Acta Med. 2016, 59: 75-78

https://doi.org/10.14712/18059694.2016.94

Droplet Digital PCR Analysis of GSTM1 Deletion Polymorphism in Psoriatic Subjects Treated with Goeckerman Therapy

Martin Beráneka,b, Zdeněk Fialac, Jan Kremláčekd, Ctirad Andrýse, Květoslava Hamákováf, Vladimír Paličkab, Lenka Borskád

aDepartment of Biochemical Sciences, Charles University in Prague, Faculty of Pharmacy in Hradec Králové, Hradec Králové, Czech Republic
bInstitute of Clinical Biochemistry and Diagnostics, Charles University Hospital and Faculty of Medicine in Hradec Králové, Hradec Králové, Czech Republic
cInstitute of Hygiene and Preventive Medicine, Charles University in Prague, Faculty of Medicine in Hradec Králové, Hradec Králové, Czech Republic
dInstitute of Pathological Physiology, Charles University in Prague, Faculty of Medicine in Hradec Králové, Hradec Králové, Czech Republic
eInstitute of Clinical Immunology and Allergology, Charles University in Prague, Faculty of Medicine in Hradec Králové, Hradec Králové, Czech Republic
fClinic of Dermal and Venereal Diseases, Charles University Hospital Hradec Králové, Hradec Králové, Czech Republic

Received May 31, 2016
Accepted June 13, 2016

Goeckerman therapy (GT) represents an effective treatment of psoriasis including a combination of pharmaceutical grade crude coal tar (CCT) and ultraviolet irradiation (UV-R). Coal tar contains a mixture of polycyclic aromatic hydrocarbons. The best known carcinogenic polyaromate – benzo[a]pyrene is metabolized into a highly reactive benzo[a]pyrene-7,8-diol-9,10-epoxide (BPDE). Glutathione S-transferase M1 (GSTM1) catalyses the conjugation of drugs, toxins and products of oxidative stress with glutathione. The aim of the study is to found possible associations between GSTM1 genotypes and the level of BPDE-DNA adducts in 46 psoriatic patients treated with GT. For genotyping, droplet digital PCR was applied. The GSTM1 copy number was normalized to β-globin reference gene. In five GSTM1*1/*1 subjects, the GSTM1 to β-globin ratio moved from 0.99 to 1.03 with a median of 1.01. GSTM1*0/*1 heterozygotes (n = 20) contained only one GSTM1 function allele which conditioned the ratio 0.47–0.53 (median 0.50). GSTM1*0/*0 individuals (n = 21) showed no amplification of the null variants because of the large deletion in GSTM1. BPDE-DNA concentrations ranged from 1.8 to 66.3 ng/µg with a median of 12.3 ng/µg. GSTM1*0/*0 and GSTM1*0/*1 genotypes showed non-significantly higher concentrations of BPDE-DNA adducts than the GSTM1*1/*1 one (12.3 and 12.4 vs 7.8 ng/µg). The non-significant relationship between BPDE-DNA adducts and GSTM1 genotypes in psoriatic patients could be associated with relatively low doses of CCT and short-term UV-R exposures used in GT.

Funding

This work is supported by the projects PRVOUK P37/09 and PRVOUK P37/11 of Charles University in Prague, Faculty of Medicine in Hradec Králové, Czech Republic

References

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