• Something wrong with this record ?

Effectiveness of human cytochrome P450 3A4 present in liposomal and microsomal nanoparticles in formation of covalent DNA adducts by ellipticine

M. Sulc, I. Mrizova, T. Cerna, E. Frei, T. Eckschlager, V. Adam, K. Kopeckova, M. Stiborova,

. 2016 ; 37 (Suppl1) : 95-102.

Language English Country Sweden

Document type Journal Article

OBJECTIVES: Ellipticine is an anticancer agent that functions through multiple mechanisms participating in cell cycle arrest and initiation of apoptosis. This drug forms covalent DNA adducts after its enzymatic activation with cytochrome P450 (CYP), which is one of the most important ellipticine DNA-damaging mechanisms of its cytotoxic effects. The improvements of cancer treatment are the major challenge in oncology research. Nanotransporters (nanoparticles) are promising approaches to target tumor cells, frequently leading to improve drug therapeutic index. Ellipticine has already been prepared in nanoparticle forms. However, since its anticancer efficiency depends on the CYP3A4-mediated metabolism in cancer cells, the aim of our research is to develop nanoparticles containing this enzyme that can be transported to tumor cells, thereby potentiating ellipticine cytotoxicity. METHODS: The CYP3A4 enzyme encapsulated into two nanoparticle forms, liposomes and microsomes, was tested to activate ellipticine to its reactive species forming covalent DNA adducts. Ellipticine-derived DNA adducts were determined by the 32P-postlabeling method. RESULTS: The CYP3A4 enzyme both in the liposome and microsome nanoparticle forms was efficient to activate ellipticine to species forming DNA adducts. Two DNA adducts, which are formed from ellipticine metabolites 12-hydroxy- and 13-hydroxyellipticine generated by its oxidation by CYP3A4, were formed by both CYP3A4 nanoparticle systems. A higher effectiveness of CYP3A4 in microsomal than in liposomal nanoparticles to form ellipticine-DNA adducts was found. CONCLUSION: Further testing in a suitable cancer cell model is encouraged to investigate whether the DNA-damaging effects of ellipticine after its activation by CYP3A4 nanoparticle forms are appropriate for active targeting of this enzyme to specific cancer cells.

000      
00000naa a2200000 a 4500
001      
bmc17023227
003      
CZ-PrNML
005      
20170720124428.0
007      
ta
008      
170720s2016 sw f 000 0|eng||
009      
AR
035    __
$a (PubMed)28263536
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a sw
100    1_
$a Sulc, Miroslav $u Department of Biochemistry, Faculty of Science, Charles University, Prague 2, Czech Republic.
245    10
$a Effectiveness of human cytochrome P450 3A4 present in liposomal and microsomal nanoparticles in formation of covalent DNA adducts by ellipticine / $c M. Sulc, I. Mrizova, T. Cerna, E. Frei, T. Eckschlager, V. Adam, K. Kopeckova, M. Stiborova,
520    9_
$a OBJECTIVES: Ellipticine is an anticancer agent that functions through multiple mechanisms participating in cell cycle arrest and initiation of apoptosis. This drug forms covalent DNA adducts after its enzymatic activation with cytochrome P450 (CYP), which is one of the most important ellipticine DNA-damaging mechanisms of its cytotoxic effects. The improvements of cancer treatment are the major challenge in oncology research. Nanotransporters (nanoparticles) are promising approaches to target tumor cells, frequently leading to improve drug therapeutic index. Ellipticine has already been prepared in nanoparticle forms. However, since its anticancer efficiency depends on the CYP3A4-mediated metabolism in cancer cells, the aim of our research is to develop nanoparticles containing this enzyme that can be transported to tumor cells, thereby potentiating ellipticine cytotoxicity. METHODS: The CYP3A4 enzyme encapsulated into two nanoparticle forms, liposomes and microsomes, was tested to activate ellipticine to its reactive species forming covalent DNA adducts. Ellipticine-derived DNA adducts were determined by the 32P-postlabeling method. RESULTS: The CYP3A4 enzyme both in the liposome and microsome nanoparticle forms was efficient to activate ellipticine to species forming DNA adducts. Two DNA adducts, which are formed from ellipticine metabolites 12-hydroxy- and 13-hydroxyellipticine generated by its oxidation by CYP3A4, were formed by both CYP3A4 nanoparticle systems. A higher effectiveness of CYP3A4 in microsomal than in liposomal nanoparticles to form ellipticine-DNA adducts was found. CONCLUSION: Further testing in a suitable cancer cell model is encouraged to investigate whether the DNA-damaging effects of ellipticine after its activation by CYP3A4 nanoparticle forms are appropriate for active targeting of this enzyme to specific cancer cells.
650    _2
$a fytogenní protinádorové látky $x metabolismus $7 D000972
650    _2
$a cytochrom P-450 CYP3A $x metabolismus $7 D051544
650    _2
$a adukty DNA $x metabolismus $7 D018736
650    _2
$a elipticiny $x metabolismus $7 D004611
650    _2
$a lidé $7 D006801
650    12
$a liposomy $7 D008081
650    12
$a mikrozomy $7 D008861
655    _2
$a časopisecké články $7 D016428
700    1_
$a Mrizova, Iveta $u Department of Biochemistry, Faculty of Science, Charles University, Prague 2, Czech Republic.
700    1_
$a Cerna, Tereza $u Department of Biochemistry, Faculty of Science, Charles University, Prague 2, Czech Republic.
700    1_
$a Frei, Eva $u Department of Biochemistry, Faculty of Science, Charles University, Prague 2, Czech Republic.
700    1_
$a Eckschlager, Tomas $u Department of Pediatric Hematology and Oncology, 2nd Medical Faculty, Charles University and University Hospital Motol, Prague 5, Czech Republic.
700    1_
$a Adam, Vojtěch $u Department of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic. $7 xx0064599
700    1_
$a Kopeckova, Katerina $u Department of Oncology, 2nd Faculty of Medicine, Charles University and University Hospital Motol, Prague 5, Czech Republic.
700    1_
$a Stiborova, Marie $u Department of Biochemistry, Faculty of Science, Charles University, Prague 2, Czech Republic.
773    0_
$w MED00168352 $t Neuro endocrinology letters $x 0172-780X $g Roč. 37, Suppl1 (2016), s. 95-102
856    41
$u https://pubmed.ncbi.nlm.nih.gov/28263536 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20170720 $b ABA008
991    __
$a 20170720124921 $b ABA008
999    __
$a ok $b bmc $g 1238908 $s 984140
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2016 $b 37 $c Suppl1 $d 95-102 $i 0172-780X $m Neuro-endocrinology letters $n Neuro-endocrinol. lett. $x MED00168352
LZP    __
$a Pubmed-20170720

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...