Transcriptional and post-transcriptional regulation of the genes encoding the small GTPases RhoA, RhoB, and RhoC: Implications for the pathogenesis of human diseases
Open accessAbstract
Rho GTPases are highly conserved proteins that play critical roles in many cellular processes including actin dynamics, vesicular trafficking, gene transcription, cell-cycle progression, and cell adhesion. The main mode of regulation of Rho GTPases is through guanine nucleotide binding (cycling between an active GTP-bound form and an inactive GDP-bound form), but transcriptional, post-transcriptional, and post-translational modes of Rho regulation have also been described. In the present review, we summarize recent progress on the mechanisms that control the expression of the three members of the Rho-like subfamily (RhoA, RhoB, and RhoC) at the level of gene transcription as well as their post-transcriptional regulation by microRNAs. We also discuss the progress made in deciphering the mechanisms of cross-talk between Rho proteins and the transforming growth factor β signaling pathway and their implications for the pathogenesis of human diseases such as cancer metastasis and fibrosis.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Several transcription factors regulate RHOA expression, including c-Myc, Max, HIF-1α, NF-κB, and STAT6, together with several miRNAs.
“Several transcription factors have been shown to regulate RHOA expression, including c-Myc, Max, hypoxia-inducible factor 1 alpha (HIF-1α), nuclear factor-κB (NF-κB), and signal transducer and activator of transcription 6 (STAT6), together with several reported miRNAs (Figure 2C) [82,83].”
From RhoA Signaling in Neurodegenerative Diseases (2022) · cites this paper as [83]
The sections on transcriptional regulation of RhoA describe Myc, NF-κB, and STAT6 as regulators, and the miRNA section identifies several miRNAs that regulate RhoA expression (page numbers unavailable). The copy does not establish Max or HIF-1α as RhoA regulators; its hypoxia passage instead concerns HIF-3α regulation of RhoC. (LLM, conf=0.87)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
No references could be resolved yet.
Research works printed but not linked: 1
- [71]71. Guan X, Chen S, Zhao Y (2018) The role of RhoC in malignant tumor invasion, metastasis and targeted therapy. Histol Histopathol 33(3):255-260
Cited by
Sorted by citations
RhoA Signaling in Neurodegenerative Diseases
Schmidt, S. I., Blaabjerg, M., Freude, K., & Meyer, M. (2022) · Cells · doi:10.3390/cells11091520 · Cited by 110 · see citing works
- Authors
- Nomikou, E., Livitsanou, M., Stournaras, C., & Kardassis, D.
- Affiliations
- University of Crete (GR)
- Corresponding author
- Kardassis, Dimitris
- Venue
- Cellular and Molecular Life Sciences
- Published
- 2018-03-02
- Volume
- 75
- Issue
- 12
- Pages
- 2111-2124
- ISSN
- 1420-682X (ISSN-L)
- 1420-9071
- PMC
- PMC11105751
- OpenAlex
- W2792349496
- Cited by
- 28
- References
- 0
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 3 · 2023: 1 · 2022: 5 · 2021: 2 · 2020: 6 · 2019: 4
- FWCI
- 0.30
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cellular and Molecular Life Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Hellenic Ministry for Education, Research and Religious Affairs (THALIS MIS 380334)
- IKY-SIEMENS RESEARCH GRANTS (N/A)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mechanisms of cancer metastasis
- Keywords
- Rho GTPases, RhoA, RhoB, RhoC, transcriptional regulation, post-transcriptional regulation, microRNA, metastasis, fibrosis, actin dynamics, cell adhesion
- MeSH terms
- rhoC GTP-Binding Protein, Animals, Gene Expression Regulation, Humans, Neoplasms, Signal Transduction, Transcriptional Activation, Transforming Growth Factor beta, rhoA GTP-Binding Protein, rhoB GTP-Binding Protein, MicroRNAs
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review