Research Topics
| M BabaSummaryAffiliation: Kagoshima University Country: Japan Publications
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Publications
Mechanism of inhibition of human immunodeficiency virus type 1 reverse transcriptase by a stavudine analogue, 4'-ethynyl stavudine triphosphateGuangwei Yang
Department of Pharmacology, School of Medicine, Yale University, 333 Cedar Street, New Haven, CT 06520, USA
Antimicrob Agents Chemother 52:2035-42. 2008..The structural basis for the higher binding affinity of 4'-Ed4TTP than of d4TTP could be the additional binding of the 4'-ethynyl group in a preformed hydrophobic pocket by A114, Y115, M184, F160, and part of D185...
Anti-HIV-1 activity and structure-activity relationship of cepharanoline derivatives in chronically infected cellsM Baba
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Japan
Antivir Chem Chemother 12:307-12. 2001..The 50% effective concentrations of this compound and cepharanthine were 0.0041 and 0.028 microg/ml (0.0060 and 0.046 microM), respectively...
Breast cancer resistance protein (BCRP/ABCG2) induces cellular resistance to HIV-1 nucleoside reverse transcriptase inhibitorsXin Wang
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Kagoshima, Japan
Mol Pharmacol 63:65-72. 2003..An analysis for intracellular metabolism of AZT suggests that the resistance is attributed to the increase of ATP-dependent efflux of its metabolites, presumably AZT 5'-monophosphate, in MT-4/DOX 500 cells...
Inhibitors of HIV-1 gene expression and transcriptionMasanori Baba
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Kagoshima 890 8520, Japan
Curr Top Med Chem 4:871-82. 2004..In addition, various compounds have been identified as inhibitors of HIV-1 gene expression and transcription, yet their precise mechanisms are still unknown...
[Recent progress in anti-HIM-1 research]Masanori Baba
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University 8 35 1, Sakuragaoka, Kagoshima 890 8544, Japan
Uirusu 54:59-66. 2004..Furthermore, clinical trials with CCR 5 (coreceptor of HIV-1) antagonists are in progress, and inhibitors of integrase, HIV-1 gene expression, and virion assembly have been identified...
TAK-652 inhibits CCR5-mediated human immunodeficiency virus type 1 infection in vitro and has favorable pharmacokinetics in humansMasanori Baba
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, 8 35 1, Sakuragaoka, Kagoshima 890 8544, Japan
Antimicrob Agents Chemother 49:4584-91. 2005..The compound displayed favorable pharmacokinetics, and its plasma concentration was 7.2 ng/ml (9.1 nM) even 24 h after the administration of 25 mg. Thus, TAK-652 is a promising candidate as a novel entry inhibitor of HIV-1...
SJ-3366 Sam Jin PharmaceuticalMasanori Baba
Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Japan
Curr Opin Investig Drugs 3:1146-8. 2002..As of June 1998, Sam Jin had been awarded a patent for SJ-3366 in South Africa, with applications pending in 22 other countries [302450]...
[Advances in antiviral chemotherapy]Masanori Baba
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Japan
Uirusu 55:69-75. 2005..Thus, it seems still mandatory to continue the search for more effective and less toxic compounds against various viral infections...
Establishment of a CCR5-expressing T-lymphoblastoid cell line highly susceptible to R5 HIV type 1M Baba
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Japan
AIDS Res Hum Retroviruses 16:935-41. 2000..These results indicate that the established cell line will be an extremely useful tool for experiments with R5 HIV-1...
Potent and selective inhibition of human immunodeficiency virus type 1 transcription by piperazinyloxoquinoline derivativesM Baba
Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Sakuragaoka, Japan
Antimicrob Agents Chemother 41:1250-5. 1997..It was not inhibitory to HIV-1 Tat or the cellular transcription factors NF-kappaB and Sp1, suggesting that the piperazinyloxoquinoline derivatives are a group of HIV-1 transcription inhibitors with a unique mechanism of action...
Marked suppression of T cells by a benzothiophene derivative in patients with human T-lymphotropic virus type I-associated myelopathy/tropical spastic paraparesisM Makino
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Kagoshima, Japan
Clin Diagn Lab Immunol 6:316-22. 1999..CI-959-A showed little toxicity toward lymphoma or HTLV-I-infected T-cell lines or toward monocytes and cultured DCs. These results suggest that CI-959-A might be a potent anti-HAM/TSP agent...
Three-drug combination of MKC-442, lamivudine and zidovudine in vitro: potential approach towards effective chemotherapy against HIV-1G Piras
Division of Human Retroviruses, Faculty of Medicine, Kagoshima University, Japan
AIDS 11:469-75. 1997..CONCLUSIONS: Our results demonstrate a potential efficacy of MKC-442 in combination with 3TC and ZDV, and the three-drug combination should be considered for treatment of AIDS patients...
Apoptosis and cell proliferation in esophageal sqamous cell carcinoma treated by chemotherapyH Okumura
First Department of Surgery, Faculty of Medicine, Kagoshima University, Kagoshima, Japan
Cancer Lett 158:211-6. 2000..60, P<0.05). In esophageal carcinoma, p53-negative tumors with highly proliferative cells might be susceptible to apoptosis induced by chemotherapy...
Inhibition of human immunodeficiency virus type 1 replication and cytokine production by fluoroquinoline derivativesM Baba
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Kagoshima 890, Japan
Mol Pharmacol 53:1097-103. 1998....
Inhibition of human immunodeficiency virus type 1 replication in acutely and chronically infected cells by EM2487, a novel substance produced by a Streptomyces speciesM Baba
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Kagoshima 890 8520, Japan
Antimicrob Agents Chemother 43:2350-5. 1999..These results suggest that the mechanism of action is attributable in part to the inhibition of Tat function...
Induction of cellular resistance to nucleoside reverse transcriptase inhibitors by the wild-type breast cancer resistance proteinXin Wang
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890-8544, Japan
Biochem Pharmacol 68:1363-70. 2004..Furthermore, the BCRP-specific inhibitor fumitremorgin C completely restored the reduction of AZT in MT-4/BCRP cells. These results indicate that, like BCRP(R482M), BCRP(WT) also plays an important role in cellular resistance to NRTIs...
How the lymph node metastases toward cervico-upper mediastinal region affect the outcome of patients with carcinoma of the thoracic esophagusS Nakano
First Department of Surgery, Faculty of Medicine, Kagoshima University, Japan
Jpn J Clin Oncol 29:248-51. 1999..The aim of this study was to establish whether the site of lymph node metastasis influences the survival of patients with carcinoma of the thoracic esophagus...
Complete inhibition of viral breakthrough by combination of MKC-442 with AZT during a long-term culture of HIV-1 infected cellsM Okamoto
Division of Human Retroviruses, Faculty of Medicine, Kagoshima University 8 35 1, Japan
Antiviral Res 31:69-77. 1996....
Effect of neoadjuvant chemotherapy for lymph node micrometastasis and tumor cell microinvolvement in the patients with esophageal carcinomaS Natsugoe
First Department of Surgery, Kagoshima University School of Medicine, 8 35 1 Sakuragaoka, Kagoshima 890 8520, Japan
Cancer Lett 159:119-25. 2000..0%; 2/20) was significantly lower than that in the surgery group (40.0%; 8/20; P=0.032). Preoperative chemotherapy in this regime was not effective, except for some patients with TCM alone...
Highly potent inhibition of human immunodeficiency virus type 1 replication by TAK-220, an orally bioavailable small-molecule CCR5 antagonistKatsunori Takashima
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1, Sakuragaoka, Kagoshima 890-8544, Japan
Antimicrob Agents Chemother 49:3474-82. 2005..At a dose of 5 mg/kg of body weight, TAK-220 showed oral bioavailabilities of 9.5 and 28.9% in rats and monkeys, respectively. Thus, TAK-220 is a promising candidate for the treatment of HIV-1 infection...
Inhibitory effects of small-molecule CCR5 antagonists on human immunodeficiency virus type 1 envelope-mediated membrane fusion and viral replicationK Takashima
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Kagoshima 890-8520, Japan
Antimicrob Agents Chemother 45:3538-43. 2001..These results indicate that the HIV-1 Env-mediated membrane fusion assay is a useful tool for the evaluation of entry inhibitors...
Isolation and characterization of human immunodeficiency virus type 1 resistant to the small-molecule CCR5 antagonist TAK-652Masanori Baba
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, 8 35 1, Sakuragaoka, Kagoshima 890 8544, Japan
Antimicrob Agents Chemother 51:707-15. 2007..Several amino acid changes not only in the V3 region but also in other Env regions seemed to be required for R5 HIV-1 to acquire complete resistance to TAK-652...
Three-drug combinations of emivirine and nucleoside reverse transcriptase inhibitors in vitro: long-term culture of HIV-1-infected cells and breakthrough virusesT Nitanda
Division of Human Retroviruses, Centre for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Kagoshima, Japan
Antivir Chem Chemother 12:161-7. 2001..These viruses had specific amino acid mutations in their reverse transcriptase...
The role of human T-lymphotropic virus type 1 (HTLV-1)-infected dendritic cells in the development of HTLV-1-associated myelopathy/tropical spastic paraparesisM Makino
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Kagoshima 890 8520, Japan
J Virol 73:4575-81. 1999..These results suggest that DCs are susceptible to HTLV-1 infection and that their cognate interaction with T cells may contribute to the development of HAM/TSP...
Inhibition of human T-lymphotropic virus type I gene expression by the Streptomyces-derived substance EM2487X Wang
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Japan
Antivir Chem Chemother 13:177-83. 2002..These results suggest that the inhibition occurred at the viral transcription level, but it cannot be attributed to the inhibition of the Tax function...
Number of lymph node metastases determined by presurgical ultrasound and endoscopic ultrasound is related to prognosis in patients with esophageal carcinomaS Natsugoe
First Department of Surgery, Kagoshima University School of Medicine, Sakuragaoka, Kagoshima, Japan
Ann Surg 234:613-8. 2001....
The role of neoadjuvant radiochemotherapy using low-dose fraction cisplatin and 5-fluorouracil in patients with carcinoma of the esophagusS Nakano
First Department of Surgery, Faculty of Medicine, Kagoshima University, Kagoshima, Japan
Jpn J Thorac Cardiovasc Surg 49:11-6. 2001..The combination of radiation and low-dose fraction CDDP/5-FU thus is first choice in neoadjuvant radiochemotherapy for the advanced esophageal carcinoma...
Anti-human immunodeficiency virus type 1 activity and resistance profile of 2',3'-didehydro-3'-deoxy-4'-ethynylthymidine in vitroTakao Nitanda
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1, Sakuragaoka, Kagoshima 890-8544, Japan
Antimicrob Agents Chemother 49:3355-60. 2005..Since 4'-Ed4T has increased anti-HIV-1 activity, decreased cytotoxicity, and a different resistance profile, it should be considered for further development as a new member of NRTIs...
Recent status of HIV-1 gene expression inhibitorsMasanori Baba
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890 8544, Japan
Antiviral Res 71:301-6. 2006....
Suppression of cytokine production and neural cell death by the anti-inflammatory alkaloid cepharanthine: a potential agent against HIV-1 encephalopathyM Okamoto
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, 8-35-1, Sakuragaoka, 890-8520, Kagoshima, Japan
Biochem Pharmacol 62:747-53. 2001..Thus, cepharanthine should be investigated further for its therapeutic and prophylactic potential in HIV-1-associated CNS disorders...
Micrometastases in the cervical lymph nodes in esophageal squamous cell carcinomaS W Qubain
First Department of Surgery, Kagoshima University, School of Medicine, Kagoshima, Japan
Dis Esophagus 14:143-8. 2001..Cervical lymph node metastasis, including micrometastasis, can be predicted by preoperative ultrasonography and the routine histologic examination of mediastinal recurrent nerve nodes...
Potent and selective inhibition of Tat-dependent HIV-1 replication in chronically infected cells by a novel naphthalene derivative JTK-101Xin Wang
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan
Antivir Chem Chemother 18:201-11. 2007..These results suggest that JTK-101 exerts its anti-HIV-1 activity through the inhibition of known or unknown Tat cofactors, presumably CDK9/cyclin T1...
Bax and Bcl-X(L) expression are not related to prognosis in patients with advanced esophageal squamous cell carcinomaS Natsugoe
First Department of Surgery, Kagoshima University School of Medicine, 8 35 1 Sakuragaoka, 890 8520, Kagoshima, Japan
Cancer Lett 174:91-7. 2001..Multiple apoptotic pathways may be associated with advanced esophageal squamous cell carcinoma...
Can sentinel node navigation surgery reduce the extent of lymph node dissection in gastric cancer?T Aikou
First Department of Surgery, Kagoshima University School of Medicine, Japan
Ann Surg Oncol 8:90S-93S. 2001..SNNS for gastric cancer is a promising technique; further study of various anatomic and pathologic factors will indicate whether it can be used to determine the extent of lymphadenectomy necessary in patients with early gastric cancer...
Expression of p21WAF1/Cip1 in the p53-dependent pathway is related to prognosis in patients with advanced esophageal carcinomaS Natsugoe
First Department of Surgery, Kagoshima University School of Medicine, Japan
Clin Cancer Res 5:2445-9. 1999..Examination of p21-positive expression in the p53-dependent pathway will help to estimate the favorable prognosis of patients with advanced esophageal carcinoma...
Long-term survivors of advanced esophageal cancer without surgical treatment: a multicenter questionnaire survey in Kyushu, JapanS Natsugoe
First Department of Surgery, Kagoshima University School of Medicine, Kagoshima, Japan
Dis Esophagus 16:239-42. 2003..To improve the prognosis of patients with advanced esophageal cancer who, for various causes, cannot undergo surgical treatment, a new protocol for adjuvant therapy is required...
Modified myeloid dendritic cells act as regulatory dendritic cells to induce anergic and regulatory T cellsKatsuaki Sato
Department of Immunology and Medical Zoology, Division of Human Retroviruses, Center for Chronic Viral Diseases, School of Medicine, Kagoshima University, Kagoshima City, Kagoshima, Japan
Blood 101:3581-9. 2003..Thus, the modulation of T cell-mediated immunity by regulatory DCs provides a novel therapeutic approach for immunopathogenic diseases...
Regulatory dendritic cells protect mice from murine acute graft-versus-host disease and leukemia relapseKatsuaki Sato
Department of Immunology and Medical Zoology, School of Medicine, Kagoshima University, 8 35 1 Sakuragaoka, Kagoshima City, 890 8520, Kagoshima, Japan
Immunity 18:367-79. 2003..Thus, the use of rDCs may be therapeutically useful for the treatment of acute GVHD and leukemia relapse in allogeneic BMT...
Novel reporter T-cell line highly susceptible to both CCR5- and CXCR4-using human immunodeficiency virus type 1 and its application to drug susceptibility testsHiroshi Miyake
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Kagoshima 890-8520, USA
J Clin Microbiol 41:2515-21. 2003..Thus, MOCHA cells are an extremely useful tool for detection of R5 and X4 HIV-1 replication and drug susceptibility tests...
The role of breast cancer resistance protein (BCRP/ABCG2) in cellular resistance to HIV-1 nucleoside reverse transcriptase inhibitorsXin Wang
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan
Antivir Chem Chemother 16:213-6. 2005..Thus, BCRP is considered to be a cellular factor that modulates the anti-HIV-1 activity of NRTIs...
Selective inhibition of porcine endogenous retrovirus replication in human cells by acyclic nucleoside phosphonatesMinyi Shi
Frontier Science Research Center, Kagoshima University, Kagoshima 890 8544, Japan
Antimicrob Agents Chemother 51:2600-4. 2007..Among the test compounds, zidovudine was found to be the most active. The order of potency was zidovudine > phosphonylmethoxyethoxydiaminopyrimidine = phosphonylmethoxypropyldiaminopurine > tenofovir > or = adefovir > stavudine...
Production of functionally deficient dendritic cells from HTLV-I-infected monocytes: implications for the dendritic cell defect in adult T cell leukemiaM Makino
Division of Human Retroviruses, Center for Chronic Viral Diseases, Kagoshima University, 8 35 1 Sakuragaoka, Kagoshima 890 8520, Japan
Virology 274:140-8. 2000..These results suggest that HTLV-I-infected monocytes cannot properly differentiate to DCs and that this might be one of the important mechanisms producing dysfunctional DCs in ATL patients...
Induction of dendritic cell-mediated immune responses against HIV-1 by antigen-capturing nanospheres in miceMasaki Kawamura
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan
J Med Virol 76:7-15. 2005..These results suggest that the use of HIV-1-NS may provide a novel and promising approach for the induction of humoral and cellular immune responses to HIV-1...
Inhibition of the tax-dependent human T-lymphotropic virus type I replication in persistently infected cells by the fluoroquinolone derivative k-37Xin Wang
Division of Human Retroviruses, Third Department of Internal Medicine, Faculty of Medicine, Kagoshima University, Kagoshima, Japan
Mol Pharmacol 61:1359-65. 2002..These results suggest that the inhibition occurred at the level of HTLV-I LTR-driven Tax expression...
Targeting of antigen to dendritic cells with poly(gamma-glutamic acid) nanoparticles induces antigen-specific humoral and cellular immunityTomofumi Uto
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, 8 35 1 Sakuragaoka, Kagoshima, Japan
J Immunol 178:2979-86. 2007..These results suggest that Ag-carrying gamma-PGA NPs are capable of inducing strong cellular and humoral immune responses and might be potentially useful as effective vaccine adjuvants for the therapy of infectious diseases...
[Basic approaches to anti-HIV resistance]Masanori Baba
Center for Chronic Viral Research, Faculty of Medicine, Kagoshima University
Nippon Rinsho 60:763-8. 2002..Furthermore, molecular mechanisms of the resistance induced by some RTIs and PIs have been well understood. Novel inhibitors effective against the resistant mutants have recently been discovered and are under clinical trials...
Colorimetric lactate dehydrogenase (LDH) assay for evaluation of antiviral activity against bovine viral diarrhoea virus (BVDV) in vitroChiaki Baba
Department of Dermatology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan
Antivir Chem Chemother 16:33-9. 2005....
Eicosapentaenoic acid reduces pulmonary edema in endotoxemic ratsS Sane
First Department of Surgery, Kagoshima University School of Medicine, 8 35 1, Sakuragaoka, Kagoshima, 890 8520, Japan
J Surg Res 93:21-7. 2000..At 6 h, wet/dry (W/D) weight ratios were calculated for the lungs to assess pulmonary edema, and neutrophils were counted in pulmonary parenchyma and peripheral blood...
Epstein-Barr virus involvement is mainly restricted to lymphoepithelial type of gastric carcinoma among various epithelial neoplasmsY Kijima
The First Department of Surgery, Faculty of Medicine, Kagoshima University, Kagoshima, Japan
J Med Virol 64:513-8. 2001..As a result, EBV was associated with only some gastric carcinomas but not with other epithelial neoplasms originating from the lung, esophagus, breast, colon, pancreas, and thyroid in southern Japan...
Modulation of gene expression related to Toll-like receptor signaling in dendritic cells by poly(gamma-glutamic acid) nanoparticlesTakayuki Hamasaki
Division of Antiviral Chemotherapy, Center for Chronic Viral Disease, Graduate School of Medical and Dental Sciences, Kagoshima University, Japan
Clin Vaccine Immunol 17:748-56. 2010..Thus, gamma-PGA NPs may be an attractive candidate to be developed further as a vaccine adjuvant...
Modulation of innate and adaptive immunity by biodegradable nanoparticlesTomofumi Uto
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan
Immunol Lett 125:46-52. 2009..Thus, gamma-PGA NPs have great potential as an efficient antigen carrier and strong adjuvant to DCs...
Long-term culture of HIV-1-infected cells with the transcription inhibitor K-37Kazunobu Yamataka
Division of Human Retroviruses, Center for Chronic Viral Diseases Faculty of Medicine, Kagoshima University, Kagoshima 890-8520, Japan
Antiviral Res 56:85-92. 2002..Furthermore, both M(1) and U(1) had a G to T nucleotide mutation at position -215 in the second nuclear factor of activated T-cells-binding domain (-215 to -203) of the HIV-1 long terminal repeat...
Inhibition of porcine endogenous retrovirus (PERV) replication by HIV-1 gene expression inhibitorsMinyi Shi
Frontier Science Research Center, Kagoshima University, Kagoshima, Japan
Antiviral Res 83:201-4. 2009..Thus, retroviral gene expression inhibitors may be able to reduce the risk of PERV transmission...
Induction of potent CD8+ T-cell responses by novel biodegradable nanoparticles carrying human immunodeficiency virus type 1 gp120Xin Wang
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, 8 35 1 Sakuragaoka, Kagoshima 890 8544, Japan
J Virol 81:10009-16. 2007..Thus, gamma-PGA NPs carrying various HIV-1 antigens may have great potential as a novel priming and/or boosting tool in current vaccination regimens for the induction of cellular immune responses...
Preserved Smad4 expression in the transforming growth factor beta signaling pathway is a favorable prognostic factor in patients with advanced gastric cancerC Xiangming
First Department of Surgery, School of Medicine, Kagoshima University, Japan
Clin Cancer Res 7:277-82. 2001..05). According to multivariate analysis, Smad4 expression acted as an independent prognostic factor. Smad4 expression, particularly in the TGF-beta pathway, is an effective predictor of outcome for patients with advanced gastric cancer...
Anti-bovine viral diarrhoea virus activity of novel diphenylmethane derivativesMohammed T A Salim
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan
Antivir Chem Chemother 20:193-200. 2010..Among them, some diphenylmethane derivatives were found to be selective inhibitors of BVDV...
Improvement of adaptive immunity by antigen-carrying biodegradable nanoparticlesTomofumi Uto
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890 8544, Japan
Biochem Biophys Res Commun 379:600-4. 2009..Strong antibody production was observed by s.c. immunization, yet no antibody was identified by intranasal immunization. Thus, gamma-PGA NPs are a safe and efficient antigen carrier with unique immunological properties...
Poly(gamma-glutamic acid) nanoparticles as an efficient antigen delivery and adjuvant system: potential for an AIDS vaccineXin Wang
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan
J Med Virol 80:11-9. 2008..Thus, gamma-PGA nanoparticles encapsulating various antigens may have great potential as novel and efficient protein-based vaccines against infectious diseases, including HIV-1 infection...
Induction of mucosal IgA following intravaginal administration of inactivated HIV-1-capturing nanospheres in miceMasaki Kawamura
Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Kagoshima, Japan
J Med Virol 66:291-8. 2002..Thus, HIV-NS may have great potential as a prophylactic HIV-1 vaccine and should be examined further for its efficacy in non-human primates...
HIV-1-infected macrophages induce astrogliosis by SDF-1alpha and matrix metalloproteinasesMika Okamoto
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Japan
Biochem Biophys Res Commun 336:1214-20. 2005..These results indicate that the activated and HIV-1-infected macrophages can indirectly induce astrocyte proliferation through up-regulating SDF-1alpha and MMP production, which implies a mechanism of astrogliosis in HAD...
Establishment of an in vitro assay system mimicking human immunodeficiency virus type 1-induced neural cell death and evaluation of inhibitors thereofMika Okamoto
Faculty of Medicine, Division of Human Retroviruses, Center for Chronic Viral Diseases, Faculty of Medicine Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima 890-8520, Japan
J Virol Methods 108:195-203. 2003..These results indicate that this system seems to be a useful tool for the evaluation of compounds against HIV-1-induced neural cell death...
Association of CD40 ligand expression on HTLV-I-infected T cells and maturation of dendritic cellsM Makino
Division of Human Retrovirus, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshima University, Japan
Scand J Immunol 54:574-81. 2001..The CD40L+ T-cell-induced maturation was blocked by anti-CD40L antibody. Therefore, the lack of CD40L expression on HTLV-I-infected T cells may be associated with the development of ATL...
Induction of thymidine phosphorylase expression by AZT contributes to enhancement of 5'-DFUR cytotoxicityKengo Tsuneyoshi
Department of Molecular Oncology, Field of Oncology, Course of Advanced Therapeutics, Graduate School of Medical and Dental Sciences, Kagoshima University, Sakuragaoka 8-35-1, Kagoshima 890-8520, Japan
Cancer Lett 244:239-46. 2006..These results suggest that AZT enhances the cytotoxic effect of 5'-DFUR on U937 cells by upregulating TP activity in addition to its inhibition of thymidine kinase (TK) activity and reduction of intracellular dTTP pools...
IgG responses to intranasal immunization with cholera-toxin-immobilized polymeric nanospheres in miceTatsuo Kaneko
Department of Nanostructured and Advanced Materials, Graduate School of Science and Engineering, Kagoshima University, 1-21-40 Korimoto, Kagoshima 890-0065, Japan
J Biomater Sci Polym Ed 15:661-9. 2004..Thus, polymeric NS may be an effective substrate to covalently immobilize antigen on their surface, steadily inducing a high level of IgG production in response to the intranasal administration...
Anti-bovine viral diarrhoea virus and hepatitis C virus activity of the cyclooxygenase inhibitor SC-560Mika Okamoto
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan
Antivir Chem Chemother 20:47-54. 2009..A number of compounds were examined for their inhibitory effect on bovine viral diarrhoea virus (BVDV) replication in cell cultures and found that some cyclooxygenase (COX) inhibitors had antiviral activity against the virus...
Highly enhanced expression of CD70 on human T-lymphotropic virus type 1-carrying T-cell lines and adult T-cell leukemia cellsMasanori Baba
Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, 8 35 1, Sakuragaoka, Kagoshima 890 8544, Japan
J Virol 82:3843-52. 2008..Since CD70 expression is strictly restricted in normal tissues, such as highly activated T and B cells, CD70 appears to be a potential target for effective antibody therapy against ATL...
High-sensitivity analysis of naturally occurring sugar chains, using a novel fluorescent linker moleculeMasaki Sato
Department of Nanostructure and Advanced Materials, Kagoshima University, Kohrimoto, Japan
J Biochem 146:33-41. 2009..Immobilization of the FLC onto gold-coated chips, and their subsequent SPR analyses were successively accomplished, as had been performed previously using non-fluorescent ligand conjugates...
Discovery of a piperidine-4-carboxamide CCR5 antagonist (TAK-220) with highly potent Anti-HIV-1 activityShinichi Imamura
Pharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Yodogawa ku, Osaka 532 8686, Japan
J Med Chem 49:2784-93. 2006..1 nM, EC(90) = 13 nM) and exhibited a good pharmacokinetic profile in monkeys (BA = 29%). This compound has been chosen as a clinical candidate for further development...
Protein direct delivery to dendritic cells using nanoparticles based on amphiphilic poly(amino acid) derivativesTakami Akagi
Department of Applied Chemistry, Graduate School of Engineering, Osaka University, 2 1 Yamadaoka, Suita 565 0871, Japan
Biomaterials 28:3427-36. 2007..This system has potential application as a universal delivery system for protein-based vaccines capable of inducing cytotoxic T lymphocyte (CTL)...
Synthesis and anti-human immunodeficiency virus activity of 4'-branched (+/-)-4'-thiostavudinesHiroki Kumamoto
School of Pharmaceutical Sciences, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan
J Med Chem 49:7861-7. 2006..6 and 0.74 microM, respectively. The activity of 29 was comparable to that of stavudine, but 29 was not as active as 4. Optical resolution of 29 was briefly examined...
Intracellular metabolism and persistence of the anti-human immunodeficiency virus activity of 2',3'-didehydro-3'-deoxy-4'-ethynylthymidine, a novel thymidine analogElijah Paintsil
Department of Pharmacology, Yale University School of Medicine, 333 Cedar Street, SHM B226, New Haven, CT 06520, USA
Antimicrob Agents Chemother 51:3870-9. 2007..4'-Ed4T is a promising antiviral candidate for HIV type 1 chemotherapy...
Synthesis and anti-HIV activity of 4'-substituted 4'-thiothymidines: a new entry based on nucleophilic substitution of the 4'-acetoxy groupKazuhiro Haraguchi
School of Pharmaceutical Sciences, Showa University, 1 5 8 Hatanodai, Shinagawa ku, Tokyo, Japan
J Med Chem 51:1885-93. 2008..It is noteworthy that 36 and 37 were also inhibitory against replication of HIV variant resistant to 3TC (HIV-1 M184V), being as potent as against HIV-1 IIIB...
Highly selective action of triphosphate metabolite of 4'-ethynyl D4T: a novel anti-HIV compound against HIV-1 RTGuangwei Yang
Department of Pharmacology, School of Medicine, Yale University, 333 Cedar Street, New Haven, CT 06520, USA
Antiviral Res 73:185-91. 2007..4'-Ed4TTP showed much less inhibitory effects toward major host DNA polymerases. Overall, our results suggest that 4'-Ed4TTP is the active form for anti-HIV-1 activity via its inhibitory effect against RT...
Highly potent and orally active CCR5 antagonists as anti-HIV-1 agents: synthesis and biological activities of 1-benzazocine derivatives containing a sulfoxide moietyMasaki Seto
Pharmaceutical Research Division, Takeda Pharmaceutical Company Limited, 2 17 85 Jusohonmachi, Yodogawa ku, Osaka 532 8686, Japan
J Med Chem 49:2037-48. 2006..The synthesis and biological activity of the 1-benzazocine compound (S)-(-)-5b and its related derivatives are described...
Studies of non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: synthesis and structure-activity relationships of 2-cyano and 2-hydroxy thiazolidenebenzenesulfonamide derivativesNaoyuki Masuda
Institute for Drug Discovery Research, Yamanouchi Pharmaceutical Co, Ltd, 21 Miyukigaoka, Tsukuba, Ibaraki 305 8585, Japan
Bioorg Med Chem 13:949-61. 2005..Compound 11g (YM-215389), a combination of 2-hydroxyphenyl and 4-chloro-5-isopropylthiazole moieties, proved to be the most active against both K103N and Y181C RTs with IC50 values of 0.043 and 0.013 microM, respectively...
Orally active CCR5 antagonists as anti-HIV-1 agents. Part 3: Synthesis and biological activities of 1-benzazepine derivatives containing a sulfoxide moietyMasaki Seto
Pharmaceutical Research Division, Takeda Pharmaceutical Company, Ltd, 2 17 85 Jusohonmachi, Yodogawa ku, Osaka 532 8686, Japan
Bioorg Med Chem 13:363-86. 2005..In addition, we established the synthesis of (S)-4r and (S)-4w by asymmetric oxidation with titanium-(S)-(-)-1,1'-bi-2-naphthol complex...
Studies of nonnucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Design and synthesis of thiazolidenebenzenesulfonamidesNaoyuki Masuda
Institute for Drug Discovery Research, Yamanouchi Pharmaceutical Co Ltd, 21 Miyukigaoka, Tsukuba, Ibaraki 305 8585, Japan
Bioorg Med Chem 12:6171-82. 2004..These results confirm the important role of the substituents at these positions and the thiazolidenebenzenesulfonamide motif as a valuable lead series for the next generation NNRTIs...
Orally active CCR5 antagonists as anti-HIV-1 agents 2: synthesis and biological activities of anilide derivatives containing a pyridine N-oxide moietyMasaki Seto
Medicinal Chemistry Research Laboratries, Pharmaceutical Research Division, Takeda Chemical Industries Ltd Osaka, Japan
Chem Pharm Bull (Tokyo) 52:818-29. 2004..In particular, compound (S)-5s showed the most potent CCR5 antagonistic activity (IC(50)=7.2 nM) and inhibitory effect (IC(50)=5.4 nM) in the fusion assay, together with good pharmacokinetic properties in rats...
Synthesis and anti-HIV activity of 4'-cyano-2',3'-didehydro-3'-deoxythymidineKazuhiro Haraguchi
School of Pharmaceutical Sciences, Showa University, Shinagawa ku, Tokyo, Japan
Nucleosides Nucleotides Nucleic Acids 23:647-54. 2004..Evaluation of the anti-HIV activity of 9 showed that this compound is much less potent than the recently reported 2',3'-didehydro-3'-deoxy-4'-(ethynyl)thymidine (1)...
CCR5 antagonists as anti-HIV-1 agents. Part 2: Synthesis and biological evaluation of N-[3-(4-benzylpiperidin-1-yl)propyl]-N,N'-diphenylureasShinichi Imamura
Pharmaceutical Research Division, Takeda Chemical Industries, Ltd, 2 17 85, Jusohonmachi, Yodogawa ku, Osaka 532 8686, Japan
Bioorg Med Chem 12:2295-306. 2004....
CCR5 antagonists as anti-HIV-1 agents. 1. Synthesis and biological evaluation of 5-oxopyrrolidine-3-carboxamide derivativesShinichi Imamura
Pharmaceutical Research Division, Takeda Chemical Industries Ltd, 2 17 85 Jusohonmachi, Yodogawa ku, Osaka 532 8686, Japan
Chem Pharm Bull (Tokyo) 52:63-73. 2004..038 microM) was found to be effective for improving CCR5 affinity. Compound 10i, 11b, and 12e also inhibited CCR5-using HIV-1 envelope-mediated membrane fusion with IC(50) values of 0.44, 0.19, and 0.49 microM, respectively...
Synthesis and anti-HIV-1 activity of novel 10-thiaisoalloxazines, a structural analog of C-5 and/or C-6 substituted pyrimidine acyclonucleosideTakanori Miyashita
Biochemical Division, Yamasa Corporation, Chiba, Japan
Chem Pharm Bull (Tokyo) 51:630-4. 2003..Among the derivatives, compounds 6, 7, and 8 bearing an alkoxymethyl moiety at the N-1 position exhibited modest inhibitory activity towards the cytotopathic effect of HIV-1...
TRAIL-transduced dendritic cells protect mice from acute graft-versus-host disease and leukemia relapseKatsuaki Sato
Laboratory for Dendritic Cell Immunobiology, Research Center for Allergy and Immunology, RIKEN Yokohama Institute, Kanagawa, Japan
J Immunol 174:4025-33. 2005..Thus, gene transfer of TRAIL to DCs is a novel modality for the treatment of acute GVHD and leukemia relapse by selective targeting of pathogenic T cells and leukemic cells...
Orally active CCR5 antagonists as anti-HIV-1 agents: synthesis and biological activity of 1-benzothiepine 1,1-dioxide and 1-benzazepine derivatives containing a tertiary amine moietyMasaki Seto
Medicinal Chemistry Research Laboratries, Pharmaceutical Research Division, Takeda Chemical Industries Ltd, Osaka, Japan
Chem Pharm Bull (Tokyo) 52:577-90. 2004..7 nM) and inhibitory effect (IC(50)=1.2 nM) on membrane fusion, together with good pharmacokinetic properties in rats. The synthesis of 1-benzothiepine 1,1-dioxide and 1-benzazepine derivatives and their biological activity are described...
4'-Ethynylstavudine (4'-Ed4T) has potent anti-HIV-1 activity with reduced toxicity and shows a unique activity profile against drug-resistant mutantsHiromichi Tanaka
School of Pharmaceutical Sciences, Showa University, Tokyo, Japan
Antivir Chem Chemother 16:217-21. 2005..The study of 4'-Ed4T against various drug-resistant HIV-1 mutants has disclosed its unique activity profile...
CCR5 antagonists as anti-HIV-1 agents. Part 3: Synthesis and biological evaluation of piperidine-4-carboxamide derivativesShinichi Imamura
Pharmaceutical Research Division, Takeda Pharmaceutical Co Ltd, 2 17 85, Jusohonmachi, Yodogawa ku, Osaka 532 8686, Japan
Bioorg Med Chem 13:397-416. 2005..The selected compound 11f showed excellent antiviral activity against CCR5-using HIV-1 replication in human peripheral blood mononuclear cells (EC50=0.59 nM) and an acceptable pharmacokinetic profile in dogs...
Synthesis of (+/-)-4'-ethynyl and 4'-cyano carbocyclic analogues of stavudine (d4T)Hiroki Kumamoto
School of Pharmaceutical Sciences, Showa University, Tokyo, Japan
Nucleosides Nucleotides Nucleic Acids 24:73-83. 2005..The ethynyl or cyano group of 8 and 9 were prepared, after the introduction of thymine base to 16, by manipulation of the ester function. Evaluation of the anti-HIV activity of 8 and 9 was also carried out...
Antiviral Chemistry & Chemotherapy's current antiviral agents FactFile 2006 (1st edition)Hugh J Field
Antivir Chem Chemother 17:111-2. 2006
Synthesis of a highly active new anti-HIV agent 2',3'-didehydro-3'-deoxy-4'-ethynylthymidineKazuhiro Haraguchi
School of Pharmaceutical Sciences, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan
Bioorg Med Chem Lett 13:3775-7. 2003..The compounds were assayed for their ability to inhibit the replication of HIV in cell culture. The 4'-ethynyl analogue (15) was found to be more potent and less toxic than the parent compound stavudine...
AIDS vaccine: Intranasal immunization using inactivated HIV-1-capturing core-corona type polymeric nanospheresTakami Akagi
Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Suita, Japan
J Control Release 109:49-61. 2005..These results suggest that HIV-NS provides an efficient vaccine delivery system for the induction of a mucosal immune response and the development of a mucosal vaccine...
Mucosal immunization with inactivated HIV-1-capturing nanospheres induces a significant HIV-1-specific vaginal antibody response in miceTakami Akagi
Japan Immunoresearch Laboratories, Takasaki, Gunma, Japan
J Med Virol 69:163-72. 2003..Intranasal immunization with HIV-NS should be further pursued for its potential as an HIV-1 prophylactic vaccine...
A new approach to the synthesis of 4'-carbon-substituted nucleosides: development of a highly active anti-HIV agent 2', 3'-didehydro-3'-deoxy-4'-ethynylthymidineKazuhiro Haraguchi
School of Pharmaceutical Sciences, Showa University, Tokyo, Japan
Nucleosides Nucleotides Nucleic Acids 24:343-7. 2005..Evaluation of their ability to inhibit the replication of HIV in cell culture showed that 4'-ethynyl-d4T (19) is more potent and less toxic than the parent compound d4T...
[Development of vaccine adjuvants using polymeric nanoparticles and their potential applications for anti-HIV vaccine]Takami Akagi
Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Yamadaoka, Suita City, Japan
Yakugaku Zasshi 127:307-17. 2007..These HIV-1-capturing nanospheres and protein-loaded gamma-PGA nanoparticles have shown unique potential as vaccine carriers...
Synthesis and antiviral activities of 1'-carbon-substituted 4'-thiothymidinesKazuhiro Haraguchi
School of Pharmaceutical Sciences, Showa University, 1 5 8 Hatanodai, Shinagawa ku, Tokyo 142 8555, Japan
Bioorg Med Chem 12:5309-16. 2004..Among the deprotected 1'-branched 4'-thiothymidines (20-25), the 1'-methyl analogue 20 showed the most potent anti-HSV-1 activity, but it was much less active than the parent compound 4'-thiothymidine...
Gamma-carboline derivatives with anti-bovine viral diarrhea virus (BVDV) activityKumiko Sako
Institute of Molecular and Cellular Biosciences, The University of Tokyo, 1 1 1 Yayoi, Bunkyo ku, Tokyo 113 0032, Japan
Bioorg Med Chem 16:3780-90. 2008..Structural development studies led to a potent anti-viral agent, SK5M (5-methyl-gamma-carboline), with the EC(50) of 0.26 microM...
Synthesis of benzodithiol-2-yl-substituted nucleoside derivatives as lead compounds having anti-bovine viral diarrhea virus activityKohji Seio
Frontier Collaborative Research Center and Department of Life Science, Tokyo Institute of Technology, Nagatsuta, Midori-ku, Yokohama 226-8501, Japan
J Med Chem 47:5265-75. 2004..Since BVDV has been recognized as a surrogate for human hepatitis C virus (HCV), the BDT-modified nucleosides might become a new class of lead compounds to find nucleoside-type anti-HCV agents such as ribavirin...
Comparison of the phosphorylation of 4'-ethynyl 2',3'-dihydro-3'-deoxythymidine with that of other anti-human immunodeficiency virus thymidine analogsChih Hung Hsu
Department of Pharmacology, Yale University School of Medicine, New Haven, CT 06520, USA
Antimicrob Agents Chemother 51:1687-93. 2007..Qualitatively, the metabolism of 4'-ethynyl D4T is more similar to that of AZT than to that of its progenitor, D4T...
Fusion of mature dendritic cells and human T-lymphotropic virus type I infected T cells: its efficiency as an antigen-presenting cellSatoshi Shimokubo
Department of Microbiology, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo, 189-0002, Japan
Virology 301:13-20. 2002..The results suggest that fusion DC-T cells produce functionally competent Ag-presenting cells and may be a likely candidate for immunotherapeutic use...
