Evidence map›Paper›PMID 30224472›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Functional profiling of circulating tumor cells with an integrated vortex capture and single-cell protease activity assay.

Manjima Dhar, Jeffrey Nam Lam, Tonya Walser, Steven M Dubinett, Matthew B Rettig, Dino Di Carlo

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

52 citing papers in PubMed, 132 citations in OpenAlex.

  1. Article
  2. Review
  3. Circulating Tumor Cells for the Monitoring of Lung Cancer Therapies.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Genetic and phenotypic profiling of single living circulating tumor cells from patients with microfluidics.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Review
  13. Article
  14. Liquid biopsy to personalize treatment for metastatic prostate cancer.American journal of translational research · 2024
    Review
  15. Review
  16. Article
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  19. Article
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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

6 authors at 1 institution in 1 country.

Manjima DharDepartment of Bioengineering, Samueli School of Engineering, University of California, Los Angeles, CA 90095.ORCID 0000-0003-1147-5450
Jeffrey Nam LamDepartment of Bioengineering, Samueli School of Engineering, University of California, Los Angeles, CA 90095.
Tonya WalserDepartment of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA 90095.
Steven M DubinettDepartment of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA 90095.
Matthew B RettigVA Greater Los Angeles Healthcare System, Los Angeles, CA 90073.
Dino Di CarloDepartment of Bioengineering, Samueli School of Engineering, University of California, Los Angeles, CA 90095; dicarlo@ucla.edu.
University of California, Los Angeles · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
The Boston University-UCLA Lung Cancer Biomarker Development LabU01CA214182 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ABERLE, DENISE R., DUBINETT, STEVEN M. · 2016 to 2021
$3.1M
Isolating circulating tumor cells using a centrifuge on a chipR33CA177456 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DI CARLO, DINO · 2013 to 2015
$719k
NCI NIH HHS P30 CA016042NCI NIH HHS R33 CA177456NCI NIH HHS U01 CA214182
6 · The paper itself

Abstract

Tumor cells are hypothesized to use proteolytic enzymes to facilitate invasion. Whether circulating tumor cells (CTCs) secrete these enzymes to aid metastasis is unknown. A quantitative and high-throughput approach to assay CTC secretion is needed to address this question. We developed an integrated microfluidic system that concentrates rare cancer cells >100,000-fold from 1 mL of whole blood into ∼50,000 2-nL drops composed of assay reagents within 15 min. The system isolates CTCs by size, exchanges fluid around CTCs to remove contaminants, introduces a matrix metalloprotease (MMP) substrate, and encapsulates CTCs into microdroplets. We found CTCs from prostate cancer patients possessed above baseline levels of MMP activity (1.7- to 200-fold). Activity of CTCs was generally higher than leukocytes from the same patient (average CTC/leukocyte MMP activity ratio, 2.6 ± 1.5). Higher MMP activity of CTCs suggests active proteolytic processes that may facilitate invasion or immune evasion and be relevant phenotypic biomarkers enabling companion diagnostics for anti-MMP therapies.

Indexed as

Cell SeparationLab-On-A-Chip DevicesMicrofluidic Analytical TechniquesA549 CellsCollagenasesHumansNeoplasm ProteinsNeoplastic Cells, CirculatingCollagenasesNeoplasm Proteinscell secretioncirculating tumor cellsliquid biopsymicrofluidicsprotease

Identifiers

PMID30224472
PMCPMC6176626
OpenAlexW2891295468

What OpenQuestion holds

Textmetadata
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.