循环肿瘤细胞
肺癌
枚举
分离(微生物学)
腺癌
癌症
肺
染色
医学
肿瘤科
病理
癌症研究
内科学
生物
生物信息学
转移
数学
组合数学
作者
Volga M Saini,Ezgi Öner,Mark P. Ward,Sinéad Hurley,Brian E. Henderson,F. Park Lewis,Stephen Finn,John O’Leary,Sharon O’Toole,Lorraine O’Driscoll,Kathy Gately
标识
DOI:10.1101/2024.02.05.578972
摘要
Abstract Circulating tumor cells (CTCs) have potential as diagnostic, prognostic and predictive biomarkers in solid tumors. Despite FDA approval of CTC devices in various cancers, their rarity and limited comparison between analysis methods hinder their clinical integration for lung cancer. This study aimed to evaluate five CTC isolation technologies using a standardized spike-in protocol: the CellMag™ (EpCAM-based enrichment), EasySep™ and RosetteSep™ (blood cell depletion), and the Parsortix® PR1 and next generation Parsortix® Plus (PX+) (size-based enrichment). The Parsortix® systems were also evaluated for any difference in recovery rates between cell harvest versus in- cassette staining. Healthy donor blood (5 mL) was spiked with 100 fluorescently labeled H1975 lung adenocarcinoma cell line, processed through each system and the isolation efficiency was calculated. All tested systems yielded discordant recovery rates with the CellMag™ having the highest mean recovery (70 ± 14%) followed by the PR1 (in-cassette staining) with a recovery of 49 ± 2% while the EasySep™ had the lowest recovery (18 ± 8%). The CellMag™ and Parsortix® PR1 may have potential clinical applications for lung cancer patients, albeit needing further optimization and validation.
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