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

被引:25
作者
Janpipatkul, Keatdamrong [1 ,2 ,3 ]
Trachu, Narumol [4 ]
Watcharenwong, Piyakarn [5 ]
Panvongsa, Wittaya [2 ,6 ]
Worakitchanon, Wittawin [1 ,2 ]
Metheetrairut, Chanatip [7 ]
Oranratnachai, Songporn [5 ,8 ]
Reungwetwattana, Thanyanan [5 ]
Chairoungdua, Arthit [1 ,2 ,6 ,9 ]
机构
[1] Mahidol Univ, Fac Sci, Dept Physiol, Rama 6 Rd, Bangkok 10400, Thailand
[2] Mahidol Univ, Excellent Ctr Drug Discovery, Bangkok, Thailand
[3] Navamindradhiraj Univ, Vajira Hosp, Dept Basic Med Sci, Fac Med, Bangkok, Thailand
[4] Mahidol Univ, Ramathibodi Hosp, Res Ctr, Fac Med, Bangkok, Thailand
[5] Mahidol Univ, Ramathibodi Hosp, Dept Med, Div Med Oncol,Fac Med, Bangkok, Thailand
[6] Mahidol Univ, Fac Sci, Toxicol Grad Program, Bangkok, Thailand
[7] Mahidol Univ, Siriraj Hosp, Dept Biochem, Fac Med, Bangkok, Thailand
[8] Chiang Mai Univ, Fac Med, Sriphat Med Ctr, Oncol Clin, Chiang Mai, Thailand
[9] Mahidol Univ, Fac Sci, Ctr Excellence Environm Hlth & Toxicol, Bangkok, Thailand
关键词
Osimertinib resistance; NSCLC; exosome; miRNA; biomarker; EGFR-TKI; EXPRESSION; ADENOCARCINOMA; WEBGESTALT; INHIBITOR; MUTATIONS; CISPLATIN; BIOLOGY;
D O I
10.3233/CBM-203075
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: 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.
引用
收藏
页码:281 / 294
页数:14
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