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      A Natural Marine Compound Extracted from the Ark Shell, Scapharca Subcrenata, Inhibits in Vivo and in Vitro Angiogenesis

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      https://www.riss.kr/link?id=A104787315

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Angiogenesis is an integral process in the growth and spread of solid tumors, and anti-angiogenesis therapy is one of the most promising therapeutic strategies for the treatment of cancer. In this study, we show that a natural marine compound extracted from ark shell, Scapharca subcrenata, has anti-angiogenic activities. Ark shell extract inhibited the proliferation, migration, invasion and tube formation of human umbilical vein endothelial cells (HUVECs), and suppressed the release of matrix metalloproteinase-2 (MMP-2) by HUVECs. In addition, ark shell extract also inhibited in vivo angiogenesis in a mouse Matrigel-plug assay. Taken together, these results suggest that ark shell extract acts as a novel angiogenesis inhibitor and could be further developed as an anticancer agent. (Cancer Prev Res 13, 47-53, 2008)
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      Angiogenesis is an integral process in the growth and spread of solid tumors, and anti-angiogenesis therapy is one of the most promising therapeutic strategies for the treatment of cancer. In this study, we show that a natural marine compound extracte...

      Angiogenesis is an integral process in the growth and spread of solid tumors, and anti-angiogenesis therapy is one of the most promising therapeutic strategies for the treatment of cancer. In this study, we show that a natural marine compound extracted from ark shell, Scapharca subcrenata, has anti-angiogenic activities. Ark shell extract inhibited the proliferation, migration, invasion and tube formation of human umbilical vein endothelial cells (HUVECs), and suppressed the release of matrix metalloproteinase-2 (MMP-2) by HUVECs. In addition, ark shell extract also inhibited in vivo angiogenesis in a mouse Matrigel-plug assay. Taken together, these results suggest that ark shell extract acts as a novel angiogenesis inhibitor and could be further developed as an anticancer agent. (Cancer Prev Res 13, 47-53, 2008)

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      참고문헌 (Reference)

      1 Folkman, J., "What is the evidence that tumors are angiogenesis dependent?" 82 : 4-6, 1990

      2 Drabkin, D.S., "Spectrophotomeric constans for common hemoglobin derivaties in human, dog and rabbit blood" 98 : 719-, 1932

      3 Fong, T.A., "SU5416 is a potent and selective inhibitor of the vascular endothelial growth factor receptor (Flk-1/KDR) that inhibits tyrosine kinase catalysis, tumor vascularization and growth of multiple tumor types" 59 : 99-106, 1999

      4 Giavazzi, R., "Preclinical development of metalloproteasis inhibitors in cancer therapy" 37 : 53-60, 2001

      5 Da Rocha, A.B., "Natural products in anticancer therapy" 1 : 364-369, 2001

      6 Bussolino, F., "Molecular mechanisms of blood vessel formation" 22 : 251-256, 1997

      7 Schwartsmann, G., "Marine- derived anticancer agents in clinical trails" 12 : 1367-1383, 2003

      8 Newman, D.J., "Marine natureal products and related compounds in clinical and advanced preclinical trails" 67 : 1216-1238, 2004

      9 Miao, R.Q., "Kallistatin is a new inhibitor of angiogenesis and tumor growth" 100 : 3245-3252, 2002

      10 Siddiqui, F.A., "Hemoglobin induces the expression and secretion of vascular endothelial growth factor from human malignant cells" 3 : 264-270, 2002

      1 Folkman, J., "What is the evidence that tumors are angiogenesis dependent?" 82 : 4-6, 1990

      2 Drabkin, D.S., "Spectrophotomeric constans for common hemoglobin derivaties in human, dog and rabbit blood" 98 : 719-, 1932

      3 Fong, T.A., "SU5416 is a potent and selective inhibitor of the vascular endothelial growth factor receptor (Flk-1/KDR) that inhibits tyrosine kinase catalysis, tumor vascularization and growth of multiple tumor types" 59 : 99-106, 1999

      4 Giavazzi, R., "Preclinical development of metalloproteasis inhibitors in cancer therapy" 37 : 53-60, 2001

      5 Da Rocha, A.B., "Natural products in anticancer therapy" 1 : 364-369, 2001

      6 Bussolino, F., "Molecular mechanisms of blood vessel formation" 22 : 251-256, 1997

      7 Schwartsmann, G., "Marine- derived anticancer agents in clinical trails" 12 : 1367-1383, 2003

      8 Newman, D.J., "Marine natureal products and related compounds in clinical and advanced preclinical trails" 67 : 1216-1238, 2004

      9 Miao, R.Q., "Kallistatin is a new inhibitor of angiogenesis and tumor growth" 100 : 3245-3252, 2002

      10 Siddiqui, F.A., "Hemoglobin induces the expression and secretion of vascular endothelial growth factor from human malignant cells" 3 : 264-270, 2002

      11 Savani, R.C., "Differential involvement of the Hyaluronan (HA) Receptors CD44 and Receptor for HA-mediated Motility in Endothelial Cell Function and Angiogenesis" 276 : 36770-36778, 2001

      12 Lee, M.S., "Angiogenic activity of pyruvic acid in in vivo and in vitro angiogenesis models" 61 : 3290-3293, 2001

      13 Liekens, S., "Angiogenesis: regulators and clinical applications" 61 : 253-270, 2001

      14 Folkman, J., "Angiogenesis in vitro" 288 : 551-556, 1980

      15 Carmeliet, P., "Angiogenesis in cancer and other diseases" 407 : 249-257, 2000

      16 Folkman, J., "Angiogenesis" 267 : 10931-10934, 1992

      17 Passaniti, A., "A simple, quantitative method for assessing antiogenesis and antiangiogenic agents using reconstituted basement membrane, heparin and fibroblast growth factor" 67 : 519-528, 1992

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      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2022 평가예정 재인증평가 신청대상 (재인증)
      2019-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2018-12-01 평가 등재후보로 하락 (계속평가) KCI등재후보
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2013-10-14 학술지명변경 외국어명 : Cancer Prevention Research -> Journal of Cancer Prevention KCI등재
      2012-10-15 학회명변경 영문명 : Korean Association of Cancer Prevention -> Korean Society of Cancer Preveniton KCI등재
      2011-04-04 학술지명변경 외국어명 : Journal of Korean Association of Cancer Prevention -> Cancer Prevention Research KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2007-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2005-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.22 0.22 0.18
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.15 0.12 0.405 0.13
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