Foekens J A, Schmitt M, van Putten W L, Peters H A, Kramer M D, Jänicke F, Klijn J G
Department of Medical Oncology, Dr Daniel den Hoed Cancer Center, Rotterdam, The Netherlands.
J Clin Oncol. 1994 Aug;12(8):1648-58. doi: 10.1200/JCO.1994.12.8.1648.
Evaluation of the relationship between plasminogen activator inhibitor-1 (PAI-1) and the metastatic potential of primary breast cancer, and to compare the prognostic impact of PAI-1 in multivariate analysis with those of conventional prognostic factors, including steroid-hormone receptors, and those of urokinase plasminogen activator (uPA), pS2-protein (PS2), and cathepsin D.
Cell biologic prognostic factors were analyzed in 657 cytosols routinely prepared from frozen-tissue biopsies that were submitted to our laboratory for the assessment of steroid-hormone receptor status. The median duration of follow-up in patients still alive at the time of analysis was 48 months. Estrogen receptor (ER) and progesterone receptor (PgR) status were assessed by radioligand binding assay, PS2, and cathepsin D by radiometric immunoassay, and uPA and PAI-1 by enzyme-linked immunosorbent assay (ELISA).
PAI-1 levels were found to be strongly positively correlated with the rates of relapse (P < .0001) and death (P < .001). Relating the levels of PAI-1 with those of other cytosolic prognostic factors, we found a positive association with the metastasis-related proteases uPA (P < .0001) and cathepsin D (P < .0001). On the other hand, PAI-1 levels were found to be negatively correlated with ER (P < .005) and PgR (P < .001), and the estrogen-regulated pS2-protein (P < .001), which are proteins associated with a favorable prognosis. In multivariate regression analysis for 5-year relapse-free survival, and using an optimized cutoff point for discrimination between PAI-1-positive and -negative, independent predictors of the rate of relapse were found to be PAI-1 (P < .0001) and uPA (P = .01) of the cytosolic parameters, and tumor size, lymph node status, and premenopausal age of the clinical parameters. In multivariate analysis in patients with node-negative disease, only PAI-1 (P < .001) and tumor size (P = .03) were positively and premenopausal age negatively (P < .001) associated with the rate of relapse. In patients with node-positive disease, PAI-1 (P < .001), uPA (P = .02), tumor size (P < .001), and the number of positive lymph nodes (P < .001) were all positively associated with the rate of relapse.
We conclude that the PAI-1 level measured in routinely prepared cytosols is an important parameter to predict the metastatic potential in both node-negative and node-positive human primary breast cancer.
评估纤溶酶原激活物抑制剂-1(PAI-1)与原发性乳腺癌转移潜能之间的关系,并在多变量分析中比较PAI-1与包括类固醇激素受体在内的传统预后因素、尿激酶型纤溶酶原激活物(uPA)、pS2蛋白(PS2)和组织蛋白酶D的预后影响。
对657份从冷冻组织活检标本中常规制备的细胞溶质进行细胞生物学预后因素分析,这些标本被送至我们实验室以评估类固醇激素受体状态。分析时仍存活患者的中位随访时间为48个月。雌激素受体(ER)和孕激素受体(PgR)状态通过放射性配体结合测定评估,PS2和组织蛋白酶D通过放射免疫测定评估,uPA和PAI-1通过酶联免疫吸附测定(ELISA)评估。
发现PAI-1水平与复发率(P <.0001)和死亡率(P <.001)呈强正相关。将PAI-1水平与其他细胞溶质预后因素的水平相关联,我们发现其与转移相关蛋白酶uPA(P <.0001)和组织蛋白酶D(P <.0001)呈正相关。另一方面,发现PAI-1水平与ER(P <.005)、PgR(P <.001)以及雌激素调节的pS2蛋白(P <.001)呈负相关,这些蛋白与良好预后相关。在对5年无复发生存率的多变量回归分析中,使用PAI-1阳性和阴性的优化分界点,发现复发率的独立预测因素在细胞溶质参数方面为PAI-1(P <.0001)和uPA(P =.01),在临床参数方面为肿瘤大小、淋巴结状态和绝经前年龄。在淋巴结阴性疾病患者的多变量分析中,仅PAI-1(P <.001)和肿瘤大小(P =.03)与复发率呈正相关,绝经前年龄与复发率呈负相关(P <.001)。在淋巴结阳性疾病患者中,PAI-1(P <.001)、uPA(P =.02)、肿瘤大小(P <.001)和阳性淋巴结数量(P <.001)均与复发率呈正相关。
我们得出结论,在常规制备的细胞溶质中测量的PAI-1水平是预测淋巴结阴性和阳性人类原发性乳腺癌转移潜能的重要参数。