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外泌体 microRNAs 作为非小细胞肺癌患者奥希替尼耐药的潜在生物标志物。

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

机构信息

Department of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand.

Excellent Center for Drug Discovery, Mahidol University, Bangkok, Thailand.

出版信息

Cancer Biomark. 2021;31(3):281-294. doi: 10.3233/CBM-203075.

Abstract

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.

摘要

背景

奥希替尼是一种表皮生长因子受体酪氨酸激酶抑制剂,专门针对癌症中的 T790M 突变。不幸的是,大多数非小细胞肺癌(NSCLC)患者会产生奥希替尼耐药性。目前,尚无用于监测奥希替尼耐药性的分子生物标志物。

目的

本研究旨在研究奥希替尼耐药性 NSCLC 患者血浆中外泌体 miRNA 的特征。

方法

通过下一代测序分析 8 例 NSCLC 患者奥希替尼敏感和奥希替尼耐药阶段的血浆外泌体 miRNA 图谱。通过 qPCR 在另一组 19 例 NSCLC 患者中验证和确认失调的外泌体 miRNA 的表达。通过 Kaplan-Meier 曲线评估外泌体 miRNA 上调与临床预后、生存分析之间的关系。

结果

与基线相比,奥希替尼耐药性 NSCLC 患者中有 10 种外泌体 miRNA 明显失调。所有 10 种候选外泌体 miRNA 的上调趋势与治疗失败潜伏期的延长和总生存期的改善相关。其中,4 种外泌体 miRNA(miR-323-3p、miR-1468-3p、miR-5189-5p 和 miR-6513-5p)明显上调,具有区分奥希替尼敏感和奥希替尼耐药 NSCLC 患者的潜力,具有较高的准确性(p<0.0001)。

结论

我们的结果强调了这些外泌体 miRNA 作为检测奥希替尼耐药性的分子生物标志物的潜在作用。

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