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Azacitidine decreases reactive oxygen species production in peripheral white blood cells:A case report

World Journal of Clinical Cases 2020年第22期8卷 5657-5662页

作者： Hidekazu Hasunuma Naomi Shimizu Hiromitsu Yokota ichiro tatsuno Department of Blood Transfusion Toho University Medical Center Sakura HospitalSakura 2858741Japan Department of Hematology Toho University Medical Center Sakura HospitalSakura 2858741Japan Clinical Laboratory Program Education Development CenterFaculty of Science Toho UniversityFunabashi 2748510Japan Center for Diabetes Metabolism and EndocrinologyToho University Medical Center Sakura HospitalSakura 2858741Japan

BACKGROUND In myelodysplastic syndrome(MDS),oxidative stress is closely related to iron overload and DNA damage.A recent study suggested the possibility that increased oxidative stress causes not only iron overload but also disease progression of MDS with DNA *** present a case of MDS with decreased reactive oxygen species(ROS)production in peripheral white blood cells(WBCs)and decreased diacron-reactive oxygen metabolites(d-ROMs)in serum after azacitidine *** SUMMARY A 74-year-old man presented to the hematological department with the chief complaint of *** vital signs were within normal limits at admission with a heart rate of 80 bpm and blood pressure of 135/60 *** tests indicated pancytopenia,a WBC count of 2190 cells/μL,a hemoglobin level of 6.2 g/dL and a platelet count of 7.4×104/μ*** patient was diagnosed with MDS with fibrosis after a bone marrow *** case showed decreased ROS production in WBCs,d-ROMs in serum and Wilms’tumor 1 after azacitidine therapy,after which his hematopoiesis *** Azacitidine therapy can improve hematopoiesis and decrease ROS and d-ROM production.

关键词： Myelodysplastic syndrome Reactive oxygen species Diacron-reactive oxygen metabolites Ferritin Azacitidine Case report

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Severe hypercholesterolemia associated with primary biliary cirrhosis in a 44-year-old Japanese woman

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World Journal of Gastroenterology 2004年第17期10卷 2607-2608页

作者： Tatsuo Kanda Osamu Yokosuka Hiroshige Kojima Fumio Imazeki Keiich Nagao ichiro tatsuno Yasushi Saito Hiromitsu Saisho First Department of Medicine Chiba University School of MedicineChiba 260-8670Japan Health Sciences CenterChiba UniversityChiba 260-8670Japan Health Sciences Center Chiba UniversityChiba 260-8670Japan Second Department of Medicine Chiba University School of MedicineChiba 260-8670Japan

A 44-year-old woman developed jaundice and was diagnosed as stage Ⅱ of primary biliary cirrhosis(PBC).She showed a severely high total cholesterol *** article focuses on atypical presentations of PBC and the need to ... 详细信息

关键词： Adult Cholesterol Female Humans Hypercholesterolemia Japan Liver Cirrhosis, Biliary Severity of Illness Index

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Characterization of NADase-Inactive NAD<sup>+</sup>Glycohydrolase in <i>Streptococcus pyogenes</i>

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Advances in Microbiology 2013年第1期3卷 91-100页

作者： ichiro tatsuno Masanori Isaka Tadao Hasegawa Department of Bacteriology Graduate School of Medical Sciences Nagoya City UniversityNagoya Japan

Background: Streptococcus pyogenes secretes NAD+ glycohydrolase (NADase, also known as SPN or Nga). All S. pyogenes strains examined to date possess the gene that encodes SPN (spn), but some strains produce SPN that lacks detectable NADase activity. Although there is much evidence to support that SPN’s NADase activity contributes to virulence, there is very little evidence that NADase-inactive SPN has detectable functions. Results: In order to characterize the NADase-inactive SPN, we firstly attempted to clone the NADase-inactive spn allele in Escherichia coli. Although we obtained recombinants which were shown to have the correct size insert, all had some mutations in the spn allele. Therefore, we attempted to change the mutated nucleotides back to the original nucleotides. While a nucleotide mutagenesis (inverse PCR method) easily changed a target nucleotide of control genes back to the original nucleotides, the mutations of NADase-inactive spn allele were never successfully converted back to the original nucleotides. Finally the mutant spn alleles were sub-cloned into another vector (pLZ12-Km2), which is maintained in both E. coli and S. pyogenes. The resultant plasmids were subjected to nucleotide mutagenesis using inverse PCR;the resultant mutagenized plasmid DNAs were used to transform both E. coli and S. pyogenes strains. We observed successful nucleotide substitutions back to the original spn nucleotide sequence in S. pyogenes transformants, but not in E. coli transformants. Thus, the NADase-inactive spn allele was successfully cloned in S. pyogenes, but not in E. coli. However, we could not find an association with NADase-inactive spn allele and virulence in a mouse infection model. Conclusions: These results suggest that NADase-inactive spn allele has some toxic effect to E. coli, but not S. pyogenes. This effect may due to an as of yet unknown function attributable to NADase-inactive SPN.

关键词： Streptococcus pyogenes NAD+ Glycohydrolase NADase SPN Streptococcal SF370

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