lncRNA TPTEP1 competitively sponges miR‑328‑5p to inhibit the proliferation of non‑small cell lung cancer cells

التفاصيل البيبلوغرافية
العنوان: lncRNA TPTEP1 competitively sponges miR‑328‑5p to inhibit the proliferation of non‑small cell lung cancer cells
المؤلفون: Yong Feng, Meiju Yang, Shuanglin Zhang, Xuefeng Wang, Zhiguo Wang, Feng Cao, Hongjun Zhu
المصدر: Oncology Reports
سنة النشر: 2019
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Cancer Research, Lung Neoplasms, Cell, Down-Regulation, Apoptosis, Biology, 03 medical and health sciences, 0302 clinical medicine, Carcinoma, Non-Small-Cell Lung, Cell Line, Tumor, microRNA, medicine, Gene silencing, Humans, non-small cell lung cancer, Aged, Cell Proliferation, Neoplasm Staging, Oncogene, Cell growth, Cancer, Computational Biology, General Medicine, Articles, long non-coding RNA TPTE pseudogene 1, Cell cycle, Middle Aged, medicine.disease, Prognosis, Molecular medicine, respiratory tract diseases, Gene Expression Regulation, Neoplastic, Adaptor Proteins, Vesicular Transport, MicroRNAs, 030104 developmental biology, medicine.anatomical_structure, Oncology, A549 Cells, 030220 oncology & carcinogenesis, Cancer research, microRNA-328-5p, Female, RNA, Long Noncoding
الوصف: Accumulating evidence suggests that lncRNAs are involved in almost all normal physiological processes and that aberrant expression of lncRNAs may be involved in the development of diseases, including non‑small cell lung cancer (NSCLC). However, the roles of lncRNA‑TPTE pseudogene 1 (TPTEP1) in lung cancer and the underlying molecular mechanisms have remained elusive. In the present study, significant downregulation of TPTEP1 in tumors compared with normal tissues from patients with NSCLC was observed. Overexpression of TPTEP1 inhibited cell proliferation and induced apoptosis in NSCLC cells. A bioinformatics analysis based on miRDB predicted microRNA (miR)‑328‑5p as a potential binding miRNA for TPTEP1. Using a dual‑luciferase reporter assay and western blot analysis, it was further validated that TPTEP1 sponged miR‑328‑5p to upregulate Src kinase signaling inhibitor 1 (SRCIN1) in NSCLC cells. Through regulation of SRCIN1, TPTEP1 was indicated to inactivate the Src and STAT3 pathways in NSCLC cells. Notably, silencing of SRCIN1 reversed the TPTEP1 overexpression‑induced inhibition of cell proliferation and increase of the apoptotic rate in NSCLC cells. Pearson correlation analysis revealed a significant positive correlation between TPTEP1 and SRCIN1 mRNA levels in NSCLC tumors. The present results provided insight into the roles of TPTEP1 in NSCLC and the underlying mechanisms.
تدمد: 1791-2431
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bd35f890db90b29448a718db1630cb8Test
https://pubmed.ncbi.nlm.nih.gov/32323798Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....3bd35f890db90b29448a718db1630cb8
قاعدة البيانات: OpenAIRE