Evidence map›Paper›PMID 32231230›Full record

ArticleScientific reports2020

Identification of Small Molecule Enhancers of Immunotherapy for Melanoma.

Christopher Dextras, Myagmarjav Dashnyam, Lesley A Mathews Griner, Janani Sundaresan, Bryan Chim, Zhiya Yu, Suman Vodnala, Chyi-Chia Richard Lee, Xin Hu, Noel Southall and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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  5. Review
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

16 authors at 3 institutions in 1 country.

Christopher DextrasDivision of Preclinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health, Rockville, Maryland, USA.ORCID http://orcid.org/0000-0002-3070-6106
Myagmarjav DashnyamDivision of Preclinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health, Rockville, Maryland, USA.ORCID http://orcid.org/0000-0003-2307-3002
Lesley A Mathews GrinerDivision of Preclinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health, Rockville, Maryland, USA.
Janani SundaresanDivision of Preclinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health, Rockville, Maryland, USA.
Bryan ChimLaboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, USA.
Zhiya YuCenter for Cancer Research, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Suman VodnalaCenter for Cancer Research, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Chyi-Chia Richard LeeCenter for Cancer Research, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Xin HuDivision of Preclinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health, Rockville, Maryland, USA.
Noel SouthallDivision of Preclinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health, Rockville, Maryland, USA.
Juan J MaruganDivision of Preclinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health, Rockville, Maryland, USA.
Ajit JadhavDivision of Preclinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health, Rockville, Maryland, USA.
Nicholas P RestifoCenter for Cancer Research, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Nicolas AcquavellaCenter for Cancer Research, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Marc FerrerDivision of Preclinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health, Rockville, Maryland, USA. marc.ferrer@nih.gov.
Anju SinghDivision of Preclinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health, Rockville, Maryland, USA. anju.singh@nih.gov.
National Institutes of Health · USNational Cancer Institute · USNational Institute of Allergy and Infectious Diseases · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small molecule based targeted therapies for the treatment of metastatic melanoma hold promise but responses are often not durable, and tumors frequently relapse. Response to adoptive cell transfer (ACT)-based immunotherapy in melanoma patients are durable but patients develop resistance primarily due to loss of antigen expression. The combination of small molecules that sustain T cell effector function with ACT could lead to long lasting responses. Here, we have developed a novel co-culture cell-based high throughput assay system to identify compounds that could potentially synergize or enhance ACT-based immunotherapy of melanoma. A BRAF

Indexed as

CD8-Positive T-LymphocytesCell Line, TumorCoculture TechniquesDrug Screening Assays, AntitumorHigh-Throughput Screening AssaysHumansImmunologic FactorsImmunotherapyImmunotherapy, AdoptiveMelanomaNeoplasm Recurrence, LocalProto-Oncogene Proteins B-rafImmunologic FactorsProto-Oncogene Proteins B-raf

Identifiers

PMID32231230
PMCPMC7105471
OpenAlexW3013557685

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.