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      KCI등재 SCIE SCOPUS

      Anti-metastatic effect of cantharidin in A549 human lung cancer cells

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      https://www.riss.kr/link?id=A103886678

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Cancer metastasis is represented by migrationand invasion of cancer cells. Cancer cells invade into theblood or lymphatic vessels and this leads to the spread ofcancer into the organs in distant sites. For cancer cells tomigrate, extracellular matrix (ECM) must be degraded.
      Cantharidin, a compound derived from blister beetles, isknown for its anti-cancer effect in several cancer cells.
      Here we report that cantharidin inhibits migration andinvasion of A549 human lung cancer cell. We found thatcantharidin inhibits activation of phosphatidylinositol3-kinase/Akt signaling pathway. This leads to the selectiveattenuation of one of the gelatinases, matrix metalloproteinase2, which can degrade components of ECM, andinhibits migration and invasion of A549 human lung cancercell.
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      Cancer metastasis is represented by migrationand invasion of cancer cells. Cancer cells invade into theblood or lymphatic vessels and this leads to the spread ofcancer into the organs in distant sites. For cancer cells tomigrate, extracellular matrix ...

      Cancer metastasis is represented by migrationand invasion of cancer cells. Cancer cells invade into theblood or lymphatic vessels and this leads to the spread ofcancer into the organs in distant sites. For cancer cells tomigrate, extracellular matrix (ECM) must be degraded.
      Cantharidin, a compound derived from blister beetles, isknown for its anti-cancer effect in several cancer cells.
      Here we report that cantharidin inhibits migration andinvasion of A549 human lung cancer cell. We found thatcantharidin inhibits activation of phosphatidylinositol3-kinase/Akt signaling pathway. This leads to the selectiveattenuation of one of the gelatinases, matrix metalloproteinase2, which can degrade components of ECM, andinhibits migration and invasion of A549 human lung cancercell.

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      참고문헌 (Reference)

      1 Chu, S. C., "Uveal melanocytes produce matrix metalloproteinases-2 and-9 in vitro" 17 : 636-642, 2004

      2 Nyberg, P., "Tumor microenvironment and angiogenesis" 13 : 6537-6553, 2008

      3 Vivanco, I., "The phosphatidylinositol 3-kinase AKT pathway in human cancer" 2 : 489-501, 2002

      4 Carnero, A., "The PTEN/PI3K/AKT signalling pathway in cancer, therapeutic implications" 8 : 187-198, 2008

      5 Sato, H., "Regulatory mechanism of 92 kDa type IV collagenase gene expression which is associated with invasiveness of tumor cells" 8 : 395-405, 1993

      6 Westermarck, J., "Regulation of matrix metalloproteinase expression in tumor invasion" 13 : 781-792, 1999

      7 Basset, P., "Matrix metalloproteinases as stromal effectors of human carcinoma progression : Therapeutic implications" 15 : 535-541, 1997

      8 Deryugina, E. I., "Matrix metalloproteinases and tumor metastasis" 25 : 9-34, 2006

      9 Nelson, A. R., "Matrix metalloproteinases : Biologic activity and clinical implications" 18 : 1135-1149, 2000

      10 Huang, C., "MAP kinases and cell migration" 117 : 4619-4628, 2004

      1 Chu, S. C., "Uveal melanocytes produce matrix metalloproteinases-2 and-9 in vitro" 17 : 636-642, 2004

      2 Nyberg, P., "Tumor microenvironment and angiogenesis" 13 : 6537-6553, 2008

      3 Vivanco, I., "The phosphatidylinositol 3-kinase AKT pathway in human cancer" 2 : 489-501, 2002

      4 Carnero, A., "The PTEN/PI3K/AKT signalling pathway in cancer, therapeutic implications" 8 : 187-198, 2008

      5 Sato, H., "Regulatory mechanism of 92 kDa type IV collagenase gene expression which is associated with invasiveness of tumor cells" 8 : 395-405, 1993

      6 Westermarck, J., "Regulation of matrix metalloproteinase expression in tumor invasion" 13 : 781-792, 1999

      7 Basset, P., "Matrix metalloproteinases as stromal effectors of human carcinoma progression : Therapeutic implications" 15 : 535-541, 1997

      8 Deryugina, E. I., "Matrix metalloproteinases and tumor metastasis" 25 : 9-34, 2006

      9 Nelson, A. R., "Matrix metalloproteinases : Biologic activity and clinical implications" 18 : 1135-1149, 2000

      10 Huang, C., "MAP kinases and cell migration" 117 : 4619-4628, 2004

      11 Attiga, F. A., "Inhibitors of prostaglandin synthesis inhibit human prostate tumor cell invasiveness and reduce the release of matrix metalloproteinases" 60 : 4629-4637, 2000

      12 Massicot, F., "In vitro assessment of renal toxicity and inflammatory events of two protein phosphatase inhibitors cantharidin and norcantharidin" 96 : 26-32, 2005

      13 Sahai, E, "Illuminating the metastatic process" 7 : 737-749, 2007

      14 Zhan, Y. P., "Clinical study on safety and efficacy of quinin-(cantharidin sodium)injection combined with chemotherapy in treating patients with gastric cancer" 13 : 4773-4776, 2012

      15 Li, W., "Cantharidin, a potent and selective PP2A inhibitor, induces an oxidative stress-independent growth inhibition of pancreatic cancer cells through G2/M cell-cycle arrest and apoptosis" 101 : 1226-1233, 2010

      16 Johnsen, M., "Cancer invasion and tissue remodeling : Common themes in proteolytic matrix degradation" 10 : 667-671, 1998

      17 Van den Steen, P. E., "Biochemistry and molecular biology of gelatinase B or matrix metalloproteinase-9(MMP-9)" 37 : 375-536, 2002

      18 Bae, I. H., "Bcl-w promotes gastric cancer cell invasion by inducing matrix metalloproteinase-2 expression via phosphoinositide 3-kinase, Akt, and Sp1" 66 : 4991-4995, 2006

      19 Kok, S. H., "Apoptotic activity of a novel synthetic cantharidin analogue on hepatoma cell lines" 17 : 945-949, 2006

      20 Chen, Y. J., "A small-molecule metastasis inhibitor, norcantharidin, downregulates matrix metalloproteinase-9 expression by inhibiting Sp1 transcriptional activity in colorectal cancer cells" 181 : 440-446, 2009

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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
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (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 1.96 0.2 1.44
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.07 0.87 0.439 0.05
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