Hudd C, LaRegina M C, Devine J E, Palmer D C, Herbold D R, Beinfeld M C, Gelder F B, Johnson F E
Department of Surgery, St. Louis University Medical Center, Missouri 63104.
Am J Surg. 1989 Apr;157(4):386-94. doi: 10.1016/0002-9610(89)90582-5.
Gastrointestinal hormones regulate growth of cancers as well as normal tissues. We investigated whether long-term cholecystokinin (CCK) administration might affect growth or metabolism of human tumors xenografted in nude mice. In each experiment, approximately 20 nude mice bearing subcutaneous xenografts of the particular cancer line being studied were used. Half received CCK and half received saline solution intraperitoneally twice daily for 14 days. Tumor volume and body weight were measured every 3 days. If the tumors produced marker substances, these were measured in nude mouse serum and also in the xenografts. Tumor growth was significantly retarded by CCK in two of the six cancers studied. In each case, DNA, RNA, and protein reflected tumor volumes. In one of these tumors (SLU 077), serum carcinoembryonic antigen (CEA) levels paralleled the tumor volumes. In another tumor (SLU 132), serum CEA levels and tumor immunolabeling for CEA and pancreatic oncofetal antigen increased in response to CCK administration, whereas tumor volumes did not. These findings suggest that exogenous highdose CCK altered the growth and metabolism in two of six human cancers studied.
胃肠激素可调节癌症以及正常组织的生长。我们研究了长期给予胆囊收缩素(CCK)是否会影响移植到裸鼠体内的人类肿瘤的生长或代谢。在每个实验中,使用了大约20只携带正在研究的特定癌症细胞系皮下异种移植物的裸鼠。一半裸鼠腹腔内注射CCK,另一半每天两次腹腔内注射生理盐水,持续14天。每3天测量肿瘤体积和体重。如果肿瘤产生标志物物质,则在裸鼠血清和异种移植物中进行测量。在研究的六种癌症中的两种中,CCK显著抑制了肿瘤生长。在每种情况下,DNA、RNA和蛋白质都反映了肿瘤体积。在其中一种肿瘤(SLU 077)中,血清癌胚抗原(CEA)水平与肿瘤体积平行。在另一种肿瘤(SLU 132)中,给予CCK后,血清CEA水平以及肿瘤对CEA和胰腺癌胚抗原的免疫标记增加,而肿瘤体积未增加。这些发现表明,外源性高剂量CCK改变了所研究的六种人类癌症中两种的生长和代谢。