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

dc.contributor.authorKeatdamrong Janpipatkulen_US
dc.contributor.authorNarumol Trachuen_US
dc.contributor.authorPiyakarn Watcharenwongen_US
dc.contributor.authorWittaya Panvongsaen_US
dc.contributor.authorWittawin Worakitchanonen_US
dc.contributor.authorChanatip Metheetrairuten_US
dc.contributor.authorSongporn Oranratnachaien_US
dc.contributor.authorThanyanan Reungwetwattanaen_US
dc.contributor.authorArthit Chairoungduaen_US
dc.contributor.otherSiriraj Hospitalen_US
dc.contributor.otherVajira Hospitalen_US
dc.contributor.otherFaculty of Medicine Ramathibodi Hospital, Mahidol Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChiang Mai Universityen_US
dc.date.accessioned2022-08-04T08:14:03Z
dc.date.available2022-08-04T08:14:03Z
dc.date.issued2021-01-01en_US
dc.description.abstractBACKGROUND: Osimertinib 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. OBJECTIVE: This study aimed to examine the profile of exosomal miRNA in the plasma of osimertinib-resistant NSCLC patients. METHODS: Plasma 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. RESULTS: In 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). CONCLUSIONS: Our results highlight the potential role of these exosomal miRNAs as molecular biomarkers for the detection of osimertinib resistance.en_US
dc.identifier.citationCancer Biomarkers. Vol.31, No.3 (2021), 281-294en_US
dc.identifier.doi10.3233/CBM-203075en_US
dc.identifier.issn18758592en_US
dc.identifier.issn15740153en_US
dc.identifier.other2-s2.0-85110118045en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/76357
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85110118045&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleExosomal microRNAs as potential biomarkers for osimertinib resistance of non-small cell lung cancer patientsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85110118045&origin=inwarden_US

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