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Semen affects the biological behavior of HeLa cells by altering ERK signaling

INTRODUCTION: The aim of the study was to investigate the effects of human semen on the proliferation, survival, migration and invasion of HeLa cervical cancer cells by analyzing the extracellular regulated protein kinase (ERK) pathway. MATERIAL AND METHODS: HeLa cells were stimulated with different...

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Autores principales: Guo, Zhi-Qiang, Zhang, Dan-Dan, Pang, Li, Wang, Yu-Ting, Cao, Pin, Zhang, Shu-Lan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286324/
https://www.ncbi.nlm.nih.gov/pubmed/32542095
http://dx.doi.org/10.5114/aoms.2019.81738
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author Guo, Zhi-Qiang
Zhang, Dan-Dan
Pang, Li
Wang, Yu-Ting
Cao, Pin
Zhang, Shu-Lan
author_facet Guo, Zhi-Qiang
Zhang, Dan-Dan
Pang, Li
Wang, Yu-Ting
Cao, Pin
Zhang, Shu-Lan
author_sort Guo, Zhi-Qiang
collection PubMed
description INTRODUCTION: The aim of the study was to investigate the effects of human semen on the proliferation, survival, migration and invasion of HeLa cervical cancer cells by analyzing the extracellular regulated protein kinase (ERK) pathway. MATERIAL AND METHODS: HeLa cells were stimulated with different concentrations of human semen. MTT assay was used to analyze the effects on cell proliferation. Apoptosis in the different experimental groups was quantified by Annexin V-FITC/PI staining. The effect of seminal plasma on in vitro invasiveness of cells was evaluated using transwell assay. Western blotting was used to evaluate ERK pathway activation. RESULTS: Human semen promoted HeLa cell proliferation; ERK1/2 phosphorylation and c-myc expression also increased with increasing semen concentration. U0126 inhibited semen-induced ERK1/2 phosphorylation, c-myc upregulation and cell proliferation. Compared with the control group, semen did not significantly affect the apoptotic rate of HeLa cells (p > 0.05). The transwell assays showed that compared with the control group, the number of invading cells increased significantly with increasing semen concentration, and the difference was significant (p < 0.05) when 1 : 50 semen was added, suggesting that semen promotes the invasion of cervical cancer cells. Western blotting indicated that ERK1/2 phosphorylation began to increase when 1 : 100 semen was added; with increasing semen concentration, ERK1/2 phosphorylation was significantly up-regulated, and the expression of its downstream target gene, c-myc, was also up-regulated (p < 0.05). CONCLUSIONS: Semen promoted the proliferation of HeLa cells by activating the ERK pathway and showed increased tumorigenic potential in vivo. Human seminal plasma might be a potential factor contributing to the development of cervical cancer.
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spelling pubmed-72863242020-06-14 Semen affects the biological behavior of HeLa cells by altering ERK signaling Guo, Zhi-Qiang Zhang, Dan-Dan Pang, Li Wang, Yu-Ting Cao, Pin Zhang, Shu-Lan Arch Med Sci Basic Research INTRODUCTION: The aim of the study was to investigate the effects of human semen on the proliferation, survival, migration and invasion of HeLa cervical cancer cells by analyzing the extracellular regulated protein kinase (ERK) pathway. MATERIAL AND METHODS: HeLa cells were stimulated with different concentrations of human semen. MTT assay was used to analyze the effects on cell proliferation. Apoptosis in the different experimental groups was quantified by Annexin V-FITC/PI staining. The effect of seminal plasma on in vitro invasiveness of cells was evaluated using transwell assay. Western blotting was used to evaluate ERK pathway activation. RESULTS: Human semen promoted HeLa cell proliferation; ERK1/2 phosphorylation and c-myc expression also increased with increasing semen concentration. U0126 inhibited semen-induced ERK1/2 phosphorylation, c-myc upregulation and cell proliferation. Compared with the control group, semen did not significantly affect the apoptotic rate of HeLa cells (p > 0.05). The transwell assays showed that compared with the control group, the number of invading cells increased significantly with increasing semen concentration, and the difference was significant (p < 0.05) when 1 : 50 semen was added, suggesting that semen promotes the invasion of cervical cancer cells. Western blotting indicated that ERK1/2 phosphorylation began to increase when 1 : 100 semen was added; with increasing semen concentration, ERK1/2 phosphorylation was significantly up-regulated, and the expression of its downstream target gene, c-myc, was also up-regulated (p < 0.05). CONCLUSIONS: Semen promoted the proliferation of HeLa cells by activating the ERK pathway and showed increased tumorigenic potential in vivo. Human seminal plasma might be a potential factor contributing to the development of cervical cancer. Termedia Publishing House 2019-01-30 /pmc/articles/PMC7286324/ /pubmed/32542095 http://dx.doi.org/10.5114/aoms.2019.81738 Text en Copyright © 2019 Termedia & Banach 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 (http://creativecommons.org/licenses/by-nc-sa/4.0/)
spellingShingle Basic Research
Guo, Zhi-Qiang
Zhang, Dan-Dan
Pang, Li
Wang, Yu-Ting
Cao, Pin
Zhang, Shu-Lan
Semen affects the biological behavior of HeLa cells by altering ERK signaling
title Semen affects the biological behavior of HeLa cells by altering ERK signaling
title_full Semen affects the biological behavior of HeLa cells by altering ERK signaling
title_fullStr Semen affects the biological behavior of HeLa cells by altering ERK signaling
title_full_unstemmed Semen affects the biological behavior of HeLa cells by altering ERK signaling
title_short Semen affects the biological behavior of HeLa cells by altering ERK signaling
title_sort semen affects the biological behavior of hela cells by altering erk signaling
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286324/
https://www.ncbi.nlm.nih.gov/pubmed/32542095
http://dx.doi.org/10.5114/aoms.2019.81738
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