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      KCI등재 SCOPUS SCIE

      KR-31831, a new synthetic anti-ischemic agent, inhibits in vivo and in vitro angiogenesis

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      https://www.riss.kr/link?id=A101634869

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Angiogenesis is considered to be an integral process to the growth and spread of solid tumors. Anti-angio-genesis therapy recently has been found to be one of the most promising anti-cancer therapeutic strategies. In this study, we provide several lines of evidences showing that KR-31831, a new ben-zopyran derivative, has anti-angiogenic activities. KR-31831 inhibited the proliferation, migration, invasion and tube formation of bovine aortic endothelial cells (BAECs), and suppressed the release of matrix metalloproteinase-2 (MMP-2) of BAECs. KR-31831 also inhibited in vivo angiogene-sis in mouse Matrigel plug assay. Furthermore, the mRNA expressions of basic fibroblast growth factor (bFGF), fibroblast growth factor receptor-2 (FGFR-2), and vascular endothelial growth factor receptor-2 (VEGFR-2) were decreased by KR-31831. Taken together, these results suggest that KR-31831 acts as a novel angiogenesis inhibitor and might be useful for treating hypervascularized cancers.
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      Angiogenesis is considered to be an integral process to the growth and spread of solid tumors. Anti-angio-genesis therapy recently has been found to be one of the most promising anti-cancer therapeutic strategies. In this study, we provide several lin...

      Angiogenesis is considered to be an integral process to the growth and spread of solid tumors. Anti-angio-genesis therapy recently has been found to be one of the most promising anti-cancer therapeutic strategies. In this study, we provide several lines of evidences showing that KR-31831, a new ben-zopyran derivative, has anti-angiogenic activities. KR-31831 inhibited the proliferation, migration, invasion and tube formation of bovine aortic endothelial cells (BAECs), and suppressed the release of matrix metalloproteinase-2 (MMP-2) of BAECs. KR-31831 also inhibited in vivo angiogene-sis in mouse Matrigel plug assay. Furthermore, the mRNA expressions of basic fibroblast growth factor (bFGF), fibroblast growth factor receptor-2 (FGFR-2), and vascular endothelial growth factor receptor-2 (VEGFR-2) were decreased by KR-31831. Taken together, these results suggest that KR-31831 acts as a novel angiogenesis inhibitor and might be useful for treating hypervascularized cancers.

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      참고문헌 (Reference)

      1 "of blood vesel formation" 22 : 251-256, 1997

      2 "What is the evidence that tumors are angiogenesis dependent? J Natl Cancer Inst" 4-6, 1990

      3 "The implications of angiogenesis for the biology and therapy of cancer metastasis" 1994

      4 "Spectrophotomeric constans for common hemoglobin derivaties in human" 1932

      5 "Preclinical development of metal-loproteasis inhibitors in cancer therapy" 37 : 53-60, 2001

      6 "Molecular mechanisms" 38 (38): 502-508, 2006

      7 "Kallistatin is a new inhibitor of angiogenesis and tumor growth" 100 : 3245-3252, 2002

      8 "Identification of a novel aniangiogenic agent; 4-(N-imidazol-2-ylmethyl)amino benzopyran analogues" 13 : 1661-1663, 2003

      9 "Differential involvement of the hyaluronan receptors CD44 and receptor for HA-mediated motility in endothelial cell function"

      10 "Clinical translation of angiogenesis inhibitors" 2 : 727-739, 2002

      1 "of blood vesel formation" 22 : 251-256, 1997

      2 "What is the evidence that tumors are angiogenesis dependent? J Natl Cancer Inst" 4-6, 1990

      3 "The implications of angiogenesis for the biology and therapy of cancer metastasis" 1994

      4 "Spectrophotomeric constans for common hemoglobin derivaties in human" 1932

      5 "Preclinical development of metal-loproteasis inhibitors in cancer therapy" 37 : 53-60, 2001

      6 "Molecular mechanisms" 38 (38): 502-508, 2006

      7 "Kallistatin is a new inhibitor of angiogenesis and tumor growth" 100 : 3245-3252, 2002

      8 "Identification of a novel aniangiogenic agent; 4-(N-imidazol-2-ylmethyl)amino benzopyran analogues" 13 : 1661-1663, 2003

      9 "Differential involvement of the hyaluronan receptors CD44 and receptor for HA-mediated motility in endothelial cell function"

      10 "Clinical translation of angiogenesis inhibitors" 2 : 727-739, 2002

      11 "Angiogenic activity of pyruvic acid in in vivo and in vitro angiogenesis models" 61 : 3290-3293, 2001

      12 "Angiogenesis: regulators and clinical applications" 61 : 253-270, 2001

      13 "Angiogenesis in vitro" 551-6, 1980

      14 "Angiogenesis in cancer and other diseases" 407 : 249-257, 2000

      15 "Angiogenesis and lung cancer: prognostic and therapeutic implications" 23 : 3243-3256, 2005

      16 "A simple, quantitative method for assessing antiogenesis and antiangiogenic agents using reconstituted basement membrane, heparin, and fibroblast growth factor" 519-28, 1992

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      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2009-09-21 학회명변경 한글명 : 대한생화학ㆍ분자생물학회 -> 생화학분자생물학회
      영문명 : Korean Society Of Medical Biochemistry And Molecular Biology -> Korean Society Of Biochemistry And Molecular Biology
      KCI등재
      2008-01-01 평가 SCI 등재 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1998-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 3.74 0.23 2.56
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.82 1.45 0.555 0.01
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