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CircMYBL1 suppressed acquired resistance to osimertinib in non-small-cell lung cancer.
Li, Yaji; Wang, Nan; Huang, Yutang; He, Shuai; Bao, Meihua; Wen, Chunjie; Wu, Lanxiang.
Affiliation
  • Li Y; Institute of Life Sciences, Chongqing Medical University, Chongqing 400016, China.
  • Wang N; Institute of Life Sciences, Chongqing Medical University, Chongqing 400016, China.
  • Huang Y; Institute of Life Sciences, Chongqing Medical University, Chongqing 400016, China.
  • He S; Institute of Life Sciences, Chongqing Medical University, Chongqing 400016, China; Molecular Medicine Diagnostic and Testing Center, Chongqing Medical University, Chongqing 400016, China.
  • Bao M; Hunan key laboratory of the research and development of novel pharmaceutical preparations, Changsha Medical University, Changsha 410219, China; Academician Workstation, Changsha Medical University, Changsha 410219, China.
  • Wen C; Institute of Life Sciences, Chongqing Medical University, Chongqing 400016, China. Electronic address: wenchunj@cqmu.edu.cn.
  • Wu L; Institute of Life Sciences, Chongqing Medical University, Chongqing 400016, China. Electronic address: lxwu@cqmu.edu.cn.
Cancer Genet ; 284-285: 34-42, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38626533
ABSTRACT
Circular RNAs (circRNAs) play an important role in the development of acquired resistance to many anticancer drugs. We developed the Non-Small-Cell Lung Cancer (NSCLC) cell lines with acquired resistance to osimertinib, a third-generation of epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs), and evaluated the different expression profiles of circRNAs in osimertinib-sensitive and -resistant NSCLC cell lines using RNA sequencing (RNA-Seq). The expression of selected differentially expressed circRNAs was verified using quantitative real-time PCR (qRT-PCR) in paired osimertinib-sensitive and -resistant NSCLC cell lines, and in plasma samples of osimertinib-sensitive and -resistant NSCLC patients. We found that circMYBL1(has_circ_0136924) was downregulated after acquired resistance to osimertinib, inhibiting circMYBL1 expression facilitated the proliferation, migration, and invasion in osimertinib-sensitive NSCLC cells. CircMYBL1 may be a novel molecular biomarker and therapeutic target for osimertinib-resistant NSCLC.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Acrylamides / Carcinoma, Non-Small-Cell Lung / Drug Resistance, Neoplasm / RNA, Circular / Aniline Compounds / Lung Neoplasms Limits: Humans Language: En Journal: Cancer Genet Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Acrylamides / Carcinoma, Non-Small-Cell Lung / Drug Resistance, Neoplasm / RNA, Circular / Aniline Compounds / Lung Neoplasms Limits: Humans Language: En Journal: Cancer Genet Year: 2024 Document type: Article Affiliation country: Country of publication: