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High expression of angiogenic factor AGGF1 is an independent prognostic factor for hepatocellular carcinoma

BACKGROUND: Angiogenesis plays a critical role in tumor growth and metastasis. Angiogenic factor with G patch and FHA domains 1 (AGGF1) has been recently identified as a novel initiator of angiogenesis. However, the function and the prognostic values of AGGF1 in hepatocellular carcinoma remain poorl...

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Autores principales: Tu, Jianfei, Ying, Xihui, Zhang, Dengke, Weng, Qiaoyou, Mao, Weibo, Chen, Li, Wu, Xulu, Tu, Chaoyong, Ji, Jiansong, Huang, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762347/
https://www.ncbi.nlm.nih.gov/pubmed/29340079
http://dx.doi.org/10.18632/oncotarget.22880
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author Tu, Jianfei
Ying, Xihui
Zhang, Dengke
Weng, Qiaoyou
Mao, Weibo
Chen, Li
Wu, Xulu
Tu, Chaoyong
Ji, Jiansong
Huang, Yuan
author_facet Tu, Jianfei
Ying, Xihui
Zhang, Dengke
Weng, Qiaoyou
Mao, Weibo
Chen, Li
Wu, Xulu
Tu, Chaoyong
Ji, Jiansong
Huang, Yuan
author_sort Tu, Jianfei
collection PubMed
description BACKGROUND: Angiogenesis plays a critical role in tumor growth and metastasis. Angiogenic factor with G patch and FHA domains 1 (AGGF1) has been recently identified as a novel initiator of angiogenesis. However, the function and the prognostic values of AGGF1 in hepatocellular carcinoma remain poorly understood. Our aim is to provide more information to assist design the angiogenesis therapy that targets AGGF1 in HCC. RESULTS: AGGF1-positive frequency in HCC tissues was significantly higher than in peritumor tissues. The high expression of AGGF1 expression in HCC tissue was well associated with the increased expression of VEGF and the high microvessel density (MVD). AGGF1 expression predicts a poor prognosis and AGGF1 was an independent prognostic factor for DFS. METHODS: The expression levels of AGGF1, vascular endothelial growth factor (VEGF) and microvessel density (MVD) were identified by immunohistochemistry in 79 HCC tumor tissues and 24 corresponding peritumor tissues. The expression level of AGGF1 and MVD were quantified by counting the positively stained endothelial cells in the HCC and the peritumor tissue on the immunohistochemically stained tissue slides. The prognostic value of AGGF1 was evaluated by survival analysis. CONCLUSIONS: Our study shows that AGGF1 is identified as the independent prognostic factor for the disease-free survival (DFS) of patients after the surgical resection. contribute to tumor angiogenesis in HCC, which indicates that AGGF1 may be a new potential therapeutic target for anti-angiogenesis treatment for patients with HCC.
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spelling pubmed-57623472018-01-16 High expression of angiogenic factor AGGF1 is an independent prognostic factor for hepatocellular carcinoma Tu, Jianfei Ying, Xihui Zhang, Dengke Weng, Qiaoyou Mao, Weibo Chen, Li Wu, Xulu Tu, Chaoyong Ji, Jiansong Huang, Yuan Oncotarget Research Paper BACKGROUND: Angiogenesis plays a critical role in tumor growth and metastasis. Angiogenic factor with G patch and FHA domains 1 (AGGF1) has been recently identified as a novel initiator of angiogenesis. However, the function and the prognostic values of AGGF1 in hepatocellular carcinoma remain poorly understood. Our aim is to provide more information to assist design the angiogenesis therapy that targets AGGF1 in HCC. RESULTS: AGGF1-positive frequency in HCC tissues was significantly higher than in peritumor tissues. The high expression of AGGF1 expression in HCC tissue was well associated with the increased expression of VEGF and the high microvessel density (MVD). AGGF1 expression predicts a poor prognosis and AGGF1 was an independent prognostic factor for DFS. METHODS: The expression levels of AGGF1, vascular endothelial growth factor (VEGF) and microvessel density (MVD) were identified by immunohistochemistry in 79 HCC tumor tissues and 24 corresponding peritumor tissues. The expression level of AGGF1 and MVD were quantified by counting the positively stained endothelial cells in the HCC and the peritumor tissue on the immunohistochemically stained tissue slides. The prognostic value of AGGF1 was evaluated by survival analysis. CONCLUSIONS: Our study shows that AGGF1 is identified as the independent prognostic factor for the disease-free survival (DFS) of patients after the surgical resection. contribute to tumor angiogenesis in HCC, which indicates that AGGF1 may be a new potential therapeutic target for anti-angiogenesis treatment for patients with HCC. Impact Journals LLC 2017-12-04 /pmc/articles/PMC5762347/ /pubmed/29340079 http://dx.doi.org/10.18632/oncotarget.22880 Text en Copyright: © 2017 Tu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Tu, Jianfei
Ying, Xihui
Zhang, Dengke
Weng, Qiaoyou
Mao, Weibo
Chen, Li
Wu, Xulu
Tu, Chaoyong
Ji, Jiansong
Huang, Yuan
High expression of angiogenic factor AGGF1 is an independent prognostic factor for hepatocellular carcinoma
title High expression of angiogenic factor AGGF1 is an independent prognostic factor for hepatocellular carcinoma
title_full High expression of angiogenic factor AGGF1 is an independent prognostic factor for hepatocellular carcinoma
title_fullStr High expression of angiogenic factor AGGF1 is an independent prognostic factor for hepatocellular carcinoma
title_full_unstemmed High expression of angiogenic factor AGGF1 is an independent prognostic factor for hepatocellular carcinoma
title_short High expression of angiogenic factor AGGF1 is an independent prognostic factor for hepatocellular carcinoma
title_sort high expression of angiogenic factor aggf1 is an independent prognostic factor for hepatocellular carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762347/
https://www.ncbi.nlm.nih.gov/pubmed/29340079
http://dx.doi.org/10.18632/oncotarget.22880
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