CCK ANTAGONISTS INTERACT WITH CCK-B RECEPTORS ON HUMAN SMALL-CELL LUNG-CANCER CELLS

被引:30
作者
STALEY, J
JENSEN, RT
MOODY, TW
机构
[1] GEORGE WASHINGTON UNIV, SCH MED & HLTH SCI, DEPT BIOCHEM & MOLEC BIOL, 2300 EYE ST NW, WASHINGTON, DC 20037 USA
[2] NIDDK, DIGEST DIS BRANCH, BETHESDA, MD 20814 USA
关键词
CCK; CCK antagonists; Cytosolic calcium; Receptors; SCLC;
D O I
10.1016/0196-9781(90)90029-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ability of cholecystokinin (CCK) receptor antagonists to interact with CCK receptors in small cell lung cancer (SCLC) cells was investigated. L-365,260, CCK-8, L-364,718, CBZ-CCK(27-32)-NH2 and proglumide analogue 10 inhibited specific 125I-CCK-8 binding to SCLC cells with IC50 values of 0.2, 2, 500, 100,000 and 500,000 nM, respectively. Gastrin-I and CCK-8 elevated the cytosolic Ca2+ when SCLC cells were loaded with Fura 2-AM. L-365,260 inhibited the cytosolic Ca2+ increase caused by 10 nM CCK-8 in a dose-dependent manner. The effects of 10 nM L-365,260 were reversed by high concentrations of CCK-8. These data indicate that L-365,260 functions as a reversible CCK-8 antagonist using SCLC cells. © 1990.
引用
收藏
页码:1033 / 1036
页数:4
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