Wilmes E, Schönberger O L, Hochstrasser K
Laryngol Rhinol Otol (Stuttg). 1979 Nov;58(11):861-4.
It's well known that increased proteolytic activity in plasma as well as in interstitial fluids is often associated with malignant tumours. There are numerous reports that cell cultures of malignant origin contain plasminogen activators responsible for an increased proteolysis. Our studies showed that patients with a carcinoma excrete in their urine a significant higher amount of an acid-stable inhibitor than healthy patients. This urine inhibitor is a split product (MW: 30,000) of the Inter-alpha-trypsin inhibitor (MW: 180,000). We conclude that the increased amount of acid-stable split products is the result of increased proteolysis in patients with malignant tumours. In contrast to other authors we do not think that the activation of plasmin by plasminogen is responsible for the proteolytic cleavage of ITI. Otherwise proteolysis by Cathepsin G and granulocytic Elastase would be reasonable. So enhanced proteolysis seems to be a sign of general enzymatic change associated with transformation.
众所周知,血浆以及组织液中蛋白水解活性的增加通常与恶性肿瘤相关。有大量报道称,恶性来源的细胞培养物中含有负责增加蛋白水解作用的纤溶酶原激活剂。我们的研究表明,癌症患者尿液中排出的酸稳定抑制剂的量明显高于健康患者。这种尿液抑制剂是α-胰蛋白酶抑制剂(分子量:180,000)的裂解产物(分子量:30,000)。我们得出结论,酸稳定裂解产物量的增加是恶性肿瘤患者蛋白水解增加的结果。与其他作者不同,我们认为纤溶酶原对纤溶酶的激活不是导致ITI蛋白水解裂解的原因。否则,组织蛋白酶G和粒细胞弹性蛋白酶引起的蛋白水解作用将是合理的。因此,增强的蛋白水解作用似乎是与细胞转化相关的一般酶变化的一个标志。