Am J Cancer Res. 2012;2(5):566-80. Epub 2012 Aug 20.
The behavior of tumor cells is influenced by the composition of the surrounding tumor environment. The importance of ascites in ovarian cancer (OC) progression is being increasingly recognized. The characterization of soluble factors in ascites is essential to understand how this environment affects OC progression. The development of cytokine arrays now allows simultaneous measurement of multiple cytokines per ascites using a single array.
We applied a multiplex cytokine array technology that simultaneously measures the level of 120 cytokines in ascites from 10 OC patients. The ascites concentration of a subset (n = 5) of cytokines that was elevated based on the multiplex array was validated by commercially available ELISA. The ascites level of these 5 cytokines was further evaluated by ELISA in a cohort of 38 patients. Kaplan-Meier analysis was used to assess the association of cytokine expression with progression-free survival (PFS) in this cohort.
We observed a wide variability of expression between different cytokines and levels of specific cytokines also varied in the 10 malignant ascites tested. Fifty-three (44%) cytokines were not detected in any of the 10 ascites. The level of several factors including, among others, angiogenin, angiopoietin-2, GRO, ICAM-1, IL-6, IL-6R, IL-8, IL-10, leptin, MCP-1, MIF NAP-2, osteprotegerin (OPG), RANTES, TIMP-2 and UPAR were elevated in most malignant ascites. Higher levels of OPG, IL-10 and leptin in OC ascites were associated with shorter PFS. IL-10 was shown to promote the anti-apoptotic activity of malignant ascites whereas OPG did not.
Our data demonstrated that there is a complex network of cytokine expression in OC ascites. Characterization of cytokine profiles in malignant ascites may provide information from which to prioritize key functional cytokines and understand the mechanism by which they alter tumor cells behavior. A better understanding of the cytokine network is essential to determine the role of ascites in OC progression.
肿瘤细胞的行为受周围肿瘤环境的组成影响。腹水在卵巢癌(OC)进展中的重要性正日益受到重视。对腹水可溶性因子的特征进行描述,对于了解这种环境如何影响 OC 进展至关重要。细胞因子阵列的发展使得现在能够通过单个阵列同时测量每例腹水的多种细胞因子的水平。
我们应用了一种多重细胞因子阵列技术,该技术可同时测量 10 名 OC 患者腹水样本中的 120 种细胞因子的水平。根据多重阵列确定的升高的细胞因子亚组(n = 5)的腹水浓度,通过商业上可获得的 ELISA 进行验证。这 5 种细胞因子的腹水水平在 38 名患者的队列中进一步通过 ELISA 进行评估。Kaplan-Meier 分析用于评估该队列中细胞因子表达与无进展生存期(PFS)的相关性。
我们观察到不同细胞因子之间的表达存在广泛的可变性,并且在测试的 10 份恶性腹水中,特定细胞因子的水平也存在差异。在 10 份腹水样本中,有 53 种(44%)细胞因子均未检测到。包括血管生成素、血管生成素-2、GRO、ICAM-1、IL-6、IL-6R、IL-8、IL-10、瘦素、MCP-1、MIF、NAP-2、骨保护素(OPG)、RANTES、TIMP-2 和 UPAR 等多种因子的水平在大多数恶性腹水中升高。OC 腹水中 OPG、IL-10 和瘦素的水平升高与较短的 PFS 相关。IL-10 被证明可促进恶性腹水的抗凋亡活性,而 OPG 则没有。
我们的数据表明,OC 腹水中存在复杂的细胞因子表达网络。对恶性腹水细胞因子谱进行特征描述,可以提供信息,从而确定关键功能细胞因子的优先级,并了解它们改变肿瘤细胞行为的机制。更深入地了解细胞因子网络对于确定腹水在 OC 进展中的作用至关重要。