酪氨酸激酶在人上消化道正常和肿瘤上皮组织中的活性。

E L Rydell, J Olofsson, S Hellem, K L Axelsson
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引用次数: 0

摘要

研究了正常粘膜和上消化道鳞状细胞癌的粗细胞质和颗粒组分中酪氨酸激酶的活性。在外源添加磷酸化底物(Glu,Tyr4:1)的情况下,肿瘤的胞质酪氨酸激酶活性比正常粘膜高6倍(p = 0.001),在颗粒组分中,肿瘤的胞质酪氨酸激酶活性比正常粘膜高8倍。不同的酪氨酸激酶抑制剂,包括染料木素、槲皮素和α -氰辛酰胺ST 638,测试了它们抑制合成酪氨酸磷酸化底物磷酸化的能力。10 μ m ST 638可使肿瘤(胞质部分)中Glu,Tyr4:1的磷酸化水平降至对照组的77.8 +/- 8.7% (p < 0.05), 100 μ m槲皮素可使Glu,Tyr4:1的磷酸化水平降至50.7 +/- 10.4% (p < 0.01)。在正常粘膜(细胞质部分)中,10 microM ST 638存在时对应值为41.7 +/- 16.6% (p < 0.05), 100 microM槲皮素存在时对应值为32.1 +/- 5.8% (p < 0.05)。这些抑制剂对颗粒部分的酪氨酸激酶活性没有影响。用sds -聚丙烯酰胺凝胶电泳法测定粗细胞质组分中内源蛋白的磷酸化情况。经这种方式处理的凝胶放射自显影显示磷酸化蛋白对应的条带,表观分子量为18,23,37 - 38,42 -44(双带),53-55(双带),61和92-94(双带)kD。槲皮素(100微米)显著降低了这些蛋白的磷酸化,而ST 638则没有作用。肝素(20微克/ml)刺激了肿瘤中3种表观分子量为39和72 kD的蛋白的磷酸化,抑制了2种分子量为92和53 kD的蛋白的磷酸化。这些特征在肿瘤和正常组织中均有观察到,除了肝素仅刺激正常黏膜的72 kD带,而在肿瘤中磷酸化程度明显更高。总之,我们的研究结果表明,与正常口腔黏膜相比,上气消化道鳞状细胞癌中酪氨酸磷酸化增加。这些差异及其起源可能对导致恶性转化的事件的调控至关重要。
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Tyrosine kinase activities in normal and neoplastic epithelia tissue of the human upper aero-digestive tract.

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.

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Measurement of protein phosphatase activity in biological samples using synthetic phosphopeptides. Phospholamban-modulated Ca2+ transport in cardiac and slow twitch skeletal muscle sarcoplasmic reticulum. Lipopolysaccharide stimulates phosphorylation of eukaryotic initiation factor-4F in macrophages and tumor necrosis factor participates in this event. Activation of G-proteins induces Ca2+ oscillations with hyperpolarizing K+ currents in pancreatic beta-cells. Heterogeneity of hepatic protein tyrosine phosphatases.
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