Gedlicka Claudia, Hager Gudrun, Weissenböck Martina, Gedlicka Wilhelm, Knerer Birgit, Kornfehl Johannes, Formanek Michael
Department of Otorhinolaryngology, Head and Neck Surgery, Medical University of Vienna, Vienna, Austria.
J Oral Pathol Med. 2006 Sep;35(8):472-8. doi: 10.1111/j.1600-0714.2006.00407.x.
1Alpha,25-dihydroxyvitamin D(3) [1,25(OH)(2) Vitamin D(3)] induces growth inhibition in squamous cell carcinoma (SCC) cell lines of the head and neck by arresting the cells in the G0/G1 phase of the cell cycle, probably due to an enhanced expression of p21, which could be demonstrated in other cell lines (JPPA, SCC9) before. In SCC25, a SCC cell line isolated from tongue, growth inhibition but no overexpression of p21 was detected. The retinoblastoma gene, as a direct target of G1 cyclin-CDK complexes, showed an obvious shift from the hyperphosphorylated to the hypophosphorylated form under 1,25(OH)(2)Vitamin D(3), which indicates that the growth inhibition takes place in the G0/G1 phase. To explore the possible pathway of growth inhibition in SCC25 we investigated other cell cycle inhibitors (p18, p19, p27).
Synchronized cells were treated with 1,25(OH)(2)Vitamin D(3) over 96 h. The cell cycle status and expression of cell cycle-regulating proteins was determined by fluorescence-activated cell sorting (FACS) and Western blotting. An overexpression of p18 in 1,25(OH)(2)Vitamin D(3) vs. ethanol-treated cells was determined until 30 h in SCC25. No influence was detectable on the expression of p27 and p19.
One mechanism by which 1,25(OH)(2)Vitamin D(3) controls cell growth might be the upregulation of p21. As p21 was unsusceptible to 1,25(OH)(2)Vitamin D(3) in SCC25, other inhibiting proteins were necessary to be tested. The proven upregulation of p18 seems to be the responsible step for growth inhibition of 1,25(OH)(2)Vitamin D(3) in SCC25.
1α,25 - 二羟基维生素D(3)[1,25(OH)₂维生素D(3)]通过使细胞停滞于细胞周期的G0/G1期来诱导头颈部鳞状细胞癌(SCC)细胞系生长抑制,这可能是由于p21表达增强,此前在其他细胞系(JPPA、SCC9)中已得到证实。在从舌部分离出的SCC细胞系SCC25中,检测到生长抑制但未检测到p21的过表达。视网膜母细胞瘤基因作为G1细胞周期蛋白 - CDK复合物的直接靶点,在1,25(OH)₂维生素D(3)作用下,显示出从高磷酸化形式到低磷酸化形式的明显转变,这表明生长抑制发生在G0/G1期。为探究SCC25中生长抑制的可能途径,我们研究了其他细胞周期抑制剂(p18、p19、p27)。
同步化细胞用1,25(OH)₂维生素D(3)处理96小时以上。通过荧光激活细胞分选(FACS)和蛋白质免疫印迹法测定细胞周期状态和细胞周期调节蛋白的表达。在SCC25中,测定1,25(OH)₂维生素D(3)处理组与乙醇处理组细胞直至30小时p18的过表达情况。未检测到对p27和p19表达的影响。
1,25(OH)₂维生素D(3)控制细胞生长的一种机制可能是p21的上调。由于在SCC25中p21对1,25(OH)₂维生素D(3)不敏感,因此需要测试其他抑制蛋白。已证实的p18上调似乎是1,25(OH)₂维生素D(3)在SCC25中抑制生长的关键步骤。