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GDI2 is a novel diagnostic and prognostic biomarker in hepatocellular carcinoma

Background: GDP Dissociation inhibitor 2 (GDI2) gene has been correlated with some important biological processes in a variety of cancers, whereas the role of GDI2 in hepatocellular carcinoma (HCC) is ill-defined. We aimed to demonstrate the relationship between GDI2 and HCC based on The Cancer Geno...

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Autores principales: Zhang, Wen, Liu, Zhongjian, Xia, Shilin, Yao, Lei, Li, Lan, Gan, Ziying, Tang, Hui, Guo, Qiang, Yan, Xinmin, Sun, Zhiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8714169/
https://www.ncbi.nlm.nih.gov/pubmed/34894398
http://dx.doi.org/10.18632/aging.203748
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author Zhang, Wen
Liu, Zhongjian
Xia, Shilin
Yao, Lei
Li, Lan
Gan, Ziying
Tang, Hui
Guo, Qiang
Yan, Xinmin
Sun, Zhiwei
author_facet Zhang, Wen
Liu, Zhongjian
Xia, Shilin
Yao, Lei
Li, Lan
Gan, Ziying
Tang, Hui
Guo, Qiang
Yan, Xinmin
Sun, Zhiwei
author_sort Zhang, Wen
collection PubMed
description Background: GDP Dissociation inhibitor 2 (GDI2) gene has been correlated with some important biological processes in a variety of cancers, whereas the role of GDI2 in hepatocellular carcinoma (HCC) is ill-defined. We aimed to demonstrate the relationship between GDI2 and HCC based on The Cancer Genome Atlas (TCGA) data mining. Methods: The expression of GDI2 was compared between cancer and normal tissues of 371 HCC patients collected from TCGA-LIHC, and verified in HCC cell lines. Gene set enrichment analysis (GSEA) was applied to annotate biological function of GDI2. Furthermore, Wilcoxon rank sum test, Logistics regression, as well as Cox regression and Kaplan-Meier survival analysis, were employed to evaluate the association of GDI2 expression with clinicopathological characteristics, and survival status of HCC patients, respectively. Results: It showed that the expression of GDI2 was much higher in tumor tissues than in normal tissues (P < 0.001) of HCC patients. And the elevated expression of GDI2 was correlated with more aggressive HCC tumor status, including severe primary tumor extent, advanced pathological stage, serious histologic grade, and mutated TP53 status (P < 0.05). Moreover, high GDI2 expression was strongly associated with a poor survival rate (P < 0.001). Both enrichment and immune infiltration analyses implied that GDI2-associated signaling mainly involve lipid metabolism and extracellular matrix (ECM) constructing pathways related to tumor microenvironment (TME) (P < 0.05). Conclusions: The elevated expression of GDI2 predicts poor prognosis in HCC patients, indicating that GDI2 could be applied as a predictive biomarker for diagnosis and prognosis of HCC.
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spelling pubmed-87141692021-12-29 GDI2 is a novel diagnostic and prognostic biomarker in hepatocellular carcinoma Zhang, Wen Liu, Zhongjian Xia, Shilin Yao, Lei Li, Lan Gan, Ziying Tang, Hui Guo, Qiang Yan, Xinmin Sun, Zhiwei Aging (Albany NY) Research Paper Background: GDP Dissociation inhibitor 2 (GDI2) gene has been correlated with some important biological processes in a variety of cancers, whereas the role of GDI2 in hepatocellular carcinoma (HCC) is ill-defined. We aimed to demonstrate the relationship between GDI2 and HCC based on The Cancer Genome Atlas (TCGA) data mining. Methods: The expression of GDI2 was compared between cancer and normal tissues of 371 HCC patients collected from TCGA-LIHC, and verified in HCC cell lines. Gene set enrichment analysis (GSEA) was applied to annotate biological function of GDI2. Furthermore, Wilcoxon rank sum test, Logistics regression, as well as Cox regression and Kaplan-Meier survival analysis, were employed to evaluate the association of GDI2 expression with clinicopathological characteristics, and survival status of HCC patients, respectively. Results: It showed that the expression of GDI2 was much higher in tumor tissues than in normal tissues (P < 0.001) of HCC patients. And the elevated expression of GDI2 was correlated with more aggressive HCC tumor status, including severe primary tumor extent, advanced pathological stage, serious histologic grade, and mutated TP53 status (P < 0.05). Moreover, high GDI2 expression was strongly associated with a poor survival rate (P < 0.001). Both enrichment and immune infiltration analyses implied that GDI2-associated signaling mainly involve lipid metabolism and extracellular matrix (ECM) constructing pathways related to tumor microenvironment (TME) (P < 0.05). Conclusions: The elevated expression of GDI2 predicts poor prognosis in HCC patients, indicating that GDI2 could be applied as a predictive biomarker for diagnosis and prognosis of HCC. Impact Journals 2021-12-11 /pmc/articles/PMC8714169/ /pubmed/34894398 http://dx.doi.org/10.18632/aging.203748 Text en Copyright: © 2021 Zhang et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/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
Zhang, Wen
Liu, Zhongjian
Xia, Shilin
Yao, Lei
Li, Lan
Gan, Ziying
Tang, Hui
Guo, Qiang
Yan, Xinmin
Sun, Zhiwei
GDI2 is a novel diagnostic and prognostic biomarker in hepatocellular carcinoma
title GDI2 is a novel diagnostic and prognostic biomarker in hepatocellular carcinoma
title_full GDI2 is a novel diagnostic and prognostic biomarker in hepatocellular carcinoma
title_fullStr GDI2 is a novel diagnostic and prognostic biomarker in hepatocellular carcinoma
title_full_unstemmed GDI2 is a novel diagnostic and prognostic biomarker in hepatocellular carcinoma
title_short GDI2 is a novel diagnostic and prognostic biomarker in hepatocellular carcinoma
title_sort gdi2 is a novel diagnostic and prognostic biomarker in hepatocellular carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8714169/
https://www.ncbi.nlm.nih.gov/pubmed/34894398
http://dx.doi.org/10.18632/aging.203748
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