Expression Profile of CYP1A1 and CYP1B1 Enzymes in Colon and Bladder Tumors

被引:68
作者
Androutsopoulos, Vasilis P. [1 ,4 ]
Spyrou, Ioannis [2 ]
Ploumidis, Achilles [3 ]
Papalampros, Alexandros Eystathios [2 ]
Kyriakakis, Michalis [1 ]
Delakas, Demetrios [3 ]
Spandidos, Demetrios A. [4 ]
Tsatsakis, Aristidis M. [1 ]
机构
[1] Univ Crete, Fac Med, Dept Morphol, Toxicol Lab, Iraklion, Crete, Greece
[2] Univ Athens, Laiko Hosp, Dept Surg 1, Athens, Greece
[3] Asklipeio Gen Hosp, Dept Urol, Athens, Greece
[4] Univ Crete, Fac Med, Dept Lab Med, Lab Clin Virol, Iraklion, Crete, Greece
关键词
ARYL-HYDROCARBON RECEPTOR; BREAST-CANCER CELLS; CYTOCHROME-P450; ENZYMES; DIFFERENTIAL EXPRESSION; METABOLIC-ACTIVATION; DRUG DEVELOPMENT; OVARIAN-CANCER; CARCINOMA; P450; P450CYP1B1;
D O I
10.1371/journal.pone.0082487
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: The cytochrome P450 CYP1A1 and CYP1B1 enzymes are involved in carcinogenesis via activation of pro-carcinogenic compounds to carcinogenic metabolites. CYP1A1 and CYP1B1 have shown elevated levels in human tumors as determined by qRT-PCR and immunohistochemical studies. However studies that have examined CYP1 expression by enzyme activity assays are limited. Results: In the current study the expression of CYP1A1 and CYP1B1 was investigated in a panel of human tumors of bladder and colorectal origin by qRT-PCR and enzyme activity assays. The results demonstrated that 35% (7/20) of bladder tumors and 35% (7/20) of colon tumors overexpressed active CYP1 enzymes. CYP1B1 mRNA was overexpressed in 65% and 60% of bladder and colon tumors respectively, whereas CYP1A1 was overexpressed in 65% and 80% of bladder and colon tumors. Mean mRNA levels of CYP1B1 and CYP1A1 along with mean CYP1 activity were higher in bladder and colon tumors compared to normal tissues (p<0.05). Statistical analysis revealed CYP1 expression levels to be independent of TNM status. Moreover, incubation of tumor microsomal protein in 4 bladder and 3 colon samples with a CYP1B1 specific antibody revealed a large reduction (72.5 +/- 5.5 % for bladder and 71.8 +/- 7.2% for colon) in catalytic activity, indicating that the activity was mainly attributed to CYP1B1 expression. Conclusions: The study reveals active CYP1 overexpression in human tumors and uncovers the potential use of CYP1 enzymes and mainly CYP1B1 as targets for cancer therapy.
引用
收藏
页数:10
相关论文
共 47 条
[1]
Functional analysis of six different polymorphic CYP1B1 enzyme variants found in an Ethiopian population [J].
Aklillu, E ;
Oscarson, M ;
Hidestrand, M ;
Leidvik, B ;
Otter, C ;
Ingelman-Sundberg, M .
MOLECULAR PHARMACOLOGY, 2002, 61 (03) :586-594
[2]
Antiproliferative and cytostatic effects of the natural product eupatorin on MDA-MB-468 human breast cancer cells due to CYP1-mediated metabolism [J].
Androutsopoulos, Vasilis ;
Arroo, Randolph R. J. ;
Hall, John F. ;
Surichan, Somchaiya ;
Potter, Gerry A. .
BREAST CANCER RESEARCH, 2008, 10 (03)
[3]
The flavonoids diosmetin and luteolin exert synergistic cytostatic effects in human hepatoma HepG2 cells via CYP1A-catalyzed metabolism, activation of JNK and ERK and P53/P21 up-regulation [J].
Androutsopoulos, Vasilis P. ;
Spandidos, Demetrios A. .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2013, 24 (02) :496-504
[4]
Proteasomal degradation of human CYP1B1: Effect of the Asn453Ser polymorphism on the post-translational regulation of CYP1B1 expression [J].
Bandiera, S ;
Weidlich, S ;
Harth, V ;
Broede, P ;
Friedberg, T .
MOLECULAR PHARMACOLOGY, 2005, 67 (02) :435-443
[5]
Coordinate Regulation of Cytochrome P450 1A1 Expression in Mouse Liver by the Aryl Hydrocarbon Receptor and the β-Catenin Pathway [J].
Braeuning, Albert ;
Koehle, Christoph ;
Buchmann, Albrecht ;
Schwarz, Michael .
TOXICOLOGICAL SCIENCES, 2011, 122 (01) :16-25
[6]
Targeting cytochrome P450 enzymes: A new approach in anti-cancer drug development [J].
Bruno, Robert D. ;
Njar, Vincent C. O. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2007, 15 (15) :5047-5060
[7]
Aryl hydrocarbon receptor activation by aminoflavone: New molecular target for renal cancer treatment [J].
Callero, Mariana A. ;
Suarez, Guadalupe V. ;
Luzzani, Gabriela ;
Itkin, Boris ;
Binh Nguyen ;
Loaiza-Perez, Andrea I. .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2012, 41 (01) :125-134
[8]
Target validation of cytochrome P450CYP1B1 in prostate carcinoma with protein expression in associated hyperplastic and premalignant tissue [J].
Carnell, DM ;
Smith, RE ;
Daley, FM ;
Barber, PR ;
Hoskin, PJ ;
Wilson, GD ;
Murray, GI ;
Everett, SA .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 58 (02) :500-509
[9]
Differential expression of CYP1A1, CYP1A2, CYP1B1 in human kidney tumours [J].
Cheung, YL ;
Kerr, AC ;
McFadyen, MCE ;
Melvin, WT ;
Murray, GI .
CANCER LETTERS, 1999, 139 (02) :199-205
[10]
12(R)-Hydroxy-5(Z),8(Z),10(E),14(Z)-eicosatetraenoic Acid [12(R)-HETE], an Arachidonic Acid Derivative, Is an Activator of the Aryl Hydrocarbon Receptor [J].
Chiaro, Christopher. R. ;
Patel, Rushang D. ;
Perdew, Gary. H. .
MOLECULAR PHARMACOLOGY, 2008, 74 (06) :1649-1656