Matrix metalloproteinase-26 is expressed in human endometrium but not in endometrial carcinoma

被引:43
作者
Isaka, K
Nishi, H
Nakai, H
Nakada, T
Li, YF
Ebihara, Y
Takayama, M
机构
[1] Tokyo Med Univ, Dept Obstet & Gynecol, Shinjuku Ku, Tokyo 1600023, Japan
[2] Tokyo Med Univ, Dept Pathol 2, Tokyo, Japan
关键词
MMP-26; (matrilysin-2; endometase); endometrial carcinoma; endometrium; MMP-7;
D O I
10.1002/cncr.11030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The human matrix metalloproteinase (MMP)-26, also called matrilysin-2 or endometase, has been isolated as a matrilysin (MMP-7) homolog. Matrix metalloproteinase-26 was expressed in tissue samples from the placenta and endometrial tumors and its expression may be related to the development of endometrial carcinomas. METHODS. Total RNAs were isolated from 5 endometrial carcinoma cell lines, 36 normal endometrial tissue samples, 4 hyperplasia tissue samples, and from 24 endometrial carcinoma tissue samples. Reverse transcription-polymerase chain reation (RT-PCR) was performed to detect MMP-26 mRNA expression. To identify MMP-26 mRNA localization and protein expression, we performed in situ RT-PCR and immunohistochemistry, respectively. RESULTS. Reverse transcription-polymerase chain reaction analysis revealed that MMP-26 mRNA was expressed in 24 of 36 normal human endometrial tissue samples. However, MMP-26 mRNA expression was not detected in endometrial carcinoma cell lines nor in endometrial carcinoma tissue samples except for one case. Western blot analysis showed similar results. In situ RT-PCR analysis revealed that MMP-26 expression was localized in the epithelial glandular cells but faint expression was observed in the stromal cells. Subsequently, we separated endometrial tissues into epithelial glandular and stromal cells. Using RT-PCR, the purified epithelial glandular cells exhibited MMP-26 mRNA expression but the purified stromal cells did not. Immunohistochemical analyses revealed that MMP-26 protein expression is also limited to endometrial epithelial glandular cells but not to cancer cells. Therefore, MMP-26 expression is limited to normal epithelial glandular cells. CONCLUSIONS. We found a significant difference in MMP-26 expression in normal and malignant endometrial tissue samples, although its function is still unknown. These data suggest that MMP-26 may be a candidate for a new tumor marker for endometrial carcinomas.
引用
收藏
页码:79 / 89
页数:11
相关论文
共 24 条
  • [1] Changing views of the role of matrix metalloproteinases in metastasis
    Chambers, AF
    Matrisian, LM
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (17) : 1260 - 1270
  • [2] de Coignac AB, 2000, EUR J BIOCHEM, V267, P3323
  • [3] Foulks M J, 1998, J Obstet Gynecol Neonatal Nurs, V27, P367, DOI 10.1111/j.1552-6909.1998.tb02660.x
  • [4] The structure of endometrial microvessels
    Hickey, M
    Fraser, IS
    [J]. HUMAN REPRODUCTION, 2000, 15 : 57 - 66
  • [5] Li H, 1998, MOL CARCINOGEN, V22, P84
  • [6] Promoter characterization of the novel human matrix metalloproteinase-26 gene: regulation by the T-cell factor-4 implies specific expression of the gene in cancer cells of epithelial origin
    Marchenko, GN
    Marchenko, ND
    Leng, J
    Strongin, AY
    [J]. BIOCHEMICAL JOURNAL, 2002, 363 : 253 - 262
  • [7] Characterization of matrix metalloproteinase-26, a novel metalloproteinase widely expressed in cancer cells of epithelial origin
    Marchenko, GN
    Ratnikov, BI
    Rozanov, DV
    Godzik, A
    Deryugina, EI
    Strongin, AY
    [J]. BIOCHEMICAL JOURNAL, 2001, 356 (356) : 705 - 718
  • [8] Matrix metalloproteinase-1 is associated with poor prognosis in colorectal cancer
    Murray, GI
    Duncan, ME
    ONeil, P
    Melvin, WT
    Fothergill, JE
    [J]. NATURE MEDICINE, 1996, 2 (04) : 461 - 462
  • [9] Matrix metalloproteinases
    Nagase, H
    Woessner, JF
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (31) : 21491 - 21494
  • [10] Matrix metalloproteinases: Biologic activity and clinical implications
    Nelson, AR
    Fingleton, B
    Rothenberg, ML
    Matrisian, LM
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (05) : 1135 - 1149