Evidence map›Paper›PMID 33896827›Full record

ArticleCancer biomarkers : section A of Disease markers2021

Exosomal microRNAs as potential biomarkers for osimertinib resistance of non-small cell lung cancer patients.

Keatdamrong Janpipatkul, Narumol Trachu, Piyakarn Watcharenwong, Wittaya Panvongsa, Wittawin Worakitchanon, Chanatip Metheetrairut, Songporn Oranratnachai, Thanyanan Reungwetwattana, Arthit Chairoungdua

Abstract read
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Article in Cancer biomarkers : section A of Disease markers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Keatdamrong JanpipatkulDepartment of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Narumol TrachuResearch Center, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Piyakarn WatcharenwongDivision of Medical Oncology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Wittaya PanvongsaExcellent Center for Drug Discovery, Mahidol University, Bangkok, Thailand.
Wittawin WorakitchanonDepartment of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Chanatip MetheetrairutDepartment of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Songporn OranratnachaiDivision of Medical Oncology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Thanyanan ReungwetwattanaDivision of Medical Oncology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Arthit ChairoungduaDepartment of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Mahidol University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsimertinib is an epidermal growth factor receptor-tyrosine kinase inhibitor that specifically targets the T790M mutation in cancer.Unfortunately, most non-small cell lung cancer (NSCLC) patients develop osimertinib resistance. Currently, the molecular biomarkers for monitoring osimertinib resistance are not available.

objectiveThis study aimed to examine the profile of exosomal miRNA in the plasma of osimertinib-resistant NSCLC patients.

methodsPlasma exosomal miRNA profiles of 8 NSCLC patients were analyzed by next-generation sequencing at osimertinib-sensitive and osimertinib-resistance stage.The expression of dysregulated exosomal miRNAs was validated and confirmed in another cohort of 19 NSCLC patients by qPCR. The relationship between exosomal miRNA upregulation and clinical prognosis, survival analysis was evaluated by Kaplan-Meier curves.

resultsIn osimertinib-resistant NSCLC patients, 10 exosomal miRNAs were significantly dysregulated compared to baseline. Upregulation of all 10 candidate exosomal miRNAs tended to correlate with increased latency to treatment failure and improved overall survival. Among them, 4 exosomal miRNAs, miR-323-3p, miR-1468-3p, miR-5189-5p and miR-6513-5p were essentially upregulated and show the potential to be markers for the discrimination of osimertinib-resistance from osimertinib-sensitive NSCLC patients with high accuracy (p< 0.0001).

conclusionsOur results highlight the potential role of these exosomal miRNAs as molecular biomarkers for the detection of osimertinib resistance.

Indexed as

AcrylamidesAdultAgedAged, 80 and overAniline CompoundsAntineoplastic AgentsBiomarkers, TumorCarcinoma, Non-Small-Cell LungDrug Resistance, NeoplasmExosomesFemaleHumansIndolesLung NeoplasmsMaleMicroRNAsAcrylamidesAniline CompoundsAntineoplastic AgentsBiomarkers, TumorIndolesMicroRNAsosimertinibPyrimidinesbiomarkerexosomemiRNANSCLCOsimertinib resistance

Identifiers

PMID33896827
PMCPMC12500004
OpenAlexW3154967890

What OpenQuestion holds

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Registered trials

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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.