Evidence map›Paper›PMID 35044655›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

In Vitro Cell Impedance Assay to Examine Antigen-Specific T-Cell-Mediated Melanoma Cell Killing to Support Cancer Immunotherapy Drug Discovery.

Elizabeth R Stirling, David R Soto-Pantoja

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

2 authors.

Elizabeth R StirlingDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
David R Soto-PantojaDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, NC, USA. dsotopan@wakehealth.edu.

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
TRAINING PROGRAM IN IMMUNOLOGY AND PATHOGENESIST32AI007401 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Martha Ann Alexander-Miller · 1991 to 2026
$4.4M
Redox Biology and Medicine Training ProgramT32GM127261 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FURDUI, CRISTINA MARIA, POOLE, LESLIE B · 2018 to 2022
$975k
NCI NIH HHS P30 CA012197NIAID NIH HHS T32 AI007401NIGMS NIH HHS T32 GM127261
6 · The paper itself

Abstract

The design of cancer immunotherapy drugs is essential for the continued investigation of novel drug regimens to improve responses and increase the survival of cancer patients. Methods to examine the interaction of effector immune cells with target cancer cells are limited by labor-intensive labeling that can be examined at specific time points. In this report, we examine an antigen-dependent model of effector cytotoxic (CD8+) T-cell-mediated cytotoxicity of target murine melanoma cells using a real-time cell impedance assay. The real-time monitoring allows measurement of viability and kinetics, allowing for a better understanding of effector/target cell interactions to support drug discovery.

Indexed as

MelanomaT-LymphocytesAnimalsCD8-Positive T-LymphocytesCell DeathCytotoxicity, ImmunologicDrug DiscoveryElectric ImpedanceHumansImmunotherapyMiceT-Lymphocytes, CytotoxicCancerImmunotherapyT cell

Identifiers

PMID35044655
PMCPMC9094138

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.