The growth inhibitory effect of new pyrrolo[1,2-alpha]benzimidazole derivatives on human gastric cancer cells

被引:3
作者
Kim, SK
Ahn, CM
Choi, SJ
Park, YS
Cho, HC
Koh, CM
机构
[1] YONSEI UNIV, WONJU COLL MED, DEPT BASIC SCI, INST BASIC MED SCI, WONJU 220701, SOUTH KOREA
[2] KWANDONG UNIV, COLL MED, DEPT MICROBIOL, KANGNUNG 210701, SOUTH KOREA
关键词
pyrrolo[1,2-alpha]benzimidazole (PBI); gastric cancer cell line; nude mouse;
D O I
10.1007/BF02973931
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In the course of screening synthetic compounds to inhibit tumor cell growth, pyrrolo[1,2-alpha] benzimidazole (PBI), an intermediate of azamitosene, was found to inhibit a proliferation of gastric cancer cell lines. Despite a potential cytotoxic activity against solid tumor cells as opposed to that against rapidly-doubled leukemic cells, there has been no report on the inhibition of gastric cancer cell line by PBI and its' derivatives. The present experiment was designed to determine if PBI derivatives can effectively inhibit the cellular proliferation of gastric cancer cells by using in vitro as well as in vivo chemosensitivity system (MTT assay, clonogenic assay and human tumor xenografted assay). Of the tested PBI derivatives, PBI (18) and PBI (20), displayed the effective growth inhibition of cultured gastric cancer cells or even in the xenografted nude mouse model.
引用
收藏
页码:410 / 413
页数:4
相关论文
共 18 条
[1]   Synthesis and in vitro antitumor activity of isoazamitosene and isoiminoazamitosene derivatives [J].
Ahn, CM ;
Kim, SK .
ARCHIVES OF PHARMACAL RESEARCH, 1996, 19 (06) :535-542
[2]  
CARMICHAEL J, 1987, CANCER RES, V47, P936
[3]  
CARRATO A, 1995, P AN M AM SOC CLIN, V14, P198
[4]  
CHA DS, 1997, J KOR CANC ASS, V29, P437
[5]   SYNTHESIS AND PHYSICAL STUDIES OF AZAMITOSENE AND IMINOAZAMITOSENE REDUCTIVE ALKYLATING-AGENTS - IMINOQUINONE HYDROLYTIC STABILITY, SYN/ANTI-ISOMERIZATION, AND ELECTROCHEMISTRY [J].
ISLAM, I ;
SKIBO, EB .
JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (10) :3195-3205
[6]   STRUCTURE ACTIVITY STUDIES OF ANTITUMOR AGENTS BASED ON PYRROLO[1,2-A]BENZIMIDAZOLES - NEW REDUCTIVE ALKYLATING DNA CLEAVING AGENTS [J].
ISLAM, I ;
SKIBO, EB ;
DORR, RT ;
ALBERTS, DS .
JOURNAL OF MEDICINAL CHEMISTRY, 1991, 34 (10) :2954-2961
[7]   MITOMYCIN-C AND PORFIROMYCIN ANALOGS WITH SUBSTITUTED ETHYLAMINES AT POSITION-7 [J].
IYENGAR, BS ;
SAMI, SM ;
REMERS, WA ;
BRADNER, WT ;
SCHURIG, JE .
JOURNAL OF MEDICINAL CHEMISTRY, 1983, 26 (01) :16-20
[8]  
Kelsen DP, 1996, SEMIN ONCOL, V23, P379
[9]   HYPOXIC TUMOR-CELL - TARGET FOR SELECTIVE CANCER-CHEMOTHERAPY [J].
KENNEDY, KA ;
TEICHER, BA ;
ROCKWELL, S ;
SARTORELLI, AC .
BIOCHEMICAL PHARMACOLOGY, 1980, 29 (01) :1-8
[10]   CHEMOTHERAPEUTIC ATTACK OF HYPOXIC TUMOR-CELLS BY THE BIOREDUCTIVE ALKYLATING AGENT MITOMYCIN-C [J].
KEYES, SR ;
HEIMBROOK, DC ;
FRACASSO, PM ;
ROCKWELL, S ;
SLIGAR, SG ;
SARTORELLI, AC .
ADVANCES IN ENZYME REGULATION, 1984, 23 :291-307