Evidence map›Paper›PMID 12208851›Full record

ArticleGenes & development2002

Interactions between Ras1, dMyc, and dPI3K signaling in the developing Drosophila wing.

David A Prober, Bruce A Edgar

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

80 citing papers in PubMed, 164 citations in OpenAlex.

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  18. International journal of molecular sciences · 2018
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20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

David A ProberMolecular and Cellular Biology Program, University of Washington, Seattle, Washington 98195, USA.
Bruce A Edgar
Fred Hutch Cancer Center · USUniversity of Washington · US

Funding

Growth Regulation during Drosophila DevelopmentR01GM051186 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ROHRSCHNEIDER, LARRY RAY · 1994 to 2011
$5.2M
NIGMS NIH HHS GMS R01-51186
6 · The paper itself

Abstract

The Ras GTPase links extracellular signals to intracellular mechanisms that control cell growth, the cell cycle, and cell identity. An activated form of Drosophila Ras (Ras(V12)) promotes these processes in the developing wing, but the effector pathways involved are unclear. Here, we present evidence indicating that Ras(V12) promotes cell growth and G(1)/S progression by increasing dMyc protein levels and activating dPI3K signaling, and that it does so via separate effector pathways. We also show that endogenous Ras is required to maintain normal levels of dMyc, but not dPI3K signaling during wing development. Finally, we show that induction of dMyc and regulation of cell identity are separable effects of Raf/MAPK signaling. These results suggest that Ras may only affect PI3K signaling when mutationally activated, such as in Ras(V12)-transformed cells, and provide a basis for understanding the synergy between Ras and other growth-promoting oncogenes in cancer.

Indexed as

DNA-Binding Proteinsras ProteinsAnimalsCell AdhesionCell CycleCell DifferentiationCell DivisionDrosophilaDrosophila ProteinsGTP-Binding ProteinsMitogen-Activated Protein KinasesModels, BiologicalMutationPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-rafReceptor Cross-TalkDNA-Binding ProteinsDrosophila ProteinsGTP-Binding ProteinsMitogen-Activated Protein KinasesMyc protein, DrosophilaPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-rafRas85D protein, Drosophilaras ProteinsTranscription Factors

Identifiers

PMID12208851
PMCPMC186666
OpenAlexW2095855911

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.