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Sema4C modulates the migration of primary tumor-associated lymphatic endothelial cells via an ERK-mediated pathway

Although lymphatic endothelial cells (LECs) serve a positive role in tumor lymphatic metastasis, the regulation of LECs undergoing migration similar to that of tumor cells remains poorly understood. A previous study revealed that semaphorin 4C (Sema4C) could be a marker of LECs in cervical cancer. T...

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Autores principales: Peng, Jin, Liu, Xijiang, Li, Chengcheng, Gao, Min, Wang, Hongyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383750/
https://www.ncbi.nlm.nih.gov/pubmed/34504556
http://dx.doi.org/10.3892/etm.2021.10535
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author Peng, Jin
Liu, Xijiang
Li, Chengcheng
Gao, Min
Wang, Hongyan
author_facet Peng, Jin
Liu, Xijiang
Li, Chengcheng
Gao, Min
Wang, Hongyan
author_sort Peng, Jin
collection PubMed
description Although lymphatic endothelial cells (LECs) serve a positive role in tumor lymphatic metastasis, the regulation of LECs undergoing migration similar to that of tumor cells remains poorly understood. A previous study revealed that semaphorin 4C (Sema4C) could be a marker of LECs in cervical cancer. Thus, the present study aimed to understand the mechanism via which Sema4C could promote the development of tumor-associated characteristics in LECs in cervical cancer. Primary tumor-associated LECs (TLECs) were distinguished from cervical cancer by flow cytometry. The promigratory ability was assessed using the Transwell assay. Lentivirus infection was used to alter the expression of Sema4C in TLECs. Confocal laser scanning was used to determine the infection efficiency of lentivirus infection. Sema4C/ERK/E-cadherin pathway was measured by reverse transcription-quantitative PCR and western blotting. The co-localization of Sema4C and the lymphatic marker lymphatic vessel endothelial hyaluronan receptor 1 was verified. Primary tumor-associated LECs (TLECs) were isolated from a mouse xenograft cervical tumor model. It was revealed that overexpressing Sema4C stimulated the migratory ability of TLECs, downregulated E-cadherin expression and stimulated ERK phosphorylation, whereas knocking down Sema4C had the opposite effects. The treatment of PD98059 (ERK inhibitor) blocked the pro-migratory ability of TLECs, which indicated a dependence on the ERK signaling pathway. It was identified that the Sema4C/ERK/E-cadherin pathway may be critical for the migration of TLECs, which may promote lymph node metastasis. Therefore, Sema4C could be a promising target for the treatment of cervical cancer with lymphatic metastasis.
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spelling pubmed-83837502021-09-08 Sema4C modulates the migration of primary tumor-associated lymphatic endothelial cells via an ERK-mediated pathway Peng, Jin Liu, Xijiang Li, Chengcheng Gao, Min Wang, Hongyan Exp Ther Med Articles Although lymphatic endothelial cells (LECs) serve a positive role in tumor lymphatic metastasis, the regulation of LECs undergoing migration similar to that of tumor cells remains poorly understood. A previous study revealed that semaphorin 4C (Sema4C) could be a marker of LECs in cervical cancer. Thus, the present study aimed to understand the mechanism via which Sema4C could promote the development of tumor-associated characteristics in LECs in cervical cancer. Primary tumor-associated LECs (TLECs) were distinguished from cervical cancer by flow cytometry. The promigratory ability was assessed using the Transwell assay. Lentivirus infection was used to alter the expression of Sema4C in TLECs. Confocal laser scanning was used to determine the infection efficiency of lentivirus infection. Sema4C/ERK/E-cadherin pathway was measured by reverse transcription-quantitative PCR and western blotting. The co-localization of Sema4C and the lymphatic marker lymphatic vessel endothelial hyaluronan receptor 1 was verified. Primary tumor-associated LECs (TLECs) were isolated from a mouse xenograft cervical tumor model. It was revealed that overexpressing Sema4C stimulated the migratory ability of TLECs, downregulated E-cadherin expression and stimulated ERK phosphorylation, whereas knocking down Sema4C had the opposite effects. The treatment of PD98059 (ERK inhibitor) blocked the pro-migratory ability of TLECs, which indicated a dependence on the ERK signaling pathway. It was identified that the Sema4C/ERK/E-cadherin pathway may be critical for the migration of TLECs, which may promote lymph node metastasis. Therefore, Sema4C could be a promising target for the treatment of cervical cancer with lymphatic metastasis. D.A. Spandidos 2021-10 2021-08-02 /pmc/articles/PMC8383750/ /pubmed/34504556 http://dx.doi.org/10.3892/etm.2021.10535 Text en Copyright: © Peng et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Peng, Jin
Liu, Xijiang
Li, Chengcheng
Gao, Min
Wang, Hongyan
Sema4C modulates the migration of primary tumor-associated lymphatic endothelial cells via an ERK-mediated pathway
title Sema4C modulates the migration of primary tumor-associated lymphatic endothelial cells via an ERK-mediated pathway
title_full Sema4C modulates the migration of primary tumor-associated lymphatic endothelial cells via an ERK-mediated pathway
title_fullStr Sema4C modulates the migration of primary tumor-associated lymphatic endothelial cells via an ERK-mediated pathway
title_full_unstemmed Sema4C modulates the migration of primary tumor-associated lymphatic endothelial cells via an ERK-mediated pathway
title_short Sema4C modulates the migration of primary tumor-associated lymphatic endothelial cells via an ERK-mediated pathway
title_sort sema4c modulates the migration of primary tumor-associated lymphatic endothelial cells via an erk-mediated pathway
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383750/
https://www.ncbi.nlm.nih.gov/pubmed/34504556
http://dx.doi.org/10.3892/etm.2021.10535
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