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Expression profiling identified IL-8 as a regulator of homotypic cell-in-cell formation
Homotypic cell-in-cell (CIC) structures forming between cancer cells were proposed to promote tumor evolution via entosis, a nonapoptotic cell death process. However, the mechanisms underlying their formation remained poorly understood. We performed a microarray analysis to identify genes associated...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Biochemistry and Molecular Biology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130832/ https://www.ncbi.nlm.nih.gov/pubmed/30021676 http://dx.doi.org/10.5483/BMBRep.2018.51.8.089 |
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author | Ruan, Banzhan Wang, Chenxi Chen, Ang Liang, Jianqing Niu, Zubiao Zheng, You Fan, Jie Gao, Lihua Huang, Hongyan Wang, Xiaoning Sun, Qiang |
author_facet | Ruan, Banzhan Wang, Chenxi Chen, Ang Liang, Jianqing Niu, Zubiao Zheng, You Fan, Jie Gao, Lihua Huang, Hongyan Wang, Xiaoning Sun, Qiang |
author_sort | Ruan, Banzhan |
collection | PubMed |
description | Homotypic cell-in-cell (CIC) structures forming between cancer cells were proposed to promote tumor evolution via entosis, a nonapoptotic cell death process. However, the mechanisms underlying their formation remained poorly understood. We performed a microarray analysis to identify genes associated with homotypic CIC formation. Cancer cells differing in their ability to form homotypic CIC structures were selected for the study. Association analysis identified 73 probe sets for 62 candidate genes potentially involved in CIC formation. Among them, twenty-one genes were downregulated while 41 genes were upregulated. Pathway analysis identified a gene interaction network centered on IL-8, which was upregulated in high CIC cells. Remarkably, CIC formation was significantly inhibited by IL-8 knockdown and enhanced upon recombinant IL-8 treatment, which correlated with altered cell-cell adhesion and expression of adhesive molecules such as P-cadherin and γ-catenin. Together, our work identified IL-8 as a positive regulator of homotypic CIC formation via enhancing intercellular adhesion. |
format | Online Article Text |
id | pubmed-6130832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-61308322018-09-12 Expression profiling identified IL-8 as a regulator of homotypic cell-in-cell formation Ruan, Banzhan Wang, Chenxi Chen, Ang Liang, Jianqing Niu, Zubiao Zheng, You Fan, Jie Gao, Lihua Huang, Hongyan Wang, Xiaoning Sun, Qiang BMB Rep Articles Homotypic cell-in-cell (CIC) structures forming between cancer cells were proposed to promote tumor evolution via entosis, a nonapoptotic cell death process. However, the mechanisms underlying their formation remained poorly understood. We performed a microarray analysis to identify genes associated with homotypic CIC formation. Cancer cells differing in their ability to form homotypic CIC structures were selected for the study. Association analysis identified 73 probe sets for 62 candidate genes potentially involved in CIC formation. Among them, twenty-one genes were downregulated while 41 genes were upregulated. Pathway analysis identified a gene interaction network centered on IL-8, which was upregulated in high CIC cells. Remarkably, CIC formation was significantly inhibited by IL-8 knockdown and enhanced upon recombinant IL-8 treatment, which correlated with altered cell-cell adhesion and expression of adhesive molecules such as P-cadherin and γ-catenin. Together, our work identified IL-8 as a positive regulator of homotypic CIC formation via enhancing intercellular adhesion. Korean Society for Biochemistry and Molecular Biology 2018-08 2018-08-31 /pmc/articles/PMC6130832/ /pubmed/30021676 http://dx.doi.org/10.5483/BMBRep.2018.51.8.089 Text en Copyright © 2018 by the The Korean Society for Biochemistry and Molecular Biology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Ruan, Banzhan Wang, Chenxi Chen, Ang Liang, Jianqing Niu, Zubiao Zheng, You Fan, Jie Gao, Lihua Huang, Hongyan Wang, Xiaoning Sun, Qiang Expression profiling identified IL-8 as a regulator of homotypic cell-in-cell formation |
title | Expression profiling identified IL-8 as a regulator of homotypic cell-in-cell formation |
title_full | Expression profiling identified IL-8 as a regulator of homotypic cell-in-cell formation |
title_fullStr | Expression profiling identified IL-8 as a regulator of homotypic cell-in-cell formation |
title_full_unstemmed | Expression profiling identified IL-8 as a regulator of homotypic cell-in-cell formation |
title_short | Expression profiling identified IL-8 as a regulator of homotypic cell-in-cell formation |
title_sort | expression profiling identified il-8 as a regulator of homotypic cell-in-cell formation |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130832/ https://www.ncbi.nlm.nih.gov/pubmed/30021676 http://dx.doi.org/10.5483/BMBRep.2018.51.8.089 |
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