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Molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell lines: less involvement of metallothionein

BACKGROUND: Heptaplatin is a new platinum derivative with anticancer activity against various cancer cell lines, including cisplatin-resistant cancer cell lines (Cancer Chemother Pharmacol 1995; 35: 441). METHODS: Molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell...

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Autores principales: Choi, Cheol-Hee, Cha, Yoon-Jung, An, Chun-San, Kim, Kyung-Jong, Kim, Kweon-Cheon, Moon, Sung-Pyo, Lee, Zang Hee, Min, Young-Don
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC533863/
https://www.ncbi.nlm.nih.gov/pubmed/15494073
http://dx.doi.org/10.1186/1475-2867-4-6
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author Choi, Cheol-Hee
Cha, Yoon-Jung
An, Chun-San
Kim, Kyung-Jong
Kim, Kweon-Cheon
Moon, Sung-Pyo
Lee, Zang Hee
Min, Young-Don
author_facet Choi, Cheol-Hee
Cha, Yoon-Jung
An, Chun-San
Kim, Kyung-Jong
Kim, Kweon-Cheon
Moon, Sung-Pyo
Lee, Zang Hee
Min, Young-Don
author_sort Choi, Cheol-Hee
collection PubMed
description BACKGROUND: Heptaplatin is a new platinum derivative with anticancer activity against various cancer cell lines, including cisplatin-resistant cancer cell lines (Cancer Chemother Pharmacol 1995; 35: 441). METHODS: Molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell lines has been investigated in connection with metallothionein (MT). Cytotoxicity was determined by an MTT assay. MT mRNA, was determined by RT-PCR assay. Transfection study was carried out to examine the function of MT. RESULTS: Of various gastric cancer cell lines, SNU-638 and SNU-601 showed the highest and lowest levels of MT mRNA, respectively, showing 80-fold difference. The IC(50 )values of SNU-638 to cisplatin, carboplatin and heptaplatin were 11.2-fold, 5.1-fold and 2.0-fold greater than those of SNU-601, respectively. Heptaplatin was more effective against cisplatin-resistant and MT-transfected gastric cancer sublines than cisplatin or carboplatin was. In addition, heptaplatin attenuated cadmium, but not zinc, induction of MT. CONCLUSION: These results indicate that molecular mechanisms of heptaplatin effective against cisplatin-resistant gastric cancer sublines is at least in part due to the less involvement of MT in heptaplatin resistance as well as its attenuation of MT induction.
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spelling pubmed-5338632004-11-26 Molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell lines: less involvement of metallothionein Choi, Cheol-Hee Cha, Yoon-Jung An, Chun-San Kim, Kyung-Jong Kim, Kweon-Cheon Moon, Sung-Pyo Lee, Zang Hee Min, Young-Don Cancer Cell Int Primary Research BACKGROUND: Heptaplatin is a new platinum derivative with anticancer activity against various cancer cell lines, including cisplatin-resistant cancer cell lines (Cancer Chemother Pharmacol 1995; 35: 441). METHODS: Molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell lines has been investigated in connection with metallothionein (MT). Cytotoxicity was determined by an MTT assay. MT mRNA, was determined by RT-PCR assay. Transfection study was carried out to examine the function of MT. RESULTS: Of various gastric cancer cell lines, SNU-638 and SNU-601 showed the highest and lowest levels of MT mRNA, respectively, showing 80-fold difference. The IC(50 )values of SNU-638 to cisplatin, carboplatin and heptaplatin were 11.2-fold, 5.1-fold and 2.0-fold greater than those of SNU-601, respectively. Heptaplatin was more effective against cisplatin-resistant and MT-transfected gastric cancer sublines than cisplatin or carboplatin was. In addition, heptaplatin attenuated cadmium, but not zinc, induction of MT. CONCLUSION: These results indicate that molecular mechanisms of heptaplatin effective against cisplatin-resistant gastric cancer sublines is at least in part due to the less involvement of MT in heptaplatin resistance as well as its attenuation of MT induction. BioMed Central 2004-10-19 /pmc/articles/PMC533863/ /pubmed/15494073 http://dx.doi.org/10.1186/1475-2867-4-6 Text en Copyright © 2004 Choi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Primary Research
Choi, Cheol-Hee
Cha, Yoon-Jung
An, Chun-San
Kim, Kyung-Jong
Kim, Kweon-Cheon
Moon, Sung-Pyo
Lee, Zang Hee
Min, Young-Don
Molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell lines: less involvement of metallothionein
title Molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell lines: less involvement of metallothionein
title_full Molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell lines: less involvement of metallothionein
title_fullStr Molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell lines: less involvement of metallothionein
title_full_unstemmed Molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell lines: less involvement of metallothionein
title_short Molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell lines: less involvement of metallothionein
title_sort molecular mechanisms of heptaplatin effective against cisplatin-resistant cancer cell lines: less involvement of metallothionein
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC533863/
https://www.ncbi.nlm.nih.gov/pubmed/15494073
http://dx.doi.org/10.1186/1475-2867-4-6
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