Rydell E L, Olofsson J, Hellem S, Axelsson K L
Department of Pharmacology, Faculty of Health Sciences, Linköping University, Sweden.
Second Messengers Phosphoproteins. 1991;13(4):217-29.
Tyrosine kinase activity was studied in the crude cytosolic and particulate fraction of normal mucosa and squamous cell carcinomas of the upper aero-digestive tract. In the presence of exogenously added phosphorylation substrate (Glu,Tyr4:1), the cytosolic tyrosine kinase activity was 6-fold higher in tumors compared to normal mucosa (p = 0.001), and in the particulate fraction the increase was 8-fold in tumors compared to normal mucosa. Different proposed tyrosine kinase inhibitors, including genistein, quercetin and the alpha-cyanocinnamide ST 638, were tested for their ability to inhibit phosphorylation of the synthetic tyrosine phosphorylation substrate. Phosphorylation of Glu,Tyr4:1 in tumors (cytosolic fraction) was reduced to 77.8 +/- 8.7% of the control value by 10 microM ST 638 (p less than 0.05), and to 50.7 +/- 10.4% by 100 microM quercetin (p less than 0.01). In normal mucosa (cytosolic fraction) the corresponding values were 41.7 +/- 16.6% in the presence of 10 microM ST 638 (p less than 0.05) and 32.1 +/- 5.8% in the presence of 100 microM quercetin (p less than 0.05). These inhibitors had no effect on the tyrosine kinase activity in the particulate fractions. Phosphorylation of endogenous proteins in the crude cytosolic fraction was evaluated by SDS-polyacrylamide gel electrophoresis after alkali treatment of the gels. Autoradiography of the gels treated in this manner revealed bands corresponding to phosphorylated proteins with apparent molecular weight of 18, 23, 37-38, 42-44 (double band), 53-55 (double band), 61 and 92-94 (double band) kD. Quercetin (100 microM) markedly reduced the phosphorylation of these proteins, while no effect of ST 638 could be seen. Heparin (20 micrograms/ml) stimulated the phosphorylation of three proteins with apparent molecular weight of 39 and about 72 kD, respectively, and inhibited the phosphorylation of 2 proteins with molecular weight of 92 and 53 kD in tumors. These features were observed in both tumors and normal tissue, with the exception that heparin only stimulated the 72 kD band in normal mucosa and that the phosphorylation was markedly higher in tumors. In summary, our results show an increased tyrosine phosphorylation in squamous cell carcinomas of the upper aero-digestive tract compared to normal oral mucosa. These differences and their origin might be of vital importance in the regulation of events leading to malignant transformation.
研究了上呼吸消化道正常黏膜和鳞状细胞癌的粗制胞质和微粒体部分中的酪氨酸激酶活性。在外源添加磷酸化底物(Glu,Tyr4:1)的情况下,肿瘤中胞质酪氨酸激酶活性比正常黏膜高6倍(p = 0.001),在微粒体部分,肿瘤中的增加量比正常黏膜高8倍。测试了不同的酪氨酸激酶抑制剂,包括染料木黄酮、槲皮素和α-氰基肉桂酰胺ST 638,以评估它们抑制合成酪氨酸磷酸化底物磷酸化的能力。10μM ST 638使肿瘤(胞质部分)中Glu,Tyr4:1的磷酸化降低至对照值的77.8±8.7%(p < 0.05),100μM槲皮素使其降低至50.7±10.4%(p < 0.01)。在正常黏膜(胞质部分)中,10μM ST 638存在时相应值为41.7±16.6%(p < 0.05),100μM槲皮素存在时为32.1±5.8%(p < 0.05)。这些抑制剂对微粒体部分的酪氨酸激酶活性没有影响。通过对凝胶进行碱处理后,用SDS-聚丙烯酰胺凝胶电泳评估粗制胞质部分中内源性蛋白质的磷酸化。以这种方式处理的凝胶的放射自显影片显示出对应于磷酸化蛋白质的条带,其表观分子量为18、23、37 - 38、42 - 44(双条带)、53 - 55(双条带)、61和92 - 94(双条带)kD。槲皮素(100μM)显著降低了这些蛋白质的磷酸化,而未观察到ST 638有此作用。肝素(20μg/ml)刺激了表观分子量分别为39和约72 kD的三种蛋白质的磷酸化,并抑制了肿瘤中分子量为92和53 kD的两种蛋白质的磷酸化。在肿瘤和正常组织中均观察到这些特征,不同之处在于肝素仅刺激正常黏膜中的72 kD条带,且肿瘤中的磷酸化明显更高。总之,我们的结果表明,与正常口腔黏膜相比,上呼吸消化道鳞状细胞癌中的酪氨酸磷酸化增加。这些差异及其来源可能在导致恶性转化的事件调节中至关重要。