I Saiki

ORCID: 0000-0002-9705-6857
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Research Areas
  • Structural Load-Bearing Analysis
  • Composite Material Mechanics
  • Cell Adhesion Molecules Research
  • Advanced Mathematical Modeling in Engineering
  • Peptidase Inhibition and Analysis
  • Structural Analysis and Optimization
  • Structural Behavior of Reinforced Concrete
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer Research and Treatments
  • Composite Structure Analysis and Optimization
  • Protease and Inhibitor Mechanisms
  • Structural Engineering and Vibration Analysis
  • Railway Engineering and Dynamics
  • Immune Cell Function and Interaction
  • Advanced Numerical Methods in Computational Mathematics
  • Chemical Synthesis and Analysis
  • Immunotherapy and Immune Responses
  • Glycosylation and Glycoproteins Research
  • Natural product bioactivities and synthesis
  • Elasticity and Material Modeling
  • Antimicrobial Peptides and Activities
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Rock Mechanics and Modeling
  • Metal Forming Simulation Techniques
  • Structural Health Monitoring Techniques

Tohoku University
2005-2022

École Nationale des Greffes
2013-2018

University of Toyama
2007-2012

Utsunomiya University
2000-2005

Tohoku Medical and Pharmaceutical University
1999-2005

Japan Society of Civil Engineers
2000-2001

Hokkaido University
1984-1996

Takara (Japan)
1990

The University of Texas MD Anderson Cancer Center
1985-1987

The University of Texas Health Science Center at Houston
1985

Mouse peritoneal macrophages were activated to become cytotoxic against B16-BL6 melanoma cells by the combination of subthreshold amounts murine interferon-gamma (IFN-gamma; 0.1 10 U/ml) and N-acetylmuramyl-L-alanyl-D-isoglutamine (MDP; 0.001 micrograms/ml), but not pH 2-treated IFN-gamma MDP, heat-treated or inactive stereoisomer N-acetyl-muramyl-D-alanyl-D-isoglutamine (MDP-D). The encapsulation intact MDP within same liposome preparation was synergistic for macrophage activation. In...

10.4049/jimmunol.135.1.684 article EN The Journal of Immunology 1985-07-01

Hydroethidine, a reduced form of ethidium bromide, was used as vital dye in fluorescence assays that allowed visual and semiquantitative monitoring uptake accumulation by microscopy, flow cytometry, image analysis, microfluorimetry. The excitation emission filters were chosen to detect hydroethidine exclude ethidium. Microscopically, there differences intensities patterns among various tumor cell lines. pattern varied from homogeneous blue the cytoplasm plus brilliant packets bluish-white...

10.1177/34.9.2426339 article EN Journal of Histochemistry & Cytochemistry 1986-09-01

Highly purified human blood monocytes, isolated by continuous Percoll density gradients under endotoxin-free conditions, and mouse peritoneal exudate macrophages (PEM) were activated in vitro the combination of muramyl dipeptide (MDP) recombinant interferon-gamma (r-IFN-gamma) to become tumoricidal against their respective tumorigenic target cells. The activation monocytes or PEM free unencapsulated r-IFN-gamma MDP was species specific: lyse allogeneic melanoma cells, but did not activate...

10.4049/jimmunol.135.6.4289 article EN The Journal of Immunology 1985-12-01

This study is designed to establish a pulmonary tumour model investigate the biology and therapy of lung cancer in mice. Current methods for forming solitary intrapulmonary nodule subsequent metastasis mediastinal lymph nodes are not well defined. Lewis carcinoma (LLC) cell suspensions were orthotopically introduced into parenchyma C57/BL6 mice via limited skin incision without thoracotomy followed by direct puncture through intercostal space. The implantation process was performed within...

10.1038/sj.bjc.6690178 article EN cc-by-nc-sa British Journal of Cancer 1999-02-12

The adjuvant and tumor-suppressive activities of the quinonyl [2,3-dimethoxy-5-methyl-6-(9'-carboxynonyl)-1,4-benzoquinone (QS-10)] derivatives N-acetyl muramyl dipeptides were examined. N-Acetyl muramyl-L-valyl-D-isoglutamine (MurNac-L-Val-D-isoGln), QS-10-MurNAc-L-Val-D-isoGln, their methyl esters shown to have potent activity on induction delayed-type hypersensitivity monoazobenzenarsonate-N-acetyl-L-tyrosine in guinea pigs primary immune response against sheep erythrocytes vitro;...

10.1128/iai.31.1.114-121.1981 article EN Infection and Immunity 1981-01-01

We studied the effects of in vivo administrations recombinant human granulocyte colony-stimulating factor (rhG-CSF) on metastasis murine hematogenous and non-hematogenous tumors spontaneous experimental models. Spontaneous lung caused by intra-footpad injections B16-BL6 melanoma Lewis-lung-carcinoma (3LL) cells were inhibited intravenous (i.v.) subcutaneous (s.c.) rhG-CSF after excision primary tumors. Recombinant hG-CSF significantly liver when administered i.v. injection L5178Y-ML25...

10.1002/ijc.2910490323 article EN International Journal of Cancer 1991-09-30

Abstract The effect of the administration recombinant interferon‐γ. (rlFN‐γ) and a synthetic lipid A subunit analog (GLA‐60) on angiogenesis induced by B16‐BL6 melanoma was examined in syngeneic C57BLJ.6 mice. Intravenous rlFN‐γ followed GLA‐60 (referred to as rIFN‐γ/GLA‐60) endogenous production tumor necrosis factor (TNF). This treatment day 3 after inoculation caused marked decrease number vessels oriented towards mass (angiogenic response) size over period 9 days. In contrast, neither...

10.1002/ijc.2910510422 article EN International Journal of Cancer 1992-06-19

The adjuvant activity of 29 kinds carbohydrate analogs N-acetylmuramyl-L-alanyl-D-isoglutamine on the induction delayed-type hypersensitivity to azobenzenearsonate-N-acetyl-L-tyrosine was examined in guinea pigs. It found that D-manno- and D-galacto-type muramyldipeptides were as active D-gluco-type muramyldipeptide (MDP). structural requirement moiety is discussed.

10.1128/iai.33.3.834-839.1981 article EN Infection and Immunity 1981-09-01

Gel was prepared from 6-O-carboxymethyl-chitin (CM-chitin) by the addition of iron(III) chloride under mild conditions without any organic solvent. The optimal for gel formation were 15 to 30 mM and 0.5 0.8 degree substitution in CM-chitin. amounts bovine serum albumin (BSA) anticancer drug doxorubicin (DOX) incorporated into CM-chitin gels more than 80% 30%, respectively described above. release BSA or DOX observed be increased lysozyme digestion a time-dependent manner. This result...

10.1248/cpb.38.506 article EN Chemical and Pharmaceutical Bulletin 1990-01-01

The immunological properties of peptidoglycan (L-PG) purified from the cell wall skeleton (L-CWS) Listeria monocytogenes strain EGD were investigated and compared with L-CWS. L-PG consisted alanine, glutamic acid, alpha, epsilon-diaminopimelic muramic glucosamine. showed potent adjuvant activities for circulating antibody formation development delayed-type hypersensitivity to bacterial alpha-amylase in vivo primary immune response sheep erythrocytes vitro, as well Both L-CWS enhanced...

10.1128/iai.38.1.58-65.1982 article EN Infection and Immunity 1982-10-01

We have reported that the selective epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, gefitinib ('Iressa', ZD1839), suppressed intrahepatic metastasis of hepatocellular carcinoma CBO140C12 cells. In this study, we focused on tumour necrosis factor-α (TNF-α) signalling pathways. Real-time reverse transcription–polymerase chain reaction showed TNF-α mRNA was expressed in large quantities implanted tumour. Gefitinib inhibited EGF- but not hepatocyte (HGF)-induced activation...

10.1038/sj.bjc.6602548 article EN cc-by-nc-sa British Journal of Cancer 2005-04-19
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