Quantitative Ultrasound Spectroscopic Imaging for Characterization of Disease Extent in Prostate Cancer Patients

Three-dimensional quantitative ultrasound spectroscopic imaging of prostate was investigated clinically for the noninvasive detection and extent characterization of disease in cancer patients and compared to whole-mount, whole-gland histopathology of radical prostatectomy specimens. Fifteen patients with prostate cancer underwent a volumetric transrectal ultrasound scan before radical prostatectomy. Conventional-frequency (~ 5 MHz) ultrasound images and radiofrequency data were collected from patients. Normalized power spectra were used as the basis of quantitative ultrasound spectroscopy. Specifically, color-coded parametric maps of 0-MHz intercept, midband fit, and spectral slope were computed and used to characterize prostate tissue in ultrasound images. Areas of cancer were identified in whole-mount histopathology specimens, and disease extent was correlated to that estimated from quantitative ultrasound parametric images. Midband fit and 0-MHz intercept parameters were found to be best associated with the presence of disease as located on histopathology whole-mount sections. Obtained results indicated a correlation between disease extent estimated noninvasively based on midband fit parametric images and that identified histopathologically on prostatectomy specimens, with an r² value of 0.71 (P < .0001). The 0-MHz intercept parameter demonstrated a lower level of correlation with histopathology. Spectral slope parametric maps offered no discrimination of disease. Multiple regression analysis produced a hybrid disease characterization model (r² = 0.764, P < .05), implying that the midband fit biomarker had the greatest correlation with the histopathologic extent of disease. This work demonstrates that quantitative ultrasound spectroscopic imaging can be used for detecting prostate cancer and characterizing disease extent noninvasively, with corresponding gross three-dimensional histopathologic correlation.     

Tetanus toxin selectively impairs anti-tumoral but not anti-microbial macrophage-mediated effector functions

Abstract The present study was designed to establish the susceptibility of macrophage-mediated effector functions to tetanus toxin (TT). Using the murine macrophage cell line, GG2EE, generated in vitro by v- raf /v- myc oncogenes, we have previously provided evidence that TT selectively inhibits interferon gamma (IFN-γ), but not basal, lysozyme activity. Here we show that while neither phagocytic nor candidacidal activities are affected by TT treatment, antitumoral activity is significantly impaired after exposure to TT. This phenomenon, which is dose-dependent, is fully ascribed to the holotoxin, as heat inactivated TT, C or A-B fragments result ineffective. Furthermore, C but not A-B fragment competes with TT in abrogating its inhibitory effects. Overall, these data indicate that TT is not a broad-spectrum, down-regulating signal on macrophage-mediated functions, thus implying that its toxic action is exerted on specific molecular targets.     

SNUAGE: an efficient platform-as-a-service security framework for the cloud

In this paper we present SNUAGE, a platform-as-a-service security framework for building secure and scalable multi-layered services based on the cloud computing model. SNUAGE ensures the authenticity, integrity, and confidentiality of data communication over the network links by creating a set of security associations between the data-bound components on the presentation layer and their respective data sources on the data persistence layer. SNUAGE encapsulates the security procedures, policies, and mechanisms in these security associations at the service development stage to form a collection of isolated and protected security domains. The secure communication among the entities in one security domain is governed and controlled by a standalone security processor and policy attached to this domain. This results into: (1) a safer data delivery mechanism that prevents security vulnerabilities in one domain from spreading to the other domains and controls the inter-domain information flow to protect the privacy of network data, (2) a reusable security framework that can be employed in existing platform-as-a-service environments and across diverse cloud computing service models, and (3) an increase in productivity and delivery of reliable and secure cloud computing services supported by a transparent programming model that relieves application developers from the intricate details of security programming. Last but not least, SNUAGE contributes to a major enhancement in the energy consumption and performance of supported cloud services by providing a suitable execution container in its protected security domains for a wide suite of energy- and performance-efficient cryptographic constructs such as those adopted by policy-driven and content-based security protocols. An energy analysis of the system shows, via real energy measurements, major savings in energy consumption on the consumer devices as well as on the cloud servers. Moreover, a sample implementation of the presented security framework is developed using Java and deployed and tested in a real cloud computing infrastructure using the Google App Engine service platform. Performance benchmarks show that the proposed framework provides a significant throughput enhancement compared to traditional network security protocols such as the Secure Sockets Layer and the Transport Layer Security protocols.     

Thermal Unfolding Pathway of PHD2 Catalytic Domain in Three Different PHD2 Species: Computational Approaches

Prolyl hydroxylase domain 2 containing protein (PHD2) is a key protein in regulation of angiogenesis and metastasis. In normoxic condition, PHD2 triggers the degradation of hypoxia-inducible factor 1 (HIF-1α) that induces the expression of hypoxia response genes. Therefore the correct function of PHD2 would inhibit angiogenesis and consequent metastasis of tumor cells in normoxic condition. PHD2 mutations were reported in some common cancers. However, high levels of HIF-1α protein were observed even in normoxic metastatic tumors with normal expression of wild type PHD2. PHD2 malfunctions due to protein misfolding may be the underlying reason of metastasis and invasion in such cases. In this study, we scrutinize the unfolding pathways of the PHD2 catalytic domain’s possible species and demonstrate the properties of their unfolding states by computational approaches. Our study introduces the possibility of aggregation disaster for the prominent species of PHD2 during its partial unfolding. This may justify PHD2 inability to regulate HIF-1α level in some normoxic tumor types.     

Age-stage,two-sex life table of the tomato looper,Chrysodeixis chalcites (Lepidoptera: Noctuidae), on different bean cultivars

The tomato looper, Chrysodeixis chalcites (Esper), is one of the polyphagous pests of several economically crops worldwide. Two-sex life table parameters of C. chalcites reared on eight bean cultivars including white kidney bean (cultivars Daneshkadeh and Dehghan), red kidney bean (cultivars Goli and Naz), common bean (cultivars Khomein, Talash and Sadra) and cowpea (cultivar Mashhad) were studied under laboratory conditions (25 ± 1 °C, 65 ± 5 % RH, a 16:8-h light–dark photoperiod). The shortest larval period of C. chalcites was 14.15 days on common bean Sadra. The longest and shortest development time of total preadult was on white kidney bean Daneshkadeh and common bean Sadra (25.77 and 23.42 days, respectively). The highest total fecundity was on common bean Sadra (674.4 eggs), and the lowest was observed on white kidney bean Daneshkadeh (136.7 eggs). The intrinsic rate of increase (r _m ) ranged from 0.0976 to 0.1599 female/female/day, which was lowest on white kidney bean Daneshkadeh and highest on common bean Sadra. The net reproductive rate (R ₀) was highest on common bean Sadra (265.82 offspring) and lowest on white kidney bean Daneshkadeh (46.88 offspring). The results revealed that the cultivar Daneshkadeh was unsuitable host to C. chalcites in comparison to the other cultivars tested.     

Comparative analysis of the methods used for finding surface energy to investigate protein interaction behavior on chromatographic supports

Hydrophobic interaction chromatography, an important and effective purification strategy, is generally used for the purification of variety of biomolecules. A basic understanding of the protein interaction behavior is required to effectively separate these biomolecules. A colloidal type extended Derjaguin, Landau, Verwey, and Overbeek calculations were utilized to study the interactions behavior of model proteins to commercially available hydrophobic chromatographic materials that is, Toyopearl Phenyl 650C and Toyopearl Butyl 650C. Physicochemical properties of selected model proteins were achieved by contact angle and zeta potential measurements. The contact angle of chromatographic materials used was achieved through sessile drop method on disrupted beads and capillary penetration method (CPM) on intact beads. The surface properties were further used to calculate the interactions of the proteins to chromatographic supports. The calculated secondary energy minimum of the proteins with the chromatographic materials (from the contact angle values determined through both methods can be correlated with the retention volumes from the real chromatography. The secondary energy minimum values are higher for each protein to the chromatographic materials calculated from the inputs derived through sessile drop method compared to CPM. For instance, immunoglobulin G has secondary energy minimum value of 0.17 kT compared to 0.11 kT, obtained through sessile drop method and CPM, respectively. Average relative values of the energy minimum calculated for all proteins are as 1.51 kT and 1.29 kT for Toyopearl Butyl 650C and Toyopearl Phenyl 650C, respectively, as a conversion factor for estimation of secondary energy minimum for both methods.     

Conjugation of a new two-photon fluorophore to poly(ethylenimine) for gene delivery imaging

We report herein the molecular engineering of an efficient two-photon absorbing (TPA) chromophore based on a donor-donor bis-stilbenyl entity to allow conjugation with biologically relevant molecules. The dye has been functionalized using an isothiocyanate moiety to conjugate it with the amine functions of poly(ethylenimine) (PEI), which is a cationic polymer commonly used for nonviral gene delivery. Upon conjugation, the basic architecture and photophysical properties of the active TPA chromophore remain unchanged. At the usual N/P ratio (ratio of the PEI positive charges to the DNA negative charges) of 10 used for transfection, the transfection efficiency and cytotoxicity of the labeled PEI/DNA complexes were found to be comparable to those of the unlabeled PEI/DNA complexes. Moreover, when used in combination with unlabeled PEI (at a ratio of 1 labeled PEI to 3 unlabeled PEI), the labeled PEI does not affect the size of the complexes with DNA. The labeled PEI was successfully used in two-photon fluorescence correlation spectroscopy measurements, showing that at N/P = 10 most PEI molecules are free and the diffusion coefficient of the complexes is consistent with the 360 nm size measured by quasielastic light scattering. Finally, two-photon images of the labeled PEI/DNA complexes confirmed that the complexes enter into the cytoplasm of HeLa cells by endocytosis and hardly escape from the endosomes. As a consequence, the functionalized TPA chromophore appears to be an adequate tool to label the numerous polyamines used in nonviral gene delivery and characterize their complexes with DNA in two-photon applications.