HERG potassium channels are more frequently expressed in human endometrial cancer as compared to non-cancerous endometrium

被引:130
作者
Cherubini, A
Taddei, GL
Crociani, O
Paglierani, M
Buccoliero, AM
Fontana, L
Noci, I
Borri, P
Borrani, E
Giachi, M
Becchetti, A
Rosati, B
Wanke, E
Olivotto, M
Arcangeli, A
机构
[1] Univ Florence, Dept Expt Pathol & Oncol, I-50134 Florence, Italy
[2] Univ Florence, Dept Human Pathol & Oncol, I-50134 Florence, Italy
[3] Univ Florence, Dept Gynecol & Human Reprod, I-50134 Florence, Italy
[4] Univ Milano Bicocca, Dept Biosci & Biotechnol, I-20126 Milan, Italy
关键词
HERG; endometrial cancer; endometrial hyperplasia; tumour markers; K+ channels;
D O I
10.1054/bjoc.2000.1497
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
HERG K+ channels. besides contributing to regulate cardiac and neuronal excitability, are preferentially expressed in tumour cell lines of different histogenesis, where their role in the development and maintenance of the neoplastic phenotype is under study. We show here that both herg gene and HERG protein are expressed with high frequency in primary human endometrial cancers, as compared to normal and hyperplastic endometrium. RT-PCR and immunohistochemistry, using specific anti-HERG antibodies developed in our laboratory, were applied to tissue specimens obtained from 18 endometrial cancers and 11 non-cancerous endometrial tissues. herg RNA and HERG protein are expressed in 67% and 82%, respectively, of cancerous, while in only 18% of non-cancerous tissues. In particular, no expression was found in endometrial hyperplasia. Moreover, electrophysiological experiments confirmed the presence of functioning HERG channels on the plasma membrane of tumour cells. On the whole, these data are the first demonstration of the presence of HERG channels in primary human neoplasias, and could candidate HERG as a potential tool capable of marking cancerous versus hyperplastic endometrial growth. (C) 2000 Cancer Research Campaign.
引用
收藏
页码:1722 / 1729
页数:8
相关论文
共 35 条
[1]  
Arcangeli A, 1999, J NEUROBIOL, V40, P214
[2]   Long term exposure to retinoic acid induces the expression of IRK1 channels in HERG channel-endowed neuroblastoma cells [J].
Arcangeli, A ;
Rosati, B ;
Cherubini, A ;
Crociani, O ;
Fontana, L ;
Passani, B ;
Wanke, E ;
Olivotto, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 244 (03) :706-711
[3]   HERG- and IRK-like inward rectifier currents are sequentially expressed during neuronal development of neural crest cells and their derivatives [J].
Arcangeli, A ;
Rosati, B ;
Cherubini, A ;
Crociani, O ;
Fontana, L ;
Ziller, C ;
Wanke, E ;
Olivotto, M .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1997, 9 (12) :2596-2604
[4]   A novel inward-rectifying K+ current with a cell-cycle dependence governs the resting potential of mammalian neuroblastoma cells [J].
Arcangeli, A ;
Bianchi, L ;
Becchetti, A ;
Faravelli, L ;
Coronnello, M ;
Mini, E ;
Olivotto, M ;
Wanke, E .
JOURNAL OF PHYSIOLOGY-LONDON, 1995, 489 (02) :455-471
[5]   INTEGRIN-MEDIATED NEURITE OUTGROWTH IN NEUROBLASTOMA-CELLS DEPENDS ON THE ACTIVATION OF POTASSIUM CHANNELS [J].
ARCANGELI, A ;
BECCHETTI, A ;
MANNINI, A ;
MUGNAI, G ;
DEFILIPPI, P ;
TARONE, G ;
DELBENE, MR ;
BARLETTA, E ;
WANKE, E ;
OLIVOTTO, M .
JOURNAL OF CELL BIOLOGY, 1993, 122 (05) :1131-1143
[6]   Inhibition of cardiac delayed rectifier K+ current by overexpression of the long-QT syndrome HERG G628S mutation in transgenic mice [J].
Babij, P ;
Askew, GR ;
Nieuwenhuijsen, B ;
Su, CM ;
Bridal, TR ;
Jow, B ;
Argentieri, TM ;
Kulik, J ;
DeGennaro, LJ ;
Spinelli, W ;
Colatsky, TJ .
CIRCULATION RESEARCH, 1998, 83 (06) :668-678
[7]  
BABIJ P, 1998, J BIOL CHEM, V273, P21061
[8]  
BACKER VV, 1996, CLIN OBSTET GYNECOL, V39, P707
[9]  
BERCHUCK A, 1995, CANCER, V76, P2034, DOI 10.1002/1097-0142(19951115)76:10+<2034::AID-CNCR2820761321>3.0.CO
[10]  
2-U