Evidence map›Paper›PMID 42466012›Full record

ArticleAdvanced biosystems2018

Profiling Heterogeneous Circulating Tumor Cells (CTC) Populations in Pancreatic Cancer Using a Serial Microfluidic CTC Carpet Chip.

Mina Zeinali, Vasudha Murlidhar, Shamileh Fouladdel, Shimeng Shao, Lili Zhao, Heather Cameron, Armand Bankhead, Jiaqi Shi, Kyle C Cuneo, Vaibhav Sahai and 5 more

Abstract read
In one paragraph

Article in Advanced biosystems, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Cell Separations and Sorting.Analytical chemistry · 2020
    Review
  8. Article
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

15 authors.

Mina ZeinaliDepartment of Chemical Engineering and Biointerfaces Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.
Vasudha MurlidharDepartment of Chemical Engineering and Biointerfaces Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.
Shamileh FouladdelBiointerfaces Institute University of Michigan 2800 Plymouth Road, NCRC Ann Arbor MI 48109 USA.
Shimeng ShaoDepartment of Chemical Engineering and Biointerfaces Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.
Lili ZhaoBiostatistics Department University of Michigan Ann Arbor MI 48109 USA.
Heather CameronDepartment of Surgery and Molecular and Integrative Physiology University of Michigan 1500 E. Medical Center Drive, 2210B Taubman Center Ann Arbor MI 48109 USA.
Armand BankheadBiostatistics Department University of Michigan Ann Arbor MI 48109 USA.
Jiaqi ShiDepartment of Pathology University of Michigan Ann Arbor MI 48109 USA.
Kyle C CuneoDepartment of Radiation Oncology University of Michigan Ann Arbor MI 48109 USA.
Vaibhav SahaiDepartment of Internal Medicine University of Michigan Ann Arbor MI 48109 USA.
Ebrahim AziziBiointerfaces Institute University of Michigan 2800 Plymouth Road, NCRC Ann Arbor MI 48109 USA.
Max S WichaBiointerfaces Institute University of Michigan 2800 Plymouth Road, NCRC Ann Arbor MI 48109 USA.
Mathias HafnerInstitute for Medical Technology of Heidelberg University & University of Applied Sciences Mannheim Mannheim 68163 Germany.
Diane M SimeoneDepartment of Surgery and Molecular and Integrative Physiology University of Michigan 1500 E. Medical Center Drive, 2210B Taubman Center Ann Arbor MI 48109 USA.
Sunitha NagrathDepartment of Chemical Engineering and Biointerfaces Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.ORCID https://orcid.org/0000-0002-1497-7977

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
Engineering sensitive microfluidic multiplex technology for isolating circulatingDP2OD006672 · OD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NAGRATH, SUNITHA · 2009 to 2009
$2.1M
NCI NIH HHS P30 CA046592NIH HHS DP2 OD006672
6 · The paper itself

Abstract

Although isolation of circulating tumor cells (CTCs) from pancreatic adenocarcinoma patients is feasible, investigating their clinical utility has proven less successful than other cancers due to the limitations of epithelial cellular adhesion molecule (EpCAM)-only based CTC assays. An integrated technology- and biology-based approach using a microfluidic "Carpet Chip" is presented to study the biological relevance of heterogeneous CTC populations. Both epithelial CTCs (EpCs) and epithelial-to-mesenchymal transition (EMT)-like CTCs (EMTCs) are isolated simultaneously from the whole blood of pancreatic cancer (PaCa) patients (

Indexed as

circulating tumor cells (CTCs)EMT‐like CTCs (EMTCs)epithelial‐to‐mesenchymal transition (EMT)microfluidicspancreatic cancer

Identifiers

PMID42466012
PMCPMC13373840

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.