Pectic polysaccharide isolated from Angelica gigas Nakai inhibits melanoma cell metastasis and growth by directly preventing cell adhesion and activating host immune functions

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dc.contributor.authorSang Bae Han-
dc.contributor.authorChang Woo Lee-
dc.contributor.authorMoo Rim Kang-
dc.contributor.authorYeo Dae Yoon-
dc.contributor.authorJong Soon Kang-
dc.contributor.authorKi Hoon Lee-
dc.contributor.authorWoon Kee Yoon-
dc.contributor.authorKiho Lee-
dc.contributor.authorSong Kyu Park-
dc.contributor.authorHwan Mook Kim-
dc.date.accessioned2017-04-19T09:05:19Z-
dc.date.available2017-04-19T09:05:19Z-
dc.date.issued2006-
dc.identifier.issn0304-3835-
dc.identifier.uri10.1016/j.canlet.2005.11.040ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/7598-
dc.description.abstractThe pectic polysaccharide (angelan) of Angelica gigas Nakai is an immunostimulator that activates the immune functions of B cells and macrophages. Here we investigated the effect of angelan on tumor growth and metastasis. Angelan was found to significantly prolong the survival rate of B16F10-implanted mice and to reduce the frequency of pulmonary metastasis of B16F10 melanoma. Moreover, the combined treatment of angelan and doxorubicin (a cytotoxic anticancer agent) more effectively inhibited tumor growth and metastasis than either compound alone. In the present study, we found that angelan directly inhibited cancer cell adhesion and invasion through the extracellular matrix, in addition to activating the immune functions of B cells and macrophages. These results suggest that angelan can inhibit tumor growth and metastasis by stimulating host immunity and directly inhibiting cancer cell adhesion.-
dc.publisherElsevier-
dc.titlePectic polysaccharide isolated from Angelica gigas Nakai inhibits melanoma cell metastasis and growth by directly preventing cell adhesion and activating host immune functions-
dc.title.alternativePectic polysaccharide isolated from Angelica gigas Nakai inhibits melanoma cell metastasis and growth by directly preventing cell adhesion and activating host immune functions-
dc.typeArticle-
dc.citation.titleCancer Letters-
dc.citation.number2-
dc.citation.endPage273-
dc.citation.startPage264-
dc.citation.volume243-
dc.contributor.affiliatedAuthorSang Bae Han-
dc.contributor.affiliatedAuthorChang Woo Lee-
dc.contributor.affiliatedAuthorMoo Rim Kang-
dc.contributor.affiliatedAuthorYeo Dae Yoon-
dc.contributor.affiliatedAuthorJong Soon Kang-
dc.contributor.affiliatedAuthorKi Hoon Lee-
dc.contributor.affiliatedAuthorWoon Kee Yoon-
dc.contributor.affiliatedAuthorKiho Lee-
dc.contributor.affiliatedAuthorSong Kyu Park-
dc.contributor.affiliatedAuthorHwan Mook Kim-
dc.contributor.alternativeName한상배-
dc.contributor.alternativeName이창우-
dc.contributor.alternativeName강무림-
dc.contributor.alternativeName윤여대-
dc.contributor.alternativeName강종순-
dc.contributor.alternativeName이기훈-
dc.contributor.alternativeName윤원기-
dc.contributor.alternativeName이기호-
dc.contributor.alternativeName박성규-
dc.contributor.alternativeName김환묵-
dc.identifier.bibliographicCitationCancer Letters, vol. 243, no. 2, pp. 264-273-
dc.identifier.doi10.1016/j.canlet.2005.11.040-
dc.subject.keywordAdhesion-
dc.subject.keywordAngelica gigas Nakai-
dc.subject.keywordInvasion-
dc.subject.keywordMetastasis-
dc.subject.keywordTumor growth-
dc.subject.localadhesion-
dc.subject.localAdhesion-
dc.subject.localAngelica gigas Nakai-
dc.subject.localangelica gigas Nakai-
dc.subject.localinvasion-
dc.subject.localInvasion-
dc.subject.localmetastasis-
dc.subject.localMetastasis-
dc.subject.localTumor growth-
dc.subject.localtumor growth-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Laboratory Animal Resource & Research Center > 1. Journal Articles
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