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miR-367-3p靶向ZEB2抑制NSCLC细胞增殖、迁移和侵袭生物学功能研究

BACKGROUND AND OBJECTIVE: microRNAs play an important role in the development and biological phenotype of lung cancer. The present study was to investigate miR-367-3p level in non-small cell lung cancer (NSCLC) patients and its biological function of NSCLC cells. METHODS: Twenty-two patients with NS...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720678/
https://www.ncbi.nlm.nih.gov/pubmed/36419391
http://dx.doi.org/10.3779/j.issn.1009-3419.2022.101.49
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description BACKGROUND AND OBJECTIVE: microRNAs play an important role in the development and biological phenotype of lung cancer. The present study was to investigate miR-367-3p level in non-small cell lung cancer (NSCLC) patients and its biological function of NSCLC cells. METHODS: Twenty-two patients with NSCLC (13 cases of adenocarcinoma and 9 cases of squamous carcinoma) admitted to our hospital and treated by surgery were included. During the operation, cancer tissue, paracancerous tissue and 5 mL peripheral blood were collected. Meanwhile, 22 healthy controls were selected and 5 mL peripheral blood was taken. Real-time PCR was applied to detected the expression of miR-367-3p in cancer tissues, peripheral blood of patients with NSCLC and healthy controls. miR-367-3p was detected in lung cancer cell lines (A549) and normal bronchial epithelial cells (BEAS-2B). The proliferation and invasion ability of A549 cells before and after infection were detected by MTT and Transwell assay after transfection with exogenous miR-367-3p. The downstream target gene of miR-367-3p was analyzed by bioinformatics. Zinc finger E-box binding homeobox 2 (ZEB2) was detected by Real-time PCR and Western blot. RESULTS: miR-367-3p in cancer tissues of 22 NSCLC patients was lower than corresponding normal tissues (P < 0.05), and the serum miR-367-3p level in healthy subjects was higher than NSCLC subjects (P < 0.05). The area under the receiver operating characteristic (ROC) curve of NSCLC was 0.95 (95%CI: 0.89-1.00) and 0.85 (95%CI: 0.74-0.97) respectively; The proliferation and migration ability of lung cancer cell line A549 transfected with exogenous miR-367-3p decreased significantly (P < 0.05); Bioinformatics predicted that the downstream target of miR-367-3p was ZEB2 and up-regulating miR-367-3p expression, ZEB2 gene was decreased (P < 0.05). The Cancer Genome Atlas (TCGA) data analysis showed that there was no significant difference in overall survival (OS) and disease free survival (DFS) between ZEB2 high expression group and low expression group (P > 0.05). ZEB2 expression was positively correlated with infiltration of B lymphocytes (r=0.32, P < 005), CD8(+) T cells (r=0.44, P < 005), CD4(+) T cells (r=0.46, P < 005), macrophages (r=0.65, P < 005), neutrophils (r=0.73, P < 005) and dendritic cells (r=0.71, P < 005) in NSCLC. CONCLUSION: The expression of miR-367-3p is down regulated in NSCLC patients and participates in the biological process of proliferation and invasion of NSCLC by targeting ZEB2 gene.
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spelling pubmed-97206782022-12-22 miR-367-3p靶向ZEB2抑制NSCLC细胞增殖、迁移和侵袭生物学功能研究 Zhongguo Fei Ai Za Zhi 临床研究 BACKGROUND AND OBJECTIVE: microRNAs play an important role in the development and biological phenotype of lung cancer. The present study was to investigate miR-367-3p level in non-small cell lung cancer (NSCLC) patients and its biological function of NSCLC cells. METHODS: Twenty-two patients with NSCLC (13 cases of adenocarcinoma and 9 cases of squamous carcinoma) admitted to our hospital and treated by surgery were included. During the operation, cancer tissue, paracancerous tissue and 5 mL peripheral blood were collected. Meanwhile, 22 healthy controls were selected and 5 mL peripheral blood was taken. Real-time PCR was applied to detected the expression of miR-367-3p in cancer tissues, peripheral blood of patients with NSCLC and healthy controls. miR-367-3p was detected in lung cancer cell lines (A549) and normal bronchial epithelial cells (BEAS-2B). The proliferation and invasion ability of A549 cells before and after infection were detected by MTT and Transwell assay after transfection with exogenous miR-367-3p. The downstream target gene of miR-367-3p was analyzed by bioinformatics. Zinc finger E-box binding homeobox 2 (ZEB2) was detected by Real-time PCR and Western blot. RESULTS: miR-367-3p in cancer tissues of 22 NSCLC patients was lower than corresponding normal tissues (P < 0.05), and the serum miR-367-3p level in healthy subjects was higher than NSCLC subjects (P < 0.05). The area under the receiver operating characteristic (ROC) curve of NSCLC was 0.95 (95%CI: 0.89-1.00) and 0.85 (95%CI: 0.74-0.97) respectively; The proliferation and migration ability of lung cancer cell line A549 transfected with exogenous miR-367-3p decreased significantly (P < 0.05); Bioinformatics predicted that the downstream target of miR-367-3p was ZEB2 and up-regulating miR-367-3p expression, ZEB2 gene was decreased (P < 0.05). The Cancer Genome Atlas (TCGA) data analysis showed that there was no significant difference in overall survival (OS) and disease free survival (DFS) between ZEB2 high expression group and low expression group (P > 0.05). ZEB2 expression was positively correlated with infiltration of B lymphocytes (r=0.32, P < 005), CD8(+) T cells (r=0.44, P < 005), CD4(+) T cells (r=0.46, P < 005), macrophages (r=0.65, P < 005), neutrophils (r=0.73, P < 005) and dendritic cells (r=0.71, P < 005) in NSCLC. CONCLUSION: The expression of miR-367-3p is down regulated in NSCLC patients and participates in the biological process of proliferation and invasion of NSCLC by targeting ZEB2 gene. 中国肺癌杂志编辑部 2022-11-20 /pmc/articles/PMC9720678/ /pubmed/36419391 http://dx.doi.org/10.3779/j.issn.1009-3419.2022.101.49 Text en 版权所有©《中国肺癌杂志》编辑部2022 https://creativecommons.org/licenses/by/3.0/This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/.
spellingShingle 临床研究
miR-367-3p靶向ZEB2抑制NSCLC细胞增殖、迁移和侵袭生物学功能研究
title miR-367-3p靶向ZEB2抑制NSCLC细胞增殖、迁移和侵袭生物学功能研究
title_full miR-367-3p靶向ZEB2抑制NSCLC细胞增殖、迁移和侵袭生物学功能研究
title_fullStr miR-367-3p靶向ZEB2抑制NSCLC细胞增殖、迁移和侵袭生物学功能研究
title_full_unstemmed miR-367-3p靶向ZEB2抑制NSCLC细胞增殖、迁移和侵袭生物学功能研究
title_short miR-367-3p靶向ZEB2抑制NSCLC细胞增殖、迁移和侵袭生物学功能研究
title_sort mir-367-3p靶向zeb2抑制nsclc细胞增殖、迁移和侵袭生物学功能研究
topic 临床研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720678/
https://www.ncbi.nlm.nih.gov/pubmed/36419391
http://dx.doi.org/10.3779/j.issn.1009-3419.2022.101.49
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