Department of Surgical and Radiological Sciences, University of California, Davis, CA 95616, USA.
Vet Comp Oncol. 2011 Dec;9(4):275-82. doi: 10.1111/j.1476-5829.2011.00264.x. Epub 2011 Mar 8.
Polyamines are essential for cell proliferation. Their production is dysregulated in many cancers and polyamine depletion leads to tumour regression in mouse models of squamous cell carcinoma (SCC). The purpose of this study was to determine the maximally tolerated dose of the polyamine transport inhibitor, MQT 1426, when combined with the ornithine decarboxylase (ODC) inhibitor, DFMO, and to determine whether this therapy results in reduction in tumour polyamine levels. Thirteen cats with oral SCC received both drugs orally and serial tumour biopsies were obtained for polyamine measurement. Cats were monitored for response to therapy and toxicity. A maximum tolerated dose (MTD) of MQT 1426 when combined with DFMO was determined. Dose-limiting toxicity was vestibular in nature, but was fully reversible. Spermidine and total polyamine levels decreased significantly in tissues, two cats experienced objective tumour regression and six cats had stable disease. These results suggest that further study of polyamine depletion therapies is warranted.
多胺对于细胞增殖至关重要。在许多癌症中,它们的产生失调,多胺耗竭会导致鳞状细胞癌 (SCC) 小鼠模型中的肿瘤消退。本研究的目的是确定多胺转运抑制剂 MQT 1426 与鸟氨酸脱羧酶 (ODC) 抑制剂 DFMO 联合使用时的最大耐受剂量,并确定这种治疗是否会导致肿瘤多胺水平降低。13 只患有口腔 SCC 的猫接受了这两种药物的口服治疗,并连续获得肿瘤活检以进行多胺测量。监测猫对治疗的反应和毒性。确定了 MQT 1426 与 DFMO 联合使用的最大耐受剂量。剂量限制毒性为前庭性质,但完全可逆。精脒和总多胺水平在组织中显著下降,有两只猫出现了客观的肿瘤消退,六只猫病情稳定。这些结果表明,有必要进一步研究多胺耗竭疗法。