Evidence map›Paper›PMID 38590190›Full record

ArticleZhongguo fei ai za zhi = Chinese journal of lung cancer2024

[Effect of CircCCND1 on the Malignant Biological Behaviors of H446 Lung Cancer Cells by Regulating the MiR-340-5p/TGIF1 Axis].

Yi Dong, Cuimin Zhu, Xin Liu, Jiwei Zhao, Qingshan Li

Open access · greenAbstract readEnglish Abstract
In one paragraph

Article in Zhongguo fei ai za zhi = Chinese journal of lung cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Yi DongDepartment of Oncology, Affiliated Hospital of Chengde Medical College, Chengde 067000, China.
Cuimin ZhuDepartment of Oncology, Affiliated Hospital of Chengde Medical College, Chengde 067000, China.
Xin LiuDepartment of Oncology, Affiliated Hospital of Chengde Medical College, Chengde 067000, China.
Jiwei ZhaoDepartment of Oncology, Affiliated Hospital of Chengde Medical College, Chengde 067000, China.
Qingshan LiDepartment of Oncology, Affiliated Hospital of Chengde Medical College, Chengde 067000, China.
Affiliated Hospital of Chengde Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer is a common malignant tumor of the lung. To explore the molecular mechanism of the occurrence and development of lung cancer is a hot topic in current research. Cyclic RNA D1 (CircCCND1) is highly expressed in lung cancer and may be a potential target for the treatment of lung cancer. The aim of this study was to investigate the effect of CircCCND1 on the malignant biological behaviors of lung cancer cells by regulating the miR-340-5p/transforming growth factor β-induced factor homeobox 1 (TGIF1) axis.

methodsThe expression of CircCCND1, miR-340-5p, and TGIF1 mRNA in human normal lung epithelial cells BEAS-2B and human lung cancer H446 cells were detected. H446 cells cultured in vitro were randomly divided into control group, CircCCND1 siRNA group, miR-340-5p mimics group, negative control group, and CircCCND1 siRNA+miR-340-5p inhibitor group. Cell proliferation, mitochondrial membrane potential, apoptosis, migration, and invasion were detected, and the expressions of CircCCND1, miR-340-5p, TGIF1 mRNA, BCL2-associated X protein (Bax), cleaved Caspase-3, N-cadherin, E-cadherin, and TGIF1 proteins in each group were detected. The targeting relationship of miR-340-5p with CircCCND1 and TGIF1 was verified.

resultsCompared with BEAS-2B cells, CircCCND1 and TGIF1 mRNA were increased in H446 cells, and miR-340-5p expression was decreased (P<0.05). Knocking down CircCCND1 or up-regulating the expression of miR-340-5p inhibited the proliferation, migration and invasion of H446 cells, decreased the expression of TGIF1 mRNA and TGIF1 protein, and promoted cell apoptosis. Down-regulation of miR-340-5p could antagonize the inhibitory effect of CircCCND1 knockdown on the malignant biological behavior of H446 lung cancer cells. CircCCND1 may target the down-regulation of miR-340-5p, and miR-340-5p may target the down-regulation of TGIF1.

conclusionsKnocking down CircCCND1 can inhibit the malignant behaviors of lung cancer H446 cells, which may be achieved through the regulation of miR-340-5p/TGIF1 axis.

Indexed as

Lung NeoplasmsMicroRNAsCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHomeodomain ProteinsHumansLungRepressor ProteinsRNA, MessengerRNA, Small InterferingHomeodomain ProteinsMicroRNAsMIRN340 microRNA, humanRepressor ProteinsRNA, MessengerRNA, Small InterferingTGIF1 protein, humanCircCCND1Lung neoplasmsMalignant biological behaviormiR-340-5p/TGIF1

Identifiers

PMID38590190
PMCPMC11002193
OpenAlexW4394758944

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.