MiR-21 and let-7 cooperation in the regulation of lung cancer

BackgroundLung cancer occurs and develops as a result of a complicated process involving numerous genes; therefore, single-gene regulation has a limited therapeutic effect. We discovered that miR-21 expression was high in lung cancer tissues and cells, whereas let-7 expression was low, and it is unc...

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Main Authors: Jinquan Bai, Zhenzhou Shi, Shuting Wang, Hong Pan, Tong Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-09-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2022.950043/full
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author Jinquan Bai
Zhenzhou Shi
Shuting Wang
Hong Pan
Tong Zhang
author_facet Jinquan Bai
Zhenzhou Shi
Shuting Wang
Hong Pan
Tong Zhang
author_sort Jinquan Bai
collection DOAJ
description BackgroundLung cancer occurs and develops as a result of a complicated process involving numerous genes; therefore, single-gene regulation has a limited therapeutic effect. We discovered that miR-21 expression was high in lung cancer tissues and cells, whereas let-7 expression was low, and it is unclear whether their combined regulation would be superior to therapy involving single regulation. The goal of our research was to investigate this situation and the regulatory mechanism that exists between these genes.MethodsTo regulate the levels of miR-21 and let-7 in these two types of lung cancer cells, we transfected miRNA mimics or inhibitors into A549 and H460 cells. Lung cancer cells were tested for proliferation, apoptosis, migration, and invasion. The results were verified using a Western blot and a qRT-PCR assay. Bioinformatics was used to investigate their potential regulatory pathways, and luciferase assays were used to confirm the binding sites.ResultsThe expression of miR-21 was increased and that of let-7 was decreased in lung cancer tissues and cells compared with paracancerous tissues and normal lung cells (p < 0.01). Tumor cells were inhibited by downregulation of miR-21 and upregulation of let-7, and cooperative regulation showed a better effect. Upregulation of miR-21 and downregulation of let-7 promoted tumor cells, and this tumor-promoting effect was amplified by cooperative regulation. MiR-21 regulated lung cancer cells directly via the Wnt/-catenin pathway, and let-7 exerted its effects via the PLAG1/GDH1 pathway. MiR-21 and let-7 cooperated to regulate lung cancer cells via the K-ras pathway.ConclusionsThe effect of cooperative regulation of miR-21 and let-7 on lung cancer is greater than that of a single miRNA. MiR-21 and let-7 are important differentially expressed genes in lung cancer that are regulated by the K-ras pathway. As a result, for multigene lung cancer, the cooperative regulation of two miRNAs will provide a new target and direction for lung cancer treatment in the future.
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spelling doaj.art-7a4f2fb1de5e4bbc91d5926e7885a5332022-12-22T04:27:15ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2022-09-011210.3389/fonc.2022.950043950043MiR-21 and let-7 cooperation in the regulation of lung cancerJinquan BaiZhenzhou ShiShuting WangHong PanTong ZhangBackgroundLung cancer occurs and develops as a result of a complicated process involving numerous genes; therefore, single-gene regulation has a limited therapeutic effect. We discovered that miR-21 expression was high in lung cancer tissues and cells, whereas let-7 expression was low, and it is unclear whether their combined regulation would be superior to therapy involving single regulation. The goal of our research was to investigate this situation and the regulatory mechanism that exists between these genes.MethodsTo regulate the levels of miR-21 and let-7 in these two types of lung cancer cells, we transfected miRNA mimics or inhibitors into A549 and H460 cells. Lung cancer cells were tested for proliferation, apoptosis, migration, and invasion. The results were verified using a Western blot and a qRT-PCR assay. Bioinformatics was used to investigate their potential regulatory pathways, and luciferase assays were used to confirm the binding sites.ResultsThe expression of miR-21 was increased and that of let-7 was decreased in lung cancer tissues and cells compared with paracancerous tissues and normal lung cells (p < 0.01). Tumor cells were inhibited by downregulation of miR-21 and upregulation of let-7, and cooperative regulation showed a better effect. Upregulation of miR-21 and downregulation of let-7 promoted tumor cells, and this tumor-promoting effect was amplified by cooperative regulation. MiR-21 regulated lung cancer cells directly via the Wnt/-catenin pathway, and let-7 exerted its effects via the PLAG1/GDH1 pathway. MiR-21 and let-7 cooperated to regulate lung cancer cells via the K-ras pathway.ConclusionsThe effect of cooperative regulation of miR-21 and let-7 on lung cancer is greater than that of a single miRNA. MiR-21 and let-7 are important differentially expressed genes in lung cancer that are regulated by the K-ras pathway. As a result, for multigene lung cancer, the cooperative regulation of two miRNAs will provide a new target and direction for lung cancer treatment in the future.https://www.frontiersin.org/articles/10.3389/fonc.2022.950043/fulllung cancermiR-21let-7K-rascooperative regulation
spellingShingle Jinquan Bai
Zhenzhou Shi
Shuting Wang
Hong Pan
Tong Zhang
MiR-21 and let-7 cooperation in the regulation of lung cancer
Frontiers in Oncology
lung cancer
miR-21
let-7
K-ras
cooperative regulation
title MiR-21 and let-7 cooperation in the regulation of lung cancer
title_full MiR-21 and let-7 cooperation in the regulation of lung cancer
title_fullStr MiR-21 and let-7 cooperation in the regulation of lung cancer
title_full_unstemmed MiR-21 and let-7 cooperation in the regulation of lung cancer
title_short MiR-21 and let-7 cooperation in the regulation of lung cancer
title_sort mir 21 and let 7 cooperation in the regulation of lung cancer
topic lung cancer
miR-21
let-7
K-ras
cooperative regulation
url https://www.frontiersin.org/articles/10.3389/fonc.2022.950043/full
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AT zhenzhoushi mir21andlet7cooperationintheregulationoflungcancer
AT shutingwang mir21andlet7cooperationintheregulationoflungcancer
AT hongpan mir21andlet7cooperationintheregulationoflungcancer
AT tongzhang mir21andlet7cooperationintheregulationoflungcancer