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Effects of HLEC on the secreted proteins of epithelial ovarian cancer cells prone to metastasize to lymph nodes
OBJECTIVE: To study explores the effect of HLEC on the secreted proteins of epithelial ovarian cancer (EOC) cells (SKOV3-PM4) with directional highly lymphatic metastasis. METHODS: Supernatants of four groups of cultured cells, namely, SKOV3 (A), SKOV3+HLEC (B), SKOV3-PM4 (C), SKOV3-PM4+HLEC (D), we...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Chinese Anti-Cancer Association
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3860345/ https://www.ncbi.nlm.nih.gov/pubmed/24349832 http://dx.doi.org/10.7497/j.issn.2095-3941.2013.04.006 |
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author | Zhang, Xin-Ying Yin, Fu-Qiang Liu, Li Gao, Ting Ruan, He-Yun Guan, Xiao Lu, Ying-Xin Li, Dan-Rong |
author_facet | Zhang, Xin-Ying Yin, Fu-Qiang Liu, Li Gao, Ting Ruan, He-Yun Guan, Xiao Lu, Ying-Xin Li, Dan-Rong |
author_sort | Zhang, Xin-Ying |
collection | PubMed |
description | OBJECTIVE: To study explores the effect of HLEC on the secreted proteins of epithelial ovarian cancer (EOC) cells (SKOV3-PM4) with directional highly lymphatic metastasis. METHODS: Supernatants of four groups of cultured cells, namely, SKOV3 (A), SKOV3+HLEC (B), SKOV3-PM4 (C), SKOV3-PM4+HLEC (D), were collected, and their proteins were detected by antibody arrays and iTRAQ-2D-LC-MALDI-TOF/TOF/MS. Significantly differential proteins were further analyzed via bioinformatics and validated in human serums and cell media via ELISA. RESULTS: Results of antibody arrays and mass spectrometry demonstrated that GRN and VEGFA were upregulated in group C (compared with group A), whereas IGFBP7 and SPARC were downregulated in group D (compared with group C). Comprehensive bioinformatics analysis results showed that IGFBP7 and VEGFA were closely linked to each other. Further validation with serums showed statistical significance in VEGFA and IGFBP7 levels among groups of patients with ovarian cancers, benign tumors, and control groups. Two proteins were upegulated in the first group. VEGFA in the control group was downregulated. For IGFBP, upregulation in the control group and down-regulation in the first group were also observed. CONCLUSION: The HLEC microenvironment is closely associated with directional metastasis to lymph nodes and with differential proteins including cell stromal proteins and adhesion factors. The upregulation of VEGFA and GRN and the downregulation of SPARC and IGFBP7 are closely associated with directional metastasis to lymph nodes in EOC cells. |
format | Online Article Text |
id | pubmed-3860345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Chinese Anti-Cancer Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-38603452013-12-17 Effects of HLEC on the secreted proteins of epithelial ovarian cancer cells prone to metastasize to lymph nodes Zhang, Xin-Ying Yin, Fu-Qiang Liu, Li Gao, Ting Ruan, He-Yun Guan, Xiao Lu, Ying-Xin Li, Dan-Rong Cancer Biol Med Original Article OBJECTIVE: To study explores the effect of HLEC on the secreted proteins of epithelial ovarian cancer (EOC) cells (SKOV3-PM4) with directional highly lymphatic metastasis. METHODS: Supernatants of four groups of cultured cells, namely, SKOV3 (A), SKOV3+HLEC (B), SKOV3-PM4 (C), SKOV3-PM4+HLEC (D), were collected, and their proteins were detected by antibody arrays and iTRAQ-2D-LC-MALDI-TOF/TOF/MS. Significantly differential proteins were further analyzed via bioinformatics and validated in human serums and cell media via ELISA. RESULTS: Results of antibody arrays and mass spectrometry demonstrated that GRN and VEGFA were upregulated in group C (compared with group A), whereas IGFBP7 and SPARC were downregulated in group D (compared with group C). Comprehensive bioinformatics analysis results showed that IGFBP7 and VEGFA were closely linked to each other. Further validation with serums showed statistical significance in VEGFA and IGFBP7 levels among groups of patients with ovarian cancers, benign tumors, and control groups. Two proteins were upegulated in the first group. VEGFA in the control group was downregulated. For IGFBP, upregulation in the control group and down-regulation in the first group were also observed. CONCLUSION: The HLEC microenvironment is closely associated with directional metastasis to lymph nodes and with differential proteins including cell stromal proteins and adhesion factors. The upregulation of VEGFA and GRN and the downregulation of SPARC and IGFBP7 are closely associated with directional metastasis to lymph nodes in EOC cells. Chinese Anti-Cancer Association 2013-12 /pmc/articles/PMC3860345/ /pubmed/24349832 http://dx.doi.org/10.7497/j.issn.2095-3941.2013.04.006 Text en 2013 Cancer Biology & Medicine This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Original Article Zhang, Xin-Ying Yin, Fu-Qiang Liu, Li Gao, Ting Ruan, He-Yun Guan, Xiao Lu, Ying-Xin Li, Dan-Rong Effects of HLEC on the secreted proteins of epithelial ovarian cancer cells prone to metastasize to lymph nodes |
title | Effects of HLEC on the secreted proteins of epithelial ovarian cancer cells prone to metastasize to lymph nodes |
title_full | Effects of HLEC on the secreted proteins of epithelial ovarian cancer cells prone to metastasize to lymph nodes |
title_fullStr | Effects of HLEC on the secreted proteins of epithelial ovarian cancer cells prone to metastasize to lymph nodes |
title_full_unstemmed | Effects of HLEC on the secreted proteins of epithelial ovarian cancer cells prone to metastasize to lymph nodes |
title_short | Effects of HLEC on the secreted proteins of epithelial ovarian cancer cells prone to metastasize to lymph nodes |
title_sort | effects of hlec on the secreted proteins of epithelial ovarian cancer cells prone to metastasize to lymph nodes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3860345/ https://www.ncbi.nlm.nih.gov/pubmed/24349832 http://dx.doi.org/10.7497/j.issn.2095-3941.2013.04.006 |
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