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High Expression of FLOT1 Is Associated with Progression and Poor Prognosis in Hepatocellular Carcinoma

BACKGROUND: The flotillin family member flotillin-1 (FLOT1) encodes a caveolae-associated, integral membrane protein that belongs to lipid raft family and involves in vesicular trafficking and signal transduction. However, the role of FLOT1 in development and progression of cancer remains largely un...

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Autores principales: Zhang, Shi-Hong, Wang, Chan-Juan, Shi, Ling, Li, Xing-Hua, Zhou, Jing, Song, Li-Bing, Liao, Wen-Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694104/
https://www.ncbi.nlm.nih.gov/pubmed/23840303
http://dx.doi.org/10.1371/journal.pone.0064709
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author Zhang, Shi-Hong
Wang, Chan-Juan
Shi, Ling
Li, Xing-Hua
Zhou, Jing
Song, Li-Bing
Liao, Wen-Ting
author_facet Zhang, Shi-Hong
Wang, Chan-Juan
Shi, Ling
Li, Xing-Hua
Zhou, Jing
Song, Li-Bing
Liao, Wen-Ting
author_sort Zhang, Shi-Hong
collection PubMed
description BACKGROUND: The flotillin family member flotillin-1 (FLOT1) encodes a caveolae-associated, integral membrane protein that belongs to lipid raft family and involves in vesicular trafficking and signal transduction. However, the role of FLOT1 in development and progression of cancer remains largely unknown. The present study was aimed to investigate the clinical and prognostic significance of FLOT1 in hepatocellular carcinoma (HCC). METHODS: Real-time PCR and western blot analyses were applied to examine FLOT1 expression in fourteen HCC cell lines and one normal hepatic cell line, ten pairs of primary HCC and matched adjacent noncancerous liver tissues from the same patient. Immunohistochemistry (IHC) was performed to examine FLOT1 protein expression in paraffin-embedded tissues from 196 HCC patients. Statistical analyses were applied to evaluate the diagnostic value and associations of FLOT1 expression with clinical parameters. RESULTS: FLOT1 expression was evidently up-regulated in HCC tissues compared with that in the matched adjacent noncancerous liver tissues. In the 196 cases of tested HCC samples, FLOT1 protein level was positively correlated with Tumor size (P = 0.025), clinical stage (P<0.002), CLIP stage (P<0.001), vascular invasion (P<0.001), relapse (P<0.001), and serum AFP levels (P = 0.025). Patients with higher FLOT1 expression had shorter overall survival time, whereas those with lower FLOT1 expression had longer survival time. CONCLUSIONS: Our study demonstrated FLOT1 is associated with aggressive characteristics of HCC, and suggested the possibility of its use as a prognostic marker in patients with HCC.
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spelling pubmed-36941042013-07-09 High Expression of FLOT1 Is Associated with Progression and Poor Prognosis in Hepatocellular Carcinoma Zhang, Shi-Hong Wang, Chan-Juan Shi, Ling Li, Xing-Hua Zhou, Jing Song, Li-Bing Liao, Wen-Ting PLoS One Research Article BACKGROUND: The flotillin family member flotillin-1 (FLOT1) encodes a caveolae-associated, integral membrane protein that belongs to lipid raft family and involves in vesicular trafficking and signal transduction. However, the role of FLOT1 in development and progression of cancer remains largely unknown. The present study was aimed to investigate the clinical and prognostic significance of FLOT1 in hepatocellular carcinoma (HCC). METHODS: Real-time PCR and western blot analyses were applied to examine FLOT1 expression in fourteen HCC cell lines and one normal hepatic cell line, ten pairs of primary HCC and matched adjacent noncancerous liver tissues from the same patient. Immunohistochemistry (IHC) was performed to examine FLOT1 protein expression in paraffin-embedded tissues from 196 HCC patients. Statistical analyses were applied to evaluate the diagnostic value and associations of FLOT1 expression with clinical parameters. RESULTS: FLOT1 expression was evidently up-regulated in HCC tissues compared with that in the matched adjacent noncancerous liver tissues. In the 196 cases of tested HCC samples, FLOT1 protein level was positively correlated with Tumor size (P = 0.025), clinical stage (P<0.002), CLIP stage (P<0.001), vascular invasion (P<0.001), relapse (P<0.001), and serum AFP levels (P = 0.025). Patients with higher FLOT1 expression had shorter overall survival time, whereas those with lower FLOT1 expression had longer survival time. CONCLUSIONS: Our study demonstrated FLOT1 is associated with aggressive characteristics of HCC, and suggested the possibility of its use as a prognostic marker in patients with HCC. Public Library of Science 2013-06-26 /pmc/articles/PMC3694104/ /pubmed/23840303 http://dx.doi.org/10.1371/journal.pone.0064709 Text en © 2013 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Shi-Hong
Wang, Chan-Juan
Shi, Ling
Li, Xing-Hua
Zhou, Jing
Song, Li-Bing
Liao, Wen-Ting
High Expression of FLOT1 Is Associated with Progression and Poor Prognosis in Hepatocellular Carcinoma
title High Expression of FLOT1 Is Associated with Progression and Poor Prognosis in Hepatocellular Carcinoma
title_full High Expression of FLOT1 Is Associated with Progression and Poor Prognosis in Hepatocellular Carcinoma
title_fullStr High Expression of FLOT1 Is Associated with Progression and Poor Prognosis in Hepatocellular Carcinoma
title_full_unstemmed High Expression of FLOT1 Is Associated with Progression and Poor Prognosis in Hepatocellular Carcinoma
title_short High Expression of FLOT1 Is Associated with Progression and Poor Prognosis in Hepatocellular Carcinoma
title_sort high expression of flot1 is associated with progression and poor prognosis in hepatocellular carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694104/
https://www.ncbi.nlm.nih.gov/pubmed/23840303
http://dx.doi.org/10.1371/journal.pone.0064709
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