Malten, a new synthetic molecule showing in vitro antiproliferative activity against tumour cells and induction of complex DNA structural alterations

被引:35
作者
Amatori, S. [1 ]
Bagaloni, I. [1 ]
Macedi, E. [2 ]
Formica, M. [2 ]
Giorgi, L. [2 ]
Fusi, V. [2 ]
Fanelli, M. [1 ]
机构
[1] Univ Urbino Carlo Bo, Dept Biomol Sci, Mol Pathol & Oncol Lab PaoLa, I-61032 Fano, PU, Italy
[2] Univ Urbino Carlo Bo, Inst Chem Sci, I-61029 Urbino, PU, Italy
关键词
antineoplastic drug; apoptosis; cell cycle; cytotoxicity; cancer therapy; LEUKEMIA-CELLS; CROSS-LINKS; APOPTOSIS; TOXICITY; LINES; ALKYLATION; EXPRESSION; GUANINE;
D O I
10.1038/sj.bjc.6605745
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
BACKGROUND: Hydroxypyrones represent several classes of molecules known for their high synthetic versatility. This family of molecules shows several interesting pharmaceutical activities and is considered as a promising source of new antineoplastic compounds. METHODS: In the quest to identify new potential anticancer agents, a new maltol (3-hydroxy-2-methyl-4-pyrone)-derived molecule, named malten (N,N'-bis((3-hydroxy-4-pyron-2-yl)methyl)-N,N'-dimethylethylendiamine), has been synthesised and analysed at both biological and molecular levels for its antiproliferative activity in eight tumour cell lines. RESULTS: Malten exposure led to a dose-dependent reduction in cell survival in all the neoplastic models studied. Sublethal concentrations of malten induce profound cell cycle changes, particularly affecting the S and/or G2-M phases, whereas exposure to lethal doses causes the induction of programmed cell death. The molecular response to malten was also investigated in JURKAT and U937 cells. It showed the modulation of genes having key roles in cell cycle progression and apoptosis. Finally, as part of the effort to clarify the action mechanism, we showed that malten is able to impair DNA electrophoretic mobility and drastically reduce both PCR amplificability and fragmentation susceptibility of DNA. CONCLUSION: Taken together, these results show that malten may exert its antiproliferative activity through the induction of complex DNA structural modifications. This evidence, together with the high synthetic versatility of maltol-derived compounds, makes malten an interesting molecular scaffold for the future design of new potential anticancer agents. British Journal of Cancer (2010) 103, 239-248. doi: 10.1038/sj.bjc.6605745 www.bjcancer.com Published online 22 June 2010 (C) 2010 Cancer Research UK
引用
收藏
页码:239 / 248
页数:10
相关论文
共 27 条
[1]
Decitabine, differently from DNMT1 silencing, exerts its antiproliferative activity through p21 upregulation in malignant pleural mesothelioma (MPM) cells [J].
Amatori, S. ;
Papalini, F. ;
Lazzarini, R. ;
Donati, B. ;
Bagaloni, I. ;
Rippo, M. R. ;
Procopio, A. ;
Pelicci, P. G. ;
Catalano, A. ;
Fanelli, M. .
LUNG CANCER, 2009, 66 (02) :184-190
[2]
Mixed-Ligand Copper(II) Maltolate Complexes: Synthesis, Characterization, DNA Binding and Cleavage, and Cytotoxicity [J].
Barve, Archika ;
Kumbhar, Avinash ;
Bhat, Menakshi ;
Joshi, Bimba ;
Butcher, Ray ;
Sonawane, Uddhavesh ;
Joshi, Rajendra .
INORGANIC CHEMISTRY, 2009, 48 (19) :9120-9132
[3]
The CULt of Caspase-8 Ubiquitination [J].
Bekes, Miklos ;
Salvesen, Guy S. .
CELL, 2009, 137 (04) :604-606
[4]
DNA UNWINDING PRODUCED BY SITE-SPECIFIC INTRASTRAND CROSS-LINKS OF THE ANTITUMOR DRUG CIS-DIAMMINEDICHLOROPLATINUM(II) [J].
BELLON, SF ;
COLEMAN, JH ;
LIPPARD, SJ .
BIOCHEMISTRY, 1991, 30 (32) :8026-8035
[5]
MUTAGENICITY OF 1,2-DICARBONYL COMPOUNDS - MALTOL, KOJIC ACID, DIACETYL AND RELATED SUBSTANCES [J].
BJELDANES, LF ;
CHEW, H .
MUTATION RESEARCH, 1979, 67 (04) :367-371
[6]
Differentiation response of acute promyelocytic leukemia cells and PML/RARα leukemogenic activity studies by real-time RT-PCR [J].
Caprodossi, S ;
Pedinotti, M ;
Amantini, C ;
Santoni, G ;
Minucci, S ;
Pelicci, PG ;
Fanelli, M .
MOLECULAR BIOTECHNOLOGY, 2005, 30 (03) :231-238
[7]
FREQUENT MUTATIONS IN THE P53 TUMOR SUPPRESSOR GENE IN HUMAN LEUKEMIA T-CELL LINES [J].
CHENG, J ;
HAAS, M .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (10) :5502-5509
[8]
Alkylation of guanine in DNA by S23906-1, a novel potent antitumor compound derived from the plant alkaloid acronycine [J].
David-Cordonnier, MH ;
Laine, W ;
Lansiaux, A ;
Kouach, M ;
Briand, G ;
Pierré, A ;
Hickman, JA ;
Bailly, C .
BIOCHEMISTRY, 2002, 41 (31) :9911-9920
[9]
Enforced expression of the tumor suppressor p53 renders human leukemia cells (U937) more sensitive to 1-[β-D-arabinofuranosyl]cytosine (ara-C)-induced apoptosis [J].
Decker, RH ;
Levin, J ;
Kramer, LB ;
Dai, Y ;
Grant, S .
BIOCHEMICAL PHARMACOLOGY, 2003, 65 (12) :1997-2008
[10]
Loss of pericentromeric DNA methylation pattern in human glioblastoma is associated with altered DNA methyltransferases expression and involves the stem cell compartment [J].
Fanelli, M. ;
Caprodossi, S. ;
Ricci-Vitiani, L. ;
Porcellini, A. ;
Tomassoni-Ardori, F. ;
Amatori, S. ;
Andreoni, F. ;
Magnani, M. ;
De Maria, R. ;
Santoni, A. ;
Minucci, S. ;
Pelicci, P. G. .
ONCOGENE, 2008, 27 (03) :358-365