Identification of compounds with preferential inhibitory activity against low-Nm23-expressing human breast carcinoma and melanoma cell lines

被引:33
作者
Freije, JMP
Lawrence, JA
Hollingshead, MG
DeLaRosa, A
Narayanan, V
Grever, M
Sausville, EA
Paull, K
Steeg, PS
机构
[1] NCI, WOMENS CANC SECT, PATHOL LAB, DIV CLIN SCI, BETHESDA, MD 20892 USA
[2] NCI, FREDERICK CANC RES & DEV CTR, BIOL TESTING BRANCH, DEV THERAPEUT PROGRAM, FREDERICK, MD 21702 USA
[3] NCI, DEV THERAPEUT PROGRAM, ROCKVILLE, MD 20852 USA
关键词
D O I
10.1038/nm0497-395
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We have used the COMPARE computer algorithm and Nm23 expression as a marker of tumor metastatic potential to examine the in vitro antiproliferative activity of chemotherapeutic drugs on human breast carcinoma and melanoma cell lines. None of 171 compounds in clinical use or under development and only 40 of 30,000 repository compounds exhibited preferential growth inhibition of low-Nm23-expressing, metastatically aggressive cell lines with a Pearson correlation coefficient of less than or equal to-0.64. Characterization of one compound, NSC 645306, is presented including in vivo activity in a hollow fiber assay. The data demonstrate a novel approach to drug identification for aggressive human tumors.
引用
收藏
页码:395 / 401
页数:7
相关论文
共 40 条
[1]
GENERATION OF A DRUG-RESISTANCE PROFILE BY QUANTITATION OF MDR-1/P-GLYCOPROTEIN IN THE CELL-LINES OF THE NATIONAL-CANCER-INSTITUTE ANTICANCER DRUG SCREEN [J].
ALVAREZ, M ;
PAULL, K ;
MONKS, A ;
HOSE, C ;
LEE, JS ;
WEINSTEIN, J ;
GREVER, M ;
BATES, S ;
FOJO, T .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (05) :2205-2214
[2]
[Anonymous], 1980, ANTICANCER AGENTS BA
[3]
BABA H, 1995, CANCER RES, V55, P1977
[4]
BAI R, 1991, J BIOL CHEM, V266, P15882
[5]
SYNTHESIS OF 2-METHYL-(Z)-4-(PHENYLIMINO)NAPHTH[2,3-D]OXAZOL-9-ONE, A MONOIMINE QUINONE WITH SELECTIVE CYTOTOXICITY TOWARD CANCER-CELLS [J].
BENEDETTIDOCTOROVICH, V ;
BURGESS, EM ;
LAMBROPOULOS, J ;
LEDNICER, D ;
VANDERVEER, D ;
ZALKOW, LH .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (05) :710-712
[6]
SOME PRACTICAL CONSIDERATIONS AND APPLICATIONS OF THE NATIONAL-CANCER-INSTITUTE IN-VITRO ANTICANCER DRUG DISCOVERY SCREEN [J].
BOYD, MR ;
PAULI, KD .
DRUG DEVELOPMENT RESEARCH, 1995, 34 (02) :91-109
[7]
NM23 NUCLEOSIDE DIPHOSPHATE KINASE - TOWARD A STRUCTURAL AND BIOCHEMICAL UNDERSTANDING OF ITS BIOLOGICAL FUNCTIONS [J].
DELAROSA, A ;
WILLIAMS, RL ;
STEEG, PS .
BIOESSAYS, 1995, 17 (01) :53-62
[8]
Ferguson AW, 1996, CANCER RES, V56, P2931
[9]
Reductase enzyme expression across the national cancer institute tumor cell line panel: Correlation with sensitivity to mitomycin C and E09 [J].
Fitzsimmons, SA ;
Workman, P ;
Grever, M ;
Paull, K ;
Camalier, R ;
Lewis, AD .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (05) :259-269
[10]
Foye W. O, 1995, CANC CHEMOTHERAPEUTI, P9