参灵兰介导的局灶黏附激酶途径抑制卵巢癌细胞迁移的临床和生物学意义

S. Owen, F. Ruge, Yunong Gao, Ying Yang, Jianli Hou, Jian Chen, J. Lane, Yongshan Gao, Hongtao Wang, Cong Wei, Yiling Wu, W. Jiang
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摘要

自20世纪70年代以来,英国卵巢癌的发病率增加了近20%,大多数病例直到晚期才被诊断出来,这时转移更有可能发生。焦点黏附激酶(FAK)是细胞迁移不可或缺的关键蛋白复合物之一,与多种实体肿瘤有关。参灵兰(SLDM)是一种传统的中草药,已被配制用于治疗实体肿瘤。本研究旨在确定SLDM对体外卵巢癌细胞中FAK的影响以及卵巢癌队列中FAK的转录水平。使用基于Kinexus™抗体的蛋白阵列鉴定SLDM治疗刺激的FAK和paxillin磷酸化事件。使用电细胞-基质阻抗传感(ECIS)评估SLDM对细胞附着和迁移的影响,同时使用免疫荧光评估局灶粘附复合物定位的变化。在卵巢癌队列中,FAK和paxillin转录物水平的差异根据关键临床参数(如分化、分期和生存结果)进行了评估。SLDM对卵巢癌细胞的体外处理导致FAK和paxillin在几个位点的磷酸化受到抑制,这似乎表现为一系列永生化卵巢癌细胞的细胞附着和迁移减少。在高级别和低分化的卵巢肿瘤以及卵巢癌相关患者的肿瘤中观察到FAK和paxillin转录本副本的增加。SLDM对卵巢癌细胞的迁移和粘附特性有深远的影响,可能是通过抑制FAK通路的激活来实现的,而FAK通路在临床卵巢癌中是异常的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The clinical and biological implications of the focal adhesion kinase pathway in ShenLingLan mediated suppression of cellular migration of ovarian cancer cells
The incidence of ovarian cancer in the UK has increased by almost twenty percent since the 1970’s and the majority of cases are not diagnosed until the late stages, when metastasis is more likely to have occurred. Focal Adhesion Kinase (FAK) is one of the key protein complexes which is integral to cell migration and has been linked to a variety of solid tumours. ShenLingLan (SLDM) is a traditional herbal medicine which has been formulated for the treatment of solid tumours. This study aimed to establish the impact of SLDM on FAK in ovarian cancer cells in vitro and transcript levels of FAK in an ovarian cancer cohort. FAK and paxillin phosphorylation events stimulated by SLDM treatment were identified using a Kinexus™ antibody based protein array. The impact of SLDM on cell attachment and migration was evaluated using Electric cell-substrate impedance sensing (ECIS), whilst the changes in focal adhesion complex localisation were assessed using immunofluorescence. In an ovarian cancer cohort, differences in FAK and paxillin transcript levels were assessed against key clinical parameters such as differentiation, stage and survival outcome. SLDM treatment of ovarian cancer cells in vitro resulted in the suppression of FAK and paxillin phosphorylation at several sites, which appeared to manifest as decreased cellular attachment and migration in a range of immortalised ovarian cancer cells. Increased FAK and paxillin transcript copies were observed in high grade and poorly differentiated ovarian tumours as well as in tumours from patients with ovarian cancer related incidence. SLDM has a profound effect on the migratory and adhesive properties of ovarian cancer cells, potentially via inhibitory effects on the activation of the FAK pathway, which is aberrant in clinical ovarian cancers.
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