Evidence map›Paper›PMID 33420321›Full record

ArticleCommunications biology2021

A biomimetic assay platform for the interrogation of antigen-dependent anti-tumor T-cell function.

Jeremy To, Doug Quackenbush, Emily Rowell, Lilin Li, Connor Reed, Frederick Lo, Shane R Horman

RetractedAbstract readEvaluation StudyRetracted Publication
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Jeremy ToDepartment of Functional Genomics, Genomics Institute of the Novartis Research Foundation (GNF), San Diego, CA, USA.
Doug QuackenbushDepartment of Online Screening, Genomics Institute of the Novartis Research Foundation (GNF), San Diego, CA, USA.
Emily RowellDepartment of Cancer Therapeutics, Genomics Institute of the Novartis Research Foundation (GNF), San Diego, CA, USA.
Lilin LiDepartment of Cancer Therapeutics, Genomics Institute of the Novartis Research Foundation (GNF), San Diego, CA, USA.
Connor ReedDepartment of Biotherapeutics and Biotechnology, Genomics Institute of the Novartis Research Foundation (GNF), San Diego, CA, USA.
Frederick LoDepartment of Cheminformatics, Genomics Institute of the Novartis Research Foundation (GNF), San Diego, CA, USA.
Shane R HormanDepartment of Functional Genomics, Genomics Institute of the Novartis Research Foundation (GNF), San Diego, CA, USA. shane.horman@takeda.com.ORCID http://orcid.org/0000-0003-2513-5721

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overcoming tumor-mediated immunosuppression and enhancing cytotoxic T-cell activity within the tumor microenvironment are two central goals of immuno-oncology (IO) drug discovery initiatives. However, exploratory assays involving immune components are often plagued by low-throughput and poor clinical relevance. Here we present an innovative ultra-high-content assay platform for interrogating T-cell-mediated killing of 3D multicellular tumor spheroids. Employing this assay platform in a chemical genomics screen of 1800 annotated compounds enabled identification of small molecule perturbagens capable of enhancing cytotoxic CD8

Indexed as

Antigen PresentationAntigens, NeoplasmBiological AssayBiomimeticsCoculture TechniquesDrug DiscoveryNeoplasmsSpheroids, CellularT-LymphocytesTumor Cells, CulturedAntigens, Neoplasm

Identifiers

PMID33420321
PMCPMC7794535

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.