Quantified postsurgical small cell size CFCs and EpCAM+ circulating tumor stem cells with cytogenetic abnormalities in hepatocellular carcinoma patients determine cancer relapse
Quantified postsurgical small cell size CFCs and EpCAM+ circulating tumor stem cells with cytogenetic abnormalities in hepatocellular carcinoma patients determine cancer relapse
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DOI:
10.1016/j.canlet.2017.10.004
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发表时间:
2018-01-01
期刊:
影响因子:
9.7
通讯作者:
Dong, Jiahong
中科院分区:
文献类型:
--
作者:
Wang, Liang;Li, Yilin;Dong, Jiahong
Detection of hepatocellular carcinoma circulating tumor cells performed with conventional strategies, is significantly limited due to inherently heterogeneous and dynamic expression of EpCAM, as well as degradation of cytokeratins during epithelial-to-mesenchymal transition, which inevitably lead to non negligible false negative detection of such "uncapturable and invisible" CTCs. A novel SE-iFISH strategy, improved for detection of HCC CTCs in this study, was applied to comprehensively detect, in situ phenotypically and karyotypically characterize hepatocellular and cholangiocarcinoma CTCs (CD45(-)/CD31(-)) in patients subjected to surgical resection. Clinical significance of diverse subtypes of CTC was systematically investigated. Existence of small cell size CFCs (= 5 cells/6 ml blood), multiploid (>= pentasomy 8) CTSCs or CTM (either one >= 1) significantly correlated to HCC patients' poor prognosis, indicating that detection of those specific subtypes of CFCs and CTSCs in post-operative patients help predict neoplasm recurrence. (C) 2017 The Authors. Published by Elsevier B.V.