INHIBITION OF P53 PROTEIN-PHOSPHORYLATION BY 9-HYDROXYELLIPTICINE - A POSSIBLE ANTICANCER MECHANISM

被引:67
作者
OHASHI, M
SUGIKAWA, E
NAKANISHI, N
机构
[1] Lead Optimization Laboratory, Tanabe Seiyaku Co, Ltd., Saitama, 335, 2-2-50 Kawagishi, Toda
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 1995年 / 86卷 / 09期
关键词
ELLIPTICINE; P53; PHOSPHORYLATION INHIBITION; APOPTOSIS INDUCTION; ANTICANCER MECHANISM;
D O I
10.1111/j.1349-7006.1995.tb03091.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Abnormality of p53, a tumor suppressor gene, is considered to be a potential cause of malignancy. We found that ellipticine and 9-hydroxyellipticine (9HE), antitumor alkaloids, caused selective inhibition of p53 protein phosphorylation in Lewis lung carcinoma and SW480 (human colon cancer cell line) in a concentration-dependent manner from 0.1 to 100 mu M. 9HE suppressed cdk2 kinase activity concentration-dependently from 1 to 100 mu M. By contrast, the inhibition of p53 protein phosphorylation by elliptinium and elliprabin (N2 substituted derivatives of 9HE) was very weak. A good correlation was observed between p53 phosphorylation inhibition and cytotoxic activity of these agents in terms of concentration-response relationships, suggesting that inhibition of p53 protein phosphorylation via kinase inhibition may be involved in the anticancer mechanism of these agents. In addition, this study demonstrated that brief exposure to 9HE caused apoptosis of cancer cells. It is suggested that accumulation of dephosphorylated mutant p53 may induce apoptosis.
引用
收藏
页码:819 / 827
页数:9
相关论文
共 52 条
[1]  
ADDISON C, 1990, ONCOGENE, V5, P423
[2]   CHROMOSOME-17 DELETIONS AND P53 GENE-MUTATIONS IN COLORECTAL CARCINOMAS [J].
BAKER, SJ ;
FEARON, ER ;
NIGRO, JM ;
HAMILTON, SR ;
PREISINGER, AC ;
JESSUP, JM ;
VANTUINEN, P ;
LEDBETTER, DH ;
BARKER, DF ;
NAKAMURA, Y ;
WHITE, R ;
VOGELSTEIN, B .
SCIENCE, 1989, 244 (4901) :217-221
[3]   HUMAN P53 IS PHOSPHORYLATED BY P60-CDC2 AND CYCLIN-B-CDC2 [J].
BISCHOFF, JR ;
FRIEDMAN, PN ;
MARSHAK, DR ;
PRIVES, C ;
BEACH, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (12) :4766-4770
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   P13SUC1 ACTS IN THE FISSION YEAST-CELL DIVISION CYCLE AS A COMPONENT OF THE P34CDC2 PROTEIN-KINASE [J].
BRIZUELA, L ;
DRAETTA, G ;
BEACH, D .
EMBO JOURNAL, 1987, 6 (11) :3507-3514
[6]   A DNA-ACTIVATED PROTEIN-KINASE FROM HELA-CELL NUCLEI [J].
CARTER, T ;
VANCUROVA, I ;
SUN, I ;
LOU, W ;
DELEON, S .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (12) :6460-6471
[7]   P53 OVER-EXPRESSION IS AN EARLY EVENT IN THE DEVELOPMENT OF HUMAN SQUAMOUS-CELL CARCINOMA OF THE LARYNX - GENETIC AND PROGNOSTIC IMPLICATIONS [J].
DOLCETTI, R ;
DOGLIONI, C ;
MAESTRO, R ;
GASPAROTTO, D ;
BARZAN, L ;
PASTORE, A ;
ROMANELLI, M ;
BOIOCCHI, M .
INTERNATIONAL JOURNAL OF CANCER, 1992, 52 (02) :178-182
[8]  
ELDEIRY WS, 1994, CANCER RES, V54, P1169
[9]   WILD-TYPE P53 CAN INHIBIT ONCOGENE-MEDIATED FOCUS FORMATION [J].
ELIYAHU, D ;
MICHALOVITZ, D ;
ELIYAHU, S ;
PINHASIKIMHI, O ;
OREN, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :8763-8767
[10]   PRESENCE OF A POTENT TRANSCRIPTION ACTIVATING SEQUENCE IN THE P53 PROTEIN [J].
FIELDS, S ;
JANG, SK .
SCIENCE, 1990, 249 (4972) :1046-1049