Mechanism of Pterostilbene-Induced Cell Death in HT-29 Colon Cancer Cells

Pterostilbene is a dietary phytochemical that has been found to possess several biological activities, such as antioxidant and anti-inflammatory. Recent studies have shown that it exhibits the hallmark characteristics of an anticancer agent. The aim of the study was to investigate the anticancer activity of pterostilbene against HT-29 human colon cancer cells, focusing on its influence on cell growth, differentiation, and the ability of this stilbene to induce cell death. To clarify the mechanism of pterostilbene activity against colon cancer cells, changes in the expression of several genes and proteins that are directly related to cell proliferation, signal transduction pathways, apoptosis, and autophagy were also evaluated. Cell growth and proliferation of cells exposed to pterostilbene (5–100 µM) were determined by SRB and BRDU assays. Flow cytometric analyses were used for cell cycle progression. Further molecular investigations were performed using quantitative real-time RT-PCR. The expression of the signaling proteins studied was determined by the ELISA method. The results revealed that pterostilbene inhibited proliferation and induced the death of HT-29 colon cancer cells. Pterostilbene, depending on concentration, caused inhibition of proliferation, G1 cell arrest, and/or triggered apoptosis in HT-29 cells. These effects were mediated by the down-regulation of the STAT3 and AKT kinase pathways. It may be concluded that pterostilbene could be considered as a potential therapeutic option in the treatment of colon cancer in the future.     

Dielectron widths of the Gamma(1S,2S,3S) resonances

We determine the dielectron widths of the Gamma(1S), Gamma(2S), and Gamma(3S) resonances with better than 2% precision by integrating the cross section of e+e- -->Gamma over the e+e- center-of-mass energy. Using e+e- energy scans of the Gamma resonances at the Cornell Electron Storage Ring and measuring Gamma production with the CLEO detector, we find dielectron widths of 1.252+/-0.004(sigma(stat))+/-0.019(sigma(syst)) keV, 0.581+/-0.004+/-0.009 keV, and 0.413+/-0.004+/-0.006 keV for the Gamma(1S), Gamma(2S), and Gamma(3S), respectively.     

Reconstructing the electron in a fractionalized quantum fluid

The low-energy physics of the fractional Hall liquid is described in terms of quasiparticles that are qualitatively distinct from electrons. We show, however, that a long-lived electronlike quasiparticle also exists in the excitation spectrum: the state obtained by the application of an electron creation operator to a fractional quantum Hall ground state has a nonzero overlap with a complex, high energy bound state containing an odd number of composite-fermion quasiparticles. The electron annihilation operator similarly couples to a bound complex of composite-fermion holes. We predict that these bound states can be observed through a conductance resonance in experiments involving a tunneling of an external electron into the fractional quantum Hall liquid. A comment is made on the origin of the breakdown of the Fermi liquid paradigm in the fractional Hall liquid.     

Evidence for the decay D0-->K(-)pi(+)pi(-)e(+)nu(e)

Using a 281 pb{-1} data sample collected at the psi(3770) with the CLEO-c detector, we present the first absolute branching fraction measurement of the decay D0-->K(-)pi(+)pi(-)e(+)nu(e) at a statistical significance of about 4.0 standard deviations. We find 10 candidates consistent with the decay D0-->K(-)pi(+)pi(-)e(+)nu(e). The probability that a background fluctuation accounts for this signal is less than 4.1 x 10{-5}. We find B(D0-->K(-)pi(+)pi(-)e(+)nu(e)) = [2.8{-1.1}{+1.4}(stat)+/-0.3(syst)]x10{-4}. By restricting the invariant mass of the hadronic system to be consistent with K1(1270), we obtain the product of branching fractions B(D{0}-->K{1}{-}(1270)e{+}nu{e})xB(K1-(1270)-->K{-}pi{+}pi{-})=[2.5{-1.0}{+1.3}(stat)+/-0.2(syst)]x10{-4}. Using B(K1-(1270)-->K{-}pi{+}pi{-})=(33+/-3)%, we obtain B(D{0}-->K{1}{-}(1270)e{+}nu{e})=[7.6{-3.0}{+4.1}(stat)+/-0.6(syst)+/-0.7]x10{-4}. The last error accounts for the uncertainties in the measured K1-(1270)-->K{-}pi{+}pi{-} branching fractions.     

Geometric programming with signomials

The difference of twoposynomials (namely, polynomials with arbitrary real exponents, but positive coefficients and positive independent variables) is termed asignomial.Each signomial program (in which a signomial is to be either minimized or maximized subject to signomial constraints) is transformed into an equivalent posynomial program in which a posynomial is to be minimized subject only to inequality posynomial constraints. The resulting class of posynomial programs is substantially larger than the class of (prototype)geometric programs (namely, posynomial programs in which a posynomial is to be minimized subject only to upper-bound inequality posynomial constraints). However, much of the (prototype) geometric programming theory is generalized by studying theequilibrium solutions to thereversed geometric programs in this larger class. Actually, some of this theory is new even when specialized to the class of prototype geometric programs. On the other hand, all of it can indirectly, but easily, be applied to the much larger class of well-posedalgebraic programs (namely, programs involving real-valued functions that are generated solely by addition, subtraction, multiplication, division, and the extraction of roots).This research was partially supported by Research Grant No. DA-AROD-31-124-6680 from the Army Research Office, Durham, North Carolina, and by a Summer Fellowship Grant from Northwestern University.     

The complementary unboundedness of dual feasible solution sets in convex programming

F.E. Clark has shown that if at least one of the feasible solution sets for a pair of dual linear programming problems is nonempty then at least one of them is both nonempty and unbounded. Subsequently, M. Avriel and A.C. Williams have obtained the same result in the more general context of (prototype posynomial) geometric programming. In this paper we show that the same result is actually false in the even more general context of convex programming — unless a certain regularity condition is satisfied.We also show that the regularity condition is so weak that it is automatically satisfied in linear programming (prototype posynomial) geometric programming, quadratic programming (with either linear or quadratic constraints),l _p -regression analysis, optimal location, roadway network analysis, and chemical equilibrium analysis. Moreover, we develop an equivalent regularity condition for each of the usual formulations of duality.Research sponsored by the Air Force Office of Scientific Research, Air Force Systems Command, USAF, under Grant Number AFOSR-73-2516.     

Synthesis of Dialkyl 5-Amino-2-hydroxy-4,6-dimethylisophthalates and Their Sulfonylation

Russian Journal of Organic Chemistry - Dimethyl 5-amino-2-hydroxy-4,6-dimethylisophthalate and dimethyl 5-amino-2-hydroxy-4,6-dimethylisophthalate were obtained in the free form for the first time....     

Heterotrimetallic Mixed-Valent Molecular Precursors Containing Periodic Table Neighbors: Assignment of Metal Positions and Oxidation States

A known trinuclear structure was used to design the heterobimetallic mixed-valent, mixed-ligand molecule [Co^II(hfac)₃−Na−Co^III(acac)₃] ( 1 ). This was used as a template structure to develop heterotrimetallic molecules [Co^II(hfac)₃−Na−Fe^III(acac)₃] ( 2 ) and [Ni^II(hfac)₃−Na−Co^III(acac)₃] ( 3 ) via isovalent site-specific substitution at either of the cobalt positions. Diffraction methods, synchrotron resonant diffraction, and multiple-wavelength anomalous diffraction were applied beyond simple structural investigation to provide an unambiguous assignment of the positions and oxidation states for the periodic table neighbors in the heterometallic assemblies. Molecules of 2 and 3 are true heterotrimetallic rather than a statistical mixture of two heterobimetallic counterparts. Trinuclear platform 1 exhibits flexibility in accommodating a variety of di- and trivalent metals, which can be further utilized in the design of molecular precursors for the NaMM′O₄ functional oxide materials.