ARHGAP20 Expression Inhibited HCC Progression by Regulating the PI3K-AKT Signaling Pathway
Gao Liu,1,2 Jia Li,1,2 Cai-Yun Zhang,1,2 Dong-Yang Huang,3 Ji-Wei Xu1,2 1Department of Hepatobiliary Surgery, Meizhou People’s Hospital, Meizhou, 514000, People’s Republic of China; 2Guangdong Provincial Key Laboratory of Precision Medicine and Clinical Translational Research of...
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Dove Medical Press
2021-04-01
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Series: | Journal of Hepatocellular Carcinoma |
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Online Access: | https://www.dovepress.com/arhgap20-expression-inhibited-hcc-progression-by-regulating-the-pi3k-a-peer-reviewed-fulltext-article-JHC |
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author | Liu G Li J Zhang CY Huang DY Xu JW |
author_facet | Liu G Li J Zhang CY Huang DY Xu JW |
author_sort | Liu G |
collection | DOAJ |
description | Gao Liu,1,2 Jia Li,1,2 Cai-Yun Zhang,1,2 Dong-Yang Huang,3 Ji-Wei Xu1,2 1Department of Hepatobiliary Surgery, Meizhou People’s Hospital, Meizhou, 514000, People’s Republic of China; 2Guangdong Provincial Key Laboratory of Precision Medicine and Clinical Translational Research of Hakka Population, Meizhou, People’s Republic of China; 3Center for Molecular Biology, Shantou University Medical College, Shantou, Guangdong, 515041, People’s Republic of ChinaCorrespondence: Dong-Yang HuangCenter for Molecular Biology, Shantou University Medical College, Shantou, Guangdong, 515041, People’s Republic of ChinaEmail huangdy@stu.edu.cnJi-Wei XuDepartment of Hepatobiliary Surgery, Meizhou People’s Hospital, No. 38 Huangtang Road, Meizhou, 514000, People’s Republic of ChinaTel +86-13823832715Email javeeht@163.comIntroduction: One of the most common cancers is hepatocellular carcinoma (HCC), which is an aggressive cancer that is associated with high mortality. The expression and role of ARHGAP20 in HCC remain unclear.Materials and Methods: The expression and clinical role of ARHGAP20 were investigated using online databases and HCC samples from Meizhou People’s Hospital. Wound healing assays, transwell migration/invasion assays, and lung metastasis models were performed using nude mice. Gene set enrichment analyses were used to further explore the potential mechanisms.Results: Inspired by expression analyses of three different public databases (ie, TIMER, Oncomine, and HCCDB database), we confirmed that ARHGAP20 was downregulated in clinical HCC tumors compared with normal controls. ARHGAP20 expression inhibited HCC migration and invasion in vitro and in vivo. Based on GSEA results, we tested markers of the PI3K-AKT signaling pathway. Interestingly, while ARHGAP20 upregulation suppressed HCC migration/invasion and phosphorylation of AKT/PI3K molecules, exposure to the PI3K-AKT pathway agonist rhIGF-1 partially rescued these phenomena. ARHGAP20 also showed a close correlation with certain components in the HCC immune microenvironment. Furthermore, we revealed that downregulated ARHGAP20 was significantly correlated with larger tumor size and vascular invasion, and could be used as an adverse independent prognostic factor for HCC OS but not RFS.Conclusion: ARHGAP20 was identified for the first time as a tumor suppressor gene that could inhibit HCC progression by regulating the PI3K-AKT signaling pathway and the immune microenvironment in HCC.Keywords: HCC, ARHGAP20, progression, PI3K-AKT, immune microenvironment |
first_indexed | 2024-12-19T19:43:44Z |
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id | doaj.art-9245f140084643a8bb2279fabfe96135 |
institution | Directory Open Access Journal |
issn | 2253-5969 |
language | English |
last_indexed | 2024-12-19T19:43:44Z |
publishDate | 2021-04-01 |
publisher | Dove Medical Press |
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series | Journal of Hepatocellular Carcinoma |
spelling | doaj.art-9245f140084643a8bb2279fabfe961352022-12-21T20:08:11ZengDove Medical PressJournal of Hepatocellular Carcinoma2253-59692021-04-01Volume 827128464131ARHGAP20 Expression Inhibited HCC Progression by Regulating the PI3K-AKT Signaling PathwayLiu GLi JZhang CYHuang DYXu JWGao Liu,1,2 Jia Li,1,2 Cai-Yun Zhang,1,2 Dong-Yang Huang,3 Ji-Wei Xu1,2 1Department of Hepatobiliary Surgery, Meizhou People’s Hospital, Meizhou, 514000, People’s Republic of China; 2Guangdong Provincial Key Laboratory of Precision Medicine and Clinical Translational Research of Hakka Population, Meizhou, People’s Republic of China; 3Center for Molecular Biology, Shantou University Medical College, Shantou, Guangdong, 515041, People’s Republic of ChinaCorrespondence: Dong-Yang HuangCenter for Molecular Biology, Shantou University Medical College, Shantou, Guangdong, 515041, People’s Republic of ChinaEmail huangdy@stu.edu.cnJi-Wei XuDepartment of Hepatobiliary Surgery, Meizhou People’s Hospital, No. 38 Huangtang Road, Meizhou, 514000, People’s Republic of ChinaTel +86-13823832715Email javeeht@163.comIntroduction: One of the most common cancers is hepatocellular carcinoma (HCC), which is an aggressive cancer that is associated with high mortality. The expression and role of ARHGAP20 in HCC remain unclear.Materials and Methods: The expression and clinical role of ARHGAP20 were investigated using online databases and HCC samples from Meizhou People’s Hospital. Wound healing assays, transwell migration/invasion assays, and lung metastasis models were performed using nude mice. Gene set enrichment analyses were used to further explore the potential mechanisms.Results: Inspired by expression analyses of three different public databases (ie, TIMER, Oncomine, and HCCDB database), we confirmed that ARHGAP20 was downregulated in clinical HCC tumors compared with normal controls. ARHGAP20 expression inhibited HCC migration and invasion in vitro and in vivo. Based on GSEA results, we tested markers of the PI3K-AKT signaling pathway. Interestingly, while ARHGAP20 upregulation suppressed HCC migration/invasion and phosphorylation of AKT/PI3K molecules, exposure to the PI3K-AKT pathway agonist rhIGF-1 partially rescued these phenomena. ARHGAP20 also showed a close correlation with certain components in the HCC immune microenvironment. Furthermore, we revealed that downregulated ARHGAP20 was significantly correlated with larger tumor size and vascular invasion, and could be used as an adverse independent prognostic factor for HCC OS but not RFS.Conclusion: ARHGAP20 was identified for the first time as a tumor suppressor gene that could inhibit HCC progression by regulating the PI3K-AKT signaling pathway and the immune microenvironment in HCC.Keywords: HCC, ARHGAP20, progression, PI3K-AKT, immune microenvironmenthttps://www.dovepress.com/arhgap20-expression-inhibited-hcc-progression-by-regulating-the-pi3k-a-peer-reviewed-fulltext-article-JHChccarhgap20progressionpi3k-aktimmune microenvironment |
spellingShingle | Liu G Li J Zhang CY Huang DY Xu JW ARHGAP20 Expression Inhibited HCC Progression by Regulating the PI3K-AKT Signaling Pathway Journal of Hepatocellular Carcinoma hcc arhgap20 progression pi3k-akt immune microenvironment |
title | ARHGAP20 Expression Inhibited HCC Progression by Regulating the PI3K-AKT Signaling Pathway |
title_full | ARHGAP20 Expression Inhibited HCC Progression by Regulating the PI3K-AKT Signaling Pathway |
title_fullStr | ARHGAP20 Expression Inhibited HCC Progression by Regulating the PI3K-AKT Signaling Pathway |
title_full_unstemmed | ARHGAP20 Expression Inhibited HCC Progression by Regulating the PI3K-AKT Signaling Pathway |
title_short | ARHGAP20 Expression Inhibited HCC Progression by Regulating the PI3K-AKT Signaling Pathway |
title_sort | arhgap20 expression inhibited hcc progression by regulating the pi3k akt signaling pathway |
topic | hcc arhgap20 progression pi3k-akt immune microenvironment |
url | https://www.dovepress.com/arhgap20-expression-inhibited-hcc-progression-by-regulating-the-pi3k-a-peer-reviewed-fulltext-article-JHC |
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