Effect of the extracts from Glycyrrhiza uralensis Fisch on the growth characteristics of human cell lines: Anti-tumor and immune activation activities
Immune modulating activity of ethanol extracts from Glycyrrhiza uralensis Fisch was investigated by conserving growth characteristics of several human cell lines. All of the samples did not show severe cytotoxicity on normal human liver cell line, WRL-68, showing less than 25% inhibition of cell gro...
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description | Immune modulating activity of ethanol extracts from Glycyrrhiza uralensis Fisch was investigated by conserving growth characteristics of several human cell lines. All of the samples did not show severe cytotoxicity on normal human liver cell line, WRL-68, showing less than 25% inhibition of cell growth. The crude extract and its fractionized samples (F1 and F3) inhibited the growth of human hepatoma, Hep3B, down to ca. 70% of normal cell growth in adding 1.0 g l(-1) of fraction F3. The result of anticancer experiments was well matched to the results of antimutagenicity using Chinese Hamster Lung cell lines(CHL V79). In adding 1.0 g l(-1) of fraction F1, the growth of human B cell was enhanced, up to 60% of control growth. The secretion of two kinds of cytokines, Interleukin-6 and Tumor Necrosis Factor-alpha from human B cells was also enhanced in adding the crude extract, but not the standards such as Glycyrrhizin (GL) or 18,beta-glycyrrhetinic acid (GM). It was found that both of the apoptosis and differentiation were more accelerated in supplementing the crude extract and fraction F1 than in adding the standards. A spot was found only in the crude extract and fractions, not standards by Thin Layer Chromatography(TLC) analysis. It tells that there must be another unknown component in crude and/or fraction F1 as a possible candidate of immune modulators. This component seems to be a derivative of a monomer, GM since its R(f) was close to the monomer. It was also interesting that glycyrrhizin, a major component in G. uralensis Fisch was biologically activated by first being hydrolyzed by an enzyme. |
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All of the samples did not show severe cytotoxicity on normal human liver cell line, WRL-68, showing less than 25% inhibition of cell growth. The crude extract and its fractionized samples (F1 and F3) inhibited the growth of human hepatoma, Hep3B, down to ca. 70% of normal cell growth in adding 1.0 g l(-1) of fraction F3. The result of anticancer experiments was well matched to the results of antimutagenicity using Chinese Hamster Lung cell lines(CHL V79). In adding 1.0 g l(-1) of fraction F1, the growth of human B cell was enhanced, up to 60% of control growth. The secretion of two kinds of cytokines, Interleukin-6 and Tumor Necrosis Factor-alpha from human B cells was also enhanced in adding the crude extract, but not the standards such as Glycyrrhizin (GL) or 18,beta-glycyrrhetinic acid (GM). It was found that both of the apoptosis and differentiation were more accelerated in supplementing the crude extract and fraction F1 than in adding the standards. A spot was found only in the crude extract and fractions, not standards by Thin Layer Chromatography(TLC) analysis. It tells that there must be another unknown component in crude and/or fraction F1 as a possible candidate of immune modulators. This component seems to be a derivative of a monomer, GM since its R(f) was close to the monomer. It was also interesting that glycyrrhizin, a major component in G. uralensis Fisch was biologically activated by first being hydrolyzed by an enzyme.</description><identifier>ISSN: 0920-9069</identifier><identifier>EISSN: 1573-0778</identifier><identifier>DOI: 10.1023/A:1016111713056</identifier><identifier>PMID: 19002915</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Antineoplastic drugs. Cytokines ; Apoptosis ; Biological and medical sciences ; Biotechnology ; Cell growth ; Cytotoxicity ; Fundamental and applied biological sciences. Psychology ; Glycyrrhiza uralensis ; Glycyrrhizin ; Health. Pharmaceutical industry ; Hepatocytes ; Hepatoma ; Immunomodulation ; Industrial applications and implications. 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All of the samples did not show severe cytotoxicity on normal human liver cell line, WRL-68, showing less than 25% inhibition of cell growth. The crude extract and its fractionized samples (F1 and F3) inhibited the growth of human hepatoma, Hep3B, down to ca. 70% of normal cell growth in adding 1.0 g l(-1) of fraction F3. The result of anticancer experiments was well matched to the results of antimutagenicity using Chinese Hamster Lung cell lines(CHL V79). In adding 1.0 g l(-1) of fraction F1, the growth of human B cell was enhanced, up to 60% of control growth. The secretion of two kinds of cytokines, Interleukin-6 and Tumor Necrosis Factor-alpha from human B cells was also enhanced in adding the crude extract, but not the standards such as Glycyrrhizin (GL) or 18,beta-glycyrrhetinic acid (GM). It was found that both of the apoptosis and differentiation were more accelerated in supplementing the crude extract and fraction F1 than in adding the standards. A spot was found only in the crude extract and fractions, not standards by Thin Layer Chromatography(TLC) analysis. It tells that there must be another unknown component in crude and/or fraction F1 as a possible candidate of immune modulators. This component seems to be a derivative of a monomer, GM since its R(f) was close to the monomer. It was also interesting that glycyrrhizin, a major component in G. uralensis Fisch was biologically activated by first being hydrolyzed by an enzyme.</description><subject>Antineoplastic drugs. Cytokines</subject><subject>Apoptosis</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cell growth</subject><subject>Cytotoxicity</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glycyrrhiza uralensis</subject><subject>Glycyrrhizin</subject><subject>Health. Pharmaceutical industry</subject><subject>Hepatocytes</subject><subject>Hepatoma</subject><subject>Immunomodulation</subject><subject>Industrial applications and implications. 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Cytokines</topic><topic>Apoptosis</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cell growth</topic><topic>Cytotoxicity</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glycyrrhiza uralensis</topic><topic>Glycyrrhizin</topic><topic>Health. Pharmaceutical industry</topic><topic>Hepatocytes</topic><topic>Hepatoma</topic><topic>Immunomodulation</topic><topic>Industrial applications and implications. Economical aspects</topic><topic>Interleukin 6</topic><topic>Lymphocytes B</topic><topic>Monomers</topic><topic>Production of active biomolecules</topic><topic>Tumor cell lines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chung, W T</creatorcontrib><creatorcontrib>Lee, S H</creatorcontrib><creatorcontrib>Kim, J D</creatorcontrib><creatorcontrib>Sung, N S</creatorcontrib><creatorcontrib>Hwang, B</creatorcontrib><creatorcontrib>Lee, S Y</creatorcontrib><creatorcontrib>Yu, C Y</creatorcontrib><creatorcontrib>Lee, H Y</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cytotechnology (Dordrecht)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chung, W T</au><au>Lee, S H</au><au>Kim, J D</au><au>Sung, N S</au><au>Hwang, B</au><au>Lee, S Y</au><au>Yu, C Y</au><au>Lee, H Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of the extracts from Glycyrrhiza uralensis Fisch on the growth characteristics of human cell lines: Anti-tumor and immune activation activities</atitle><jtitle>Cytotechnology (Dordrecht)</jtitle><addtitle>Cytotechnology</addtitle><date>2001-09-01</date><risdate>2001</risdate><volume>37</volume><issue>1</issue><spage>55</spage><epage>64</epage><pages>55-64</pages><issn>0920-9069</issn><eissn>1573-0778</eissn><abstract>Immune modulating activity of ethanol extracts from Glycyrrhiza uralensis Fisch was investigated by conserving growth characteristics of several human cell lines. All of the samples did not show severe cytotoxicity on normal human liver cell line, WRL-68, showing less than 25% inhibition of cell growth. The crude extract and its fractionized samples (F1 and F3) inhibited the growth of human hepatoma, Hep3B, down to ca. 70% of normal cell growth in adding 1.0 g l(-1) of fraction F3. The result of anticancer experiments was well matched to the results of antimutagenicity using Chinese Hamster Lung cell lines(CHL V79). In adding 1.0 g l(-1) of fraction F1, the growth of human B cell was enhanced, up to 60% of control growth. The secretion of two kinds of cytokines, Interleukin-6 and Tumor Necrosis Factor-alpha from human B cells was also enhanced in adding the crude extract, but not the standards such as Glycyrrhizin (GL) or 18,beta-glycyrrhetinic acid (GM). It was found that both of the apoptosis and differentiation were more accelerated in supplementing the crude extract and fraction F1 than in adding the standards. A spot was found only in the crude extract and fractions, not standards by Thin Layer Chromatography(TLC) analysis. It tells that there must be another unknown component in crude and/or fraction F1 as a possible candidate of immune modulators. This component seems to be a derivative of a monomer, GM since its R(f) was close to the monomer. It was also interesting that glycyrrhizin, a major component in G. uralensis Fisch was biologically activated by first being hydrolyzed by an enzyme.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>19002915</pmid><doi>10.1023/A:1016111713056</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antineoplastic drugs. Cytokines Apoptosis Biological and medical sciences Biotechnology Cell growth Cytotoxicity Fundamental and applied biological sciences. Psychology Glycyrrhiza uralensis Glycyrrhizin Health. Pharmaceutical industry Hepatocytes Hepatoma Immunomodulation Industrial applications and implications. Economical aspects Interleukin 6 Lymphocytes B Monomers Production of active biomolecules Tumor cell lines |
title | Effect of the extracts from Glycyrrhiza uralensis Fisch on the growth characteristics of human cell lines: Anti-tumor and immune activation activities |
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