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接受8-甲氧基补骨脂素和紫外线A光治疗的患者体内的8-甲氧基补骨脂素-DNA加合物

8-Methoxypsoralen-DNA adducts in patients treated with 8-methoxypsoralen and ultraviolet A light.

作者信息

Yang X Y, Gasparro F P, DeLeo V A, Santella R M

机构信息

Comprehensive Cancer Center, Columbia University, New York 10032.

出版信息

J Invest Dermatol. 1989 Jan;92(1):59-63. doi: 10.1111/1523-1747.ep13071224.

DOI:10.1111/1523-1747.ep13071224
PMID:2642513
Abstract

The combination of 8-methoxypsoralen (8-MOP) plus ultraviolet A light (320-400 nm), termed PUVA, is used in the treatment of psoriasis, a hyperproliferative disease of the skin. This treatment results in the formation of specific 8-MOP adducts with cellular DNA. We have previously developed monoclonal antibodies which recognize these 8-MOP photoadducts. We now report the use of these antibodies in an indirect immunofluorescence technique to study human skin biopsies. Nuclei in 3 of 5 skin biopsies from psoriasis patients undergoing PUVA therapy were positive for adducts. The presence of adducts by immunofluorescence did not correlate with plasma levels of 8-MOP. Enzyme-linked immunosorbent assays, used to determine whether 8-MOP photoadducts could be detected in DNA isolated from the lymphocytes of psoriasis patients after PUVA therapy, were negative.

摘要

8-甲氧基补骨脂素(8-MOP)与紫外线A光(320 - 400纳米)联合使用,即PUVA疗法,用于治疗银屑病,一种皮肤过度增殖性疾病。这种治疗会导致8-MOP与细胞DNA形成特定加合物。我们之前已开发出可识别这些8-MOP光加合物的单克隆抗体。我们现在报告这些抗体在间接免疫荧光技术中用于研究人类皮肤活检样本的情况。接受PUVA治疗的银屑病患者的5份皮肤活检样本中有3份的细胞核加合物呈阳性。通过免疫荧光检测到的加合物的存在与8-MOP的血浆水平无关。用于确定PUVA治疗后银屑病患者淋巴细胞分离出的DNA中是否能检测到8-MOP光加合物的酶联免疫吸附测定结果为阴性。

相似文献

1
8-Methoxypsoralen-DNA adducts in patients treated with 8-methoxypsoralen and ultraviolet A light.接受8-甲氧基补骨脂素和紫外线A光治疗的患者体内的8-甲氧基补骨脂素-DNA加合物
J Invest Dermatol. 1989 Jan;92(1):59-63. doi: 10.1111/1523-1747.ep13071224.
2
Detection and quantification of 8-methoxypsoralen-DNA adducts.8-甲氧基补骨脂素-DNA加合物的检测与定量
IARC Sci Publ. 1988(89):333-40.
3
Immunological detection and visualization of 8-methoxypsoralen-DNA photoadducts.8-甲氧基补骨脂素-DNA光加合物的免疫检测与可视化
Cancer Res. 1987 May 1;47(9):2451-5.
4
Autoradiographic localization of 8-methoxypsoralen in psoriasis skin in vitro.8-甲氧基补骨脂素在体外银屑病皮肤中的放射自显影定位
Acta Derm Venereol. 1981;61(6):481-5.
5
Cytochrome P450 CYP1B1 interacts with 8-methoxypsoralen (8-MOP) and influences psoralen-ultraviolet A (PUVA) sensitivity.细胞色素 P450 CYP1B1 与 8-甲氧基补骨脂素(8-MOP)相互作用,并影响补骨脂素-长波紫外线 A(PUVA)的敏感性。
PLoS One. 2013 Sep 23;8(9):e75494. doi: 10.1371/journal.pone.0075494. eCollection 2013.
6
Intraindividual and interindividual variability in 8-methoxypsoralen kinetics and effect in psoriatic patients.银屑病患者中8-甲氧基补骨脂素动力学及效应的个体内和个体间变异性。
Clin Pharmacol Ther. 1983 Jul;34(1):117-24. doi: 10.1038/clpt.1983.139.
7
DNA repair elicited by UVB during PUVA therapy for psoriasis.银屑病光化学疗法(PUVA)中紫外线B(UVB)引发的DNA修复
Arch Dermatol Res. 1985;278(1):25-30. doi: 10.1007/BF00412491.
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Detection of DNA-psoralen photoadducts in mammalian skin.哺乳动物皮肤中DNA-补骨脂素光加合物的检测。
J Invest Dermatol. 1986 Mar;86(3):308-15. doi: 10.1111/1523-1747.ep12285506.
9
Systemic allergic contact dermatitis to 8-methoxypsoralen (8-MOP).对8-甲氧基补骨脂素(8-MOP)的全身性过敏性接触性皮炎。
J Am Acad Dermatol. 2001 Dec;45(6 Suppl):S218-9. doi: 10.1067/mjd.2001.103644.
10
A reappraisal of the use of 5-methoxypsoralen in the therapy of psoriasis.5-甲氧基补骨脂素在银屑病治疗中应用的重新评估。
Exp Dermatol. 1992 Jul;1(1):46-51. doi: 10.1111/j.1600-0625.1992.tb00071.x.

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Human DNA adduct measurements: state of the art.人类DNA加合物测量:现状
Environ Health Perspect. 1996 Oct;104 Suppl 5(Suppl 5):883-93. doi: 10.1289/ehp.96104s5883.
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Platinum drug-DNA interactions in human tissues measured by cisplatin-DNA enzyme-linked immunosorbent assay and atomic absorbance spectroscopy.
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Environ Health Perspect. 1993 Mar;99:149-54. doi: 10.1289/ehp.9399149.
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Cell Biol Toxicol. 1988 Dec;4(4):511-6. doi: 10.1007/BF00117779.
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