RHO GTPase-Related Long Noncoding RNAs in Human Cancers

RHO GTPases are critical signal transducers that regulate cell adhesion, polarity, and migration through multiple signaling pathways. While all these cellular processes are crucial for the maintenance of normal cell homeostasis, disturbances in RHO GTPase-associated signaling pathways contribute to...

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Main Authors: Mahsa Saliani, Amin Mirzaiebadizi, Niloufar Mosaddeghzadeh, Mohammad Reza Ahmadian
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/13/21/5386
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author Mahsa Saliani
Amin Mirzaiebadizi
Niloufar Mosaddeghzadeh
Mohammad Reza Ahmadian
author_facet Mahsa Saliani
Amin Mirzaiebadizi
Niloufar Mosaddeghzadeh
Mohammad Reza Ahmadian
author_sort Mahsa Saliani
collection DOAJ
description RHO GTPases are critical signal transducers that regulate cell adhesion, polarity, and migration through multiple signaling pathways. While all these cellular processes are crucial for the maintenance of normal cell homeostasis, disturbances in RHO GTPase-associated signaling pathways contribute to different human diseases, including many malignancies. Several members of the RHO GTPase family are frequently upregulated in human tumors. Abnormal gene regulation confirms the pivotal role of lncRNAs as critical gene regulators, and thus, they could potentially act as oncogenes or tumor suppressors. lncRNAs most likely act as sponges for miRNAs, which are known to be dysregulated in various cancers. In this regard, the significant role of miRNAs targeting RHO GTPases supports the view that the aberrant expression of lncRNAs may reciprocally change the intensity of RHO GTPase-associated signaling pathways. In this review article, we summarize recent advances in lncRNA research, with a specific focus on their sponge effects on RHO GTPase-targeting miRNAs to crucially mediate gene expression in different cancer cell types and tissues. We will focus in particular on five members of the RHO GTPase family, including RHOA, RHOB, RHOC, RAC1, and CDC42, to illustrate the role of lncRNAs in cancer progression. A deeper understanding of the widespread dysregulation of lncRNAs is of fundamental importance for confirmation of their contribution to RHO GTPase-dependent carcinogenesis.
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spelling doaj.art-0e9046a061174c0aa96307e152689a2a2023-11-22T20:34:29ZengMDPI AGCancers2072-66942021-10-011321538610.3390/cancers13215386RHO GTPase-Related Long Noncoding RNAs in Human CancersMahsa Saliani0Amin Mirzaiebadizi1Niloufar Mosaddeghzadeh2Mohammad Reza Ahmadian3Institute of Biochemistry and Molecular Biology II, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine University, 40225 Düsseldorf, GermanyInstitute of Biochemistry and Molecular Biology II, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine University, 40225 Düsseldorf, GermanyInstitute of Biochemistry and Molecular Biology II, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine University, 40225 Düsseldorf, GermanyInstitute of Biochemistry and Molecular Biology II, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine University, 40225 Düsseldorf, GermanyRHO GTPases are critical signal transducers that regulate cell adhesion, polarity, and migration through multiple signaling pathways. While all these cellular processes are crucial for the maintenance of normal cell homeostasis, disturbances in RHO GTPase-associated signaling pathways contribute to different human diseases, including many malignancies. Several members of the RHO GTPase family are frequently upregulated in human tumors. Abnormal gene regulation confirms the pivotal role of lncRNAs as critical gene regulators, and thus, they could potentially act as oncogenes or tumor suppressors. lncRNAs most likely act as sponges for miRNAs, which are known to be dysregulated in various cancers. In this regard, the significant role of miRNAs targeting RHO GTPases supports the view that the aberrant expression of lncRNAs may reciprocally change the intensity of RHO GTPase-associated signaling pathways. In this review article, we summarize recent advances in lncRNA research, with a specific focus on their sponge effects on RHO GTPase-targeting miRNAs to crucially mediate gene expression in different cancer cell types and tissues. We will focus in particular on five members of the RHO GTPase family, including RHOA, RHOB, RHOC, RAC1, and CDC42, to illustrate the role of lncRNAs in cancer progression. A deeper understanding of the widespread dysregulation of lncRNAs is of fundamental importance for confirmation of their contribution to RHO GTPase-dependent carcinogenesis.https://www.mdpi.com/2072-6694/13/21/5386carcinogenesislncRNAsmiRNAsRHO GTPasessignal transductionsponge effect
spellingShingle Mahsa Saliani
Amin Mirzaiebadizi
Niloufar Mosaddeghzadeh
Mohammad Reza Ahmadian
RHO GTPase-Related Long Noncoding RNAs in Human Cancers
Cancers
carcinogenesis
lncRNAs
miRNAs
RHO GTPases
signal transduction
sponge effect
title RHO GTPase-Related Long Noncoding RNAs in Human Cancers
title_full RHO GTPase-Related Long Noncoding RNAs in Human Cancers
title_fullStr RHO GTPase-Related Long Noncoding RNAs in Human Cancers
title_full_unstemmed RHO GTPase-Related Long Noncoding RNAs in Human Cancers
title_short RHO GTPase-Related Long Noncoding RNAs in Human Cancers
title_sort rho gtpase related long noncoding rnas in human cancers
topic carcinogenesis
lncRNAs
miRNAs
RHO GTPases
signal transduction
sponge effect
url https://www.mdpi.com/2072-6694/13/21/5386
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AT aminmirzaiebadizi rhogtpaserelatedlongnoncodingrnasinhumancancers
AT niloufarmosaddeghzadeh rhogtpaserelatedlongnoncodingrnasinhumancancers
AT mohammadrezaahmadian rhogtpaserelatedlongnoncodingrnasinhumancancers