Expression of multidrug resistance-related genes in oral squamous cell carcinomas

被引:13
作者
Cho, YS
Kim, MJ
机构
[1] Seoul Natl Univ, Sch Dent, Dept Oral & Maxillofacial Surg, Jongro Gu, Seoul 110460, South Korea
[2] Chungbuk Natl Univ, Coll Med, Dept Oral & Maxillofacial Surg, Heungdeok Gu, Chonju 361240, Chungbuk, South Korea
[3] Chungbuk Natl Univ, Med Res Inst, Heungdeok Gu, Chonju 361240, Chungbuk, South Korea
来源
ORAL ONCOLOGY | 2001年 / 37卷 / 08期
关键词
multidrug resistance-related genes; oral squamous cell carcinoma; RT-PCR;
D O I
10.1016/S1368-8375(00)00128-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To characterize the multidrug resistance (MDR) phenotype in human oral squamous cell carcinomas (OSCCs), the expression levels of four MDR-related genes (multidrug resistance, mdr1, multidrug resistance-associated protein, MRP; glutathione S-transferase-pi, GST-pi; and DNA topoisomerase II, topoII) were analyzed in OSCCs. Fifty-two OSCC tissues and 22 normal oral mucosal tissues were involved in this study. The expression of each gene was analyzed with a reverse-transcript ion polymerase chain reaction (RT-PCR) method using beta (2)m microglobulin (beta (2)m) mRNA as an endogenous control. The mean values of mdr1, MRP, GST-pi, and topoII gene expression relative to the beta (2)m gene in OSCC tissues were 0.37, 0.75, 0.66, and 1.11, those of normal oral mucosa were 0.40, 0.27, 0.62, and 0.91, respectively. The averaged expression levels of the MRP and topoII gene in OSCC tissues were higher than those of normal oral mucosas (P=0.001 and P=0.02, respectively). The expression levels of four MDR-related genes in OSCCs were not related with the degree of histologic cell differentiation, tumor stage, primary or recurred tumor, or the presence or absence of chemotherapy. Linear regression analysis showed a correlation between the expression levels of MRP and GST-pi in normal oral mucosas (r=0.596, P=0.003) and in OSCCs (r=0.287, P=0.039). The results Suggest that MRP expression is activated during the tumorigenesis of OSCCs and that this may play a role in de novo drug resistance in OSCCs. These results should provide further insight into the complex role postulated for MDR-related genes in chemotherapy, carcinogenesis and tumor progression. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:652 / 659
页数:8
相关论文
共 35 条
[1]  
ARAO S, 1994, CANCER RES, V54, P1355
[2]  
BORDOW SB, 1994, CANCER RES, V54, P5036
[3]   TRANSFORMATION OF RAT-LIVER EPITHELIAL-CELLS WITH V-H-RAS OR V-RAF CAUSES EXPRESSION OF MDR-1, GLUTATHIONE-S-TRANSFERASE-P AND INCREASED RESISTANCE TO CYTO-TOXIC CHEMICALS [J].
BURT, RK ;
GARFIELD, S ;
JOHNSON, K ;
THORGEIRSSON, SS .
CARCINOGENESIS, 1988, 9 (12) :2329-2332
[4]   Evaluation of glutathione S-transferase activity in human buccal epithelial dysplasias and squamous cell carcinomas [J].
Chen, YK ;
Lin, LM .
INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 1997, 26 (03) :205-209
[5]   MODULATION OF ACTIVITY OF THE PROMOTER OF THE HUMAN MDR1 GENE BY RAS AND P53 [J].
CHIN, KV ;
UEDA, K ;
PASTAN, I ;
GOTTESMAN, MM .
SCIENCE, 1992, 255 (5043) :459-462
[6]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[7]  
DEFFIE AM, 1989, CANCER RES, V49, P58
[8]  
Endo K, 1996, CANCER, V77, P1681
[9]  
FARBER E, 1984, CANCER RES, V44, P5463
[10]   A GENETIC MODEL FOR COLORECTAL TUMORIGENESIS [J].
FEARON, ER ;
VOGELSTEIN, B .
CELL, 1990, 61 (05) :759-767