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The effect of mast cells on the biological characteristics of prostate cancer cells

AIM OF THE STUDY: To investigate the effects of mast cells on the proliferation, invasion, and metastasis of prostate cancer cells. MATERIAL AND METHODS: The mast cell P815 and prostate cancer LNCaP cells were chosen using a Transwell chamber to construct a two-cell cocultured in vitro model to obse...

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Autores principales: Ma, Zhifang, Yue, Liang, Xu, Zhaoliang, Zeng, Sheng, Ma, Yukun, Li, Zhuoping, Li, Wei, Wang, Dongwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Society of Experimental and Clinical Immunology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5927167/
https://www.ncbi.nlm.nih.gov/pubmed/29731687
http://dx.doi.org/10.5114/ceji.2018.74867
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author Ma, Zhifang
Yue, Liang
Xu, Zhaoliang
Zeng, Sheng
Ma, Yukun
Li, Zhuoping
Li, Wei
Wang, Dongwen
author_facet Ma, Zhifang
Yue, Liang
Xu, Zhaoliang
Zeng, Sheng
Ma, Yukun
Li, Zhuoping
Li, Wei
Wang, Dongwen
author_sort Ma, Zhifang
collection PubMed
description AIM OF THE STUDY: To investigate the effects of mast cells on the proliferation, invasion, and metastasis of prostate cancer cells. MATERIAL AND METHODS: The mast cell P815 and prostate cancer LNCaP cells were chosen using a Transwell chamber to construct a two-cell cocultured in vitro model to observe the migration of mast cells to prostate cancer cells. RESULTS: In the migration experiment, the migration rate of mast cells from the experimental group (%) was 10.167 ±0.833, the mast cell migration rate (%) of the control group was 0.833 ±0.208, and the difference was statistically significant (p < 0.05). The MTT test showed that the OD value of cells in each group over time increased gradually, and 24 h after LNCaP cells were cocultured with different concentrations of mast cells, the OD value was significantly higher than that of the control group (p < 0.05). QRT-PCR and western blot results showed that, compared with the control group, E-cad expression from the experimental group was significantly weakened; N-cad and vimentin expression increased (p < 0.05), and c-kit and SCF expression from experimental group were significantly higher than that of the control group (p < 0.05). After the addition of c-kit neutralising antibodies, compared with the control group, the mast cell migration rate of experimental group decreased significantly and prostate cancer cell proliferation significantly decreased (p < 0.05). CONCLUSIONS: Mast cells could promote the proliferation of prostate cancer cells and the occurrence of epithelial mesenchymal transition (EMT), which could promote the invasion and metastasis of prostate cancer cells.
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spelling pubmed-59271672018-05-04 The effect of mast cells on the biological characteristics of prostate cancer cells Ma, Zhifang Yue, Liang Xu, Zhaoliang Zeng, Sheng Ma, Yukun Li, Zhuoping Li, Wei Wang, Dongwen Cent Eur J Immunol Experimental Immunology AIM OF THE STUDY: To investigate the effects of mast cells on the proliferation, invasion, and metastasis of prostate cancer cells. MATERIAL AND METHODS: The mast cell P815 and prostate cancer LNCaP cells were chosen using a Transwell chamber to construct a two-cell cocultured in vitro model to observe the migration of mast cells to prostate cancer cells. RESULTS: In the migration experiment, the migration rate of mast cells from the experimental group (%) was 10.167 ±0.833, the mast cell migration rate (%) of the control group was 0.833 ±0.208, and the difference was statistically significant (p < 0.05). The MTT test showed that the OD value of cells in each group over time increased gradually, and 24 h after LNCaP cells were cocultured with different concentrations of mast cells, the OD value was significantly higher than that of the control group (p < 0.05). QRT-PCR and western blot results showed that, compared with the control group, E-cad expression from the experimental group was significantly weakened; N-cad and vimentin expression increased (p < 0.05), and c-kit and SCF expression from experimental group were significantly higher than that of the control group (p < 0.05). After the addition of c-kit neutralising antibodies, compared with the control group, the mast cell migration rate of experimental group decreased significantly and prostate cancer cell proliferation significantly decreased (p < 0.05). CONCLUSIONS: Mast cells could promote the proliferation of prostate cancer cells and the occurrence of epithelial mesenchymal transition (EMT), which could promote the invasion and metastasis of prostate cancer cells. Polish Society of Experimental and Clinical Immunology 2018-03-30 2018 /pmc/articles/PMC5927167/ /pubmed/29731687 http://dx.doi.org/10.5114/ceji.2018.74867 Text en Copyright: © 2018 Polish Society of Experimental and Clinical Immunology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Experimental Immunology
Ma, Zhifang
Yue, Liang
Xu, Zhaoliang
Zeng, Sheng
Ma, Yukun
Li, Zhuoping
Li, Wei
Wang, Dongwen
The effect of mast cells on the biological characteristics of prostate cancer cells
title The effect of mast cells on the biological characteristics of prostate cancer cells
title_full The effect of mast cells on the biological characteristics of prostate cancer cells
title_fullStr The effect of mast cells on the biological characteristics of prostate cancer cells
title_full_unstemmed The effect of mast cells on the biological characteristics of prostate cancer cells
title_short The effect of mast cells on the biological characteristics of prostate cancer cells
title_sort effect of mast cells on the biological characteristics of prostate cancer cells
topic Experimental Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5927167/
https://www.ncbi.nlm.nih.gov/pubmed/29731687
http://dx.doi.org/10.5114/ceji.2018.74867
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