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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Veröffentlicht in:Acta pharmacologica Sinica 2008-07, Vol.29 (7), p.861-869
Hauptverfasser: Tong, Qiang-song, Jiang, Guo-song, Zheng, Li-duan, Tang, Shao-tao, Cai, Jia-bin, Liu, Yuan, Zeng, Fu-qing, Dong, Ji-hua
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container_title Acta pharmacologica Sinica
container_volume 29
creator Tong, Qiang-song
Jiang, Guo-song
Zheng, Li-duan
Tang, Shao-tao
Cai, Jia-bin
Liu, Yuan
Zeng, Fu-qing
Dong, Ji-hua
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. 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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><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 - biosynthesis</subject><subject>Microtubule-Associated Proteins - genetics</subject><subject>original-article</subject><subject>Oxylipins - chemistry</subject><subject>Oxylipins - pharmacology</subject><subject>Pharmacology/Toxicology</subject><subject>Proliferating Cell Nuclear Antigen - biosynthesis</subject><subject>Proto-Oncogene Proteins c-myc - biosynthesis</subject><subject>Structure-Activity Relationship</subject><subject>Tumor Stem Cell Assay</subject><subject>Vaccine</subject><subject>X-Linked Inhibitor of Apoptosis Protein - biosynthesis</subject><subject>X-Linked Inhibitor of Apoptosis Protein - genetics</subject><subject>X线性抑制剂</subject><subject>增生细胞核</subject><subject>成神经细胞瘤</subject><subject>茉莉酮酸酯</subject><issn>1671-4083</issn><issn>1745-7254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkctu1TAQhiMEoqXwCshiwS7B1yReogooUgWLwqIry3YmJwmJfeqLKDw9Di1UYoOl0Vgzn-fiv6oQwQ0p583SkI6LuqOCNxTjvilGeHP7qDr9m3hc7m1Hao57dlI9i3HBmFFG5NPqhPSiFbTvTqufn3TKQa9o0XHzTieIyI9omMcRAriEYgrZFqTEYz4ei48oTYAOwX9P085OedMOOcjBm1XH5DeNLKwrWmcH6OqivroW10i7Ac0pog3spN0ct_i8ejLqNcKLe39WfX3_7sv5RX35-cPH87eXtWWcp5oTDrjVZrQEgGEjmdS9bYns2ECGTtJhNFIbSzQYYHTsNSGSm8EMWAhiGTurXt_VPQZ_kyEmtc1xH1A78DmqVlIqGe3_C1Lcd0ISWcBX_4CLz8GVJRQlDNNOir3ty3somw0GdQzzpsMP9efvCyDvgFhS7gDhoQrBatdZLWqXU-1yql1n9VtndfswgZ28O9yU58po-22cV1ClfVs2Z-wXhh-myA</recordid><startdate>20080701</startdate><enddate>20080701</enddate><creator>Tong, Qiang-song</creator><creator>Jiang, Guo-song</creator><creator>Zheng, Li-duan</creator><creator>Tang, Shao-tao</creator><creator>Cai, Jia-bin</creator><creator>Liu, Yuan</creator><creator>Zeng, Fu-qing</creator><creator>Dong, Ji-hua</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>20080701</creationdate><title>Natural jasmonates of different structures suppress the growth of human neuroblastoma cell line SH-SY5Y and its mechanisms</title><author>Tong, Qiang-song ; 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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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