha-GaOOH rods coated by silk fibroin (SF) have been prepared via a facile biomineralization process in the template of SF peptide. The carbon-coated alpha-Ga(2)O(3) and beta-Ga(2)O(3) rods are obtained by thermal treatment of the alpha-GaOOH rods at 600 and 800 degrees C, respectively. In vitro cytotoxicity studies of these gallium oxide rods showed no significant effect leading to restraint of cell proliferation of L929, Hela, and HaCat cells in less than 0.

Characterization and bacterial response of zinc oxide particles prepared by a biomineralization process.

In this paper, olive-like ZnO particles were successfully synthesized via a facile biomineralization process in the template of silk fibroin (SF) peptide at room temperature. The coat of SF peptide on the surface of ZnO particles had a substantial influence on their morphology during the biomineralization. Room-temperature photoluminescence behavior of ZnO particles indicated that the visible blue emission peak centered at 410 nm was enhanced with the mineralization time.

Preparation and characterization of the biomineralized zinc oxide particles in spider silk peptides.

In this work, hierarchical ZnO particles were prepared using a biomineralization strategy at room temperature in the presence of peptides acidified from spider silk proteins. A mechanism of the mineralization of the ZnO particles was that the affinity of original ZnO nanoparticles and zinc ions in the peptide chains played an important role in controlling the biocrystallizing formation of the pore ZnO particles. The intensity of their visible green luminescence was enhanced with increases of the mineralization time due to the porous surface defects.

Toxicological effect of ZnO nanoparticles based on bacteria.

Streptococcus agalactiae and Staphylococcus aureus are two pathogenetic agents of several infective diseases in humans. Biocidal effects and cellular internalization of ZnO nanoparticles (NPs) on two bacteria are reported, and ZnO NPs have a good bacteriostasis effect. ZnO NPs were synthesized in the EG aqueous system through the hydrolysis of ionic Zn2+ salts.