JP2009526861A5 - - Google Patents

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Publication number
JP2009526861A5
JP2009526861A5 JP2008555380A JP2008555380A JP2009526861A5 JP 2009526861 A5 JP2009526861 A5 JP 2009526861A5 JP 2008555380 A JP2008555380 A JP 2008555380A JP 2008555380 A JP2008555380 A JP 2008555380A JP 2009526861 A5 JP2009526861 A5 JP 2009526861A5
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JP
Japan
Prior art keywords
seq
lec3
ednra
cxcr4
polypeptide
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JP2008555380A
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Japanese (ja)
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JP2009526861A (en
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Priority claimed from PCT/US2007/004114 external-priority patent/WO2007095353A2/en
Publication of JP2009526861A publication Critical patent/JP2009526861A/en
Publication of JP2009526861A5 publication Critical patent/JP2009526861A5/ja
Pending legal-status Critical Current

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Claims (17)

以下から選択されたポリヌクレオチドを備える単離された発現ベクターと、薬学的に受容可能なキャリアとを備える、動物における血管新生を促進するための医薬品組成物を調製する方法:
(a)配列番号1、配列番号3、配列番号5、配列番号7、配列番号9及び配列番号11、並びに、
(b)配列番号2、配列番号4、配列番号6、配列番号8、配列番号10及び配列番号12のアミノ酸配列を有するポリペプチドをコードする配列。
A method of preparing a pharmaceutical composition for promoting angiogenesis in an animal comprising an isolated expression vector comprising a polynucleotide selected from: and a pharmaceutically acceptable carrier :
(A) SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9 and SEQ ID NO: 11, and
(B) A sequence encoding a polypeptide having the amino acid sequence of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10 and SEQ ID NO: 12.
配列番号10のアミノ酸配列を備えるポリペプチドに高い親和力で特異的に結合する抗体。 An antibody that specifically binds to a polypeptide comprising the amino acid sequence of SEQ ID NO: 10 with high affinity. 配列番号4のアミノ酸配列を備えるポリペプチドの細胞外部分に高い親和力で特異的に結合する抗体。 An antibody that specifically binds with high affinity to the extracellular portion of a polypeptide comprising the amino acid sequence of SEQ ID NO: 4. 前記抗体はモノクローナルである請求項2又は3の抗体。 4. The antibody of claim 2 or 3 , wherein the antibody is monoclonal. 前記抗体はポリクロナールである請求項2又は3の抗体。 The antibody according to claim 2 or 3 , wherein the antibody is a polyclonal. ゼブラフィッシュLEC3、CXCR4又はEDNRAの全部又は一部を生産する方法であって、
発現制御配列に操作可能に結合された配列番号1、配列番号3、配列番号5、配列番号7、配列番号9又は配列番号11の配列を備える発現ベクターを備える宿主細胞を、ゼブラフィッシュLEC3、CXCR4又はEDNRAの全部又は一部の発現に適した培養条件下で培養し、
前記LEC3、CXCR4又はEDNRAの全部又は一部を単離すること、
を備える方法。
A method for producing all or part of zebrafish LEC3, CXCR4 or EDNRA,
A host cell comprising an expression vector comprising the sequence of SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9 or SEQ ID NO: 11 operably linked to an expression control sequence is transformed into zebrafish LEC3, CXCR4. Or cultured under culture conditions suitable for the expression of all or part of EDNRA,
Isolating all or part of the LEC3, CXCR4 or EDNRA;
A method comprising:
LEC3、CXCR4及びEDNRAの全部又は一部をコードする核酸配列を備える単離されたポリヌクレオチドと、薬学的に受容可能なキャリアとを備える治療用組成物。 A therapeutic composition comprising an isolated polynucleotide comprising a nucleic acid sequence encoding all or part of LEC3, CXCR4 and EDNRA, and a pharmaceutically acceptable carrier. 請求項3の抗体と薬学的に受容可能なキャリアとを備える治療用組成物。 A therapeutic composition comprising the antibody of claim 3 and a pharmaceutically acceptable carrier. 配列番号2、配列番号4、配列番号6、配列番号8、配列番号10及び配列番号12から成る群から選択された少なくとも1つのアミノ酸配列を備えるポリペプチドと、薬学的に受容可能なキャリアとを備える治療用組成物。 A polypeptide comprising at least one amino acid sequence selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10 and SEQ ID NO: 12, and a pharmaceutically acceptable carrier. A therapeutic composition comprising. LEC3の発現を抑制する血管新生を抑制するのに十分な量のポリヌクレオチドと、薬学的に受容可能なキャリアとを備える、血管新生関連の疾病を治療するための医薬品組成物を調製する方法 A method for preparing a pharmaceutical composition for treating angiogenesis-related diseases, comprising a sufficient amount of a polynucleotide to suppress angiogenesis that suppresses LEC3 expression and a pharmaceutically acceptable carrier . LEC3、CXCR4及びEDNRAポリペプチドの全部又は一部をコードする有効量の第1のポリヌクレオチドと、VEGFポリペプチドをコードする有効量の第2のポリヌクレオチドと、薬学的に受容可能なキャリアとを備える、必要とする動物の血管新生を促進するための医薬品組成物を調製する方法。 An effective amount of a first polynucleotide encoding all or a portion of the LEC 3, CXCR4 and EDNRA polypeptides; an effective amount of a second polynucleotide encoding a VEGF polypeptide; and a pharmaceutically acceptable carrier. A method of preparing a pharmaceutical composition for promoting angiogenesis in an animal in need thereof . LEC3、CXCR4及び/又はEDNRA活性を抑制する化合物を同定する方法であって、試験化合物をLEC3、CXCR4及び/又はEDNRAポリペプチドと接触させ、前記試験化合物がLEC3、CXCR4及び/又はEDNRA活性を抑制するかどうか判断することを備え、LEC3、CXCR4及び/又はEDNRAの活性を抑制する試験化合物は、LEC3、CXCR4及び/又はEDNRAのアンタゴニストであると同定される方法。 A method of identifying a compound that inhibits LEC3, CXCR4 and / or EDNRA activity, wherein the test compound is contacted with LEC3, CXCR4 and / or EDNRA polypeptide, said test compound inhibits LEC3, CXCR4 and / or EDNRA activity A test compound that inhibits the activity of LEC3, CXCR4 and / or EDNRA is identified as an antagonist of LEC3, CXCR4 and / or EDNRA. LEC3、CXCR4及び/又はEDNRAの前記生物活性は、LEC3、CXCR4及び/又はEDNRAに前記試験化合物を結合することにより測定される請求項12の方法。 13. The method of claim 12 , wherein the biological activity of LEC3, CXCR4 and / or EDNRA is measured by binding the test compound to LEC3, CXCR4 and / or EDNRA. LEC3、CXCR4及び/又はEDNRAの生物学的な機能を抑制する有効量の細胞浸透性ペプチドを細胞に投与することを備える血管新生を抑制する方法。 A method for inhibiting angiogenesis, comprising administering to a cell an effective amount of a cell-penetrating peptide that inhibits the biological function of LEC3, CXCR4 and / or EDNRA. VEGFの発現又は生物学的機能を抑制する化合物の投与をさらに備える請求項14の方法。 15. The method of claim 14 , further comprising administration of a compound that inhibits VEGF expression or biological function. 以下から成る群から選択された化合物と、薬学的に受容可能なキャリアとを備える、血管新生を促進するための医薬品組成物を調製する方法:
(a) 配列番号41、配列番号43、配列番号45、配列番号47、配列番号のヌクレオチド配列を有するポリヌクレオチドを備える単離された発現ベクター、
(b) 配列番号42、配列番号44、配列番号46、配列番号48、配列番号50、配列番号52、配列番号54、配列番号56及び配列番号58のアミノ酸配列を有するポリペプチドをコードする配列を有するポリヌクレオチドを備える単離された発現ベクター、
(c) 配列番号42、配列番号44、配列番号46、配列番号48、配列番号50、配列番号52、配列番号54、配列番号56及び配列番号58のアミノ酸配列を備えるポリペプチド。
Methods of preparing the following or et consisting of compounds selected from the group, and a pharmaceutically acceptable carrier, a pharmaceutical composition for promoting angiogenesis:
(A) an isolated expression vector comprising a polynucleotide having the nucleotide sequence of SEQ ID NO: 41, SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, SEQ ID NO:
(B) a sequence encoding a polypeptide having the amino acid sequence of SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56 and SEQ ID NO: 58; An isolated expression vector comprising a polynucleotide having
(C) A polypeptide comprising the amino acid sequences of SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, and SEQ ID NO: 58.
血管新生を抑制するのに十分な量のSDF−1又はET−1に結合する抗体と、薬学的に受容可能なキャリアとを備える、血管新生関連の疾病を治療するための医薬品組成物を調製する方法 Preparation of a pharmaceutical composition for treating angiogenesis-related diseases comprising an antibody that binds to SDF-1 or ET-1 in an amount sufficient to inhibit angiogenesis and a pharmaceutically acceptable carrier How to do .
JP2008555380A 2006-02-14 2007-02-14 GPCR as an angiogenic target Pending JP2009526861A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US77299106P 2006-02-14 2006-02-14
PCT/US2007/004114 WO2007095353A2 (en) 2006-02-14 2007-02-14 Gpcrs as angiogenesis targets

Publications (2)

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JP2009526861A JP2009526861A (en) 2009-07-23
JP2009526861A5 true JP2009526861A5 (en) 2010-04-02

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EP (1) EP1996619A4 (en)
JP (1) JP2009526861A (en)
WO (1) WO2007095353A2 (en)

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ES2822924T3 (en) 2014-09-26 2021-05-05 Helixmith Co Ltd Composition to prevent or treat peripheral arterial disease using hepatocyte growth factor and stromal cell-derived factor 1a
FR3077574B1 (en) * 2018-02-07 2022-04-01 Commissariat Energie Atomique ANTIBODIES DIRECTED AGAINST ENDOTHELIN RECEPTOR SUBTYPE A AND THEIR USES.

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ATE164884T1 (en) * 1992-11-17 1998-04-15 Icos Corp NEW SEVEN TRANSMEMBRANE RECEPTOR V28
WO1997028258A1 (en) * 1996-01-30 1997-08-07 The National Institutes Of Health Cells expressing both human cd4 and cxcr4
US6479256B1 (en) * 1998-03-04 2002-11-12 Icos Corporation Lectomedin materials and methods
WO1999047158A2 (en) * 1998-03-13 1999-09-23 The University Of British Columbia Therapeutic chemokine receptor antagonists
US20020107196A1 (en) * 1998-07-21 2002-08-08 Smithkline Beecham Corporation Method for inducing chemotaxis in endothelial cells by administering stromal cell derived factor-1alpha
JP2004531249A (en) * 2001-02-14 2004-10-14 プロテイン デザイン ラブス インコーポレイティド Method for diagnosing angiogenesis, composition, and method for screening angiogenesis modulator
US20040009171A1 (en) * 2001-10-18 2004-01-15 Genentech, Inc. Methods for the treatment of carcinoma

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