Document Detail


Involvement of apoptosis and cyclin D1 gene repression in growth inhibition of T-47D human breast cancer cells by methylglyoxal bis(cyclopentylamidinohydrazone).
MedLine Citation:
PMID:  9852627     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Polyamines are considered to be important intracellular molecules for the proliferation of the cancer cells. In this study, effects of methylglyoxal bis(cyclopentylamidinohydrazone) (MGBCP), a potent inhibitor of the polyamine biosynthetic pathway, on the growth and cell cycle of T-47D human breast cancer cells were investigated. MGBCP dose-dependently inhibited the growth of T-47D cells, in which the contents of spermine, spermidine and putrescine decreased concomitantly. The gene expression of cyclin D1 was also repressed by the MGBCP treatment. The MGBCP-treated cells clearly exhibited morphological changes indicating the blebbing and chromatin condensation which are characteristic of apoptosis. Flow cytometric analysis showed hypo-diploid subpopulations due to apoptotic cells, and characteristic oligonucleosomal-sized DNA fragments were clearly observed for MGBCP-treated cells as the concentration of the drug was increased. These findings suggest that the inhibition of polyamine synthesis results in the repressions of cyclin D1 expression and cell cycle progression, eventually inducing apoptosis in these human breast cancer cells.
Authors:
H Kaneko; H Hibasami; N Satoh; H Wakabayashi; H Ikeda; N Tsuge; K Yonemaru; A Muraki; Y Kawarada; K Nakashima
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  International journal of molecular medicine     Volume:  1     ISSN:  1107-3756     ISO Abbreviation:  Int. J. Mol. Med.     Publication Date:  1998 Jun 
Date Detail:
Created Date:  2000-06-29     Completed Date:  2000-06-29     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  9810955     Medline TA:  Int J Mol Med     Country:  GREECE    
Other Details:
Languages:  eng     Pagination:  931-6     Citation Subset:  IM    
Affiliation:
Department of Biochemistry and First Surgery, Faculty of Medicine, Mie University, Tsu-city, Mie 514-8507, Japan.
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MeSH Terms
Descriptor/Qualifier:
Antineoplastic Agents / pharmacology*
Apoptosis / drug effects*
Breast Neoplasms / drug therapy*,  genetics,  pathology
Cell Cycle / drug effects
Cell Division / drug effects*
Cyclin D1 / genetics*
DNA Fragmentation / drug effects
Dose-Response Relationship, Drug
Flow Cytometry
Gene Expression Regulation, Neoplastic / drug effects
Humans
Mitoguazone / analogs & derivatives*,  pharmacology
Polyamines / metabolism
RNA, Messenger / drug effects,  genetics,  metabolism
Time Factors
Tumor Cells, Cultured / cytology,  drug effects,  metabolism
Chemical
Reg. No./Substance:
0/Antineoplastic Agents; 0/Polyamines; 0/RNA, Messenger; 123035-67-6/methylglyoxal bis(cyclopentylamidinohydrazone); 136601-57-5/Cyclin D1; 459-86-9/Mitoguazone

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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