Pyroptosis of MCF7 Cells Induced by the Secreted Factors of hUCMSCs

Human umbilical cord mesenchymal stem cells (hUCMSCs) are superior to other sources of mesenchymal stem/stromal cells (MSCs), and they are used as a novel tool for cell-based cancer therapy. However, the mechanism underlying hUCMSC-induced cancer cell death is not clear. In the present study, we aim...

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Main Authors: Yang Jiao, Hongbo Zhao, Guodong Chen, Xiongbo Sang, Luhan Yang, Zongliu Hou, Wei Si, Bingrong Zheng
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2018/5912194
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spelling doaj-04372ecf992e4b2a8802d57938c158d32020-11-24T21:01:38ZengHindawi LimitedStem Cells International1687-966X1687-96782018-01-01201810.1155/2018/59121945912194Pyroptosis of MCF7 Cells Induced by the Secreted Factors of hUCMSCsYang Jiao0Hongbo Zhao1Guodong Chen2Xiongbo Sang3Luhan Yang4Zongliu Hou5Wei Si6Bingrong Zheng7School of Medicine, Yunnan University, Kunming, 650091 Yunnan, ChinaYunnan Key Laboratory of Stem Cell and Regenerative Medicine, Institute of Molecular and Clinical medicine, Kunming Medical University, Kunming, 650500 Yunnan, ChinaSchool of Medicine, Yunnan University, Kunming, 650091 Yunnan, ChinaSchool of Medicine, Yunnan University, Kunming, 650091 Yunnan, ChinaSchool of Medicine, Yunnan University, Kunming, 650091 Yunnan, ChinaYan’an Hospital of Kunming City, Kunming, 650051 Yunnan, ChinaYunnan Key Laboratory of Primate Biomedical Research, Institute of Primate Translational Medicine, Kunming University of Science and Technology, Kunming, 650500 Yunnan, ChinaSchool of Medicine, Yunnan University, Kunming, 650091 Yunnan, ChinaHuman umbilical cord mesenchymal stem cells (hUCMSCs) are superior to other sources of mesenchymal stem/stromal cells (MSCs), and they are used as a novel tool for cell-based cancer therapy. However, the mechanism underlying hUCMSC-induced cancer cell death is not clear. In the present study, we aimed to evaluate the effect of secreted factors of hUCMSCs on the breast cancer cell line MCF7 by exposing them to the conditioned medium (CM) of hUCMSCs. We evaluated the morphological changes, cell viability, cell cycle, apoptosis, DNA fragmentation, and interleukin-1β (IL-1β) secretion of CM-exposed MCF7 cells. The results showed that the secreted factors of hUCMSCs could cause MCF7 cell death by inducing pyroptosis. We also sequenced the total RNA, and the differentially expressed genes (DEGs) were subjected to the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. A total of 2597 (1822 upregulated and 775 downregulated) genes were identified and 14 pathways were significantly enriched. The results showed that the expression of the pyroptosis-related genes NLRP1 and CASP4 and the inflammation-related pathways changed significantly in MCF7 cells exposed to the CM. To the best of our knowledge, this study is the first to report that the secreted factors of hUCMSCs can cause MCF7 cell pyroptosis. Furthermore, it is the first to examine the global gene expression in MCF7 cells exposed to CM. These results will provide valuable information for further studies on the mechanism of MCF7 cell pyroptosis induced by the secreted factors of hUCMSCs. It will also help understand the effect of hUCMSCs on cell-based breast cancer therapy.http://dx.doi.org/10.1155/2018/5912194
collection DOAJ
language English
format Article
sources DOAJ
author Yang Jiao
Hongbo Zhao
Guodong Chen
Xiongbo Sang
Luhan Yang
Zongliu Hou
Wei Si
Bingrong Zheng
spellingShingle Yang Jiao
Hongbo Zhao
Guodong Chen
Xiongbo Sang
Luhan Yang
Zongliu Hou
Wei Si
Bingrong Zheng
Pyroptosis of MCF7 Cells Induced by the Secreted Factors of hUCMSCs
Stem Cells International
author_facet Yang Jiao
Hongbo Zhao
Guodong Chen
Xiongbo Sang
Luhan Yang
Zongliu Hou
Wei Si
Bingrong Zheng
author_sort Yang Jiao
title Pyroptosis of MCF7 Cells Induced by the Secreted Factors of hUCMSCs
title_short Pyroptosis of MCF7 Cells Induced by the Secreted Factors of hUCMSCs
title_full Pyroptosis of MCF7 Cells Induced by the Secreted Factors of hUCMSCs
title_fullStr Pyroptosis of MCF7 Cells Induced by the Secreted Factors of hUCMSCs
title_full_unstemmed Pyroptosis of MCF7 Cells Induced by the Secreted Factors of hUCMSCs
title_sort pyroptosis of mcf7 cells induced by the secreted factors of hucmscs
publisher Hindawi Limited
series Stem Cells International
issn 1687-966X
1687-9678
publishDate 2018-01-01
description Human umbilical cord mesenchymal stem cells (hUCMSCs) are superior to other sources of mesenchymal stem/stromal cells (MSCs), and they are used as a novel tool for cell-based cancer therapy. However, the mechanism underlying hUCMSC-induced cancer cell death is not clear. In the present study, we aimed to evaluate the effect of secreted factors of hUCMSCs on the breast cancer cell line MCF7 by exposing them to the conditioned medium (CM) of hUCMSCs. We evaluated the morphological changes, cell viability, cell cycle, apoptosis, DNA fragmentation, and interleukin-1β (IL-1β) secretion of CM-exposed MCF7 cells. The results showed that the secreted factors of hUCMSCs could cause MCF7 cell death by inducing pyroptosis. We also sequenced the total RNA, and the differentially expressed genes (DEGs) were subjected to the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. A total of 2597 (1822 upregulated and 775 downregulated) genes were identified and 14 pathways were significantly enriched. The results showed that the expression of the pyroptosis-related genes NLRP1 and CASP4 and the inflammation-related pathways changed significantly in MCF7 cells exposed to the CM. To the best of our knowledge, this study is the first to report that the secreted factors of hUCMSCs can cause MCF7 cell pyroptosis. Furthermore, it is the first to examine the global gene expression in MCF7 cells exposed to CM. These results will provide valuable information for further studies on the mechanism of MCF7 cell pyroptosis induced by the secreted factors of hUCMSCs. It will also help understand the effect of hUCMSCs on cell-based breast cancer therapy.
url http://dx.doi.org/10.1155/2018/5912194
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