Projects per year
Abstract
The RASSF (Ras-association domain family) has recently gained several new members and now contains ten proteins (RASSF1–10), several of which are potential tumour suppressors. The family can be split into two groups, the classical RASSF proteins (RASSF1–6) and the four recently added N-terminal RASSF proteins (RASSF7–10). The N-terminal RASSF proteins have a number of differences from the classical RASSF members and represent a newly defined set of potential Ras effectors. They have been linked to key biological processes, including cell death, proliferation, microtubule stability, promoter methylation, vesicle trafficking and response to hypoxia. Two members of the N-terminal RASSF family have also been highlighted as potential tumour suppressors. The present review will summarize what is known about the N-terminal RASSF proteins, addressing their function and possible links to cancer formation. It will also compare the N-terminal RASSF proteins with the classical RASSF proteins and ask whether the N-terminal RASSF proteins should be considered as genuine members or imposters in the RASSF family.
Original language | English |
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Pages (from-to) | 303-311 |
Number of pages | 9 |
Journal | Biochemical Journal |
Volume | 425 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2010 |
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- 2 Finished
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THE ROLE OF ORIENTED CELL DIVISION AND CELL POLARITY IN ESTA BLISHING CELL FATE DIVERSITY IN THE EARLY VERTEBRATE EMBRYO
Chalmers, A. (PI)
1/09/05 → 31/03/08
Project: Research council
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COOPERATIVE GROUP IN ORGANOGENESIS, GROWTH AND REGENERATION
Ward, A. (PI), Holman, G. (CoI), Hurst, L. (CoI), Kelsh, R. (CoI), Slack, J. (CoI) & Tosh, D. (CoI)
21/06/04 → 20/06/09
Project: Research council