O'Grady R L, Harrop P J, Cameron D A
Pathology. 1982 Apr;14(2):135-8. doi: 10.3109/00313028209061286.
Five carcinomas and 5 sarcomas were investigated in relation to their production of neutral proteases capable of digesting polymeric collagen. The carcinomas were far more active than the sarcomas but all the malignant tumours produced enzymes which were capable of causing collagenolysis in vitro. collagenolytic enzymes were recovered from extracts of neoplastic cells from long-term culture, from the media in which these cells were cultured, from the media of mixed cell cultures (neoplastic, stromal and inflammatory cells from minced tumours), and from normal fibroblasts cultures. In contrast to the cultures of non-neoplastic fibroblasts, the tumour cells produced active enzymes, since limited proteolysis with trypsin or treatment with p-aminophenyl-mercuric acetate (APMA) caused no increase in enzyme activity. These tumours possess collagenolytic ability in vitro which may be partly responsible for their invasive nature in vivo.
对5例癌和5例肉瘤进行了研究,观察它们产生能够消化聚合胶原的中性蛋白酶的情况。癌比肉瘤的活性高得多,但所有恶性肿瘤都产生了能够在体外引起胶原溶解的酶。从长期培养的肿瘤细胞提取物、这些细胞培养的培养基、混合细胞培养物(来自切碎肿瘤的肿瘤细胞、基质细胞和炎性细胞)的培养基以及正常成纤维细胞培养物中都回收了胶原olytic酶。与非肿瘤性成纤维细胞培养物不同,肿瘤细胞产生活性酶,因为用胰蛋白酶进行有限的蛋白水解或用对氨基苯基汞乙酸盐(APMA)处理不会导致酶活性增加。这些肿瘤在体外具有胶原olytic能力,这可能部分解释了它们在体内的侵袭性。