Evidence map›Paper›PMID 35664056›Full record

ArticleTheranostics2022

Continuous centrifugal microfluidics (CCM) isolates heterogeneous circulating tumor cells via full automation.

Hyeong Jung Woo, Seung-Hoon Kim, Hyo Jung Kang, Soo-Hwan Lee, Seung Joon Lee, Jong Man Kim, Ogan Gurel, Soo Yeol Kim, Hye Ran Roh, Jungmin Lee and 14 more

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.5field-weighted citation impact, top 6% of its field
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

13 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
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

24 authors at 5 institutions in 1 country.

Hyeong Jung WooDepartment of New Biology, DGIST, Daegu 42988, Korea.
Seung-Hoon KimCTCELLS Inc., 206-C, R7, DGIST, Daegu 42988, Korea.
Hyo Jung KangCTCELLS Inc., 206-C, R7, DGIST, Daegu 42988, Korea.
Soo-Hwan LeeJE-UK Institute for Cancer Research, JEUK Co. Ltd., Gumi-si 39418, Korea.
Seung Joon LeeCTCELLS Inc., 206-C, R7, DGIST, Daegu 42988, Korea.
Jong Man KimCTCELLS Inc., 206-C, R7, DGIST, Daegu 42988, Korea.
Ogan GurelCTCELLS Inc., 206-C, R7, DGIST, Daegu 42988, Korea.
Soo Yeol KimDepartment of New Biology, DGIST, Daegu 42988, Korea.
Hye Ran RohCTCELLS Inc., 206-C, R7, DGIST, Daegu 42988, Korea.
Jungmin LeeCTCELLS Inc., 206-C, R7, DGIST, Daegu 42988, Korea.
Yeonsoo ParkDepartment of New Biology, DGIST, Daegu 42988, Korea.
Hyun Young ShinCTCELLS Inc., 206-C, R7, DGIST, Daegu 42988, Korea.
Yong-Il ShinResearch Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Korea.
Sun Min LeeDepartment of Rehabilitation Medicine, Pusan National University School of Medicine, Yangsan 50612, Korea.
So Yeon OhMedical Oncology & Hematology, Department of Internal Medicine, Pusan National University Yangsan Hospital, Yangsan 50612, Korea.
Young Zoon KimDivision of Neurooncology and Department of Neurosurgery, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon 51353, Korea.
Jung-Il ChaeDepartment of Dental Pharmacology, School of Dentistry, Jeonbuk National University, Jeonju 54896, Korea.
Seoyoung LeeDivision of Medical Oncology, Department of Internal Medicine, Yonsei University College of Medicine, Gangnam Severance Hospital, Seoul 06273, Korea.
Min Hee HongDivision of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul 03722, Korea.
Byoung Chul ChoDivision of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul 03722, Korea.
Eun Sook LeeCenter for Breast Cancer, National Cancer Center, Goyang 10408, Korea.
Klaus PantelInstitute of Tumour Biology, University Medical Centre Hamburg-Eppendorf, Hamburg 20246, Germany.
Hye Ryun KimDivision of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul 03722, Korea.
Minseok S KimDepartment of New Biology, DGIST, Daegu 42988, Korea.
Daegu Gyeongbuk Institute of Science and Technology · KRYonsei University · KRJeonbuk National University · KRNational Cancer Center · KRPusan National University Yangsan Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding cancer heterogeneity is essential to finding diverse genetic mutations in metastatic cancers. Thus, it is critical to isolate all types of CTCs to identify accurate cancer information from patients. Moreover, full automation robustly capturing the full spectrum of CTCs is an urgent need for CTC diagnosis to be routine clinical practice.

Indexed as

Neoplastic Cells, CirculatingAutomationCell Line, TumorCell SeparationEpithelial Cell Adhesion MoleculeErbB ReceptorsHumansMicrofluidicsEpithelial Cell Adhesion MoleculeErbB Receptorscancer heterogeneitycirculating tumor cellscontinuous centrifugal microfluidicsfull automationunbiased isolation

Identifiers

PMID35664056
PMCPMC9131262
OpenAlexW4285136821

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.