삼령백출산가미방(蔘笭白朮散加味方)의 항암(抗癌) 및 항전이(抗轉移) 활성(活性)에 관(關)한 연구(硏究)
To evaluate the antitumor activity, antimetastatic and immunomodulatory effects of samryongbakchulsankamibang(SBSK) studies were done experimentally, In cytotoxicity against P388, A549. SK-OV-3, B16-F10 and SK-MEL-2. concentration inhibiting cell growth up to below 40% of control was recognized at $...
Gespeichert in:
Veröffentlicht in: | 大韓韓醫學會誌 1999, Vol.20 (2), p.128-140 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | kor |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 140 |
---|---|
container_issue | 2 |
container_start_page | 128 |
container_title | 大韓韓醫學會誌 |
container_volume | 20 |
creator | 김성훈 전기석 Kim, Sung-Hoon Jeon, Ki-Seok |
description | To evaluate the antitumor activity, antimetastatic and immunomodulatory effects of samryongbakchulsankamibang(SBSK) studies were done experimentally, In cytotoxicity against P388, A549. SK-OV-3, B16-F10 and SK-MEL-2. concentration inhibiting cell growth up to below 40% of control was recognized at $10^{-3}g/ml$ of SBSK. In Inhibitory effect on activity of DNA topoisomerase I. the $IC_{50}$ was shown $200-400{\mu}g/ml$ of SBSK. The T/C was 154% in SBSK-treated group in S-180 bearing ICR mice, The concentration inhibiting adhesion of A549 and B16-F10 to complex extracellular matrix up to below 30% of control was recognized at $5{\times}10^{-4}$, $1{\times}10^{-3}\;g/ml$ of SBSK. In pumonary colonization assay with B16-BL/6, a number of colonies in the lungs were decreased significantly in SBSK-treated group as compared with control group, In hematological changes in B16-BL/6 injected C57BL/6, numbers of WBC and platelet were not changed significantly in SBSK-treated groups, In CAM and in vitro neovascularization assay, angiogenesis was inhibited significantly in SBSK-treated group as compared with control group. From above results it was concluded that SBSK could be usefully applied for the prevention and treatment of cancer. |
format | Article |
fullrecord | <record><control><sourceid>kisti</sourceid><recordid>TN_cdi_kisti_ndsl_JAKO199904637287724</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JAKO199904637287724</sourcerecordid><originalsourceid>FETCH-kisti_ndsl_JAKO1999046372877243</originalsourceid><addsrcrecordid>eNpjYeA0NDA00DUwszTlYOAtLs5MMjCwMDE1NDMy52ToetO05_WCna83bHyzbc6bpg2vNjS8Xr_j9YaVGi-mzHi-Zu3zmXufzVn3bOrip10Lnk7c_GzaTs03c2covJ269s3UKRrPuqY_n9mjqfB6Qz9YaEHLm7lbQKIv9nY-X75bU-HtzDlvWjZqPNuy-1nDcs030ycovNrSoPFy-hzNt1PnKLyZvuHV1jUazxf2P1-5TZOHgTUtMac4lRdKczOourmGOHvoZmcWl2TG56UU58R7OXr7G1paWhqYmBmbG1mYmxuZGBOrDgBkS3kT</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>삼령백출산가미방(蔘笭白朮散加味方)의 항암(抗癌) 및 항전이(抗轉移) 활성(活性)에 관(關)한 연구(硏究)</title><source>Alma/SFX Local Collection</source><creator>김성훈 ; 전기석 ; Kim, Sung-Hoon ; Jeon, Ki-Seok</creator><creatorcontrib>김성훈 ; 전기석 ; Kim, Sung-Hoon ; Jeon, Ki-Seok</creatorcontrib><description>To evaluate the antitumor activity, antimetastatic and immunomodulatory effects of samryongbakchulsankamibang(SBSK) studies were done experimentally, In cytotoxicity against P388, A549. SK-OV-3, B16-F10 and SK-MEL-2. concentration inhibiting cell growth up to below 40% of control was recognized at $10^{-3}g/ml$ of SBSK. In Inhibitory effect on activity of DNA topoisomerase I. the $IC_{50}$ was shown $200-400{\mu}g/ml$ of SBSK. The T/C was 154% in SBSK-treated group in S-180 bearing ICR mice, The concentration inhibiting adhesion of A549 and B16-F10 to complex extracellular matrix up to below 30% of control was recognized at $5{\times}10^{-4}$, $1{\times}10^{-3}\;g/ml$ of SBSK. In pumonary colonization assay with B16-BL/6, a number of colonies in the lungs were decreased significantly in SBSK-treated group as compared with control group, In hematological changes in B16-BL/6 injected C57BL/6, numbers of WBC and platelet were not changed significantly in SBSK-treated groups, In CAM and in vitro neovascularization assay, angiogenesis was inhibited significantly in SBSK-treated group as compared with control group. From above results it was concluded that SBSK could be usefully applied for the prevention and treatment of cancer.</description><identifier>ISSN: 1010-0695</identifier><language>kor</language><ispartof>大韓韓醫學會誌, 1999, Vol.20 (2), p.128-140</ispartof><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4024</link.rule.ids></links><search><creatorcontrib>김성훈</creatorcontrib><creatorcontrib>전기석</creatorcontrib><creatorcontrib>Kim, Sung-Hoon</creatorcontrib><creatorcontrib>Jeon, Ki-Seok</creatorcontrib><title>삼령백출산가미방(蔘笭白朮散加味方)의 항암(抗癌) 및 항전이(抗轉移) 활성(活性)에 관(關)한 연구(硏究)</title><title>大韓韓醫學會誌</title><addtitle>Journal of Korean Oriental Medicine</addtitle><description>To evaluate the antitumor activity, antimetastatic and immunomodulatory effects of samryongbakchulsankamibang(SBSK) studies were done experimentally, In cytotoxicity against P388, A549. SK-OV-3, B16-F10 and SK-MEL-2. concentration inhibiting cell growth up to below 40% of control was recognized at $10^{-3}g/ml$ of SBSK. In Inhibitory effect on activity of DNA topoisomerase I. the $IC_{50}$ was shown $200-400{\mu}g/ml$ of SBSK. The T/C was 154% in SBSK-treated group in S-180 bearing ICR mice, The concentration inhibiting adhesion of A549 and B16-F10 to complex extracellular matrix up to below 30% of control was recognized at $5{\times}10^{-4}$, $1{\times}10^{-3}\;g/ml$ of SBSK. In pumonary colonization assay with B16-BL/6, a number of colonies in the lungs were decreased significantly in SBSK-treated group as compared with control group, In hematological changes in B16-BL/6 injected C57BL/6, numbers of WBC and platelet were not changed significantly in SBSK-treated groups, In CAM and in vitro neovascularization assay, angiogenesis was inhibited significantly in SBSK-treated group as compared with control group. From above results it was concluded that SBSK could be usefully applied for the prevention and treatment of cancer.</description><issn>1010-0695</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>JDI</sourceid><recordid>eNpjYeA0NDA00DUwszTlYOAtLs5MMjCwMDE1NDMy52ToetO05_WCna83bHyzbc6bpg2vNjS8Xr_j9YaVGi-mzHi-Zu3zmXufzVn3bOrip10Lnk7c_GzaTs03c2covJ269s3UKRrPuqY_n9mjqfB6Qz9YaEHLm7lbQKIv9nY-X75bU-HtzDlvWjZqPNuy-1nDcs030ycovNrSoPFy-hzNt1PnKLyZvuHV1jUazxf2P1-5TZOHgTUtMac4lRdKczOourmGOHvoZmcWl2TG56UU58R7OXr7G1paWhqYmBmbG1mYmxuZGBOrDgBkS3kT</recordid><startdate>1999</startdate><enddate>1999</enddate><creator>김성훈</creator><creator>전기석</creator><creator>Kim, Sung-Hoon</creator><creator>Jeon, Ki-Seok</creator><scope>JDI</scope></search><sort><creationdate>1999</creationdate><title>삼령백출산가미방(蔘笭白朮散加味方)의 항암(抗癌) 및 항전이(抗轉移) 활성(活性)에 관(關)한 연구(硏究)</title><author>김성훈 ; 전기석 ; Kim, Sung-Hoon ; Jeon, Ki-Seok</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kisti_ndsl_JAKO1999046372877243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>1999</creationdate><toplevel>online_resources</toplevel><creatorcontrib>김성훈</creatorcontrib><creatorcontrib>전기석</creatorcontrib><creatorcontrib>Kim, Sung-Hoon</creatorcontrib><creatorcontrib>Jeon, Ki-Seok</creatorcontrib><collection>KoreaScience</collection><jtitle>大韓韓醫學會誌</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>김성훈</au><au>전기석</au><au>Kim, Sung-Hoon</au><au>Jeon, Ki-Seok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>삼령백출산가미방(蔘笭白朮散加味方)의 항암(抗癌) 및 항전이(抗轉移) 활성(活性)에 관(關)한 연구(硏究)</atitle><jtitle>大韓韓醫學會誌</jtitle><addtitle>Journal of Korean Oriental Medicine</addtitle><date>1999</date><risdate>1999</risdate><volume>20</volume><issue>2</issue><spage>128</spage><epage>140</epage><pages>128-140</pages><issn>1010-0695</issn><abstract>To evaluate the antitumor activity, antimetastatic and immunomodulatory effects of samryongbakchulsankamibang(SBSK) studies were done experimentally, In cytotoxicity against P388, A549. SK-OV-3, B16-F10 and SK-MEL-2. concentration inhibiting cell growth up to below 40% of control was recognized at $10^{-3}g/ml$ of SBSK. In Inhibitory effect on activity of DNA topoisomerase I. the $IC_{50}$ was shown $200-400{\mu}g/ml$ of SBSK. The T/C was 154% in SBSK-treated group in S-180 bearing ICR mice, The concentration inhibiting adhesion of A549 and B16-F10 to complex extracellular matrix up to below 30% of control was recognized at $5{\times}10^{-4}$, $1{\times}10^{-3}\;g/ml$ of SBSK. In pumonary colonization assay with B16-BL/6, a number of colonies in the lungs were decreased significantly in SBSK-treated group as compared with control group, In hematological changes in B16-BL/6 injected C57BL/6, numbers of WBC and platelet were not changed significantly in SBSK-treated groups, In CAM and in vitro neovascularization assay, angiogenesis was inhibited significantly in SBSK-treated group as compared with control group. From above results it was concluded that SBSK could be usefully applied for the prevention and treatment of cancer.</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1010-0695 |
ispartof | 大韓韓醫學會誌, 1999, Vol.20 (2), p.128-140 |
issn | 1010-0695 |
language | kor |
recordid | cdi_kisti_ndsl_JAKO199904637287724 |
source | Alma/SFX Local Collection |
title | 삼령백출산가미방(蔘笭白朮散加味方)의 항암(抗癌) 및 항전이(抗轉移) 활성(活性)에 관(關)한 연구(硏究) |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T02%3A12%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-kisti&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=%EC%82%BC%EB%A0%B9%EB%B0%B1%EC%B6%9C%EC%82%B0%EA%B0%80%EB%AF%B8%EB%B0%A9(%E8%94%98%E7%AC%AD%E7%99%BD%E6%9C%AE%E6%95%A3%E5%8A%A0%E5%91%B3%E6%96%B9)%EC%9D%98%20%ED%95%AD%EC%95%94(%E6%8A%97%E7%99%8C)%20%EB%B0%8F%20%ED%95%AD%EC%A0%84%EC%9D%B4(%E6%8A%97%E8%BD%89%E7%A7%BB)%20%ED%99%9C%EC%84%B1(%E6%B4%BB%E6%80%A7)%EC%97%90%20%EA%B4%80(%E9%97%9C)%ED%95%9C%20%EC%97%B0%EA%B5%AC(%E7%A1%8F%E7%A9%B6)&rft.jtitle=%E5%A4%A7%E9%9F%93%E9%9F%93%E9%86%AB%E5%AD%B8%E6%9C%83%E8%AA%8C&rft.au=%EA%B9%80%EC%84%B1%ED%9B%88&rft.date=1999&rft.volume=20&rft.issue=2&rft.spage=128&rft.epage=140&rft.pages=128-140&rft.issn=1010-0695&rft_id=info:doi/&rft_dat=%3Ckisti%3EJAKO199904637287724%3C/kisti%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |