Elevated 8-isoprostane levels in basal cell carcinoma and in UVA irradiated skin

被引:31
作者
Belli, R
Amerio, P
Brunetti, L
Orlando, G
Toto, P
Proietto, G
Vacca, M
Tulli, A
机构
[1] Univ G DAnnunzio, Dept Dermatol, Chieti, Italy
[2] Univ G DAnnunzio, Dept Drug Sci, Chieti, Italy
[3] Univ G dAnnunzio, Ctr Sci Aging, Chieti, Italy
关键词
isoprostanes; basal cell carcinoma; ROS;
D O I
10.1177/039463200501800309
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Isoprostanes are prostaglandin isomers produced from the peroxidation of polyunsaturated fatty acids from the cellular membrane. They have been used as a specific index of cellular lipoperoxidation and as an indirect measure of oxidative stress. However, these molecules also present several biological activities. An oxidative environment measured as the presence of other indirect measurements of reactive oxygen species lipoperoxidation has recently been described in basal cell carcinoma, the most frequent type of non-melanoma skin cancer. This study aims to measure the levels of 8-isoprostaglandin F2 alpha, an isoprostane widely studied in other models as a by-product of ROS-induced lipid peroxidation, in basal cell carcinoma and in UVA irradiated healthy skin. We found that 8-iso-PGF2 alpha is present in higher levels in BCC specimens compared to healthy non sun-exposed skin, confirming previous studies on the production of lipoperoxidation in this tumor. Moreover, we demonstrated that topical pre-treatment with a compound containing vitamin E is capable of reducing 8-iso-PGF2 alpha formation in UV irradiated skin suggesting a role for isoprostanes in UV induced inflammation and eventually carcinogenesis and confirming the function of vitamin E as an antioxidant in this model.
引用
收藏
页码:497 / 502
页数:6
相关论文
共 27 条
[11]  
Luczaj W, 2003, CELL MOL BIOL LETT, V8, P391
[12]   Toxic effects of ultraviolet radiation on the skin [J].
Matsumura, Y ;
Ananthaswamy, HN .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2004, 195 (03) :298-308
[13]   Measurement of lipid peroxidation [J].
Moore, K ;
Roberts, LJ .
FREE RADICAL RESEARCH, 1998, 28 (06) :659-671
[14]   A SERIES OF PROSTAGLANDIN-F2-LIKE COMPOUNDS ARE PRODUCED INVIVO IN HUMANS BY A NONCYCLOOXYGENASE, FREE RADICAL-CATALYZED MECHANISM [J].
MORROW, JD ;
HILL, KE ;
BURK, RF ;
NAMMOUR, TM ;
BADR, KF ;
ROBERTS, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (23) :9383-9387
[15]   THE F2-ISOPROSTANE, 8-EPI-PROSTAGLANDIN-F2-ALPHA, A POTENT AGONIST OF THE VASCULAR THROMBOXANE ENDOPEROXIDE RECEPTOR, IS A PLATELET THROMBOXANE ENDOPEROXIDE RECEPTOR ANTAGONIST [J].
MORROW, JD ;
MINTON, TA ;
ROBERTS, LJ .
PROSTAGLANDINS, 1992, 44 (02) :155-163
[16]   Parameters related to oxygen free radicals in human skin:: A study comparing healthy epidermis and skin cancer tissue [J].
Nogués, MR ;
Giralt, M ;
Cervelló, I ;
Del Castillo, D ;
Espeso, O ;
Argany, N ;
Aliaga, A ;
Mallol, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2002, 119 (03) :645-652
[17]   Measurement of F2-isoprostanes as an index of oxidative stress in vivo [J].
Roberts, LJ ;
Morrow, JD .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (04) :505-513
[18]   Reactive oxygen species as intracellular messengers during cell growth and differentiation [J].
Sauer, H ;
Wartenberg, M ;
Hescheler, J .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2001, 11 (04) :173-186
[19]   8-Isoprostane increases expression of interleukin-8 in human macrophages through activation of mitogen-activated protein kinases [J].
Scholz, H ;
Yndestad, A ;
Damås, JK ;
Wæhre, T ;
Tonstad, S ;
Aukrust, P ;
Halvorsen, B .
CARDIOVASCULAR RESEARCH, 2003, 59 (04) :945-954
[20]   PERSISTENT OXIDATIVE STRESS IN CANCER [J].
TOYOKUNI, S ;
OKAMOTO, K ;
YODOI, J ;
HIAI, H .
FEBS LETTERS, 1995, 358 (01) :1-3