RETRACTED: Cyclooxygenase-2 (COX-2) expression in high-risk premalignant oral lesions (Retracted Article. See vol 43, pg 420, 2007)

被引:51
作者
Sudbo, J [1 ]
Ristimäki, A
Sondresen, JE
Kildal, W
Boysen, M
Koppang, HS
Reith, A
Risberg, B
Nesland, JM
Bryne, M
机构
[1] Norwegian Radium Hosp, Dept Med Oncol & Radiotherapy, N-0310 Oslo, Norway
[2] Univ Helsinki, Dept Pathol, Helsinki Univ Cent Hosp, FIN-00014 Helsinki, Finland
[3] Univ Helsinki, Mol & Canc Biol Res Program, FIN-00014 Helsinki, Finland
[4] Dept Oral Biol, Oslo, Norway
[5] Norwegian Radium Hosp, Dept Pathol, Oslo, Norway
[6] Univ Oslo, Natl Hosp, Dept Otorhinolaryngol, Oslo, Norway
[7] Univ Oslo, Dept Clin Dent, Oslo, Norway
[8] Univ Oslo, Dept Pathol & Forens Odontol, Oslo, Norway
关键词
oral precancer; premalignancy; oral carcinoma; risk markers; cyclooxygenase-2; chemoprevention; coxibs; DNA content; aneuploidy;
D O I
10.1016/S1368-8375(03)00012-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Emerging data indicate a link between genetic instability and up-regulation of cyclooxygenase-2 (COX-2). To see if individuals at high risk of oral cancer are candidates for treatment with selective COX-2 inhibitors (coxibs), levels of COX-2 expression in healthy, premalignant and cancerous oral mucosa were compared with the occurrence of DNA ploidy status as a genetic risk marker of oral cancer. COX-2 gene product was evaluated immunohistochemically in 30 healthy persons, in 22 patients with dysplastic lesions without previous or concomitant carcinomas, and in 29 patients with oral carcinomas. The immunohistochemical findings were verified by western blotting. COX-2 expression was correlated to DNA content as a genetic risk marker of oral cancer. COX-2 was up-regulated from healthy to premalignant to cancerous oral mucosa. Thus, COX-2 expression was found in 1 case of healthy oral mucosa (3%). All specimens from healthy mucosa had a normal DNA content. In patients with premalignancies. In 29 patients with oral carcinomas, cyclooxygenase-2 expression was observed in 26 (88%), and aneuploidy was observed in 25 cases (94%, P=0.04). Notably, of 22 patients with dysplastic lesions, COX-2 was exclusively expressed in a subgroup of nine patients (41%) identified to be at high risk of cancer by the aberrant DNA content of their lesions. Seven of these patients were followed for 5 years or more. An oral carcinoma developed in six of them (85%; P=0.02). These findings emphasize the need to determine whether coxibs can reduce the risk of oral cancer in patients with high-risk precancerous lesions. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
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页码:497 / 505
页数:9
相关论文
共 54 条
[1]  
Bartsch H, 2001, ADV EXP MED BIOL, V500, P675
[2]   Ultrasensitive and specific detection methods for exocylic DNA adducts: Markers for lipid peroxidation and oxidative stress [J].
Bartsch, H ;
Nair, J .
TOXICOLOGY, 2000, 153 (1-3) :105-114
[3]  
BARTSCH H, 2000, MUTAT RES, V462, P25579
[4]   2ND MALIGNANT NEOPLASMS IN PATIENTS WITH HEAD AND NECK SQUAMOUS-CELL CARCINOMAS [J].
BOYSEN, M ;
LOVEN, JO .
ACTA ONCOLOGICA, 1993, 32 (03) :283-288
[5]   CHANGING TRENDS IN THE MANAGEMENT OF SQUAMOUS CARCINOMA OF THE TONGUE [J].
CALLERY, CD ;
SPIRO, RH ;
STRONG, EW .
AMERICAN JOURNAL OF SURGERY, 1984, 148 (04) :449-454
[6]  
Chan G, 1999, CANCER RES, V59, P991
[7]   Cyclooxygenase-2: a novel target for cancer chemotherapy? [J].
Dempke, W ;
Rie, C ;
Grothey, A ;
Schmoll, HJ .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2001, 127 (07) :411-417
[8]   CHEMOPREVENTION IN THE MANAGEMENT OF ORAL-CANCER - EUROSCAN AND OTHER STUDIES [J].
DEVRIES, N ;
VANZANDWIJK, N ;
PASTORINO, U .
ORAL ONCOLOGY-EUROPEAN JOURNAL OF CANCER PART B, 1992, 28B (02) :153-157
[9]   Cyclooxygenase in biology and disease [J].
Dubois, RN ;
Abramson, SB ;
Crofford, L ;
Gupta, RA ;
Simon, LS ;
Van De Putte, LBA ;
Lipsky, PE .
FASEB JOURNAL, 1998, 12 (12) :1063-1073
[10]  
Ghadimi BM, 2000, GENE CHROMOSOME CANC, V27, P183, DOI 10.1002/(SICI)1098-2264(200002)27:2<183::AID-GCC10>3.3.CO