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MiR-451 suppresses the growth, migration, and invasion of prostate cancer cells by targeting macrophage migration inhibitory factor

BACKGROUND: Metastasis is the most common cause of death of prostate cancer patients. Identification of key regulators in prostate cancer metastasis is essential for improved management of the disease. Accumulation of evidence suggests that miRNAs play important roles in cancer metastasis. Here, we...

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Autores principales: Wang, Gang, Yao, Lixia, Yang, Tao, Guo, Liuxiong, Gu, Shouyi, Liu, Junjiang, Yang, Kuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798350/
https://www.ncbi.nlm.nih.gov/pubmed/35116797
http://dx.doi.org/10.21037/tcr.2019.03.28
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author Wang, Gang
Yao, Lixia
Yang, Tao
Guo, Liuxiong
Gu, Shouyi
Liu, Junjiang
Yang, Kuo
author_facet Wang, Gang
Yao, Lixia
Yang, Tao
Guo, Liuxiong
Gu, Shouyi
Liu, Junjiang
Yang, Kuo
author_sort Wang, Gang
collection PubMed
description BACKGROUND: Metastasis is the most common cause of death of prostate cancer patients. Identification of key regulators in prostate cancer metastasis is essential for improved management of the disease. Accumulation of evidence suggests that miRNAs play important roles in cancer metastasis. Here, we investigated the role of miR-451 in prostate cancer progression and metastasis. METHODS: In this study, we performed reverse transcription-quantitative PCR analysis to examine the expression of miR-451 in clinical prostate cancer samples and cell lines. TargetScan Release 7.0 programs, luciferase reporter assay, and a rescue experiment were used to validate the direct target of miR-451. The protein expression of the miR-451 target was detected by Western blot. MTS cell viability assay, transwell migration assay, and modified Boyden chamber invasion assay were used to demonstrate the effects of increased miR-451 expression on prostate cancer cell growth, migration and invasiveness. RESULTS: We identified the decreased expression of miR-451 in clinical metastatic prostate cancer compared to localized primary prostate cancer and benign prostate. Consistently, we also observed the decreased expression of miR-451 in highly metastatic prostate cancer cell lines (C4-2 and PC3M) compared to their low metastatic counterparts (LNCaP and PC3). Furthermore, we confirmed the macrophage migration inhibitory factor (MIF) is a direct target of miR-451 in prostate cancer and demonstrated a negative correlation between miR-451 and MIF expression in clinical prostate cancer samples. Functional studies showed increased miR-451 expression significantly suppressed cell growth, migration and invasiveness via targeting MIF. The effect of increased miR-451 expression can be reversed by overexpressing MIF in prostate cancer cells. CONCLUSIONS: These findings suggest that miR-451 suppresses prostate cancer cell growth, migration and metastasis, which provides insight into the development of novel therapeutic approaches for prostate cancer treatment.
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spelling pubmed-87983502022-02-02 MiR-451 suppresses the growth, migration, and invasion of prostate cancer cells by targeting macrophage migration inhibitory factor Wang, Gang Yao, Lixia Yang, Tao Guo, Liuxiong Gu, Shouyi Liu, Junjiang Yang, Kuo Transl Cancer Res Original Article BACKGROUND: Metastasis is the most common cause of death of prostate cancer patients. Identification of key regulators in prostate cancer metastasis is essential for improved management of the disease. Accumulation of evidence suggests that miRNAs play important roles in cancer metastasis. Here, we investigated the role of miR-451 in prostate cancer progression and metastasis. METHODS: In this study, we performed reverse transcription-quantitative PCR analysis to examine the expression of miR-451 in clinical prostate cancer samples and cell lines. TargetScan Release 7.0 programs, luciferase reporter assay, and a rescue experiment were used to validate the direct target of miR-451. The protein expression of the miR-451 target was detected by Western blot. MTS cell viability assay, transwell migration assay, and modified Boyden chamber invasion assay were used to demonstrate the effects of increased miR-451 expression on prostate cancer cell growth, migration and invasiveness. RESULTS: We identified the decreased expression of miR-451 in clinical metastatic prostate cancer compared to localized primary prostate cancer and benign prostate. Consistently, we also observed the decreased expression of miR-451 in highly metastatic prostate cancer cell lines (C4-2 and PC3M) compared to their low metastatic counterparts (LNCaP and PC3). Furthermore, we confirmed the macrophage migration inhibitory factor (MIF) is a direct target of miR-451 in prostate cancer and demonstrated a negative correlation between miR-451 and MIF expression in clinical prostate cancer samples. Functional studies showed increased miR-451 expression significantly suppressed cell growth, migration and invasiveness via targeting MIF. The effect of increased miR-451 expression can be reversed by overexpressing MIF in prostate cancer cells. CONCLUSIONS: These findings suggest that miR-451 suppresses prostate cancer cell growth, migration and metastasis, which provides insight into the development of novel therapeutic approaches for prostate cancer treatment. AME Publishing Company 2019-04 /pmc/articles/PMC8798350/ /pubmed/35116797 http://dx.doi.org/10.21037/tcr.2019.03.28 Text en 2019 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Wang, Gang
Yao, Lixia
Yang, Tao
Guo, Liuxiong
Gu, Shouyi
Liu, Junjiang
Yang, Kuo
MiR-451 suppresses the growth, migration, and invasion of prostate cancer cells by targeting macrophage migration inhibitory factor
title MiR-451 suppresses the growth, migration, and invasion of prostate cancer cells by targeting macrophage migration inhibitory factor
title_full MiR-451 suppresses the growth, migration, and invasion of prostate cancer cells by targeting macrophage migration inhibitory factor
title_fullStr MiR-451 suppresses the growth, migration, and invasion of prostate cancer cells by targeting macrophage migration inhibitory factor
title_full_unstemmed MiR-451 suppresses the growth, migration, and invasion of prostate cancer cells by targeting macrophage migration inhibitory factor
title_short MiR-451 suppresses the growth, migration, and invasion of prostate cancer cells by targeting macrophage migration inhibitory factor
title_sort mir-451 suppresses the growth, migration, and invasion of prostate cancer cells by targeting macrophage migration inhibitory factor
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798350/
https://www.ncbi.nlm.nih.gov/pubmed/35116797
http://dx.doi.org/10.21037/tcr.2019.03.28
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