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MiR-96-5p is an oncogene in lung adenocarcinoma and facilitates tumor progression through ARHGAP6 downregulation

  • Human Genetics • Original Paper
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Abstract

Accumulating investigations illustrated that miRNA acts as a key regulator in tumor progression, whereas regulatory role of miR-96-5p in lung adenocarcinoma (LUAD) is warranted. Thus, we sought to probe mechanism of miR-96-5p in this disease. Through bioinformatics analysis, miR-96-5p level in normal tissue and LUAD tissue in TCGA database were obtained. Meanwhile, mRNA expression dataset was analyzed to obtain downregulated mRNAs binding to miR-96-5p. qRT-PCR assessed miR-96-5p and ARHGAP6 mRNA in LUAD. Western blot assessed protein level of ARHGAP6 in LUAD. Dual-luciferase reporter gene detection verified targeting relationship of miR-96-5p and ARHGAP6. Biological functional experiments such as CCK-8, colony formation, scratch healing, and Transwell assessed cell proliferation, migration, and invasion. MiR-96-5p was overexpressed, which fostered LUAD cell proliferation, migration, and invasion. ARHGAP6 was downregulated in LUAD and targeted by miR-96-5p. ARHGAP6 upregulation prominently restored promotion of miR-96-5p on cell progression. MiR-96-5p could stimulate LUAD progression through targeting ARHGAP6. This study generates a novel direction and lays a theoretical basis for targeted therapy.

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Data availability

The data used to support the findings of this study are included within the article. The data and materials in the current study are available from the corresponding author on reasonable request.

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Funding

1. This study was supported by the funds from 2020 Zhejiang Medical and Health Science and Technology Program (above item). Funds: 2020KY053.

2. This study was supported by the funds from Zhejiang Lung Cancer center.

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Contributions

ZF contributed to the study design. BZ conducted the literature search. YC and SW acquired the data. CH wrote the article. FY performed data analysis. EL drafted. ZF and ZB revised the article and gave the final approval of the version to be submitted. All authors read and approved the final manuscript.

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Correspondence to Bing Zhou.

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The authors declare no competing interests.

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Communicated by Michal Witt

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Liu, Z., Cui, Y., Wang, S. et al. MiR-96-5p is an oncogene in lung adenocarcinoma and facilitates tumor progression through ARHGAP6 downregulation . J Appl Genetics 62, 631–638 (2021). https://doi.org/10.1007/s13353-021-00652-1

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