Gershtein E S, Mushtenko S V, Ermilova V D, Levchenko N E, Kushlinskii N E
N. N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, Moscow, Russia.
Bull Exp Biol Med. 2018 May;165(1):75-79. doi: 10.1007/s10517-018-4103-0. Epub 2018 May 24.
In patients with endometrial cancer (N=94), endometrial polyps (N=28), endometrial hyperplasia (N=25), and healthy women (N=77), the serum contents of MMP-2, MMP-7, MMP-9, TIMP-1, and TIMP-2 were measured by ELISA. Both carcinoma and benign neoplasms were accompanied by significant elevation of MMP-7 and TIMP-2 in blood serum. The greatest elevation (in comparison with the control) was observed for MMP-7, although serum concentration of this marker was practically identical in patients with carcinoma and benign tumors. In contrast, the levels of MMP-2 and TIMP-1 were lower in cancer patients in comparison with the control; in these patients, the levels of MMP-9 and TIMP-1 were also lower than the corresponding levels in patients with polyps and endometrial hyperplasia. There were no significant correlations between the levels of examined markers with tumor metastasizing, its histological structure, and differentiation degree of endometrial cancer. No differences were observed between examined serological markers in patients with polyps and endometrial hyperplasia of various severities. The examined MMPs and TIMPs cannot be advanced as potential diagnostic markers of endometrial cancer, but they can be used to monitor and prognosticate the disease and to assess effectiveness of the targeted therapy.
在子宫内膜癌患者(N = 94)、子宫内膜息肉患者(N = 28)、子宫内膜增生患者(N = 25)以及健康女性(N = 77)中,采用酶联免疫吸附测定法(ELISA)检测血清中基质金属蛋白酶-2(MMP-2)、基质金属蛋白酶-7(MMP-7)、基质金属蛋白酶-9(MMP-9)、金属蛋白酶组织抑制因子-1(TIMP-1)和金属蛋白酶组织抑制因子-2(TIMP-2)的含量。癌组织和良性肿瘤组织患者血清中的MMP-7和TIMP-2均显著升高。尽管该标志物在癌症患者和良性肿瘤患者中的血清浓度实际上相同,但MMP-7升高幅度最大(与对照组相比)。相比之下,癌症患者血清中的MMP-2和TIMP-1水平低于对照组;在这些患者中,MMP-9和TIMP-1的水平也低于息肉和子宫内膜增生患者的相应水平。所检测标志物的水平与肿瘤转移、组织学结构以及子宫内膜癌的分化程度之间均无显著相关性。不同严重程度的息肉和子宫内膜增生患者的血清学标志物之间未观察到差异。所检测的基质金属蛋白酶和金属蛋白酶组织抑制因子不能作为子宫内膜癌的潜在诊断标志物,但可用于监测和预测疾病以及评估靶向治疗的效果。