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微流控芯片检测肺癌患者循环肿瘤细胞的临床意义。

Clinical significance of circulating tumor cells from lung cancer patients using microfluidic chip.

机构信息

Center of Laboratory Medicine, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, China.

Vip Ward, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, China.

出版信息

Clin Exp Med. 2018 May;18(2):191-202. doi: 10.1007/s10238-018-0485-6. Epub 2018 Feb 14.

Abstract

Circulating tumor cells (CTCs) exist in the peripheral blood and have an important role in the disease development, tumor metastasis and clinical surveillance, especially in the process of metastasis. However, the technology of detecting CTCs still had a large challenge since they were rare in the peripheral blood. Here, we developed a size-based microfluidic chip, which contained array and filter channel array that could enrich CTCs from blood samples more quickly and conveniently. Combined with clinical specimen, we analyzed CTCs in 200 lung cancer patients by this microfluidic chip. The microfluidic device has high specificity and sensitivity in detecting CTCs (86.0% sensitivity and 98% specificity). Furthermore, the number of CTCs showed a increasing trend according to the stage of the disease (the mean number of I stage 5.0 ± 5.121 versus II stage 8.731 ± 6.36 versus III stage 16.81 ± 9.556 versus IV stage 28.72 ± 17.39 cells/mL, P < 0.05). The number of CTCs was concurrent with the condition of pathological type and metastasis patients. Compared to conventional markers like CEA, CY211, SCC, CTCs showed a higher positive rate in diagnosed patients. The advanced microfluidic device could capture tumor cells without reliance on cell surface expression markers and provide a fast, convenient, economical method in detecting CTCs, thereby offering potential to design effective and individualized cancer therapies.

摘要

循环肿瘤细胞(CTCs)存在于外周血液中,在疾病发展、肿瘤转移和临床监测中具有重要作用,尤其是在转移过程中。然而,由于外周血中 CTC 数量稀少,检测 CTC 的技术仍然存在很大的挑战。在这里,我们开发了一种基于尺寸的微流控芯片,该芯片包含阵列和过滤通道阵列,可以更快速、更方便地从血液样本中富集 CTC。我们结合临床标本,通过这种微流控芯片分析了 200 例肺癌患者的 CTC。微流控装置在检测 CTC 方面具有很高的特异性和灵敏度(86.0%的灵敏度和 98%的特异性)。此外,根据疾病的分期,CTCs 的数量呈上升趋势(I 期的平均数量为 5.0±5.121 个,II 期为 8.731±6.36 个,III 期为 16.81±9.556 个,IV 期为 28.72±17.39 个/毫升,P<0.05)。CTCs 的数量与病理类型和转移患者的情况相一致。与 CEA、CY211、SCC 等常规标志物相比,CTCs 在诊断患者中具有更高的阳性率。这种先进的微流控装置可以在不依赖于细胞表面表达标志物的情况下捕获肿瘤细胞,为 CTC 的检测提供了快速、方便、经济的方法,从而为设计有效的个体化癌症治疗方法提供了潜力。

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