Sallot M, Lascombe I, Bermont L, Jouvenot M
Institut d'Etude et de Transfert de Gènes, Besançon, France.
Anticancer Res. 1997 Sep-Oct;17(5A):3499-504.
This study was designed to evaluate if c-myc expression could influence RL95-2 cell proliferation after EGF or fetal calf serum (FCS) stimulation. Upon FCS addition, c-myc mRNAs slightly increased in the first 30 minutes, peaked at 75 minutes (2.2 fold induction) and returned to the control value within 24 hours. This slight and transient FCS effect on c-myc expression contrasted with the marked and long-lasting EGF effect (17 fold induction up to 48 hours). The increase of cell number by FCS was partially but significantly reduced in the presence of c-myc antisense oligodeoxynucleotides (ODNs). The EGF inhibitory effect on cell growth was not reversed by c-myc antisense ODNs whatever the backbone may be (phosphorothioate or phosphodiester). It appears that EGF and FCS have differential effects on c-myc and RL95-2 cell proliferation and that c-myc is necessary but insufficient for proliferation.
本研究旨在评估c-myc表达是否会在表皮生长因子(EGF)或胎牛血清(FCS)刺激后影响RL95-2细胞的增殖。添加FCS后,c-myc mRNA在前30分钟略有增加,在75分钟时达到峰值(诱导2.2倍),并在24小时内恢复到对照值。FCS对c-myc表达的这种轻微且短暂的影响与EGF显著且持久的影响(长达48小时诱导17倍)形成对比。在存在c-myc反义寡脱氧核苷酸(ODN)的情况下,FCS引起的细胞数量增加部分但显著减少。无论骨架如何(硫代磷酸酯或磷酸二酯),c-myc反义ODN均不能逆转EGF对细胞生长 的抑制作用。似乎EGF和FCS对c-myc和RL95-2细胞增殖具有不同的影响,并且c-myc对于增殖是必要的,但并不充分。