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RASSF4/AD037 is a potential ras effector/tumor suppressor of the RASSF family.
- Source :
-
Cancer research [Cancer Res] 2004 Dec 01; Vol. 64 (23), pp. 8688-93. - Publication Year :
- 2004
-
Abstract
- Activated Ras proteins interact with a broad range of effector proteins to induce a diverse series of biological consequences. Although typically associated with enhanced growth and transformation, activated Ras may also induce growth antagonistic effects such as senescence or apoptosis. It is now apparent that some of the growth-inhibitory properties of Ras are mediated via the RASSF family of Ras effector/tumor suppressors. To date, four members of this family have been identified (Nore1, RASSF1, RASSF2, and RASSF3). We now identify a fifth member of this group, RASSF4 (AD037). RASSF4 shows approximately 25% identity with RASSF1A and 60% identity with RASSF2. RASSF4 binds directly to activated K-Ras in a GTP-dependent manner via the effector domain, thus exhibiting the basic properties of a Ras effector. Overexpression of RASSF4 induces Ras-dependent apoptosis in 293-T cells and inhibits the growth of human tumor cell lines. Although broadly expressed in normal tissue, RASSF4 is frequently down-regulated by promoter methylation in human tumor cells. Thus, RASSF4 appears to be a new member of the RASSF family of potential Ras effector/tumor suppressors.
- Subjects :
- Amino Acid Sequence
Apoptosis physiology
Base Sequence
Cell Line, Tumor
DNA Methylation
Down-Regulation
Gene Silencing
Guanosine Triphosphate metabolism
Humans
Molecular Sequence Data
Promoter Regions, Genetic
Protein Structure, Tertiary
Sequence Alignment
Transfection
Tumor Suppressor Proteins biosynthesis
Tumor Suppressor Proteins metabolism
Tumor Suppressor Proteins physiology
Tumor Suppressor Proteins genetics
ras Proteins genetics
ras Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0008-5472
- Volume :
- 64
- Issue :
- 23
- Database :
- MEDLINE
- Journal :
- Cancer research
- Publication Type :
- Academic Journal
- Accession number :
- 15574778
- Full Text :
- https://doi.org/10.1158/0008-5472.CAN-04-2065