Saydjari R, Alexander R W, Upp J R, Poston G J, Barranco S C, Townsend C M, Thompson J C
Department of Surgery, University of Texas Medical Branch, Galveston 77550.
Cancer Invest. 1991;9(4):415-9. doi: 10.3109/07357909109084639.
Polyamines are essential for cell growth of normal and neoplastic tissue, alpha-Difluoromethylornithine (DFMO) is a known irreversible inhibitor or ornithine decarboxylase (ODC), the rate-limiting enzyme in polyamine biosynthesis. The purpose of this study was to examine the effects of tumor burden on ODC in tissues of tumor-bearing compared with tumor-free mice. Twenty-eight male Balb/c mice were divided into four groups of 7 each. Groups 1 and 2 were inoculated subcutaneously with 10 x 10(6) MC-26 mouse colon adenocarcinoma cells. Groups 3 and 4 were kept as tumor-free controls. Ten days after inoculation, groups 2 and 4 were injected with DFMO (200 mg/kg) intraperitoneally (IP) while Groups 1 and 3 received saline. Two hours after the injection of DFMO the animals were sacrificed. The tumor, pancreas, kidney, and liver were excised and analyzed for ODC activity. DFMO caused a significant reduction (compared with controls that did not receive DFMO) in the ODC activity of tumors; however, ODC activity of the kidney, pancreas, and liver of tumor-bearing mice was not affected. Additionally, the basal ODC activity in the kidney, liver, and pancreas of tumor-bearing mice was significantly lower compared with tumor-free controls. DFMO lowered ODC activity in the kidney, pancreas, and liver of tumor-free mice. These results suggest that the presence of MC-26 tumor causes systemic effects that alter ODC activity and the response to a known inhibitor of ODC.
多胺对正常组织和肿瘤组织的细胞生长至关重要,α-二氟甲基鸟氨酸(DFMO)是一种已知的鸟氨酸脱羧酶(ODC)不可逆抑制剂,鸟氨酸脱羧酶是多胺生物合成中的限速酶。本研究的目的是检测与无肿瘤小鼠相比,肿瘤负荷对荷瘤小鼠组织中ODC的影响。28只雄性Balb/c小鼠被分为四组,每组7只。第1组和第2组皮下接种10×10⁶个MC-26小鼠结肠腺癌细胞。第3组和第4组作为无肿瘤对照。接种10天后,第2组和第4组腹腔注射DFMO(200mg/kg),而第1组和第3组注射生理盐水。注射DFMO两小时后处死动物。切除肿瘤、胰腺、肾脏和肝脏并分析ODC活性。DFMO导致肿瘤的ODC活性显著降低(与未接受DFMO的对照组相比);然而,荷瘤小鼠肾脏、胰腺和肝脏的ODC活性未受影响。此外,荷瘤小鼠肾脏、肝脏和胰腺的基础ODC活性与无肿瘤对照相比显著降低。DFMO降低了无肿瘤小鼠肾脏、胰腺和肝脏的ODC活性。这些结果表明,MC-26肿瘤的存在会引起全身效应,改变ODC活性以及对已知ODC抑制剂的反应。