Ferroptosis: A New Road towards Cancer Management

Ferroptosis is a recently described programmed cell death mechanism that is characterized by the buildup of iron (Fe)-dependent lipid peroxides in cells and is morphologically, biochemically, and genetically distinct from other forms of cell death, having emerged to play an important role in cancer biology. Ferroptosis has significant importance during cancer treatment because of the combination of factors, including suppression of the glutathione peroxidase 4 (Gpx4), cysteine deficiency, and arachidonoyl (AA) peroxidation, which cause cells to undergo ferroptosis. However, the physiological significance of ferroptosis throughout development is still not fully understood. This current review is focused on the factors and molecular mechanisms with the diagrammatic illustrations of ferroptosis that have a role in the initiation and sensitivity of ferroptosis in various malignancies. This knowledge will open a new road for research in oncology and cancer management.     

A new form of symplectically invariant multimode uncertainty relations

We derive symplectically invariant uncertainty relations for a set of canonically conjugated variables. The uncertainty relations obtained are multimode analogs of the Robertson–Schrödinger inequalities. Our uncertainty relations are equivalent to the necessary and sufficient conditions for a matrix to be a correlation matrix of some quantum state, obtained by R. Simon and coauthors. The advantage of our inequalities, compared to that suggested by Simon, consists in its simplicity and more obvious symplectic invariance. We derive our inequalities for the case of a two-mode system in explicit form. Particular cases of small and large degrees of correlation between the first and second modes are analyzed in detail.     

Extraction of trivalent europium and americium by the synergistic mixture of bis-1,2-dicarbollylcobaltate and N,N,N′,N′-tetraoctyl diglycolamide in highly polar 3-nitro-α,α,α-trifluorotoluene solvent

Journal of Radioanalytical and Nuclear Chemistry - The extraction of trivalent europium and americium in the system water—HNO3—3-nitro-α,α,α-trifluorotoluene...     

Diazoacetonitrile (N2CHCN): A Long Forgotten but Valuable Reagent for Organic Synthesis

Diazoacetonitrile (N₂CHCN) is a small reactive diazoalkane. It has been synthesized for the first time already in 1898 by Theodor Curtius, however, did not gain much recognition in organic synthesis until recently. Only in 2015, after introduction of in situ and flow protocols for the safe generation of diazoacetonitrile, it started gaining popularity. In this minireview, the synthetic properties and applications of this valuable reagent are discussed.     

CASPT2 and CCSD(T) calculations of dipole moments and polarizabilities of acetone in excited states

The acetone molecule is investigated in its ground state and valence ^1,3n-π*, ^1,3π-π*, and ^1,3σ-π* excited states and Rydberg ^1,3n-3s, ^1,3π-3?, ^1,3n-3p_y and ^1,3π-3p_y states using the CASSCF, CASPT2, and CCSD(T) methods. Equilibrium geometries of excited states are obtained and their changes with respect to the ground state are discussed. For most excited states the C_2v symmetry of the ground state is lowered to the C_s symmetry. A series of valence vertical and adiabatic excitation energies is presented along with excitation energies for Rydberg states. The main body of the paper contains Finite-Field Perturbation Theory (FFPT) calculations of electric properties of the vertically as well as geometry relaxed excited states. Dipole moments of valence excited states decrease significantly upon excitation, being about one half of the ground state dipole moment. Polarizabilities usually change upon excitation much less (increase by about 30%) but hyperpolarizabilities are enhanced up to one or two orders of magnitude. The orientation of the dipole moment is reversed in some vertically excited Rydberg states. Properties of the ground and excited states are discussed considering alterations of the electronic structure and shifts in the geometry.     

Simple Concepts

To talk about simple concepts presupposes that the notion of concept has been aptly explicated. I argue that a most adequate explication should abandon the set-theoretical paradigm and use a procedural approach. Such a procedural approach is offered by Tichý´s Transparent Intensional Logic (TIL). Some main notions and principles of TIL are briefly presented, and as a result, concepts are explicated as a kind of abstract procedure. Then it can be shown that simplicity, as applied to concepts, is well definable as a property relative to conceptual systems, each of which is determined by a finite set of simple (‘primitive’) concepts. Refinement as a method of replacing simple concepts by compound concepts is defined.     

Matrix-free interior point method for compressed sensing problems

We consider a class of optimization problems for sparse signal reconstruction which arise in the field of compressed sensing (CS). A plethora of approaches and solvers exist for such problems, for example GPSR, FPC_AS, SPGL1, NestA, $\mathbf{\ell _1\_\ell _s}$ , PDCO to mention a few. CS applications lead to very well conditioned optimization problems and therefore can be solved easily by simple first-order methods. Interior point methods (IPMs) rely on the Newton method hence they use the second-order information. They have numerous advantageous features and one clear drawback: being the second-order approach they need to solve linear equations and this operation has (in the general dense case) an ${\mathcal {O}}(n^3)$ computational complexity. Attempts have been made to specialize IPMs to sparse reconstruction problems and they have led to interesting developments implemented in $\mathbf{\ell _1\_\ell _s}$ and PDCO softwares. We go a few steps further. First, we use the matrix-free IPM, an approach which redesigns IPM to avoid the need to explicitly formulate (and store) the Newton equation systems. Secondly, we exploit the special features of the signal processing matrices within the matrix-free IPM. Two such features are of particular interest: an excellent conditioning of these matrices and the ability to perform inexpensive (low complexity) matrix–vector multiplications with them. Computational experience with large scale one-dimensional signals confirms that the new approach is efficient and offers an attractive alternative to other state-of-the-art solvers.     

Phase behaviour,structural properties and intermolecular interactions of systems based on substituted thiacalix[4]arene and nonionic surfactants

Supramolecular organised materials were prepared from nonionic surfactants and the following macrocyclic ionic liquids: n-tert-butylthiacalix[4]arenes containing quaternary ammonium fragments with amino acid substituents. Tetraethylene glycol monododecyl ether and decadiethylene glycol monododecyl ether were used as nonionic surfactants. They form lamellar and hexagonal mesophases in aqueous media, respectively. Liquid crystal and structural properties of these systems were studied. Intermolecular interactions of system components leading to formation of lyomesophases were estimated. Molecular structure of thiacalixarene contributes to the formation of a hydrogen bonding with surfactants. This process, in turn, initiates formation of a denser packed hexagonal structure.