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Cited by 559

The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.

Rho GTPases: Regulation and roles in cancer cell biology

Open access
Haga, Raquel B., Ridley, Anne J.·2016·Small GTPases

Abstract

Rho GTPases are well known for their roles in regulating cell migration, and also contribute to a variety of other cellular responses. They are subdivided into 2 groups: typical and atypical. The typical Rho family members, including RhoA, Rac1 and Cdc42, cycle between an active GTP-bound and inactive GDP-bound conformation, and are regulated by GEFs, GAPs and GDIs, whereas atypical Rho family members have amino acid substitutions that alter their ability to interact with GTP/GDP and hence are regulated by different mechanisms. Both typical and atypical Rho GTPases contribute to cancer progression. In a few cancers, RhoA or Rac1 are mutated, but in most cancers expression levels and/or activity of Rho GTPases is altered. Rho GTPase signaling could therefore be therapeutically targeted in cancer treatment.

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Metadata

Authors
Haga, R. B., & Ridley, A. J.
Venue
Small GTPases
Published
2016-09-26
Volume
7
Issue
4
Pages
207-221
ISSN
  • 2154-1248 (ISSN-L)
  • 2154-1256
OpenAlex
W2520842278
Cited by
559
References
14
FWCI
11.29
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Rho GTPases: Regulation and roles in cancer cell biology. https://app.cochat.ai/papers/10.1080/21541248.2016.1232583
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Haga, R. B., & Ridley, A. J. (2016). Rho GTPases: Regulation and roles in cancer cell biology. Small GTPases. https://doi.org/10.1080/21541248.2016.1232583

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.