Shimazoe T, Funakoshi A, Kono A
Chemotherapy Division of Research Institute, National Kyushu Cancer Center, Fukuoka, Japan.
Gan To Kagaku Ryoho. 1992 Aug;19(9):1321-5.
Effects of caerulein (CCK), 5-FU and CCK antagonist, loxiglumide (CR1505), were studied on the growth of human pancreatic cancer cell line, KP-1 N, in vitro. And effects of UFT and CR 1505 were also studied on liver metastasis in nude mice. The growth of KP-1 N was stimulated approximately 40% by addition of 10(-10) M of CCK in vitro. CR1505 antagonized the action of CCK, that is, the 40% growth rate increase was suppressed by addition of 25 microM of CR1505. Moreover, the growth rate of the cells dose-dependently decreased by the addition of CR1505. 5-FU also dose-dependently inhibited the growth of KP-1 N in culture. 5-FU additionally decreased the growth rate of KP-1 N in combination with CR1505. A number of metastatic nodules were found in the liver of nude mice a month after injections of KP-1 N cells into the spleen CR1505 suppressed the liver metastasis in nude mice which were administered with UFT. These results suggest that CR1505 would be useful for the treatment of human pancreatic cancer in combination with UFT.
研究了蛙皮素(CCK)、5-氟尿嘧啶(5-FU)及CCK拮抗剂洛西丁胺(CR1505)对人胰腺癌细胞系KP-1 N体外生长的影响。同时也研究了优福定(UFT)和CR1505对裸鼠肝转移的影响。体外实验中,添加10^(-10) M的CCK可使KP-1 N的生长刺激约40%。CR1505可拮抗CCK的作用,即添加25 μM的CR1505可抑制40%的生长率增加。此外,添加CR1505后细胞生长率呈剂量依赖性下降。5-FU也呈剂量依赖性抑制培养中的KP-1 N生长。5-FU与CR1505联合使用还可降低KP-1 N的生长率。将KP-1 N细胞注射到裸鼠脾脏一个月后,在其肝脏中发现了许多转移瘤结节。CR1505可抑制给予优福定的裸鼠的肝转移。这些结果表明,CR1505与优福定联合使用可能对治疗人类胰腺癌有用。