Huang Hong-jie, Ping Fei-yun, Hu Ji-an, Zhao Shi-fang
Department of Stomatology, Affiliated Hospital of Medical School, Hangzhou Normal University, Hangzhou 310015, China.
Zhonghua Yi Xue Za Zhi. 2009 Dec 15;89(46):3289-94.
To investigate the cross-talk between Notch1 and epidermal growth factor receptor (EGFR) signaling in regulating the cellular proliferation of human tongue squamous cell carcinoma (SCC).
Human tongue SCC cell line Tca8113 cells was transiently transfected with the vector encoding exogenous intracellular fragment of Notch1 and the vector encoding the specific short hairpin RNA (shRNA) targeting EGFR respectively and were treated by AG1478, an inhibitor of receptor tyrosine kinases, for elucidating the effects of constitutive activation, EGFR gene silencing and blocking EGFR signaling upon cellular proliferation and expression of Notch1 and EGFR. The mRNA and protein levels of Notch1 and EGFR were detected by reverse transcriptase polymerase chain reaction (RT-PCR) and Western blot, respectively. The cellular proliferation was evaluated by methyl thiazolyl tetrazolium (MTT) assay.
Constitutive activation of Notch1 resulted in inhibition of cellular proliferation, and up-regulation of Notch1 (1.102 +/- 0.135, 0.243 +/- 0.032, P < 0.05) but down-regulation of EGFR (0.083 +/- 0.009, 0.605 +/- 0.075, P < 0.05) at the the mRNA and protein levels. Silencing of EGFR gene resulted in inhibition of cell proliferation, and down-regulation of EGFR (0.148 +/- 0.019, 1.175 +/- 0.132, P < 0.05) but up-regulation of Notch1 (0.978 +/- 0.115, 0.083 +/- 0.009, P < 0.05) at the mRNA and protein levels. Blocking EGFR signaling had no significant effect upon EGFR expression (P > 0.05), but resulted in inhibition of cellular proliferation and up-regulation of Notch1 (P < 0.05) at the mRNA and protein levels.
There might be a cross-talk of bi-directional control between Notch1 and EGFR signaling in regulating the cellular proliferation of human tongue SCC cells.
研究Notch1与表皮生长因子受体(EGFR)信号通路在调节人舌鳞状细胞癌(SCC)细胞增殖中的相互作用。
分别用编码Notch1胞内段的载体和编码靶向EGFR的特异性短发夹RNA(shRNA)的载体瞬时转染人舌SCC细胞系Tca8113细胞,并用受体酪氨酸激酶抑制剂AG1478处理,以阐明Notch1组成性激活、EGFR基因沉默及阻断EGFR信号通路对细胞增殖以及Notch1和EGFR表达的影响。分别采用逆转录聚合酶链反应(RT-PCR)和蛋白质印迹法检测Notch1和EGFR的mRNA及蛋白水平。采用噻唑蓝(MTT)法评估细胞增殖情况。
Notch1的组成性激活导致细胞增殖受到抑制,在mRNA和蛋白水平上Notch1上调(1.102±0.135,0.243±0.032,P<0.05),而EGFR下调(0.083±0.009,0.605±0.075,P<0.05)。EGFR基因沉默导致细胞增殖受到抑制,在mRNA和蛋白水平上EGFR下调(0.148±0.019,1.175±0.132,P<0.05),而Notch1上调(0.978±0.115,0.083±0.009,P<0.05)。阻断EGFR信号通路对EGFR表达无显著影响(P>0.05),但导致细胞增殖受到抑制,在mRNA和蛋白水平上Notch1上调(P<0.05)。
在调节人舌SCC细胞增殖过程中,Notch1与EGFR信号通路之间可能存在双向控制的相互作用。