The Ras-related protein AGS1/RASD1 suppresses cell growth

Title

The Ras-related protein AGS1/RASD1 suppresses cell growth

Creator

Vaidyanathan G; Cismowski M J; Wang G S; Vincent T S; Brown K D; Lanier S M

Publisher

Oncogene

Date

2004
2004-07

Description

AGS1/RASD1 is a Ras-related protein identified as a dexamethasone-inducible cDNA and as a signal regulator in various functional and protein-interaction screens. As an initial approach to define the role of AGS1/RASD1 as a Ras-family member, we determined its influence on cell growth/survival. In clonogenic assays with NIH-3T3 murine fibroblast cells, the MCF-7 human breast cancer cell line and the human lung adenocarcinoma cell line A549, AGS1/RASD1 markedly diminished the number of G418-resistant colonies, whereas the Ras subgroup member K-Ras was without effect. A549 cell infection with adenovirus engineered to express AGS1/RASD1 (Ad.AGS1) inhibited log phase growth in vitro and increased the percentage of cells undergoing apoptosis. The anti-growth action was also observed in vivo as the expression of AGS1/RASD1 inhibited the subcutaneous tumor growth of A549 cells in athymic nude mice. These data indicate that AGS1/RASD1, a member of the Ras superfamily of small G-proteins that often promotes cell growth and tumor expansion, plays an active role in preventing aberrant cell growth.

Subject

activation; AGS1; apoptosis; binding protein; Biochemistry & Molecular Biology; cancer; Cell Biology; coupled receptors; Dexras1; Dexras1; G protein; gene; Genetics &; Heredity; hormone; identification; Integration; Oncology; RASD1; signal-transduction

Format

Journal Article

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Rights

Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).

Pages

5858-5863

Issue

34

Volume

23

Citation

Vaidyanathan G; Cismowski M J; Wang G S; Vincent T S; Brown K D; Lanier S M, “The Ras-related protein AGS1/RASD1 suppresses cell growth,” NEOMED Bibliography Database, accessed April 25, 2024, https://neomed.omeka.net/items/show/7381.