van der Stappen J W, Hendriks T, Wobbes T
Department of General Surgery, St. Radboud University Hospital, Nijmegen, The Netherlands.
Int J Cancer. 1990 Jun 15;45(6):1071-8. doi: 10.1002/ijc.2910450616.
Collagenolytic activity, extracted from 55 tumor and healthy corresponding intestinal control samples, was determined by 3 different assays using soluble type I and fibrillar type I and III collagen, respectively, as substrate. The enzyme extracted from tumor-digested collagen type I reconstituted fibrils and yielded the three-quarter segments characteristic for the action of one of the matrix metalloproteinases: MMP-I or mammalian collagenase. Metal-chelating agents such as EDTA and O-phenanthrolin indeed inhibited this activity. Collagenolytic activities were calculated on the basis of wet weight, total DNA and total extracted protein. Correlations were sought between levels of activity and both clinicopathological stage (Dukes' staging) and grade of histological differentiation. In all the assays applied, significant correlations were found between grade of histological differentiation and collagenolytic activity expressed as the tumor/control ratios: poorly differentiated tumors exhibited a higher tumor/control ratio than well-differentiated tumors. Also, tumors penetrating into the serosa showed a higher tumor/control ratio than tumors invading the muscularis propria only. A relation between collagenolytic activity and clinico-pathological stage was observed only if activities were calculated on a DNA basis. These results confirm a relationship between the histological appearance of a tumor and its enzymatic potential to degrade interstitial collagens.
从55个肿瘤样本及其相应的健康肠道对照样本中提取胶原酶活性,分别使用可溶性I型胶原以及纤维状I型和III型胶原作为底物,通过3种不同的检测方法进行测定。从肿瘤消化的I型胶原重构原纤维中提取的酶产生了四分之三段,这是基质金属蛋白酶之一(MMP-I或哺乳动物胶原酶)作用的特征性片段。金属螯合剂如EDTA和邻菲罗啉确实抑制了这种活性。胶原酶活性是根据湿重、总DNA和总提取蛋白计算得出的。研究了活性水平与临床病理分期(Dukes分期)和组织学分化程度之间的相关性。在所有应用的检测方法中,组织学分化程度与以肿瘤/对照比值表示的胶原酶活性之间均存在显著相关性:低分化肿瘤的肿瘤/对照比值高于高分化肿瘤。此外,穿透至浆膜的肿瘤的肿瘤/对照比值高于仅侵犯固有肌层的肿瘤。仅当基于DNA计算活性时,才观察到胶原酶活性与临床病理分期之间的关系。这些结果证实了肿瘤的组织学表现与其降解间质胶原的酶活性潜力之间的关系。