Literature DB >> 16757362

Use of conditionally active ras fusion proteins to study epidermal growth, differentiation, and neoplasia.

Jason A Reuter1, Paul A Khavari.   

Abstract

Ras proteins are membrane-bound GTPases that play a central role in transmitting signals from the cell surface to the nucleus and affect a wide array of biological processes. The overall cellular response to Ras activation varies with cell type, experimental conditions, signal strength, and signal duration. Most current studies, however, rely on expression of constitutively active protein to study Ras function and thus ignore temporal variables, as well as signal strength. These experiments may provide contradictory results, as seen in the case of epidermal keratinocytes. In this setting, Ras has been shown to both promote and oppose proliferation and differentiation. By providing control over timing, duration, and signal magnitude, conditional systems allow for more precise investigation of the role of Ras in carcinogenesis, as well as normal cellular physiology. This chapter focuses on use of a ligand-responsive steroid hormone receptor fusion of Ras, ER-Ras, to study aspects of cellular transformation in epidermal keratinocytes.

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Year:  2006        PMID: 16757362     DOI: 10.1016/S0076-6879(05)07054-0

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  2 in total

1.  Modeling inducible human tissue neoplasia identifies an extracellular matrix interaction network involved in cancer progression.

Authors:  Jason A Reuter; Susana Ortiz-Urda; Markus Kretz; John Garcia; Florence A Scholl; Anna M G Pasmooij; David Cassarino; Howard Y Chang; Paul A Khavari
Journal:  Cancer Cell       Date:  2009-06-02       Impact factor: 31.743

2.  Mitotic Stress Is an Integral Part of the Oncogene-Induced Senescence Program that Promotes Multinucleation and Cell Cycle Arrest.

Authors:  Dina Dikovskaya; John J Cole; Susan M Mason; Colin Nixon; Saadia A Karim; Lynn McGarry; William Clark; Rachael N Hewitt; Morgan A Sammons; Jiajun Zhu; Dimitris Athineos; Joshua D G Leach; Francesco Marchesi; John van Tuyn; Stephen W Tait; Claire Brock; Jennifer P Morton; Hong Wu; Shelley L Berger; Karen Blyth; Peter D Adams
Journal:  Cell Rep       Date:  2015-08-20       Impact factor: 9.423

  2 in total

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