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<i>RHAMM</i> regulates the growth and migration of lung adenocarcinoma A549 cell line by regulating <i>Cdc2/CyclinB1</i> and <i>MMP9</i> genes
Author(s) -
Feng Chen,
Xuqing Zhu,
Jing Zheng,
Ting-Ting Xu,
Kuan Wu,
Chuhui Ru
Publication year - 2020
Publication title -
mathematical biosciences and engineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.451
H-Index - 45
eISSN - 1551-0018
pISSN - 1547-1063
DOI - 10.3934/mbe.2020114
Subject(s) - a549 cell , cell cycle , cell growth , cyclin dependent kinase 1 , cell culture , gene silencing , cell migration , microbiology and biotechnology , cancer research , cd44 , gene knockdown , epithelial–mesenchymal transition , chemistry , flow cytometry , biology , cell , downregulation and upregulation , genetics , biochemistry , gene
Objective : The study aims to explore the effects of receptor of hyaluronan mediated motility ( RHAMM ) on the proliferation, invasion and migration of the lung adenocarcinoma (LUAD) cell line A549 and its targeted regulatory pathway. Methods : Bioinformatics was used to analyze the differentially expressed genes in LUAD chips. The mRNA and protein expression level of Cdc2, CyclinB1, MMPs and epithelial-mesenchymal transition (EMT) related markers E-cadherin and Vimentin were tested by qRT-PCR and western blot in A549 cell line after silencing RHAMM . Cell proliferation, cell division cycle, migration and invasion abilities were tested in RHAMM knockdown A549 cells by flow cytometry and in vitro assays. Results : Silencing RHAMM inhibited EMT, proliferation, migration and invasion of A549 cell line and induced cells to cluster at G2/M phase. In addition, after silencing RHAMM , the mRNA and protein expressions of Cdc2 and CyclinB1 were decreased while those of MMP9 were increased. Conclusion : The findings suggest tha RHAMM regulates cell division cycle by regulating Cdc2 and CyclinB1 , and regulates extracellular matrix degradation by regulating MMP9 . These targeted modulations regulate the occurrence and development of LUAD cells.

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