Gröne A, Weckmann M T, Capen C C, Rosol T J
Department of Veterinary Biosciences, The Ohio State University, Columbus, USA.
Exp Toxicol Pathol. 1998 Sep;50(4-6):365-70. doi: 10.1016/S0940-2993(98)80017-1.
The regulation of parathyroid hormone-related protein expression by colchicine, vinblastine, nocodazole, taxol, transforming growth factor-beta1 (TGFbeta1), and epidermal growth factor (EGF) was investigated in a canine squamous carcinoma cell line (SCC 2/88 cells). SCC 2/88 cells were stably transfected with a human P2/P3 PTHrP promoter-luciferase reporter gene construct and gene expression was measured after chemical treatments. The greatest increase in reporter gene expression was observed after colchicine treatment and small increases occurred after treatment with vinblastine, taxol, TGFbeta1, or EGF. Nocodazole had no significant effect on reporter gene expression. Colchicine also increased PTHrP steady state mRNA expression and PTHrP secretion by SCC 2/88 cells. These results demonstrated that PTHrP production was increased in SCC 2/88 cells by colchicine and suggested that factors or events during mitosis are capable of stimulating PTHrP production. An increase in PTHrP production during mitosis of malignant epithelial cells may be important in the pathogenesis of humoral hypercalcemia of malignancy.
在犬鳞状癌细胞系(SCC 2/88细胞)中研究了秋水仙碱、长春碱、诺考达唑、紫杉醇、转化生长因子-β1(TGFβ1)和表皮生长因子(EGF)对甲状旁腺激素相关蛋白表达的调节作用。用人类P2/P3甲状旁腺激素相关蛋白(PTHrP)启动子-荧光素酶报告基因构建体稳定转染SCC 2/88细胞,化学处理后测量基因表达。秋水仙碱处理后观察到报告基因表达增加最为显著,长春碱、紫杉醇、TGFβ1或EGF处理后有小幅度增加。诺考达唑对报告基因表达无显著影响。秋水仙碱还增加了SCC 2/88细胞中PTHrP的稳态mRNA表达和PTHrP分泌。这些结果表明,秋水仙碱可增加SCC 2/88细胞中PTHrP的产生,并提示有丝分裂期间的因素或事件能够刺激PTHrP的产生。恶性上皮细胞有丝分裂期间PTHrP产生的增加可能在恶性肿瘤体液性高钙血症的发病机制中起重要作用。