Wang Shuyi, Zhang Chunxiao, Wang Guozhou, Cheng Boran, Wang Yulei, Chen Fangfang, Chen Yuanyuan, Feng Maohui, Xiong Bin
Department of Oncology, Zhongnan Hospital of Wuhan University; Hubei Key Laboratory of Tumor Biological Behaviors & Hubei Cancer Clinical Study Center, Wuhan 430071, P. R. China;
Department of Oncology, Zhongnan Hospital of Wuhan University; Hubei Key Laboratory of Tumor Biological Behaviors & Hubei Cancer Clinical Study Center, Wuhan 430071, P. R. China;; Department of Oncology, Peking University Shenzhen Hospital, No. 1120, Lianhua Road, Futain District, Shenzhen 518036, Guangdong Province, P. R. China.
Theranostics. 2016 Aug 7;6(11):1877-86. doi: 10.7150/thno.15284. eCollection 2016.
Circulating tumor cells (CTCs) have been considered as the origin of cancer metastasis. Thus, detection of CTCs in peripheral blood is of great value in different types of solid tumors. However, owing to extremely low abundance of CTCs, detection of them has been technically challenging. To establish a simple and efficient method for CTCs detection in patients with hepatocellular carcinoma (HCC), we applied biocompatible and transparent HA/CTS (Hydroxyapatite/chitosan) nanofilm to achieve enhanced topographic interactions with nanoscale cellular surface components, and we used sLex-AP (aptamer for carbohydrate sialyl Lewis X) to coat onto HA/CTS nanofilm for efficient capture of HCC CTCs, these two functional components combined to form our CTC-(BioT)Chip platform. Using this platform, we realized HCC CTCs' capture and identification, the average recovery rate was 61.6% or more at each spiking level. Importantly, our platform identified CTCs (2±2 per 2 mL) in 25 of 42 (59.5%) HCC patients. Moreover, both the positivity rate and the number of detected CTCs were significantly correlated with tumor size, portal vein tumor thrombus, and the TNM (tumor-node-metastasis) stage. In summary, our CTC-(BioT)Chip platform provides a new method allowing for simple but efficient detection of CTCs in HCC patients, and it holds potential of clinically usefulness in monitoring HCC prognosis and guiding individualized treatment in the future.
循环肿瘤细胞(CTCs)被认为是癌症转移的起源。因此,在外周血中检测CTCs在不同类型的实体瘤中具有重要价值。然而,由于CTCs的丰度极低,对其进行检测在技术上具有挑战性。为了建立一种简单有效的检测肝细胞癌(HCC)患者CTCs的方法,我们应用了生物相容性和透明的HA/CTS(羟基磷灰石/壳聚糖)纳米膜,以增强与纳米级细胞表面成分的形貌相互作用,并使用sLex-AP(用于sLex-AP(碳水化合物唾液酸化路易斯X适配体)包被在HA/CTS纳米膜上,以有效捕获HCC CTCs,这两种功能成分结合形成了我们的CTC-(BioT)芯片平台。使用该平台,我们实现了HCC CTCs的捕获和鉴定,每个加标水平的平均回收率均在61.6%或更高。重要的是,我们的平台在42例HCC患者中的25例(59.5%)中鉴定出了CTCs(每2 mL 2±2个)。此外,检测到的CTCs的阳性率和数量均与肿瘤大小、门静脉癌栓以及TNM(肿瘤-淋巴结-转移)分期显著相关。总之,我们的CTC-(BioT)芯片平台提供了一种新方法,可简单有效地检测HCC患者的CTCs,并且在未来监测HCC预后和指导个体化治疗方面具有临床应用潜力。