Natural jasmonates of different structures suppress the growth of human neuroblastoma cell line SH-SY5Y and its mechanisms
Aim: Recent evidence has indicated that members of natural jasmonates, a family of plant stress hormones, exhibit anticancer activity. The current study was undertaken to investigate the effects of jasmonates on the in vitro growth of human neuroblastomas, one of the most common solid tumors in chil...
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description | Aim: Recent evidence has indicated that members of natural jasmonates, a family of plant stress hormones, exhibit anticancer activity. The current study was undertaken to investigate the effects of jasmonates on the in vitro growth of human neuroblastomas, one of the most common solid tumors in children. Methods: Cellular proliferation was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide colorimetry and colony formation assay. Apoptosis was detected by Hoechst 33258 staining and flow cytometry. Western blotting was applied to assay gene expression. Results: The administration of natural jasmonates, methyl jasmonate, cis-jasmone, and jasmonic acid to cultured neuro- blastoma cell line SH-SY5Y, resulted in a decrease of cell proliferation in a doseand time-dependent manner. However, the in vitro growth of cultured human embryonic kidney (HEK) cell line HEK 293 was not affected by jasmonates. The cell cycles of jasmonate-treated SH-SY5Y cells were arrested at the G2/M phase. The incubation of SH-SY5Y cells with jasmonates resulted in characteristic changes of apoptosis. The anticancer activities of natural jasmonates on SH-SY5Y cells are as follows: methyl jasmonate〉cis-jasmone〉jasmonic acid. In addition, the expressions of proliferating cell nuclear antigen and N-myc were downregulated by methyl jasmonate. Moreover, methyl jasmonate decreased the expression of the X- linked inhibitor of apoptosis protein and survivin, critical members of inhibitors of the apoptosis protein family, in SH-SY5Y cells. Conclusion: Jasmonates suppress the growth of human neuroblastoma cell line SH-SY5Y via inhibiting cell proliferation and inducing apoptosis, which lays the groundwork for further investigation into the anticancer activities and its mechanisms of natural jasmonates on human neuroblastomas. |
doi_str_mv | 10.1111/j.1745-7254.2008.00814.x |
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The current study was undertaken to investigate the effects of jasmonates on the in vitro growth of human neuroblastomas, one of the most common solid tumors in children. Methods: Cellular proliferation was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide colorimetry and colony formation assay. Apoptosis was detected by Hoechst 33258 staining and flow cytometry. Western blotting was applied to assay gene expression. Results: The administration of natural jasmonates, methyl jasmonate, cis-jasmone, and jasmonic acid to cultured neuro- blastoma cell line SH-SY5Y, resulted in a decrease of cell proliferation in a doseand time-dependent manner. However, the in vitro growth of cultured human embryonic kidney (HEK) cell line HEK 293 was not affected by jasmonates. The cell cycles of jasmonate-treated SH-SY5Y cells were arrested at the G2/M phase. The incubation of SH-SY5Y cells with jasmonates resulted in characteristic changes of apoptosis. The anticancer activities of natural jasmonates on SH-SY5Y cells are as follows: methyl jasmonate〉cis-jasmone〉jasmonic acid. In addition, the expressions of proliferating cell nuclear antigen and N-myc were downregulated by methyl jasmonate. Moreover, methyl jasmonate decreased the expression of the X- linked inhibitor of apoptosis protein and survivin, critical members of inhibitors of the apoptosis protein family, in SH-SY5Y cells. Conclusion: Jasmonates suppress the growth of human neuroblastoma cell line SH-SY5Y via inhibiting cell proliferation and inducing apoptosis, which lays the groundwork for further investigation into the anticancer activities and its mechanisms of natural jasmonates on human neuroblastomas.</description><identifier>ISSN: 1671-4083</identifier><identifier>EISSN: 1745-7254</identifier><identifier>DOI: 10.1111/j.1745-7254.2008.00814.x</identifier><identifier>PMID: 18565287</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Animals ; Antineoplastic Agents, Phytogenic - chemistry ; Antineoplastic Agents, Phytogenic - pharmacology ; Apoptosis - drug effects ; Biomedical and Life Sciences ; Biomedicine ; Cell Cycle - drug effects ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Cyclopentanes - chemistry ; Cyclopentanes - pharmacology ; Humans ; Immunology ; Inhibitor of Apoptosis Proteins ; Internal Medicine ; Jasminum - chemistry ; Medical Microbiology ; Mice ; Mice, Inbred C57BL ; Microtubule-Associated Proteins - biosynthesis ; Microtubule-Associated Proteins - genetics ; original-article ; Oxylipins - chemistry ; Oxylipins - pharmacology ; Pharmacology/Toxicology ; Proliferating Cell Nuclear Antigen - biosynthesis ; Proto-Oncogene Proteins c-myc - biosynthesis ; Structure-Activity Relationship ; Tumor Stem Cell Assay ; Vaccine ; X-Linked Inhibitor of Apoptosis Protein - biosynthesis ; X-Linked Inhibitor of Apoptosis Protein - genetics ; X线性抑制剂 ; 增生细胞核 ; 成神经细胞瘤 ; 茉莉酮酸酯</subject><ispartof>Acta pharmacologica Sinica, 2008-07, Vol.29 (7), p.861-869</ispartof><rights>CPS and SIMM 2008</rights><rights>Copyright Nature Publishing Group Jul 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c344t-414e06abfc1ee30b939a8c61973d1d792dfb9abc1aebe32f8a1194bdbd0551c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/95561A/95561A.jpg</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18565287$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tong, Qiang-song</creatorcontrib><creatorcontrib>Jiang, Guo-song</creatorcontrib><creatorcontrib>Zheng, Li-duan</creatorcontrib><creatorcontrib>Tang, Shao-tao</creatorcontrib><creatorcontrib>Cai, Jia-bin</creatorcontrib><creatorcontrib>Liu, Yuan</creatorcontrib><creatorcontrib>Zeng, Fu-qing</creatorcontrib><creatorcontrib>Dong, Ji-hua</creatorcontrib><title>Natural jasmonates of different structures suppress the growth of human neuroblastoma cell line SH-SY5Y and its mechanisms</title><title>Acta pharmacologica Sinica</title><addtitle>Acta Pharmacol Sin</addtitle><addtitle>Acta Pharmacologica Sinica</addtitle><description>Aim: Recent evidence has indicated that members of natural jasmonates, a family of plant stress hormones, exhibit anticancer activity. The current study was undertaken to investigate the effects of jasmonates on the in vitro growth of human neuroblastomas, one of the most common solid tumors in children. Methods: Cellular proliferation was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide colorimetry and colony formation assay. Apoptosis was detected by Hoechst 33258 staining and flow cytometry. Western blotting was applied to assay gene expression. Results: The administration of natural jasmonates, methyl jasmonate, cis-jasmone, and jasmonic acid to cultured neuro- blastoma cell line SH-SY5Y, resulted in a decrease of cell proliferation in a doseand time-dependent manner. However, the in vitro growth of cultured human embryonic kidney (HEK) cell line HEK 293 was not affected by jasmonates. The cell cycles of jasmonate-treated SH-SY5Y cells were arrested at the G2/M phase. The incubation of SH-SY5Y cells with jasmonates resulted in characteristic changes of apoptosis. The anticancer activities of natural jasmonates on SH-SY5Y cells are as follows: methyl jasmonate〉cis-jasmone〉jasmonic acid. In addition, the expressions of proliferating cell nuclear antigen and N-myc were downregulated by methyl jasmonate. Moreover, methyl jasmonate decreased the expression of the X- linked inhibitor of apoptosis protein and survivin, critical members of inhibitors of the apoptosis protein family, in SH-SY5Y cells. Conclusion: Jasmonates suppress the growth of human neuroblastoma cell line SH-SY5Y via inhibiting cell proliferation and inducing apoptosis, which lays the groundwork for further investigation into the anticancer activities and its mechanisms of natural jasmonates on human neuroblastomas.</description><subject>Animals</subject><subject>Antineoplastic Agents, Phytogenic - chemistry</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Apoptosis - drug effects</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Cycle - drug effects</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Cyclopentanes - chemistry</subject><subject>Cyclopentanes - pharmacology</subject><subject>Humans</subject><subject>Immunology</subject><subject>Inhibitor of Apoptosis Proteins</subject><subject>Internal Medicine</subject><subject>Jasminum - chemistry</subject><subject>Medical Microbiology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microtubule-Associated Proteins - 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chemistry</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Apoptosis - drug effects</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Cycle - drug effects</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Cyclopentanes - chemistry</topic><topic>Cyclopentanes - pharmacology</topic><topic>Humans</topic><topic>Immunology</topic><topic>Inhibitor of Apoptosis Proteins</topic><topic>Internal Medicine</topic><topic>Jasminum - chemistry</topic><topic>Medical Microbiology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microtubule-Associated Proteins - biosynthesis</topic><topic>Microtubule-Associated Proteins - genetics</topic><topic>original-article</topic><topic>Oxylipins - chemistry</topic><topic>Oxylipins - pharmacology</topic><topic>Pharmacology/Toxicology</topic><topic>Proliferating Cell Nuclear Antigen - biosynthesis</topic><topic>Proto-Oncogene Proteins c-myc - 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Academic</collection><jtitle>Acta pharmacologica Sinica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tong, Qiang-song</au><au>Jiang, Guo-song</au><au>Zheng, Li-duan</au><au>Tang, Shao-tao</au><au>Cai, Jia-bin</au><au>Liu, Yuan</au><au>Zeng, Fu-qing</au><au>Dong, Ji-hua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Natural jasmonates of different structures suppress the growth of human neuroblastoma cell line SH-SY5Y and its mechanisms</atitle><jtitle>Acta pharmacologica Sinica</jtitle><stitle>Acta Pharmacol Sin</stitle><addtitle>Acta Pharmacologica Sinica</addtitle><date>2008-07-01</date><risdate>2008</risdate><volume>29</volume><issue>7</issue><spage>861</spage><epage>869</epage><pages>861-869</pages><issn>1671-4083</issn><eissn>1745-7254</eissn><abstract>Aim: Recent evidence has indicated that members of natural jasmonates, a family of plant stress hormones, exhibit anticancer activity. The current study was undertaken to investigate the effects of jasmonates on the in vitro growth of human neuroblastomas, one of the most common solid tumors in children. Methods: Cellular proliferation was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide colorimetry and colony formation assay. Apoptosis was detected by Hoechst 33258 staining and flow cytometry. Western blotting was applied to assay gene expression. Results: The administration of natural jasmonates, methyl jasmonate, cis-jasmone, and jasmonic acid to cultured neuro- blastoma cell line SH-SY5Y, resulted in a decrease of cell proliferation in a doseand time-dependent manner. However, the in vitro growth of cultured human embryonic kidney (HEK) cell line HEK 293 was not affected by jasmonates. The cell cycles of jasmonate-treated SH-SY5Y cells were arrested at the G2/M phase. The incubation of SH-SY5Y cells with jasmonates resulted in characteristic changes of apoptosis. The anticancer activities of natural jasmonates on SH-SY5Y cells are as follows: methyl jasmonate〉cis-jasmone〉jasmonic acid. In addition, the expressions of proliferating cell nuclear antigen and N-myc were downregulated by methyl jasmonate. Moreover, methyl jasmonate decreased the expression of the X- linked inhibitor of apoptosis protein and survivin, critical members of inhibitors of the apoptosis protein family, in SH-SY5Y cells. Conclusion: Jasmonates suppress the growth of human neuroblastoma cell line SH-SY5Y via inhibiting cell proliferation and inducing apoptosis, which lays the groundwork for further investigation into the anticancer activities and its mechanisms of natural jasmonates on human neuroblastomas.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>18565287</pmid><doi>10.1111/j.1745-7254.2008.00814.x</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Antineoplastic Agents, Phytogenic - chemistry Antineoplastic Agents, Phytogenic - pharmacology Apoptosis - drug effects Biomedical and Life Sciences Biomedicine Cell Cycle - drug effects Cell Line, Tumor Cell Proliferation - drug effects Cyclopentanes - chemistry Cyclopentanes - pharmacology Humans Immunology Inhibitor of Apoptosis Proteins Internal Medicine Jasminum - chemistry Medical Microbiology Mice Mice, Inbred C57BL Microtubule-Associated Proteins - biosynthesis Microtubule-Associated Proteins - genetics original-article Oxylipins - chemistry Oxylipins - pharmacology Pharmacology/Toxicology Proliferating Cell Nuclear Antigen - biosynthesis Proto-Oncogene Proteins c-myc - biosynthesis Structure-Activity Relationship Tumor Stem Cell Assay Vaccine X-Linked Inhibitor of Apoptosis Protein - biosynthesis X-Linked Inhibitor of Apoptosis Protein - genetics X线性抑制剂 增生细胞核 成神经细胞瘤 茉莉酮酸酯 |
title | Natural jasmonates of different structures suppress the growth of human neuroblastoma cell line SH-SY5Y and its mechanisms |
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