Targeting non-coding RNAs to overcome osimertinib resistance in EGFR-mutated non-small cell lung cancer

被引:1
作者
Zeng, Beilei [1 ,2 ]
Gan, Kelun [1 ]
Yu, Yuanhang [1 ]
Hu, Jianping [1 ,2 ]
Deng, Qiao [1 ,2 ]
Yin, Chong [3 ,4 ]
Gao, Xi [1 ,2 ]
机构
[1] North Sichuan Med Coll, Dept Oncol, Affiliated Hosp, Nanchong, Sichuan, Peoples R China
[2] North Sichuan Med Coll, Sch Med Imaging, Nanchong, Sichuan, Peoples R China
[3] North Sichuan Med Coll, Dept Clin Lab, Affiliated Hosp, Nanchong, Sichuan, Peoples R China
[4] North Sichuan Med Coll, Translat Med Res Ctr, Dept Lab Med, Nanchong, Sichuan, Peoples R China
关键词
non-small cell lung cancer; EGFR; ncRNA; osimertinib resistance; mechanism; CIRCULAR RNA; EXOSOMES; SENSITIVITY; BIOMARKERS; INHIBITORS; EXPRESSION; THERAPIES;
D O I
10.3389/fonc.2024.1442237
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osimertinib, a third-generation inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase, exhibits remarkable efficacy in prolonging the survival of patients with non-small cell lung cancer (NSCLC) carrying EGFR mutations, surpassing the efficacy of first- and second-generation EGFR tyrosine kinases. Nevertheless, the emergence of osimertinib resistance is inevitable, necessitating an investigation into the underlying mechanisms. Increasing evidence has revealed that non-coding RNAs (ncRNAs), including microRNAs, long ncRNAs, and circular RNAs, play a significant role in the development and progression of lung cancer. These ncRNAs regulate essential signaling pathways, offering a novel avenue for understanding the fundamental mechanisms of osimertinib resistance. Recent studies have reported the significant impact of ncRNAs on osimertinib resistance, achieved through various mechanisms that modulate treatment sensitivity. We provide a concise overview of the functions and underlying mechanisms of extensively researched ncRNAs in the development of osimertinib resistance and emphasize their potential clinical application in EGFR-mutated NSCLC resistant to osimertinib. Finally, we discuss the obstacles that must be addressed to effectively translate ncRNA-based approaches into clinical practice.
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页数:10
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共 86 条
[1]   Systemic Therapy for Locally Advanced and Metastatic Non-Small Cell Lung Cancer A Review [J].
Arbour, Kathryn C. ;
Riely, Gregory J. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2019, 322 (08) :764-774
[2]   Emerging Insights into Targeted Therapy-Tolerant Persister Cells in Cancer [J].
Cabanos, Heidie Frisco ;
Hata, Aaron N. .
CANCERS, 2021, 13 (11)
[3]   Targeting apoptosis in cancer therapy [J].
Carneiro, Benedito A. ;
El-Deiry, Wafik S. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2020, 17 (07) :395-417
[4]   Targeting non-coding RNAs to overcome cancer therapy resistance [J].
Chen, BaoQing ;
Dragomir, Mihnea P. ;
Yang, Chen ;
Li, Qiaoqiao ;
Horst, David ;
Calin, George A. .
SIGNAL TRANSDUCTION AND TARGETED THERAPY, 2022, 7 (01)
[5]   Characterization of circRNAs in established osimertinib-resistant non-small cell lung cancer cell lines [J].
Chen, Xin ;
Gu, Jingyao ;
Huang, Jiali ;
Wen, Kang ;
Zhang, Ge ;
Chen, Zhenyao ;
Wang, Zhaoxia .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2023, 52 (05)
[6]   Hsa_circ_0007312 Promotes Third-Generation Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitor Resistance through Pyroptosis and Apoptosis via the MiR-764/MAPK1 Axis in Lung Adenocarcinoma Cells [J].
Dai, Chenyue ;
Ma, Zeming ;
Si, Jiahui ;
An, Guo ;
Zhang, Wenlong ;
Li, Shaolei ;
Ma, Yuanyuan .
JOURNAL OF CANCER, 2022, 13 (09) :2798-2809
[7]   Exosomal long non-coding RNA MSTRG.292666.16 is associated with osimertinib (AZD9291) resistance in non-small cell lung cancer [J].
Deng, Qinfang ;
Fang, Qiyu ;
Xie, Boxiong ;
Sun, Hui ;
Bao, Yuchen ;
Zhou, Songwen .
AGING-US, 2020, 12 (09) :8001-8015
[8]   Classical and noncanonical functions of miRNAs in cancers [J].
Dragomir, Mihnea P. P. ;
Knutsen, Erik ;
Calin, George A. A. .
TRENDS IN GENETICS, 2022, 38 (04) :379-394
[9]   Therapeutic strategies for EGFR-mutated non-small cell lung cancer patients with osimertinib resistance [J].
Fu, Kai ;
Xie, Fachao ;
Wang, Fang ;
Fu, Liwu .
JOURNAL OF HEMATOLOGY & ONCOLOGY, 2022, 15 (01)
[10]   Glycogen synthase kinase-3 inhibition overcomes epithelial-mesenchymal transition-associated resistance to osimertinib inEGFR-mutant lung cancer [J].
Fukuda, Koji ;
Takeuchi, Shinji ;
Arai, Sachiko ;
Kita, Kenji ;
Tanimoto, Azusa ;
Nishiyama, Akihiro ;
Yano, Seiji .
CANCER SCIENCE, 2020, 111 (07) :2374-2384