Bcl-xL confers multi-drug resistance in several squamous cell carcinoma cell lines

被引:42
作者
Noutomi, T
Chiba, H
Itoh, M
Toyota, H
Mizuguchi, J
机构
[1] Tokyo Med Univ Hosp, Dept Immunol, Shinjuku Ku, Tokyo 1600022, Japan
[2] Tokyo Med Univ, Dept Immunol, Shinjuku Ku, Tokyo 1600022, Japan
[3] Tokyo Med Univ, Intractable Dis Res Ctr, Tokyo, Japan
关键词
squamous cell carcinoma; apoptosis; carboplatin; Bcl-x(L); Bax-alpha;
D O I
10.1016/S1368-8375(00)00098-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Carboplatin (CBDCA) alone or in combination with irradiation and other chemotherapeutic agents has been used for the treatment of oral Squamous carcinoma. However, there are some limitations for such therapy because of inherent or acquired resistance to CBDCA, To gain some insights into the association of CBDCA resistance with Bcl-2 family level or p53 status, we established eight carcinoma cell lines, consisting of two resistant (MIT8, MIT16), two sensitive (MIT6. MIT7), and four intermediate lines. All of the five cell lines with p53 mutation belonged to the resistant similar to intermediate group, whereas two of three other lines with Wildtype p53 were in the sensitive group. Interestingly, both of the two resistant cell lines showed elevated levels of Bcl-x(L), almost double that of sensitive line (MIL5), whereas either Bcl-2 or Bax-alpha level did not correlate with the CBDCA-resistance. To further verify the association between the Bcl-x(L) level and the drug resistance, two transformants (x(L)-3, x(L)-6) overexpressing BCl-x(L) in the CBDCA-sensitive cell line MIT7 were established using the gene transfer method. Both clones showed resistance to multiple chemotherapeutic agents, including CBDCA, actinomycin D, etoposide, and mitomycin C, Moreover, MIT8 and MT16 also displayed cross-resistance to these agents. These findings suggest that BCl-x(L) may function as one of the key components conferring Multiple drug-resistance in squamous cell carcinomas. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:41 / 48
页数:8
相关论文
共 45 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]   ACTIVATION OF PROGRAMMED CELL-DEATH (APOPTOSIS) BY CISPLATIN, OTHER ANTICANCER DRUGS, TOXINS AND HYPERTHERMIA [J].
BARRY, MA ;
BEHNKE, CA ;
EASTMAN, A .
BIOCHEMICAL PHARMACOLOGY, 1990, 40 (10) :2353-2362
[3]   BCL-X, A BCL-2-RELATED GENE THAT FUNCTIONS AS A DOMINANT REGULATOR OF APOPTOTIC CELL-DEATH [J].
BOISE, LH ;
GONZALEZGARCIA, M ;
POSTEMA, CE ;
DING, LY ;
LINDSTEN, T ;
TURKA, LA ;
MAO, XH ;
NUNEZ, G ;
THOMPSON, CB .
CELL, 1993, 74 (04) :597-608
[4]  
Burger H, 1997, INT J CANCER, V73, P592, DOI 10.1002/(SICI)1097-0215(19971114)73:4<592::AID-IJC22>3.3.CO
[5]  
2-7
[6]   BCL-2 FAMILY: Regulators of cell death [J].
Chao, DT ;
Korsmeyer, SJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1998, 16 :395-419
[7]   QUANTITATIVE-ANALYSIS OF DOSE-EFFECT RELATIONSHIPS - THE COMBINED EFFECTS OF MULTIPLE-DRUGS OR ENZYME-INHIBITORS [J].
CHOU, TC ;
TALALAY, P .
ADVANCES IN ENZYME REGULATION, 1984, 22 :27-55
[8]   Human Bcl-2 antisense therapy for lymphomas [J].
Cotter, FE ;
Waters, J ;
Cunningham, D .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1999, 1489 (01) :97-106
[9]  
Decaudin D, 1997, CANCER RES, V57, P62
[10]  
DEIMLING AV, 1992, CANCER RES, V52, P2987