Evidence map›Paper›PMID 35693293›Full record

ArticleTranslational lung cancer research2022

Elevated expression of miR-494-3p is associated with resistance to osimertinib in EGFR T790M-positive non-small cell lung cancer.

Dominika Kaźmierczak, Inger Johanne Zwicky Eide, Radosveta Gencheva, Yi Lai, Rolf Lewensohn, Georgios Tsakonas, Oscar Grundberg, Luigi de Petris, Marc McGowan, Odd Terje Brustugun and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Translational lung cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

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  13. Exosomal microRNA Therapy for Non-Small-Cell Lung Cancer.Technology in cancer research & treatment
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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

12 authors at 5 institutions in 2 countries.

Dominika Kaźmierczak *Department of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Inger Johanne Zwicky Eide *Section of Oncology, Drammen Hospital, Vestre Viken Hospital Trust, Drammen, Norway.
Radosveta GenchevaDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Yi LaiDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Rolf LewensohnDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Georgios TsakonasDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Oscar GrundbergThoracic Oncology Center, Karolinska University Hospital, Stockholm, Sweden.
Luigi de PetrisDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Marc McGowanSection of Cancer Genetics, Inst of Cancer Research, Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.
Odd Terje Brustugun *Section of Oncology, Drammen Hospital, Vestre Viken Hospital Trust, Drammen, Norway.
Simon Ekman *Department of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Per Hydbring *Department of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Karolinska Institutet · SEKarolinska University Hospital · SEDrammen Hospital · NONorwegian Cancer Society · NOUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Non-small cell lung cancer (NSCLC) harboring activating mutations in the gene encoding epidermal growth factor receptor ( Methods: We combined miRNA expression profiling with miRNA-inhibitory screening to identify miRNAs involved in conferring resistance to osimertinib. Finally, we validated our top miRNA candidate by profiling longitudinal plasma exosomal RNA from patients receiving osimertinib as second-line therapy in a clinical trial. Results: Various miRNAs displayed differential expression in parental versus osimertinib-refractory NSCLC cells. miRNA-inhibitory screening revealed miR-494-3p to partially confer resistance to osimertinib Conclusions: Our results highlight the need for further therapeutic exploration of miR-494-3p in

Indexed as

epidermal growth factor receptor (EGFR)microRNA (miRNA)Non-small cell lung cancer (NSCLC)osimertinibresistance

Identifiers

PMID35693293
PMCPMC9186160
OpenAlexW4282931981

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.