Tomita T, Iwata K
Department of Pathology, University of Kansas Medical Center, Kansas City 66160, USA.
Dis Colon Rectum. 1996 Nov;39(11):1255-64. doi: 10.1007/BF02055119.
Colonic adenocarcinomas evolve through a multistep process from tubular adenomas to invasive adenocarcinomas. Matrix metalloproteinases (MMPs) have been implicated in proteolysis of basement membrane for initiation of metastatic cascade.
By immunocytochemical staining, hyperplastic polyps, tubular adenomas, tubovillous adenomas, villous adenomas to adenocarcinomas were systematically examined for the presence of MMP-2 (gelatinase A) and MMP-9 (gelatinase B) and tissue inhibitor of MMP (TIMP)-1 and TIMP-2, respectively.
MMP-2 and MMP-9, and TIMP-1 and TIMP-2 were immunolocalized in scattered stromal cells, whereas epithelial cells of normal mucosa and hyperplastic polyps were weakly stained. From tubular adenomas to villous adenomas, immunolocalization of gelatinases and TIMPs showed increasing gradually, and in situ carcinomas showed a definite positive, immunolocalization of gelatinases and TIMPs.
Increasing immunolocalization of gelatinases and TIMPs from tubular adenomas to adenocarcinomas coincides with a multistep process of colonic tumorigenesis.
结肠腺癌通过从管状腺瘤到浸润性腺癌的多步骤过程演变。基质金属蛋白酶(MMPs)参与基底膜的蛋白水解,启动转移级联反应。
通过免疫细胞化学染色,系统检查增生性息肉、管状腺瘤、绒毛状管状腺瘤、绒毛状腺瘤至腺癌中MMP-2(明胶酶A)和MMP-9(明胶酶B)以及MMP组织抑制剂(TIMP)-1和TIMP-2的存在情况。
MMP-2和MMP-9以及TIMP-1和TIMP-2免疫定位在散在的基质细胞中,而正常黏膜和增生性息肉的上皮细胞染色较弱。从管状腺瘤到绒毛状腺瘤,明胶酶和TIMP的免疫定位逐渐增加,原位癌中明胶酶和TIMP的免疫定位呈明确阳性。
从管状腺瘤到腺癌,明胶酶和TIMP的免疫定位增加与结肠肿瘤发生的多步骤过程一致。