Evidence map›Paper›PMID 16818603›Full record

ArticleGenes & development2006

A positive feedback loop couples Ras activation and CD44 alternative splicing.

Chonghui Cheng, Michael B Yaffe, Phillip A Sharp

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing 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

92 citing papers in PubMed, 146 citations in OpenAlex.

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  19. The role of alternative splicing in human cancer progression.American journal of cancer research · 2021
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32 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

3 authors at 1 institution in 1 country.

Chonghui ChengCenter for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139, USA.
Michael B Yaffe
Phillip A Sharp
Center for Cancer Research · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Ras signaling pathway is important in both cell proliferation and tumor progression. Alternatively spliced isoforms of CD44 containing variable exon 6 (v6) can serve as coreceptors for growth factor receptors that activate Ras. Here we use v6-specific small interfering RNA (siRNA) to investigate the role of CD44 alternative splicing in Ras signaling. We identify a positive feedback loop in which Ras signaling promotes CD44v6 splicing, and CD44v6 then sustains late Ras signaling, which is important for cell cycle progression. These results are the first demonstration of a positive feedback loop linking signaling-dependent alternative splicing to mitogenic progression.

Indexed as

Alternative SplicingFeedback, PhysiologicalCell CycleCell LineEnzyme ActivationEpidermal Growth FactorGlycoproteinsHepatocyte Growth FactorHumansHyaluronan ReceptorsMitogen-Activated Protein Kinasesras GTPase-Activating ProteinsRNA, Small InterferingSignal TransductionUp-RegulationCD44v6 antigenEpidermal Growth FactorGlycoproteinsHepatocyte Growth FactorHyaluronan ReceptorsMitogen-Activated Protein Kinasesras GTPase-Activating ProteinsRNA, Small Interfering

Identifiers

PMID16818603
PMCPMC1522067
OpenAlexW2050276211

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.