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AIF-1, a potential biomarker of aggressive tumor behavior in patients with non-small cell lung cancer
Allogeneic inflammatory factor-1 (AIF-1) overexpression has been reported to be associated with tumorigenesis and tumor metastasis. This study aimed to investigate the role of AIF-1 in the development and progression of non-small cell lung cancer (NSCLC). AIF-1, IL-6, and VEGF expressions in human N...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9754194/ https://www.ncbi.nlm.nih.gov/pubmed/36520870 http://dx.doi.org/10.1371/journal.pone.0279211 |
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author | Wang, Lingling Zhao, Xing Zheng, Huachuan Zhu, Cuimin Liu, Yanhong |
author_facet | Wang, Lingling Zhao, Xing Zheng, Huachuan Zhu, Cuimin Liu, Yanhong |
author_sort | Wang, Lingling |
collection | PubMed |
description | Allogeneic inflammatory factor-1 (AIF-1) overexpression has been reported to be associated with tumorigenesis and tumor metastasis. This study aimed to investigate the role of AIF-1 in the development and progression of non-small cell lung cancer (NSCLC). AIF-1, IL-6, and VEGF expressions in human NSCLC tissue were examined by immunofluorescence staining. Bioinformatics analyses were performed to identify AIF-1-related molecules and pathways in NSCLC. Human lung cancer A549 cell proliferation was assessed by CCK-8 assay, and cell migration was evaluated with wound-healing assay. IL-6 and VEGF secretions in A549 cell culture supernatants were quantified using the Elecsys IL-6 immunoassay kit and Vascular Endothelial Growth Factor Assay Kit. RT-PCR and western blot were performed to quantify the expressions of AIF-1, IL-6, and VEGF mRNAs and proteins involved in p38-MAPK and JAK/STAT3 signaling such as p-p38 and p-STAT3. The effects of AIF-1 on A549 cell proliferation and the expressions of IL-6 and VEGF were assessed using SB203580 and ruxolitinib. The results showed that AIF-1 expression was higher in human NSCLC tissue than that in paracancer tissue. High AIF-1 expression was associated with metastasis, higher TNM stage, and poorer survival. Bioinformatics connected AIF-1 to JAK/STAT signaling in NSCLC. AIF-1 increased A549 cell proliferation, migration, IL-6 secretion and, VEGF secretion, and these effects were attenuated by inhibition of p38-MAPK or JAK/STAT3 signaling. In conclusion, AIF-1 may promote aggressive NSCLC behavior via activation of p38-MAPK and JAK/STAT signaling. |
format | Online Article Text |
id | pubmed-9754194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-97541942022-12-16 AIF-1, a potential biomarker of aggressive tumor behavior in patients with non-small cell lung cancer Wang, Lingling Zhao, Xing Zheng, Huachuan Zhu, Cuimin Liu, Yanhong PLoS One Research Article Allogeneic inflammatory factor-1 (AIF-1) overexpression has been reported to be associated with tumorigenesis and tumor metastasis. This study aimed to investigate the role of AIF-1 in the development and progression of non-small cell lung cancer (NSCLC). AIF-1, IL-6, and VEGF expressions in human NSCLC tissue were examined by immunofluorescence staining. Bioinformatics analyses were performed to identify AIF-1-related molecules and pathways in NSCLC. Human lung cancer A549 cell proliferation was assessed by CCK-8 assay, and cell migration was evaluated with wound-healing assay. IL-6 and VEGF secretions in A549 cell culture supernatants were quantified using the Elecsys IL-6 immunoassay kit and Vascular Endothelial Growth Factor Assay Kit. RT-PCR and western blot were performed to quantify the expressions of AIF-1, IL-6, and VEGF mRNAs and proteins involved in p38-MAPK and JAK/STAT3 signaling such as p-p38 and p-STAT3. The effects of AIF-1 on A549 cell proliferation and the expressions of IL-6 and VEGF were assessed using SB203580 and ruxolitinib. The results showed that AIF-1 expression was higher in human NSCLC tissue than that in paracancer tissue. High AIF-1 expression was associated with metastasis, higher TNM stage, and poorer survival. Bioinformatics connected AIF-1 to JAK/STAT signaling in NSCLC. AIF-1 increased A549 cell proliferation, migration, IL-6 secretion and, VEGF secretion, and these effects were attenuated by inhibition of p38-MAPK or JAK/STAT3 signaling. In conclusion, AIF-1 may promote aggressive NSCLC behavior via activation of p38-MAPK and JAK/STAT signaling. Public Library of Science 2022-12-15 /pmc/articles/PMC9754194/ /pubmed/36520870 http://dx.doi.org/10.1371/journal.pone.0279211 Text en © 2022 Wang et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wang, Lingling Zhao, Xing Zheng, Huachuan Zhu, Cuimin Liu, Yanhong AIF-1, a potential biomarker of aggressive tumor behavior in patients with non-small cell lung cancer |
title | AIF-1, a potential biomarker of aggressive tumor behavior in patients with non-small cell lung cancer |
title_full | AIF-1, a potential biomarker of aggressive tumor behavior in patients with non-small cell lung cancer |
title_fullStr | AIF-1, a potential biomarker of aggressive tumor behavior in patients with non-small cell lung cancer |
title_full_unstemmed | AIF-1, a potential biomarker of aggressive tumor behavior in patients with non-small cell lung cancer |
title_short | AIF-1, a potential biomarker of aggressive tumor behavior in patients with non-small cell lung cancer |
title_sort | aif-1, a potential biomarker of aggressive tumor behavior in patients with non-small cell lung cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9754194/ https://www.ncbi.nlm.nih.gov/pubmed/36520870 http://dx.doi.org/10.1371/journal.pone.0279211 |
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