Review Article: The Role of Ras Superfamily Proteins in Bladder Cancer Progression
Abstract
Purpose The prognosis of patients with bladder cancer is strongly dependent on whether the lesion is superficial or invasive at initial presentation. In addition, a significant fraction of patients presenting with superficial disease have invasive tumor during followup. Understanding how superficial bladder cancer progresses to invasive forms of the disease is of paramount importance for early diagnosis and successful treatment. Molecular mechanisms underlying bladder cancer progression are being elucidated. We reviewed the roles that members of the Ras superfamily of monomeric G proteins, an important class of cellular regulator, have in bladder cancer and its progression. Materials and methods We performed MEDLINE searches focusing on members of the Ras superfamily of monomeric G proteins and their involvement in transitional cell carcinoma, which is the most common form of bladder cancer. General involvement in cancer of key superfamily members, focusing on mechanisms and downstream pathways, was also reviewed through MEDLINE and manual bibliographic searches. Results With more than 100 members in humans the Ras superfamily is a diverse group of monomeric G proteins. These proteins regulate many cellular processes, such as cell cycle progression, actin cytoskeletal dynamics and membrane traffic. Members of the Ras and Rho family are also known to be involved in human cancer through mutation, over expression and dysregulation. In this review we focus on bladder cancer. In p…
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Overactivation of RHO subfamily GTPases such as RAC1 and CDC42 promotes hyperactivation of critical signaling cascades leading to cancer.
“However, overactivation of the RHO subfamily such as RAS-related C3 botulinum toxin substrate 1 (RAC1) and cell division cycle 42 homolog (CDC42) are also known to promote the hyperactivation of critical signaling cascades leading to cancer (10, 13, 17).”
From RHO to the DOCK for GDP disembarking: Structural insights into the DOCK GTPase nucleotide exchange factors (2021) · cites this paper as [13]
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Thompson, A. P., Bitsina, C., Gray, J. L., von Delft, F., & Brennan, P. E. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100521 · Cited by 21 · see citing works
- Authors
- OXFORD, G., & THEODORESCU, D.
- Affiliations
- University of Virginia (US)
- ORCID
- THEODORESCU, DAN
- Venue
- Journal of Urology
- Published
- 2003-11
- Volume
- 170
- Issue
- 5
- Pages
- 1987-1993
- ISSN
- 0022-5347 (ISSN-L)
- 1527-3792
- OpenAlex
- W2040543332
- Cited by
- 86
- References
- 2
- Citations by year
- 2025: 2 · 2024: 2 · 2022: 1 · 2021: 4 · 2020: 2 · 2019: 2 · 2018: 1 · 2017: 4 · 2016: 4 · 2015: 3 · 2014: 1 · 2013: 3 · 2012: 10
- FWCI
- 1.37
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Urology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Health Sciences › Medicine › Surgery › Bladder and Urothelial Cancer Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Keywords
- Ras superfamily, bladder cancer progression, H-Ras, RhoGDI2, Rho family, urothelial carcinoma, epidermal growth factor receptor, p53, PTEN, signaling pathways, therapeutic target
- MeSH terms
- Urinary Bladder, Urinary Bladder Neoplasms, Carcinoma, Transitional Cell, Humans, Neoplasm Invasiveness, Signal Transduction, Disease Progression, ras Proteins, Monomeric GTP-Binding Proteins
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