Satisfaction with mammography in the National Cancer Screening Programme participants of age 40s in Korea

JEON, B.Y.,LEE, H‐,Y.,PARK, E‐,C.,CHOI, K.S.,JUN, J.K.,KIM, Y.,HAN, M.A.,YOON, N‐,H.,KIM, E.J.,JEON, S.M. Blackwell Publishing Ltd 2011 European journal of cancer care Vol.20 No.6

<P>JEON B.Y., LEE H‐Y., PARK E‐C., CHOI K.S., JUN J.K., KIM Y., HAN M.A., YOON N‐H., KIM E.J. & JEON S.M. (2011) <I>European Journal of Cancer Care</I><B>20</B>, 803–809</P><P><B>Satisfaction with mammography in the National Cancer Screening Programme participants of age 40s in Korea</B></P><P>The aim of this study was to evaluate satisfaction with the National Cancer Screening Programme of mammography in Korea and to examine the association between subscales of satisfaction and general satisfaction. We conducted a cross‐sectional telephone survey for women who had obtained a National Cancer Screening Programme mammographic screening at general hospitals between May and October 2008. The present study included 2005 women in their forties. We performed multivariate linear regression using dependent variable as general satisfaction and independent variables as subscales of satisfaction, such as pre‐screening information transfer, staff interpersonal skills, physical surroundings and results reporting. Participants were stratified according to the result of their mammogram as negative or positive. Mean score of satisfaction was above 2.5 of 4 for all subscales. Women who received positive results were less satisfied with all of subscale factors. Staff interpersonal skills were the most important factor that contributed to general satisfaction. Future efforts such as staff training programme of communication/attitude skills, ensuring privacy and explanation of possible discomfort of the screening would be needed.</P>

Mucilaginibacter oryzae sp. nov., isolated from soil of a rice paddy

Jeon, Y.,Lee, S.-S.,Chung, B. S.,Kim, J. M.,Bae, J.-W.,Park, S. K.,Jeon, C. O. Microbiology Society 2009 International journal of systematic and evolutiona Vol.59 No.6

<P>A Gram-negative-staining, non-spore-forming bacterium devoid of flagella, designated strain B9(T), was isolated from rice paddy soil associated with the roots of Oryza sativa collected from Jinju, South Korea. Cells were straight rods, were catalase- and oxidase-positive and were able to hydrolyse pectin, xylan and laminarin. Growth of strain B9(T) was observed between 15 and 35 degrees C (optimum 25-30 degrees C) and between pH 5.0 and 8.0 (optimum pH 6.5-7.5). Strain B9(T) contained menaquinone-7 (MK-7) as a major isoprenoid quinone and summed feature 3 (C(16 : 1)omega7c and/or iso-C(15 : 0) 2-OH), iso-C(15 : 0) and C(16 : 0) as major fatty acids. The G+C content of the genomic DNA was 44.4 mol%. Comparative 16S rRNA gene sequence analysis showed that strain B9(T) belonged to the genus Mucilaginibacter, a member of the family Sphingobacteriaceae, and was most closely related to Mucilaginibacter kameinonensis SCK(T) (95.9 % sequence similarity). On the basis of chemotaxonomic data and molecular properties, strain B9(T) represents a novel species of the genus Mucilaginibacter, for which the name Mucilaginibacter oryzae sp. nov. is proposed. The type strain is B9(T) (=KACC 12816(T) =DSM 19975(T)).</P>

Influences of Enzyme Complex Supplementation on Growth, Ileal and Apparent Fecal Digestibility and Morphology of Small Intestine in Pigs

Kim, B.G.,Tian, J.Z.,Lim, J.S.,Kil, D.Y.,Jeon, H.Y.,Chung, Y.K.,Kim, Y.Y. Asian Australasian Association of Animal Productio 2004 Animal Bioscience Vol.17 No.12

A total of 140 weaning pigs were used to determine the effects of digestive enzyme supplementation to corn-soybean meal diets on growth performance, physiological changes of small intestine, microorganisms and pH in the gastrointestinal tract. Two kinds of enzyme complex (A, B) were used in this experiment. Pigs were allotted in a completely random design (CRD) to five replicates with four pigs per pen. Diets and water were provided for ad libitum consumption. Treatments included 1) Control: without enzyme supplementation, 2) Enzyme A 0.05%, 3) Enzyme A 0.10%, 4) Enzyme A 0.15%, 5) Enzyme B 0.05%, 6) Enzyme B 0.10%, 7) Enzyme B 0.15% in the diets. A total of 24 crossbred barrows 25.78${\pm}$0.55 kg BW fitted with simple ileal T-cannulas were used to evaluate the effect the enzyme addition on the nutrient digstibility. Pigs were allotted 4 treatments (No enzyme, enzyme A 0.05%, enzyme A 0.1%, enzyme A 0.15%), 6 replicates according to a completely random design (CRD). Another digestibility trial was followed for enzyme complex B. Twenty pigs, average 31.92${\pm}$0.37 kg BW, fitted with simple ileal T-cannulas for digestibility trial. Neither enzyme A nor enzyme B affected on fecal or ileal digestibility of dry matter, gross energy, crude protein, crude fat and crude ash (p>0.05). The apparent fecal digestibilities of all the nutrients were higher in total feces collection method than in indirect method. At the end of feeding trial, 21 pigs were slaughtered for examining the morphological changes of small intestine and the concentration of microorganisms in the ileum and the colon. Growth performance, intestinal morphology and pH of ileum and colon were not affected by the either enzyme complex supplementation (p>0.05). These results suggested that enzyme complex A and enzyme complex B were of no benefit to early-weaned pigs when corn-soybean meal based diet was provided.

Enhanced antitumor immunotherapeutic effect of B-cell-based vaccine transduced with modified adenoviral vector containing type 35 fiber structures

Kim, E-K,Seo, H-S,Chae, M-J,Jeon, I-S,Song, B-Y,Park, Y-J,Ahn, H M,Yun, C-O,Kang, C-Y Macmillan Publishers Limited 2014 Gene therapy Vol.21 No.1

For successful clinical tumor immunotherapy outcomes, strong immune responses against tumor antigens must be generated. Cell-based vaccines compromise one strategy with which to induce appropriate strong immune responses. Previously, we established a natural killer T-cell (NKT) ligand-loaded, adenoviral vector-transduced B-cell-based anticancer cellular vaccine. To enhance tumor antigen delivery to B cells, we established a modified adenoviral vector (Ad-k35) that encoded a truncated form of the breast cancer antigen Her2/neu (Ad-k35HM) in which fiber structure was substituted with adenovirus serotype 35. We observed increased tumor antigen expression with Ad-k35HM in both human and murine B cells. In addition, an Ad-k35HM-transduced B-cell vaccine elicited strong antigen-specific cellular and humoral immune responses that were further enhanced with the additional loading of soluble NKT ligand KBC009. An Ad-k35HM-transduced, KBC009-loaded B-cell vaccine efficiently suppressed the in vivo growth of established tumors in a mouse model. Moreover, the vaccine elicited human leukocyte antigen (HLA)-A2 epitope-specific cytotoxic T-cell responses in B6.Cg (CB)-Tg (HLA-A/H2-D) 2Enge/Jat mice. These findings indicated that the Ad-k35 could be appropriate for the preclinical and clinical development of B-cell-based anticancer immunotherapies.

Thymosin beta-4 promotes mesenchymal stem cell proliferation via an interleukin-8-dependent mechanism

Jeon, B.J.,Yang, Y.,Kyung Shim, S.,Yang, H.M.,Cho, D.,Ik Bang, S. Academic Press 2013 Experimental cell research Vol.319 No.17

Mesenchymal stem cells (MSCs) hold great promise for the field of tissue regeneration. Because only a limited number of MSCs can be obtained from each donor site, it is important to establish standard methods for MSC expansion using growth and trophic factors. Thymosin β4 (Tβ4) is a novel trophic factor that has antimicrobial effects and the potential to promote tissue repair. Tβ4 is a ubiquitous, naturally-occurring peptide in the wound bed. Therefore, the relationship between Tβ4 and MSCs, especially adjacent adipose tissue-derived stem cells (ASCs), merits consideration. Exogenous Tβ4 treatment enhanced the proliferation of human ASCs, resulting in prominent nuclear localization of PCNA immunoreactivity. In addition, exogenous Tβ4 also increased IL-8 secretion and blocking of IL-8 with neutralizing antibodies decreased Tβ4-induced ASC proliferation, suggesting that IL-8 is a critical mediator of Tβ4-enhanced proliferation. Moreover, Tβ4 activated phosphorylation of ERK½ and increased the nuclear translocation of NF-κB. These observation provide that Tβ4 promotes the expansion of human ASCs via an IL-8-dependent mechanism that involves the ERK and NF-κB pathways. Therefore, Tβ4 could be used as a tool for MSC expansion in cell therapeutics.

Charge and mass transport properties of La₂Ni_0.95Al_0.05O_4.025+δ

Jeon, S.Y.,Singh, B.,Im, H.N.,Seong, K.P.,Song, S.J. Elsevier Sequoia 2014 Journal of alloys and compounds Vol.589 No.-

<P>In this work, mass and charge transport properties of acceptor doped lanthanum nickelate, La2Ni0.95Al0.05O4.025+delta d (LNAO), were analyzed. The thermal expansion, electrical conductivity and thermoelectric power of LNAO were measured as a function of temperature in 25-1000 degrees C range and oxygen partial pressure ( pO(2)) in -14 <= log (pO(2)/atm)6 <= -1 range. The average thermal expansion coefficient was 13.77 x 10 (6) K (1). The electrical conductivity was analyzed in relation to the thermoelectric power to elucidate the positive deviation of the activity coefficient of hole on the basis of the delocalized electron model. The thermoelectric power measurement shows a p-type to n- type transition. The chemical diffusion coefficient (D-chem) and surface exchange coefficient (ksurf.) were calculated by 4-probe DC conductivity measurement and ksurf. was slightly higher than ((D) over tilde Dchem). The best- estimated hole-mobility values showed very weak temperature dependence. The results were compared with the literature results on La2NiO4+ d. (C) 2013 Elsevier B.V. All rights reserved.</P>

The heat-shock protein 90 inhibitor, geldanamycin, induces apoptotic cell death in Epstein–Barr virus-positive NK/T-cell lymphoma by Akt down-regulation

Jeon, YK,Park, CH,Kim, K-Y,Li, YC,Kim, J,Kim, YA,Paik, J-H,Park, B-K,Kim, C-W,Kim, Y-N John Wiley Sons, Ltd. 2007 The Journal of pathology Vol.213 No.2

<P>NK/T-cell lymphoma (NKTL) is strongly associated with latent Epstein–Barr virus (EBV) infection. Recently, latent membrane protein 1 (LMP1), an EBV oncoprotein, was reported to activate the phosphatidylinositol-3 kinase (PI3K)/Akt pathway for cell survival. Because geldanamycin (GA) and its derivative, 17-allylamino-17-demethoxygeldanamycin (17-AAG), exhibit anti-tumour activity by degrading HSP90 client proteins, including Akt, we investigated the effect of GA and 17-AAG on the survival of NKTL cell lines. EBV-positive NKTL cell lines, Hank-1 and NK-YS, and an EBV-negative NK leukaemia cell line, NK-L, were treated with PI3K and Akt inhibitors, GA, and 17-AAG, and were subjected to apoptosis and cell viability assays, and immunoblot analysis. EBV-positive B-lymphoblastoid cell lines IM9 and LMP1-transfected IM9 (IM9-LMP1) were also included. Hank-1 and NK-YS cell viability was compromised and apoptosis was induced by LY294002 (PI3K inhibitor) or Akt inhibitor II. GA or 17-AAG administration resulted in the apoptosis of NKTL cells, accompanied by Akt and pAkt down-regulation, caspase 3 activation, and mitochondrial membrane potential disruption. The intrinsic level of pAkt was higher in EBV-positive NKTL cells than in EBV-negative NK-L, and GA or 17-AAG decreased the viability of NKTL cells more efficiently than NK-L. Moreover, IM9-LMP1 was more sensitive to Akt inhibitor II or HSP90 inhibitors than IM9. Importantly, GA showed little effect on the viability of normal peripheral NK cells as non-neoplastic counterparts for comparison. In conclusion, this study suggests that the PI3K/Akt pathway is frequently activated in EBV-positive NKTL and that therapeutic modalities based on targeting the PI3K/Akt pathway with HSP90 inhibitors could be useful for achieving NKTL control. Copyright © 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</P>

Synthesis of silver nanoparticles in an eco-friendly way using <i>Phyllanthus amarus</i> leaf extract: Antimicrobial and catalytic activity

Ajitha, B.,Reddy, Y. Ashok Kumar,Jeon, Hwan-Jin,Ahn, Chi Won VSP 2018 Advanced powder technology Vol.29 No.1

<P><B>Abstract</B></P> <P>In the present study, silver nanoparticles (AgNPs) with a flower-like structure were synthesized through an easy, rapid and eco-friendly pathway using <I>Phyllanthus amarus</I> leaf extract. The obtained AgNPs were characterized using ultraviolet–visible (UV–Vis) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), and transmission electron microscopy (TEM). In addition, the antimicrobial and catalytic activities of the bio-synthesized AgNPs were carried out. Our results indicated that the concentration of the Ag precursor and the volume of the leaf extract played key roles in the formation of the flower-shaped AgNPs. Morphology study confirms the shape of the obtained bio-AgNPs as flower like structure. This study also showed the presence of clear capping layers surrounding and apparently interacting with the nanoparticles. Moreover, our studies indicated this interaction to involve bio-organic capping agents in the leaf extract. UV–Vis absorption spectra confirmed the formation of AgNPs with an optimized size. The zeta (ζ) potential of the AgNPs attests the stability of the nanoparticles. FTIR spectra provided evidence for the presence of biomolecules responsible for the reduction as well as capping of the AgNPs. Finally, the bio-synthesized AgNPs were shown to be an excellent microbial activity against the selected pathogens and enhanced catalyst of the reduction of rhodamine B.</P> <P><B>Highlights</B></P> <P> <UL> <LI> <I>Phyllanthus amarus</I> is an exceptional sink for biosynthesis of silver nanoparticles. </LI> <LI> Biomolecules of leaf extract are found to play an active role in AgNPs formation. </LI> <LI> Zeta potential value attested the higher stability of biosynthesized AgNPs. </LI> <LI> Excellent antimicrobial and catalytic activities were obtained in an eco-friendly way. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>

Poly-paclitaxel/cyclodextrin-SPION nano-assembly for magnetically guided drug delivery system

Jeon, H.,Kim, J.,Lee, Y.M.,Kim, J.,Choi, H.W.,Lee, J.,Park, H.,Kang, Y.,Kim, I.S.,Lee, B.H.,Hoffman, A.S.,Kim, W.J. Elsevier Science Publishers 2016 Journal of controlled release Vol.231 No.-

<P>This work demonstrates the development of magnetically guided drug delivery systems and its potential on efficient anticancer therapy. The magnetically guided drug delivery system was successfully developed by utilizing superparamagnetic iron oxide nanoparticle, beta-cyclodextrin, and polymerized paclitaxel. Multivalent host-guest interactions between beta-cyclodextrin-conjugated superparamagnetic iron oxide nanoparticle and polymerized paclitaxel allowed to load the paclitaxel and the nanoparticle into the nano-assembly. Clusterized superparamagnetic iron oxide nanoparticles in the nano-assembly permitted the rapid and efficient targeted drug delivery. Compared to the control groups, the developed nano-assembly showed the enhanced anticancer effects in vivo as well as in vitro. Consequently, the strategy of the use of superparamagnetic nanoparticles and multivalent host-guest interactions has a promising potential for developing the efficient drug delivery systems. (C) 2016 Elsevier B.V. All rights reserved.</P>

Salmonella Typhi균의 분자역학적 연구

이복권,강연호,박미선,유재연,김성한,김준영,전형근 국립보건연구원 1999 국립보건원보 Vol.36 No.-