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Correlation between serum IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients

BACKGROUND: IL-1β is an essential factor of inflammation initiation, and it also promotes malignant transformation, indicating its tumorigenic property. We aimed to investigate the correlation between IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients. RESULTS: The IL-...

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Autores principales: Wu, Chen, Xu, Bin, Zhou, You, Ji, Mei, Zhang, Dachuan, Jiang, Jingting, Wu, Changping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349881/
https://www.ncbi.nlm.nih.gov/pubmed/27811377
http://dx.doi.org/10.18632/oncotarget.13042
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author Wu, Chen
Xu, Bin
Zhou, You
Ji, Mei
Zhang, Dachuan
Jiang, Jingting
Wu, Changping
author_facet Wu, Chen
Xu, Bin
Zhou, You
Ji, Mei
Zhang, Dachuan
Jiang, Jingting
Wu, Changping
author_sort Wu, Chen
collection PubMed
description BACKGROUND: IL-1β is an essential factor of inflammation initiation, and it also promotes malignant transformation, indicating its tumorigenic property. We aimed to investigate the correlation between IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients. RESULTS: The IL-1β level in both LUAD and LUSC patients was significantly higher than that of healthy donors (P < 0.001). In both populations, patients with low IL-1β level had better prognosis than high IL-1β level (P < 0.001 and P = 0.010, respectively). In A549 cells, miR-144 showed the biggest expression change (−4.38 fold) after IL-1β exposure. In LUAD patients, a negative correlation was detected between IL-1β and miR-144-3p (r = –0.540, P < 0.001) and the high miR-144-3p group had better prognosis (P = 0.003), which was validated by TCGA data. Clinical stage, IL-1β and miR-144-3p were independent risk factors in LUAD patients. In vitro, IL-1β and miR-144-3p antagomir could enhance proliferation and miR-144-3p mimics would attenuate the promoting effect of IL-1β. MATERIALS AND METHODS: ELISA and qRT-PCR were applied respectively to detected cytokines and miR-144-3p in 129 LUAD, 54 LUSC and 40 healthy donors. Moreover, miRNA array was carried out for miRNA profiling. TCGA database was employed for validation, and follow up data were collected for prognosis evaluation. MTT assay and western-blot were carried out for proliferation evaluation. CONCLUSIONS: In LUAD patients, the serum IL-1β level was correlated with miR-144-3p may affect miR-144-3p at transcriptional level. Both of them were independent risk factors for LUAD prognosis. In addition, IL-1β and miR-144-3p might mediate inflammation-promoted tumorigenesis in LUAD patients.
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spelling pubmed-53498812017-04-06 Correlation between serum IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients Wu, Chen Xu, Bin Zhou, You Ji, Mei Zhang, Dachuan Jiang, Jingting Wu, Changping Oncotarget Research Paper BACKGROUND: IL-1β is an essential factor of inflammation initiation, and it also promotes malignant transformation, indicating its tumorigenic property. We aimed to investigate the correlation between IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients. RESULTS: The IL-1β level in both LUAD and LUSC patients was significantly higher than that of healthy donors (P < 0.001). In both populations, patients with low IL-1β level had better prognosis than high IL-1β level (P < 0.001 and P = 0.010, respectively). In A549 cells, miR-144 showed the biggest expression change (−4.38 fold) after IL-1β exposure. In LUAD patients, a negative correlation was detected between IL-1β and miR-144-3p (r = –0.540, P < 0.001) and the high miR-144-3p group had better prognosis (P = 0.003), which was validated by TCGA data. Clinical stage, IL-1β and miR-144-3p were independent risk factors in LUAD patients. In vitro, IL-1β and miR-144-3p antagomir could enhance proliferation and miR-144-3p mimics would attenuate the promoting effect of IL-1β. MATERIALS AND METHODS: ELISA and qRT-PCR were applied respectively to detected cytokines and miR-144-3p in 129 LUAD, 54 LUSC and 40 healthy donors. Moreover, miRNA array was carried out for miRNA profiling. TCGA database was employed for validation, and follow up data were collected for prognosis evaluation. MTT assay and western-blot were carried out for proliferation evaluation. CONCLUSIONS: In LUAD patients, the serum IL-1β level was correlated with miR-144-3p may affect miR-144-3p at transcriptional level. Both of them were independent risk factors for LUAD prognosis. In addition, IL-1β and miR-144-3p might mediate inflammation-promoted tumorigenesis in LUAD patients. Impact Journals LLC 2016-11-03 /pmc/articles/PMC5349881/ /pubmed/27811377 http://dx.doi.org/10.18632/oncotarget.13042 Text en Copyright: © 2016 Wu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Wu, Chen
Xu, Bin
Zhou, You
Ji, Mei
Zhang, Dachuan
Jiang, Jingting
Wu, Changping
Correlation between serum IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients
title Correlation between serum IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients
title_full Correlation between serum IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients
title_fullStr Correlation between serum IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients
title_full_unstemmed Correlation between serum IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients
title_short Correlation between serum IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients
title_sort correlation between serum il-1β and mir-144-3p as well as their prognostic values in luad and lusc patients
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349881/
https://www.ncbi.nlm.nih.gov/pubmed/27811377
http://dx.doi.org/10.18632/oncotarget.13042
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