Evidence map›Paper›PMID 28198402›Full record

ArticleScientific reports2017

An integrated microfluidic device for rapid and high-sensitivity analysis of circulating tumor cells.

Jianing Jiang, Hui Zhao, Weiliang Shu, Jing Tian, Yuqing Huang, Yongxin Song, Ruoyu Wang, Encheng Li, Dennis Slamon, Dongmei Hou and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed.

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  8. Circulating tumor cells in colorectal cancer in the era of precision medicine.Journal of molecular medicine (Berlin, Germany) · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Jianing JiangDepartment of Respiratory Medicine, The Second Hospital Affiliated to Dalian Medical University, Dalian 116027, China.
Hui ZhaoDepartment of Respiratory Medicine, The Second Hospital Affiliated to Dalian Medical University, Dalian 116027, China.
Weiliang ShuShenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Jing TianDepartment of Respiratory Medicine, The Second Hospital Affiliated to Dalian Medical University, Dalian 116027, China.
Yuqing HuangLABVIV Technology(Shenzhen) Co., Ltd, Shenzhen 518055, China.
Yongxin SongCollege of Marine Engineering, Dalian Maritime University, Dalian 116026, China.
Ruoyu WangDepartment of Respiratory Medicine, Affiliated Zhongshan Hospital of Dalian University, Dalian 116001, China.
Encheng LiDepartment of Respiratory Medicine, The Second Hospital Affiliated to Dalian Medical University, Dalian 116027, China.
Dennis SlamonDepartment of Medicine, Division of Hematology Oncology, Medical School of University of California at Los Angeles, Los Angeles 90095, CA, USA.
Dongmei HouDepartment of Medicine, Division of Hematology Oncology, Medical School of University of California at Los Angeles, Los Angeles 90095, CA, USA.
Xiaohui DuDepartment of Respiratory Medicine, The Second Hospital Affiliated to Dalian Medical University, Dalian 116027, China.
Lichuan ZhangDepartment of Respiratory Medicine, Affiliated Zhongshan Hospital of Dalian University, Dalian 116001, China.
Yan ChenShenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Qi WangDepartment of Respiratory Medicine, The Second Hospital Affiliated to Dalian Medical University, Dalian 116027, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently there has been a more focus on the development of an efficient technique for detection of circulating tumor cells (CTCs), due to their significance in prognosis and therapy of metastatic cancer. However, it remains a challenge because of the low count of CTCs in the blood. Herein, a rapid and high-sensitivity approach for CTCs detection using an integrated microfluidic system, consisting of a deterministic lateral displacement (DLD) isolating structure, an automatic purifying device with CD45-labeled immunomagnetic beads and a capturing platform coated with rat-tail collagen was reported. We observed high capture rate of 90%, purity of about 50% and viability of more than 90% at the high throughput of 1 mL/min by capturing green fluorescent protein (GFP)-positive cells from blood. Further capturing of CTCs from metastatic cancers patients revealed a positive capture rate of 83.3%. Furthermore, our device was compared with CellSearch system via parallel analysis of 30 cancer patients, to find no significant difference between the capture efficiency of both methods. However, our device displayed advantage in terms of time, sample volume and cost for analysis. Thus, our integrated device with sterile environment and convenient use will be a promising platform for CTCs detection with potential clinical application.

Indexed as

Lab-On-A-Chip DevicesMicrofluidic Analytical TechniquesAgedAged, 80 and overBiomarkersCase-Control StudiesCell Line, TumorCell SurvivalCombined Modality TherapyFemaleFluorescent Antibody TechniqueHumansMaleMicroscopy, FluorescenceMiddle AgedNeoplasmsBiomarkers

Identifiers

PMID28198402
PMCPMC5309797

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.