Two Main Cancer Biomarkers as Molecular Targets of Binase Antitumor Activity.

Cancer is frequently coupled with the disturbance of key signaling pathways. Aberrant activation of the mitogen-activated protein kinase (MAPK) signaling cascade, occurring in over 85% of cancers, is mainly caused by the genetic alterations of its main components-oncogenes EGFR and RAS, and plays a crucial role in cell fate. The importance of EGFR and RAS proteins in a variety of tumors suggests that they would be good therapeutic targets, but at present, no effective targeted therapy against these two oncogenes has been proven.

[Efficiency of Escherichia coli and Bacillus subtilis Expression Systems for Production of Binase Mutants].

Bacillus pumilus ribonuclease (binase) exhibits cytotoxic and oncolytic properties, while causing genotoxic effects at high concentrations. Mutants that have reduced catalytic activity and preserve the antitumor properties of the native enzyme could exert lower toxic side effects. Mutant binase forms with the Lys26Ala and His101Glu single substitutions were obtained by site-directed mutagenesis.

On the effectiveness of random walks for modeling epidemics on networks.

Random walks on graphs are often used to analyse and predict epidemic spreads and to investigate possible control actions to mitigate them. In this study, we first show that models based on random walks with a single stochastic agent (such as Google's popular PageRank) may provide a poor description of certain features of epidemic spread: most notably, spreading times. Then, we discuss another Markov chain based method that does reflect the correct mean infection times for the disease to spread between individuals in a network, and we determine a procedure that allows one to compute them efficiently via a sampling strategy.

Structural and Functional Differences between Homologous Bacterial Ribonucleases.

Small cationic guanyl-preferring ribonucleases (RNases) produced by the species share a similar protein tertiary structure with a high degree of amino acid sequence conservation. However, they form dimers that differ in conformation and stability. Here, we have addressed the issues (1) whether the homologous RNases also have distinctions in catalytic activity towards different RNA substrates and interactions with the inhibitor protein barstar, and (2) whether these differences correlate with structural features of the proteins.

The Cytotoxicity of RNase-Derived Peptides.

Bacterial ribonuclease binase exhibits a cytotoxic effect on tumor cells possessing certain oncogenes. The aim of this study was to identify the structural parts of the binase molecule that exert cytotoxicity. Out of five designed peptides, the peptides representing the binase regions 21-50 and 74-94 have the highest cytotoxic potential toward human cervical HeLa and breast BT-20 and MCF-7 cancer cells.