Literature DB >> 29235843

Self-Sterilizing and Regeneratable Microchip for the Precise Capture and Recovery of Viable Circulating Tumor Cells from Patients with Cancer.

Lanlan Hui1,2, Yi Su1,2, Tingting Ye1,2, Zhao Liu, Qingchang Tian1,2, Chuanjiang He1,2, Yueqi Zhao, Pu Chen3, Xiaojia Wang4, Weidong Han5, Yan Luo6, Ben Wang1,2.   

Abstract

Cancer cells metastasize and are transported in the bloodstream, easily reaching any site in the body through the blood circulation. A method designed to assess the number of circulating tumor cells (CTCs) should be validated as a clinical tool for predicting the response to therapy and monitoring the disease progression in patients with cancer. Although CTCs are detectable in many cases, they remain unavailable for clinic usage because of their high testing cost, tedious operation, and poor clinical relevance. Herein, we developed a regeneratable microchip for isolating CTCs, which is available for robust cell heterogeneity assays on-site without the need for a sterile environment. The ivy-like hierarchical roughened zinc oxide (ZnO) nanograss interface was synthesized and directly integrated into the microfluidic devices and enables effective CTC capture and flexible, nontoxic CTC release during incubation in a mildly acidic solution, thus enabling cellular and molecular analyses. The microchip can be regenerated and recycled to capture CTCs with the remaining ZnO without affecting the efficiency, even after countless cycles of cell release. Moreover, microbial infection is avoided during its storage, distribution, and even in the open space usage, which ideally appeals to the demands of point-of-care (POC) and home testing and meets to the requirements for blood examinations in undeveloped or resource-limited settings. Furthermore, the findings generated using this platform based on the cocktail of antiepithelial cell adhesion molecule and antivimentin antibodies indicate that CTC capture was more precise and reasonable for patients with advanced cancer.

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Keywords:  antibacterial; circulating tumor cells (CTCs); epithelial to mesenchymal transition (EMT); polydimethylsiloxane (PDMS); recyclable; zinc oxide

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Year:  2017        PMID: 29235843     DOI: 10.1021/acsami.7b15406

Source DB:  PubMed          Journal:  ACS Appl Mater Interfaces        ISSN: 1944-8244            Impact factor:   9.229


  2 in total

1.  3D microfluidic in vitro model and bioinformatics integration to study the effects of Spatholobi Caulis tannin in cervical cancer.

Authors:  Nijia Wang; Jiayi Wang; Xiansheng Meng; Yongrui Bao; Shuai Wang; Tianjiao Li
Journal:  Sci Rep       Date:  2018-08-16       Impact factor: 4.379

2.  ARHGAP10 inhibits the epithelial-mesenchymal transition of non-small cell lung cancer by inactivating PI3K/Akt/GSK3β signaling pathway.

Authors:  Lan-Lan Lin; Fan Yang; Dong-Huan Zhang; Cong Hu; Sheng Yang; Xiang-Qi Chen
Journal:  Cancer Cell Int       Date:  2021-06-26       Impact factor: 5.722

  2 in total

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