MMP-2 expression associates with CA 125 and clinical course in endometrial carcinoma

被引:31
作者
Honkavuori, M.
Talvensaari-Mattila, A.
Soini, Y.
Turpeenniemi-Hujanen, T.
Santala, M.
机构
[1] Univ Oulu, Dept Obstet & Gynecol, Oulu 90014, Finland
[2] Univ Oulu, Dept Pathol, Oulu 90014, Finland
[3] Univ Oulu, Dept Radiotherapy & Oncol, Oulu 90014, Finland
关键词
CA; 125; endometrial cancer; prognosis; MMP-2; MMP-9;
D O I
10.1016/j.ygyno.2006.08.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Objective. Matrix metalloproteinases have long been associated with aggressive behavior of several malignancies, but their role in endometrial cancer has not been conclusively established. This study aimed to evaluate the roles of matrix metalloproteinase-2 (MMP-2) and -9 (MMP-9) as prognostic factors in endometrial carcinoma and their association with CA 125 and other conventional prognostic markers. Methods. The MMP-2 and MMP-9 immunoreactive proteins were evaluated from primary tumors of endometrial carcinoma in 266 specimens by using a specific monoclonal antibody in immunohistochemical stainings. The median follow-up time was 79 months. Results. Expression of the MMP-2 and MMP-9 proteins was found in 88% and 70% of the primary tumors, respectively. Positive MMP-2 immunostaining was associated with a shortened recurrence-free (P=0.04) and cancer-specific survival (P=0.05). MMP-2 negativity was linked with a favorable prognosis; only one patient developed recurrent disease and died during the follow-up. Preoperative serum levels of CA 125 were higher in the patients presenting with tumors positive for MMP-2 than in those with negative immunostaining (P = 0.03). Conclusions. We suggest that MMP-2 is linked with biologically aggressive nature of this cancer type. It seems that MMP-2, but not MMP-9, has some prognostic value in endometrial carcinoma. However, the conventional prognostic markers are superior to MMP-2 in assessing aggressive behavior and cancer-specific survival in endometrial cancer. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:217 / 221
页数:5
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