JP2010511597A5 - - Google Patents

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JP2010511597A5
JP2010511597A5 JP2009524035A JP2009524035A JP2010511597A5 JP 2010511597 A5 JP2010511597 A5 JP 2010511597A5 JP 2009524035 A JP2009524035 A JP 2009524035A JP 2009524035 A JP2009524035 A JP 2009524035A JP 2010511597 A5 JP2010511597 A5 JP 2010511597A5
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JP
Japan
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usa
gene
cells
histone
vpa
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JP2009524035A
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JP4887427B2 (ja
JP2010511597A (ja
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Priority claimed from PCT/JP2007/074067 external-priority patent/WO2008069349A1/en
Publication of JP2010511597A publication Critical patent/JP2010511597A/ja
Publication of JP2010511597A5 publication Critical patent/JP2010511597A5/ja
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ヒトの乳癌細胞株、MCF−7細胞およびHMC−1細胞を用いて、100nM TSA(Sigma,USA)存在下24時間または4mM VPA(Sigma,USA)存在下48時間、それぞれ培養した後、メーカー(Upstate Inc.,USA)の使用説明書に従って、細胞からクロマチンを抽出し抗アセチル化ヒストンH3抗体(Upstate Inc.,USA)を用いてクロマチンの免疫沈降を行った(Assam El−Osta et al.,(2002)MOLECULAR AND CELLULAR BIOLOGY 22(6)p1844−1857を参照のこと)。アセチル化ヒストンと結合している遺伝子を、B2M遺伝子特異的プライマー(GAAAACGGGAAAGTCCCTCT;配列番号1、およびAGATCCAGCCCTGGACTAGC;配列番号2)を用いてPCRにて増幅し、1%アガロースゲルで電気泳動後、臭化エチジウムの存在下、トランスイルミネータで検出した。この結果、いずれの癌細胞においてもB2M遺伝子領域のヒストンは脱アセチル化していることが示された。TSAやVPAのようなHDAC阻害剤の作用によってヒストンアセチル化が促進されると、アセチル化ヒストンとともにB2M遺伝子が検出された(図1)。
JP2009524035A 2006-12-06 2007-12-06 ヒストン脱アセチル化酵素阻害活性を有する物質を用いた細胞性免疫増強剤 Expired - Fee Related JP4887427B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US87322306P 2006-12-06 2006-12-06
US60/873,223 2006-12-06
PCT/JP2007/074067 WO2008069349A1 (en) 2006-12-06 2007-12-06 Potentiation of cellular immunity using histone deacetylase (hdac) inhibitors

Publications (3)

Publication Number Publication Date
JP2010511597A JP2010511597A (ja) 2010-04-15
JP2010511597A5 true JP2010511597A5 (ja) 2010-06-03
JP4887427B2 JP4887427B2 (ja) 2012-02-29

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JP2009524035A Expired - Fee Related JP4887427B2 (ja) 2006-12-06 2007-12-06 ヒストン脱アセチル化酵素阻害活性を有する物質を用いた細胞性免疫増強剤

Country Status (7)

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US (1) US20100093862A1 (ja)
EP (1) EP2091525A1 (ja)
JP (1) JP4887427B2 (ja)
CN (1) CN101626763A (ja)
AU (1) AU2007328872A1 (ja)
CA (1) CA2671649A1 (ja)
WO (1) WO2008069349A1 (ja)

Families Citing this family (8)

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Publication number Priority date Publication date Assignee Title
JP2014505076A (ja) * 2011-01-27 2014-02-27 ザ トラスティーズ オブ プリンストン ユニバーシティ 抗ウイルス剤としてのmTORキナーゼの阻害剤
US9821054B2 (en) * 2011-03-11 2017-11-21 Turnstone Limited Partnership Method of vaccination comprising a histone deacetylase inhibitor
US10335482B2 (en) 2012-06-06 2019-07-02 Bionor Immuno As Method of inducing an anti-HIV-1 immune response comprising administering a C5/TM-GP41 peptide dimer
WO2014082114A1 (en) 2012-11-30 2014-06-05 Commonwealth Scientific And Industrial Research Organisation Wireless backhaul system
CA2905070A1 (en) 2013-03-14 2014-09-25 Genentech, Inc. Methods of treating cancer and preventing cancer drug resistance
CN105617381B (zh) * 2014-10-30 2019-07-05 中国科学院上海巴斯德研究所 组蛋白去乙酰化酶抑制剂治疗β亚科疱疹病毒的新用途
WO2018213699A1 (en) * 2017-05-19 2018-11-22 Memorial Sloan Kettering Cancer Center Methods for modifying endoplasmic reticulum processing of protein
CN111671742B (zh) * 2020-05-17 2023-08-25 中国人民解放军军事科学院军事医学研究院 丙戊酸钠在制备人冠状病毒感染肺炎治疗药物中的应用

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999011659A1 (fr) * 1997-09-02 1999-03-11 Japan Energy Corporation Derives tetrapeptides cycliques et leur utilisation medicinale
US6518012B1 (en) * 1999-04-02 2003-02-11 Health Research, Inc. Method for regulating the expression of MHC antigens and CD40 by inhibitors of histone deacetylation
EP1170008A1 (en) * 2000-07-07 2002-01-09 Chemotherapeutisches Forschungsinstitut Georg-Speyer-Haus Valproic acid and derivatives thereof as histone deacetylase inhibitors
EP1293205A1 (en) * 2001-09-18 2003-03-19 G2M Cancer Drugs AG Valproic acid and derivatives thereof for the combination therapy of human cancers, for the treatment of tumour metastasis and minimal residual disease
ES2308065T3 (es) * 2004-04-30 2008-12-01 Topotarget Germany Ag Formulacion que comprende un inhibidor de histona desacetilasa, que exhibe una liberacion bifasica.
EP2018366A4 (en) * 2006-05-16 2010-08-04 Univ Mcgill HYBRID MOLECULES HAVING MIXED PROPERTIES OF VITAMIN D RECEPTOR AGONISM AND HISTONE DEACETYLASE INHIBITOR

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