Cargando…

Dysregulation of GTPase IMAP family members in hepatocellular cancer

Hepatocellular carcinoma (HCC) is one of the most life-threatening diseases in the world. Members of the GTPase of the immunity-associated protein (GIMAP) family are important in regulating apoptosis in cancer cells. However, the basic mechanism of GIMAP in HCC remains to be fully elucidated. The pr...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Zhen, Zhang, Wei, Gao, Chunhai, Ji, Baoju, Chi, Xiuwen, Zheng, Wei, Wang, Hai Lan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5101897/
https://www.ncbi.nlm.nih.gov/pubmed/27667392
http://dx.doi.org/10.3892/mmr.2016.5764
_version_ 1782466373294751744
author Huang, Zhen
Zhang, Wei
Gao, Chunhai
Ji, Baoju
Chi, Xiuwen
Zheng, Wei
Wang, Hai Lan
author_facet Huang, Zhen
Zhang, Wei
Gao, Chunhai
Ji, Baoju
Chi, Xiuwen
Zheng, Wei
Wang, Hai Lan
author_sort Huang, Zhen
collection PubMed
description Hepatocellular carcinoma (HCC) is one of the most life-threatening diseases in the world. Members of the GTPase of the immunity-associated protein (GIMAP) family are important in regulating apoptosis in cancer cells. However, the basic mechanism of GIMAP in HCC remains to be fully elucidated. The present study was performed to investigate the dysregulation of GIMAP family members in HCC. The techniques of polymerase chain reaction analysis, immunohistochemistry and ELISA were used to analyze the expression of GIMAP5 and GIMAP6 in HCC tissues, in matched noncancerous tissue samples, and in blood samples obtained from patients with HCC and healthy subjects. It was found that the mRNA expression levels of GIMAP5 and GIMAP6 were significantly downregulated in the HCC tumor samples, compared with the levels of expression in the matched non-tumor tissue samples. Similarly, the mRNA expression levels of GIMAP5 and GIMAP6 were also significantly downregulated in the blood samples from patients with HCC, compared with the expression levels in the blood from healthy subjects. At the protein level, it was found that the GIMAP5 and GIMAP6 proteins were expressed at lower levels in the tumor tissue samples, compared with the matched normal tissue samples, and their expression levels were also lower in the blood samples from patients with HCC, compared with the blood samples from the healthy subjects. These data, demonstrating the downregulation of the mRNA and protein expression levels of GIMAP5 and GIMAP6 in the tumor tissues and blood of patients with HCC, suggested the involvement of GIMAP5 and GIMAP6 in the pathogenesis of HCC, and indicate their possible use as diagnostic markers for HCC.
format Online
Article
Text
id pubmed-5101897
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-51018972016-11-22 Dysregulation of GTPase IMAP family members in hepatocellular cancer Huang, Zhen Zhang, Wei Gao, Chunhai Ji, Baoju Chi, Xiuwen Zheng, Wei Wang, Hai Lan Mol Med Rep Articles Hepatocellular carcinoma (HCC) is one of the most life-threatening diseases in the world. Members of the GTPase of the immunity-associated protein (GIMAP) family are important in regulating apoptosis in cancer cells. However, the basic mechanism of GIMAP in HCC remains to be fully elucidated. The present study was performed to investigate the dysregulation of GIMAP family members in HCC. The techniques of polymerase chain reaction analysis, immunohistochemistry and ELISA were used to analyze the expression of GIMAP5 and GIMAP6 in HCC tissues, in matched noncancerous tissue samples, and in blood samples obtained from patients with HCC and healthy subjects. It was found that the mRNA expression levels of GIMAP5 and GIMAP6 were significantly downregulated in the HCC tumor samples, compared with the levels of expression in the matched non-tumor tissue samples. Similarly, the mRNA expression levels of GIMAP5 and GIMAP6 were also significantly downregulated in the blood samples from patients with HCC, compared with the expression levels in the blood from healthy subjects. At the protein level, it was found that the GIMAP5 and GIMAP6 proteins were expressed at lower levels in the tumor tissue samples, compared with the matched normal tissue samples, and their expression levels were also lower in the blood samples from patients with HCC, compared with the blood samples from the healthy subjects. These data, demonstrating the downregulation of the mRNA and protein expression levels of GIMAP5 and GIMAP6 in the tumor tissues and blood of patients with HCC, suggested the involvement of GIMAP5 and GIMAP6 in the pathogenesis of HCC, and indicate their possible use as diagnostic markers for HCC. D.A. Spandidos 2016-11 2016-09-22 /pmc/articles/PMC5101897/ /pubmed/27667392 http://dx.doi.org/10.3892/mmr.2016.5764 Text en Copyright: © Huang et al. 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
Huang, Zhen
Zhang, Wei
Gao, Chunhai
Ji, Baoju
Chi, Xiuwen
Zheng, Wei
Wang, Hai Lan
Dysregulation of GTPase IMAP family members in hepatocellular cancer
title Dysregulation of GTPase IMAP family members in hepatocellular cancer
title_full Dysregulation of GTPase IMAP family members in hepatocellular cancer
title_fullStr Dysregulation of GTPase IMAP family members in hepatocellular cancer
title_full_unstemmed Dysregulation of GTPase IMAP family members in hepatocellular cancer
title_short Dysregulation of GTPase IMAP family members in hepatocellular cancer
title_sort dysregulation of gtpase imap family members in hepatocellular cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5101897/
https://www.ncbi.nlm.nih.gov/pubmed/27667392
http://dx.doi.org/10.3892/mmr.2016.5764
work_keys_str_mv AT huangzhen dysregulationofgtpaseimapfamilymembersinhepatocellularcancer
AT zhangwei dysregulationofgtpaseimapfamilymembersinhepatocellularcancer
AT gaochunhai dysregulationofgtpaseimapfamilymembersinhepatocellularcancer
AT jibaoju dysregulationofgtpaseimapfamilymembersinhepatocellularcancer
AT chixiuwen dysregulationofgtpaseimapfamilymembersinhepatocellularcancer
AT zhengwei dysregulationofgtpaseimapfamilymembersinhepatocellularcancer
AT wanghailan dysregulationofgtpaseimapfamilymembersinhepatocellularcancer