基于加权酶芯片阵列的自动芯片球装置检测外周血治疗靶点KRAS突变体的新技术

Suz-Kai Hsiung , Hui-Jen Chang , Ming-Je Yang , Ming-Sung Chang , Der-An Tsao , Hua-Hsien Chiu , Yi-Fang Chen , Tian-Lu Cheng , Shiu-Ru Lin
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引用次数: 7

摘要

逆转录酶和实时聚合酶链反应被广泛用于基因过表达的检测。然而,当需要检测多个遗传靶点时,会出现各种缺点和局限性。在前期研究中,我们实验室成功建立了一种带有诊断生物芯片的膜阵列操作平台,用于筛选肿瘤患者循环肿瘤细胞的基因过表达。为了有效缩短反应时间,我们对传统的RNA提取方法进行了改进。在芯片阵列读取过程中引入权重概念,建立了加权酶芯片阵列平台。我们利用流体工程技术开发了全自动基因芯片分析仪Chipball,该分析仪在WEnCA平台上自动运行。这两个系统的组合被命名为WEnCA-Chipball系统。为了了解WEnCA-Chipball和WEnCA-manual操作的实际差异,我们使用WEnCA-manual分析了200例癌症患者样本中KRAS相关基因的过表达,以建立激活KRAS检测芯片的截止值。具体而言,采用WEnCA-manual和WEnCA-Chipball对209例肺癌患者血液样本中活化的KRAS表达进行分析和比较。定义WEnCAChipball的临床适用性,包括敏感性、特异性和准确性。结果显示,209例患者中,71例患者WEnCA-Chipball阳性KRAS活化表达,敏感性89%,特异性94%,准确性92%。此外,《WEnCA-Chipball》的平均总分比《WEnCA-manual》低4.7分。WEnCA-Chipball只需要7.5小时的操作时间,大约是wenca -手动操作时间的九分之一,成本是wenca -手动操作时间的五分之一。两种系统的检测限无显著差异。这方面已经取得了很大的进展。WEnCA-Chipball操作系统具有临床应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Novel Technique for Detecting the Therapeutic Target, KRAS Mutant, From Peripheral Blood Using the Automatic Chipball Device With Weighted Enzymatic Chip Array

Reverse transcriptase and real-time polymerase chain reactions are widely used for the detection of gene overexpression. However, various disadvantages and limitations arise when the detection of multiple genetic targets is required. In previous studies, our laboratory successfully established a membrane array operation platform with a diagnostic biochip for the screening of gene overexpression by circulating tumor cells in cancer patients. To effectively shorten the reaction time, we improved the conventional RNA extraction method. The concept of weightedness was included in the reading procedure of the chip array and a weighted enzymatic chip array (WEnCA) platform was established. We used fluid engineering to develop a fully automatic gene chip analyzer named Chipball, which runs automatically on the WEnCA platform. The combination of the two systems is named the WEnCA-Chipball system. To understand the actual differences between the operations of WEnCA-Chipball and WEnCA-manual, we used the WEnCA-manual to analyze KRAS-associated gene overexpression in 200 samples from cancer patients to establish a cutoff value for activating the KRAS Detection Chip. Specifically, the activated KRAS expression in blood samples of 209 lung cancer patients was analyzed by both WEnCA-manual and WEnCA-Chipball and compared. The clinical applicability of WEnCAChipball was defined, including the sensitivity, specificity, and accuracy. The results showed that among 209 samples, 71 patients were positive for activated KRAS expression by WEnCA-Chipball with a sensitivity of 89%, specificity of 94%, and accuracy of 92%. In addition, the average total score of WEnCA-Chipball was 4.7 lower than that of the WEnCA-manual. The WEnCA-Chipball required an operation time of only 7.5 hours, approximately one-ninth of the WEnCA-manual operation time and one-fifth of the cost of WEnCA-manual. No significant difference was found between the detection limitations of the two systems. Great strides have been made in this development. The WEnCA-Chipball operation system has potential for clinical applications.

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