Elevated expression of vacuolar proton pump genes and cellular pH in cisplatin resistance

被引:124
作者
Murakami, T
Shibuya, I
Ise, T
Chen, ZS
Akiyama, S
Nakagawa, M
Izumi, H
Nakamura, T
Matsuo, K
Yamada, Y
Kohno, K
机构
[1] Univ Occupat & Environm Hlth, Fac Med, Dept Mol Biol, Yahatanishi Ku, Fukuoka 8078555, Japan
[2] Univ Occupat & Environm Hlth, Dept Mol Biol, Yahatanishi Ku, Kitakyushu, Fukuoka 807, Japan
[3] Univ Occupat & Environm Hlth, Dept Orthoped Surg, Yahatanishi Ku, Kitakyushu, Fukuoka 807, Japan
[4] Univ Occupat & Environm Hlth, Dept Physiol 1, Yahatanishi Ku, Kitakyushu, Fukuoka 807, Japan
[5] Kagoshima Univ, Inst Canc Res, Dept Canc Chemotherapy, Kagoshima 890, Japan
[6] Kagoshima Univ, Fac Med, Dept Urol, Kagoshima 890, Japan
[7] Taiho Pharmaceut Co, Hanno Res Ctr, Saitama, Japan
关键词
V-ATPase; cisplatin; drug resistance; intracellular pH; vacuolar proton pump gene;
D O I
10.1002/ijc.1418
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
V-ATPases are proton-translocating enzymes, which are found not only in numerous intracellular organelles but also in the plasma membranes of many eukaryotic cells. Using differential display, we have identified one of the proton pump subunit genes, ATP6C, as a cisplatin-inducible gene. Northern blot analysis demonstrated that expression of other members of the subunit is inducible by cisplatin treatment. Proton pump gene expression is also upregulated in 3 independent cisplatin-resistant cell lines but not in vincristine- or etoposide-resistant cell lines. Cellular PH was significantly higher in cisplatin-resistant cells than in sensitive parental cells. In vitro DNA-binding activity of cisplatin was markedly increased in acidic conditions, suggesting that the cytotoxicity of cisplatin is modulated by cellular pH. Furthermore, the proton pump inhibitor bafilomycin can synergistically potentiate the cytotoxicity of cisplatin but not of etoposide or camptothecin. These results indicate that cellular pH is one of the critical parameters for effective cancer chemotherapy with cisplatin. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:869 / 874
页数:6
相关论文
共 40 条
[1]   DNA repair: Enzymatic mechanisms and relevance to drug response [J].
Chaney, SG ;
Sancar, A .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (19) :1346-1360
[2]   Cisplatin efflux, binding and intracellular pH in the HTB56 human lung adenocarcinoma cell line and the E-8/0.7 cisplatin-resistant variant [J].
Chau, Q ;
Stewart, DJ .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1999, 44 (03) :193-202
[3]   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
[4]  
CHU G, 1994, J BIOL CHEM, V269, P787
[5]  
CRIDER BP, 1994, J BIOL CHEM, V269, P17379
[6]   Structure and properties of the vacuolar (H+)-ATPases [J].
Forgac, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (19) :12951-12954
[7]   Structure, function and regulation of the vacuolar (H+)-ATPases [J].
Forgac, M .
FEBS LETTERS, 1998, 440 (03) :258-263
[8]   ACTIVE EFFLUX SYSTEM FOR CISPLATIN IN CISPLATIN-RESISTANT HUMAN KB CELLS [J].
FUJII, R ;
MUTOH, M ;
NIWA, K ;
YAMADA, K ;
AIKOU, T ;
NAKAGAWA, M ;
KUWANO, M ;
AKIYAMA, S .
JAPANESE JOURNAL OF CANCER RESEARCH, 1994, 85 (04) :426-433
[9]   Tumor pH: Implications for treatment and novel drug design [J].
Gerweck, LE .
SEMINARS IN RADIATION ONCOLOGY, 1998, 8 (03) :176-182
[10]   CELL ACIDIFICATION IN APOPTOSIS - GRANULOCYTE-COLONY-STIMULATING FACTOR DELAYS PROGRAMMED CELL-DEATH IN NEUTROPHILS BY UP-REGULATING THE VACUOLAR H+-ATPASE [J].
GOTTLIEB, RA ;
GIESING, HA ;
ZHU, JY ;
ENGLER, RL ;
BABIOR, BM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (13) :5965-5968