O'Grady R L, Upfold L I, Stephens R W
Int J Cancer. 1981 Oct 15;28(4):509-15. doi: 10.1002/ijc.2910280418.
A spontaneous mammary adenocarcinoma (AC) from an inbred female rat was investigated with regard to secretion of neutral proteases. Cultures of neoplastic epithelial cells derived from the tumour secreted an enzyme that fulfilled the criteria for a specific collagenase. In contrast to cultures of non-neoplastic cells, tumour collagenase was present as an active enzyme, since treatment with trypsin or p-aminophenylmercuric acetate (APMA) did not increase activity. The neoplastic cells were also prolific producers of plasminogen activator (PA). Dexamethasone (Dex) (10(-6)M) markedly reduced the levels of both enzymes. Addition of tranexamic acid (TA), an inhibitor of plasmin and of plasminogen activation, did not affect collagenase activity, even at 10(-1)M TA, nor did latent collagenase accumulate. Latent collagenase was secreted in culture by normal fibroblasts from neonatal rat lungs. This latent enzyme was activated by the addition of tumour cell medium plus plasminogen, but this effect was inhibited by the addition of TA. These results demonstrate that the neoplastic cells themselves secrete collagenase as an active enzyme. PA is also secreted, is not involved with tumour collagenase, but is capable, in the presence of plasminogen, of activating latent collagenase produced by the non-neoplastic cells within the tumour or in the surrounding tissue. This tumour possesses potent collagenolytic ability in vitro which may be partly responsible for its rapid invasion in vivo.
对一只近交系雌性大鼠的自发性乳腺腺癌(AC)进行了中性蛋白酶分泌方面的研究。源自该肿瘤的肿瘤上皮细胞培养物分泌出一种符合特定胶原酶标准的酶。与非肿瘤细胞培养物不同,肿瘤胶原酶以活性酶的形式存在,因为用胰蛋白酶或对氨基苯基汞乙酸盐(APMA)处理并不会增加其活性。肿瘤细胞也是纤溶酶原激活物(PA)的大量生产者。地塞米松(Dex)(10^(-6)M)显著降低了这两种酶的水平。添加氨甲环酸(TA),一种纤溶酶和纤溶酶原激活的抑制剂,即使在10^(-1)M TA时也不影响胶原酶活性,也不会积累潜伏性胶原酶。潜伏性胶原酶由新生大鼠肺的正常成纤维细胞在培养物中分泌。这种潜伏性酶通过添加肿瘤细胞培养基加纤溶酶原而被激活,但这种作用被添加TA所抑制。这些结果表明肿瘤细胞自身分泌活性形式的胶原酶。PA也被分泌,它与肿瘤胶原酶无关,但在纤溶酶原存在的情况下,能够激活肿瘤内或周围组织中非肿瘤细胞产生的潜伏性胶原酶。这种肿瘤在体外具有强大的胶原溶解能力,这可能部分解释了其在体内的快速侵袭。