Zhang Y J, Li Y, DeLeo V A, Santella R M
Cancer Center, School of Public Health, Columbia University, New York, N.Y.
Skin Pharmacol. 1990;3(3):171-9. doi: 10.1159/000210867.
A clinical therapy for psoriasis, a hyperproliferative disease of the skin, utilizes topical application of crude coal tar sometimes followed by UV irradiation (Goeckerman therapy). To investigate the formation of covalent DNA adducts resulting from this therapy, skin biopsies were obtained from treated patients and controls. Indirect immunofluorescence staining with antisera generated against benzo(a)pyrene diol epoxide-modified DNA was used to investigate cell-specific localization of adduct formation. Specific nuclear staining was detected in the epidermal cells of all biopsies from treated patients but not from control biopsies obtained from untreated individuals. 32P postlabeling of DNA isolated from the biopsies was used to determine the spectrum of hydrophobic adducts present. A pattern of multiple adducts was detected in the samples obtained from the treated patients but not from controls.
一种用于治疗银屑病(一种皮肤过度增殖性疾病)的临床疗法是局部应用粗煤焦油,有时随后进行紫外线照射(格克曼疗法)。为了研究这种疗法导致的共价DNA加合物的形成,从接受治疗的患者和对照组获取了皮肤活检样本。使用针对苯并(a)芘二醇环氧化物修饰的DNA产生的抗血清进行间接免疫荧光染色,以研究加合物形成的细胞特异性定位。在所有来自接受治疗患者的活检样本的表皮细胞中检测到特异性核染色,但在从未经治疗个体获得的对照活检样本中未检测到。对从活检样本中分离的DNA进行³²P后标记,以确定存在的疏水加合物谱。在从接受治疗患者获得的样本中检测到多种加合物模式,但在对照组中未检测到。