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1.
Antimicrob Agents Chemother ; 66(11): e0102922, 2022 11 15.
Article in English | MEDLINE | ID: mdl-36222537

ABSTRACT

Vancomycin-resistant Enterococcus faecium carrying the vanD1 gene on plasmid pEF-D was isolated from a fecal sample of a hospitalized patient in Japan. The strain JH5687 showed moderate resistance to vancomycin (MIC, 16 µg/mL) but remained susceptible to teicoplanin (MIC, 1 µg/mL). The backbone gene organization of pEF-D was highly homologous to that of conjugative plasmid pMG1 or pHTß. The calculated conjugation frequency of JH5687 was 10-4 to 10-5 per donor cell.


Subject(s)
Enterococcus faecium , Gram-Positive Bacterial Infections , Vancomycin-Resistant Enterococci , Humans , Vancomycin/pharmacology , Vancomycin Resistance/genetics , Anti-Bacterial Agents/pharmacology , Plasmids/genetics , Vancomycin-Resistant Enterococci/genetics , Gram-Positive Bacterial Infections/drug therapy , Microbial Sensitivity Tests
2.
Int J Cancer ; 112(6): 927-33, 2004 Dec 20.
Article in English | MEDLINE | ID: mdl-15386364

ABSTRACT

In order to clarify the roles of tumor necrosis factor (TNF)-alpha in lung metastasis, we injected Renca cells intravenously into TNF receptor p55-deficient (TNF-Rp55 KO) and wild-type (WT) mice. Microscopic and macroscopic metastasis foci appeared in lungs at 7 and 14 days after the tumor injection, respectively. Moreover, metastasis foci expanded at similar rates in both WT and TNF-Rp55 KO mice until 21 days, and lungs were occupied with metastasis foci. However, later than 21 days after the injection, metastasis foci spontaneously regressed in TNF-Rp55 KO mice, whereas WT mice exhibited a progressive growth of metastasis foci. Moreover, metastasis foci remained reduced sizes in TNF-Rp55 KO mice even at 26 days, when all WT mice died with lungs filled with metastasis foci. Later than 21 days after the tumor injection, the number of apoptotic tumor cells was increased in TNF-Rp55 KO mice. In contrast, neovascularization was less evident in TNF-Rp55 KO than WT mice, with depressed hepatocyte growth factor (HGF) gene in TNF-Rp55 KO mice at 21 days after the tumor injection. Thus, TNF-Rp55-mediated signals can maintain tumor neovascularization at least partly by inducing HGF expression, and eventually support lung metastasis process.


Subject(s)
Carcinoma, Renal Cell/metabolism , Carcinoma, Renal Cell/secondary , Hepatocyte Growth Factor/metabolism , Lung Neoplasms/metabolism , Lung Neoplasms/secondary , Neovascularization, Pathologic/prevention & control , Receptors, Tumor Necrosis Factor, Type I/metabolism , Animals , Carcinoma, Renal Cell/blood supply , Female , Gene Expression Regulation, Neoplastic , Hepatocyte Growth Factor/genetics , Immunohistochemistry , In Situ Nick-End Labeling , Injections, Intravenous , Kidney Neoplasms/metabolism , Kidney Neoplasms/pathology , Lung Neoplasms/blood supply , Mice , Mice, Inbred BALB C , Mice, Knockout , Neovascularization, Pathologic/drug therapy , Polymerase Chain Reaction , Receptors, Tumor Necrosis Factor, Type I/deficiency , Receptors, Tumor Necrosis Factor, Type I/genetics , Time Factors , Tumor Cells, Cultured , Tumor Necrosis Factor-alpha/metabolism
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