Evidence map›Paper›PMID 28982179›Full record

ArticlePloS one2017

A study of PD-L1 expression in KRAS mutant non-small cell lung cancer cell lines exposed to relevant targeted treatments.

Anna Minchom, Parames Thavasu, Zai Ahmad, Adam Stewart, Alexandros Georgiou, Mary E R O'Brien, Sanjay Popat, Jaishree Bhosle, Timothy A Yap, Johann de Bono and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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  11. The intracellular signalosome of PD-L1 in cancer cells.Signal transduction and targeted therapy
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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

11 authors at 3 institutions in 1 country.

Anna MinchomThe Lung Unit, Department of Medicine, The Royal Marsden, Sutton, United Kingdom.ORCID http://orcid.org/0000-0002-9339-7101
Parames ThavasuThe Drug Development Unit, The Institute of Cancer Research and The Royal Marsden, London, United Kingdom.
Zai AhmadThe Drug Development Unit, The Institute of Cancer Research and The Royal Marsden, London, United Kingdom.
Adam StewartThe Drug Development Unit, The Institute of Cancer Research and The Royal Marsden, London, United Kingdom.
Alexandros GeorgiouThe Drug Development Unit, The Institute of Cancer Research and The Royal Marsden, London, United Kingdom.
Mary E R O'BrienThe Lung Unit, Department of Medicine, The Royal Marsden, Sutton, United Kingdom.
Sanjay PopatThe Lung Unit, The Royal Marsden, London, United Kingdom.
Jaishree BhosleThe Lung Unit, Department of Medicine, The Royal Marsden, Sutton, United Kingdom.
Timothy A YapThe Drug Development Unit, The Institute of Cancer Research and The Royal Marsden, London, United Kingdom.
Johann de BonoThe Drug Development Unit, The Institute of Cancer Research and The Royal Marsden, London, United Kingdom.
Udai BanerjiThe Drug Development Unit, The Institute of Cancer Research and The Royal Marsden, London, United Kingdom.
Institute of Cancer Research · GBRoyal Marsden NHS Foundation Trust · GBRoyal Marsden Hospital · GB

Funding

Cancer Research UK 11566
6 · The paper itself

Abstract

We investigated PD-L1 changes in response to MEK and AKT inhibitors in KRAS mutant lung adenocarcinoma (adeno-NSCLC). PD-L1 expression was quantified using immunofluorescence and co-culture with a jurkat cell-line transfected with NFAT-luciferase was used to study if changes in PD-L1 expression in cancer cell lines were functionally relevant. Five KRAS mutant cell lines with high PD-L1 expression (H441, H2291, H23, H2030 and A549) were exposed to GI50 inhibitor concentrations of a MEK inhibitor (trametinib) and an AKT inhibitor (AZD5363) for 3 weeks. Only 3/5 (H23, H2030 and A549) and 2/5 cell lines (H441 and H23) showed functionally significant increases in PD-L1 expression when exposed to trametinib or AZD5363 respectively. PD-L1 overexpression is not consistent and is unlikely to be an early mechanism of resistance to KRAS mutant adeno-NSCLC treated with MEK or AKT inhibitors.

Indexed as

Genes, rasMutationB7-H1 AntigenCarcinoma, Non-Small-Cell LungCell Line, TumorCoculture TechniquesHumansLung NeoplasmsB7-H1 AntigenCD274 protein, human

Identifiers

PMID28982179
PMCPMC5628934
OpenAlexW2761835541

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.