Yu H, Levesque M A, Khosravi M J, Papanastasiou-Diamandi A, Clark G M, Diamandis E P
Section of Cancer Prevention and Control, Feist-Weiller Cancer Center, Louisiana State University Medical Center, Shreveport, USA.
Int J Cancer. 1998 Dec 18;79(6):624-8. doi: 10.1002/(sici)1097-0215(19981218)79:6<624::aid-ijc12>3.0.co;2-9.
Insulin-like growth factors (IGFs) are potent mitogens involved in the regulation of cell proliferation and apoptosis. The action of IGFs is mediated through a specific cell membrane receptor (IGF-IR), and the interactions between IGFs and this receptor are regulated by IGF-binding proteins (IGFBPs). IGFBP-3 is one such protein which either suppresses or enhances the actions of IGFs. Findings from most in vitro studies suggest that IGFBP-3 inhibits breast cancer cell growth and facilitates apoptosis, but clinical studies have found that high levels of IGFBP-3 in breast cancer tissues are associated with unfavourable prognostic indicators of the disease, such as large tumour size, low levels of steroid hormone receptors, elevated S-phase fraction and DNA aneuploidy. To further examine the role of IGFBP-3 in breast cancer recurrence and survival, we conducted the following nested case-control study. From a cohort of 1,000 women treated surgically for primary breast cancer, we consecutively selected 100 patients who developed recurrent disease after surgery and 100 age- and year of diagnosis-matched patients who had no relapse. Concentrations of IGFBP-3 in breast tissue extracts were determined with an ELISA. Inverse correlations of IGFBP-3 were revealed with estrogen receptor expression and patient age but not with tumour size or S-phase fraction. Levels of IGFBP-3 in breast tissues were slightly higher in the recurrent patients than in controls, but the differences were not statistically significant. No significant association was found between IGFBP-3 and breast cancer recurrence. Survival analysis, however, indicated that the risk of death was increased with higher IGFBP-3 levels, and the association was independent of other prognostic markers. In conclusion, our results demonstrate that high levels of IGFBP-3 are associated with unfavourable prognostic features of breast cancer.
胰岛素样生长因子(IGFs)是参与细胞增殖和凋亡调节的强效促有丝分裂原。IGFs的作用通过特定的细胞膜受体(IGF-IR)介导,并且IGFs与该受体之间的相互作用受胰岛素样生长因子结合蛋白(IGFBPs)调节。IGFBP-3就是这样一种蛋白,它既可以抑制也可以增强IGFs的作用。大多数体外研究结果表明,IGFBP-3抑制乳腺癌细胞生长并促进细胞凋亡,但临床研究发现,乳腺癌组织中高水平的IGFBP-3与该疾病的不良预后指标相关,如肿瘤体积大、类固醇激素受体水平低、S期分数升高和DNA非整倍体。为了进一步研究IGFBP-3在乳腺癌复发和生存中的作用,我们进行了以下巢式病例对照研究。从1000名接受原发性乳腺癌手术治疗的女性队列中,我们连续选择了100例术后出现复发性疾病的患者和100例年龄及诊断年份匹配且无复发的患者。用酶联免疫吸附测定法(ELISA)测定乳腺组织提取物中IGFBP-3的浓度。结果显示IGFBP-3与雌激素受体表达和患者年龄呈负相关,但与肿瘤大小或S期分数无关。复发患者乳腺组织中IGFBP-3水平略高于对照组,但差异无统计学意义。未发现IGFBP-3与乳腺癌复发之间存在显著关联。然而,生存分析表明,IGFBP-3水平越高,死亡风险越高,且这种关联独立于其他预后标志物。总之,我们的结果表明,高水平的IGFBP-3与乳腺癌的不良预后特征相关。