Misugi Fumiko, Sumi Toshiyuki, Okamoto Eri, Nobeyama Hiroyuki, Hattori Kanae, Yoshida Hiroyuki, Matsumoto Yoshinari, Yasui Tomoyo, Honda Ken-Ichi, Ishiko Osamu
Department of Obstetrics and Gynecology, Osaka City University Graduate School of Medicine, 1-4-3 Asahimachi, Abenoku, Osaka 545-8585, Japan.
Int J Mol Med. 2005 Oct;16(4):541-6.
Matrix metalloproteinases (MMPs) are associated with invasion and metastasis of several human malignant tumors, in particular MMP-7, which is mainly produced by the cancer cell itself. We examined the expression of MMP-2, 7 and 9, and tissue inhibitors of metalloproteinase (TIMP)-1 and 2 in uterine endometrial carcinoma, and compared the expression with clinicopathological characteristics in uterine endometrial carcinoma (UEC). A group of 256 patients with UEC received surgery at the Osaka City University Medical School Hospital, and 196 tumor samples were immunohistochemically stained to examine the expression of MMP-2, 7 and 9, and TIMP-1 and 2. Additionally, the invasion ability of cell stain established from UEC was examined using an in vitro invasion assay. The expression of MMP-2, 7 and 9, and TIMP-1 and 2 was observed in the cytoplasm, and the expression of MMP-2 and 7, and TIMP-1 and 2 was observed in stromal cells around the tumor cells. The expression of MMP-7 was significantly stronger in higher-grade than lower-grade tumors (P<0.05). The invasion assay showed that the invasion of cells derived from UECs was significantly inhibited by TIMP-1 and 2. The disease-free interval was significantly shorter when MMP-7 expression was intense. This increased expression of MMP-7 in high grade UECs may be associated with tumor invasion and metastasis, and MMP-7 could serve as a prognostic maker in UEC.
基质金属蛋白酶(MMPs)与多种人类恶性肿瘤的侵袭和转移相关,尤其是MMP - 7,其主要由癌细胞自身产生。我们检测了子宫内膜癌中MMP - 2、7和9以及金属蛋白酶组织抑制剂(TIMP)- 1和2的表达,并将其表达与子宫内膜癌(UEC)的临床病理特征进行比较。一组256例UEC患者在大阪市立大学医学院附属医院接受了手术,对196份肿瘤样本进行免疫组织化学染色,以检测MMP - 2、7和9以及TIMP - 1和2的表达。此外,使用体外侵袭试验检测了从UEC建立的细胞株的侵袭能力。MMP - 2、7和9以及TIMP - 1和2的表达在细胞质中观察到,MMP - 2和7以及TIMP - 1和2的表达在肿瘤细胞周围的基质细胞中观察到。MMP - 7在高级别肿瘤中的表达明显强于低级别肿瘤(P<0.05)。侵袭试验表明,TIMP - 1和2可显著抑制UEC来源细胞的侵袭。当MMP - 7表达强烈时,无病生存期明显缩短。高级别UEC中MMP - 7表达的增加可能与肿瘤侵袭和转移相关,并且MMP - 7可作为UEC的预后标志物。