Evidence map›Paper›PMID 34015194›Full record

ArticleAdvanced biology2021

Apoptotic Bodies in the Pancreatic Tumor Cell Culture Media Enable Label-Free Drug Sensitivity Assessment by Impedance Cytometry.

Carlos Honrado, Sara J Adair, John H Moore, Armita Salahi, Todd W Bauer, Nathan S Swami

Open access · greenAbstract read
In one paragraph

Article in Advanced biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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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.

Carlos HonradoElectrical & Computer Engineering, University of Virginia, Charlottesville, VA, 22904, USA.ORCID 0000-0002-4151-2147
Sara J AdairSurgery, School of Medicine, University of Virginia, Charlottesville, VA, 22904, USA.ORCID 0000-0002-9973-4252
John H MooreElectrical & Computer Engineering, University of Virginia, Charlottesville, VA, 22904, USA.ORCID 0000-0002-9696-233X
Armita SalahiElectrical & Computer Engineering, University of Virginia, Charlottesville, VA, 22904, USA.
Todd W BauerSurgery, School of Medicine, University of Virginia, Charlottesville, VA, 22904, USA.ORCID 0000-0002-9516-1848
Nathan S SwamiElectrical & Computer Engineering, University of Virginia, Charlottesville, VA, 22904, USA.ORCID 0000-0002-0492-1160
University of Virginia · US

Funding

The integrated Translational Health Research Institute of Virginia (iTHRIV): Using Data to Improve HealthUL1TR003015 · NCATS · UNIVERSITY OF VIRGINIA · PI BROWN, DONALD E, JOHNSTON, KAREN C. · 2019 to 2023
$20.3M
NCATS NIH HHS UL1 TR003015NCI NIH HHS L30 CA124093
6 · The paper itself

Abstract

The ability to rapidly and sensitively predict drug response and toxicity using in vitro models of patient-derived tumors is essential for assessing chemotherapy efficacy. Currently, drug sensitivity assessment for solid tumors relies on imaging adherent cells or by flow cytometry of cells lifted from drug-treated cultures after fluorescent staining for apoptotic markers. Subcellular apoptotic bodies (ABs), including microvesicles that are secreted into the culture media under drug treatment can potentially serve as markers for drug sensitivity, without the need to lift cells under culture. However, their stratification to quantify cell disassembly is challenging due to their compositional diversity, with tailored labeling strategies currently needed for the recognition and cytometry of each AB type. It is shown that the high frequency impedance phase versus size distribution of ABs determined by high-throughput single-particle impedance cytometry of supernatants in the media of gemcitabine-treated pancreatic tumor cultures exhibits phenotypic resemblance to lifted apoptotic cells and enables shape-based stratification within distinct size ranges, which is not possible by flow cytometry. It is envisioned that this tool can be applied in conjunction with the appropriate pancreatic tumor microenvironment model to assess drug sensitivity and toxicity of patient-derived tumors, without the need to lift cells from cultures.

Indexed as

Extracellular VesiclesPancreatic NeoplasmsPharmaceutical PreparationsCell Culture TechniquesCell Line, TumorElectric ImpedanceHumansTumor MicroenvironmentPharmaceutical Preparationsapoptosiscancercytometryextracellular vesiclesmicrofluidicspancreatic ductal adenocarcinoma

Identifiers

PMID34015194
PMCPMC8349864
OpenAlexW3160293344

What OpenQuestion holds

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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.