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Overexpression of CXCL2 inhibits cell proliferation and promotes apoptosis in hepatocellular carcinoma
C-X-C motif chemokine ligand 2 (CXCL2) is a small secreted protein that exhibits a structure similar to the proangiogenic subgroup of the CXC chemokine family. Recently, accumulating evidence suggests that chemokines play a pivotal role in cancer progression and carcinogenesis. We examined the expre...
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/PMC6330937/ https://www.ncbi.nlm.nih.gov/pubmed/30293547 http://dx.doi.org/10.5483/BMBRep.2018.51.12.140 |
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author | Ding, Jun Xu, Kangdi Zhang, Jie Lin, Bingyi Wang, Yubo Yin, Shengyong Xie, Haiyang Zhou, Lin Zheng, Shusen |
author_facet | Ding, Jun Xu, Kangdi Zhang, Jie Lin, Bingyi Wang, Yubo Yin, Shengyong Xie, Haiyang Zhou, Lin Zheng, Shusen |
author_sort | Ding, Jun |
collection | PubMed |
description | C-X-C motif chemokine ligand 2 (CXCL2) is a small secreted protein that exhibits a structure similar to the proangiogenic subgroup of the CXC chemokine family. Recently, accumulating evidence suggests that chemokines play a pivotal role in cancer progression and carcinogenesis. We examined the expression levels of 7 types of ELR(+) CXCLs messenger RNA (mRNA) in 264 clinical samples. We found that CXCL2 expression was stably down-regulated in 94% of hepatocellular carcinoma (HCC) specimens compared with paired adjacent normal liver tissues and some HCC cell lines. Moreover, CXCL2 overexpression profoundly attenuated HCC cell proliferation and growth and induced apoptosis in vitro. In animal studies, we found that overexpressing CXCL2 by lentivirus also apparently inhibited the size and weight of subcutaneous tumours in nude mice. Furthermore, we demonstrated that CXCL2 induced HCC cell apoptosis via both nuclear and mitochondrial apoptosis pathways. Our results indicate that CXCL2 negatively regulates the cell cycle in HCC cells via the ERK1/2 signalling pathway. These results provide new insights into HCC and may ultimately lead to the discovery of innovative therapeutic approaches of HCC. |
format | Online Article Text |
id | pubmed-6330937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-63309372019-01-22 Overexpression of CXCL2 inhibits cell proliferation and promotes apoptosis in hepatocellular carcinoma Ding, Jun Xu, Kangdi Zhang, Jie Lin, Bingyi Wang, Yubo Yin, Shengyong Xie, Haiyang Zhou, Lin Zheng, Shusen BMB Rep Articles C-X-C motif chemokine ligand 2 (CXCL2) is a small secreted protein that exhibits a structure similar to the proangiogenic subgroup of the CXC chemokine family. Recently, accumulating evidence suggests that chemokines play a pivotal role in cancer progression and carcinogenesis. We examined the expression levels of 7 types of ELR(+) CXCLs messenger RNA (mRNA) in 264 clinical samples. We found that CXCL2 expression was stably down-regulated in 94% of hepatocellular carcinoma (HCC) specimens compared with paired adjacent normal liver tissues and some HCC cell lines. Moreover, CXCL2 overexpression profoundly attenuated HCC cell proliferation and growth and induced apoptosis in vitro. In animal studies, we found that overexpressing CXCL2 by lentivirus also apparently inhibited the size and weight of subcutaneous tumours in nude mice. Furthermore, we demonstrated that CXCL2 induced HCC cell apoptosis via both nuclear and mitochondrial apoptosis pathways. Our results indicate that CXCL2 negatively regulates the cell cycle in HCC cells via the ERK1/2 signalling pathway. These results provide new insights into HCC and may ultimately lead to the discovery of innovative therapeutic approaches of HCC. Korean Society for Biochemistry and Molecular Biology 2018-12 2018-12-31 /pmc/articles/PMC6330937/ /pubmed/30293547 http://dx.doi.org/10.5483/BMBRep.2018.51.12.140 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 Ding, Jun Xu, Kangdi Zhang, Jie Lin, Bingyi Wang, Yubo Yin, Shengyong Xie, Haiyang Zhou, Lin Zheng, Shusen Overexpression of CXCL2 inhibits cell proliferation and promotes apoptosis in hepatocellular carcinoma |
title | Overexpression of CXCL2 inhibits cell proliferation and promotes apoptosis in hepatocellular carcinoma |
title_full | Overexpression of CXCL2 inhibits cell proliferation and promotes apoptosis in hepatocellular carcinoma |
title_fullStr | Overexpression of CXCL2 inhibits cell proliferation and promotes apoptosis in hepatocellular carcinoma |
title_full_unstemmed | Overexpression of CXCL2 inhibits cell proliferation and promotes apoptosis in hepatocellular carcinoma |
title_short | Overexpression of CXCL2 inhibits cell proliferation and promotes apoptosis in hepatocellular carcinoma |
title_sort | overexpression of cxcl2 inhibits cell proliferation and promotes apoptosis in hepatocellular carcinoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330937/ https://www.ncbi.nlm.nih.gov/pubmed/30293547 http://dx.doi.org/10.5483/BMBRep.2018.51.12.140 |
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