μ3 opiate receptor expression in lung and lung carcinoma:: ligand binding and coupling to nitric oxide release

被引:31
作者
Fimiani, C
Arcuri, E
Santoni, A
Rialas, CM
Bilfinger, TV
Peter, D
Salzet, B
Stefano, GB [1 ]
机构
[1] SUNY Coll Old Westbury, Neurosci Res Inst, Old Westbury, NY 11568 USA
[2] Univ Roma La Sapienza, Dept Expt Med, Lab Cellular & Nat Immun, I-00185 Rome, Italy
[3] Regina Elena Inst Canc Res, Intens Care Unit & Pain Therapy, I-00161 Rome, Italy
[4] SUNY Stony Brook, Hlth Sci Ctr, Dept Surg, Div Cardiothorac Surg, Stony Brook, NY 11794 USA
[5] Univ Sci & Tech Lille Flandres Artois, Lab Neuroimmun Annelides, Ctr Biol Cellulaire, F-59655 Villeneuve Dascq, France
关键词
opioid receptor transcript; mu neoplasia; nitric oxide; morphine; cancer; alternative splicing; lung;
D O I
10.1016/S0304-3835(99)00227-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The mu 3 opiate receptor subtype is expressed in human surgical specimens of both normal lung and non-small-cell lung carcinoma. Nitric oxide (NO) release is mediated through the mu 3 receptor, and in lung carcinoma, morphine-stimulated NO release is significantly higher and prolonged than in normal lung. Using reverse transcriptase-polymerase chain reaction (RT-PCR) and Southern blot analysis we show that specific mu opioid receptor transcripts are present in lung carcinoma and other cells with the mu 3 profile. Our findings identify a unique role for the mu 3 opiate receptor in opiate-mediated NO release and suggest that endogenous opiates, through their release of NO, may play a role in cancer progression. (C) 1999 Elsevier Science ireland Ltd. All rights reserved.
引用
收藏
页码:45 / 51
页数:7
相关论文
共 27 条
[1]
ANTITUMOR-ACTIVITY OF NALTREXONE AND CORRELATION WITH STEROID-HORMONE RECEPTORS [J].
ABOUISSA, H ;
TEJWANI, GA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 175 (02) :625-630
[2]
Vascular endothelial growth factor and nitric oxide synthase expression in human lung cancer and the relation to p53 [J].
Ambs, S ;
Bennett, WP ;
Merriam, WG ;
Ogunfusika, MO ;
Oser, SM ;
Khan, MA ;
Jones, RT ;
Harris, CC .
BRITISH JOURNAL OF CANCER, 1998, 78 (02) :233-239
[3]
EXPRESSION OF 2 VARIANTS OF THE HUMAN MU-OPIOID RECEPTOR MESSENGER-RNA IN SK-N-SH CELLS AND HUMAN BRAIN [J].
BARE, LA ;
MANSSON, E ;
YANG, DM .
FEBS LETTERS, 1994, 354 (02) :213-216
[4]
Cryopreserved veins in myocardial revascularization: Possible mechanism for their increased failure [J].
Bilfinger, TV ;
Hartman, AR ;
Liu, Y ;
Magazine, HI ;
Stefano, GB .
ANNALS OF THORACIC SURGERY, 1997, 63 (04) :1063-1069
[5]
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]
MU-OPIOID RECEPTOR GENE-EXPRESSION IN IMMUNE CELLS [J].
CHUANG, TK ;
KILLAM, KF ;
CHUANG, LF ;
KUNG, HF ;
SHENG, WS ;
CHAO, CC ;
YU, L ;
CHUANG, RY .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 216 (03) :922-930
[7]
NITRIC-OXIDE INDUCES OXIDATIVE DAMAGE IN ADDITION TO DEAMINATION IN MACROPHAGE DNA [J].
DEROJASWALKER, T ;
TAMIR, S ;
JI, H ;
WISHNOK, JS ;
TANNENBAUM, SR .
CHEMICAL RESEARCH IN TOXICOLOGY, 1995, 8 (03) :473-477
[8]
Elliott Jackie, 1994, European Journal of Pharmacology Molecular Pharmacology Section, V16, P447
[9]
Nitric oxide reduces tumor cell adhesion to isolated rat postcapillary venules [J].
Kong, LP ;
Dunn, GD ;
Keefer, LK ;
Korthuis, RJ .
CLINICAL & EXPERIMENTAL METASTASIS, 1996, 14 (04) :335-343
[10]
LEJEUNE P, 1994, J IMMUNOL, V152, P5077