Evidence map›Paper›PMID 17297469›Full record

ArticleOncogene2007

Hypermethylation of Ron proximal promoter associates with lack of full-length Ron and transcription of oncogenic short-Ron from an internal promoter.

D Angeloni, A Danilkovitch-Miagkova, T Ivanova, E Braga, E Zabarovsky, M I Lerman

Abstract read
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In one paragraph

Article in Oncogene, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.1field-weighted citation impact, top 24% of its field
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

25 citing papers in PubMed, 51 citations in OpenAlex.

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  7. Journal of virology · 2017
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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

6 authors at 3 institutions in 2 countries.

D AngeloniLaboratory of Immunobiology, Center for Cancer Research, National Cancer Institute, Frederick, MD, USA. angeloni@ifc.cnr.it
A Danilkovitch-Miagkova
T Ivanova
E Braga
E Zabarovsky
M I Lerman
Center for Cancer Research · USKarolinska Institutet · SENational Cancer Institute · US

Funding

Functional Analysis of Cancer Genes from Human Chromosome 3pZ01BC008579 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LERMAN, MICHAEL · 1996 to 2008
$804k
Intramural NIH HHS
6 · The paper itself

Abstract

The gene for tyrosine-kinase receptor Ron (MST1R) resides in the chromosome 3p21.3 region, frequently affected in common human malignancies. The gene generates two transcripts, 5 and 2 kb-long, full-length Ron (flRon) and short-form Ron (sfRon), respectively. Here, we show for the first time that the variegated Ron expression is associated with variations in the methylation patterns of two distinct CpG islands in Ron proximal promoter. Widespread hypermethylation associates with lack of flRon whereas hypermethylation of the distal island associates with transcription of sfRon, a constitutively active tyrosine-kinase that drives cell proliferation. sfRon inhibition with kinase-dead transgenes decreases cancer cell growth and induces cellular differentiation. sfRon could be a new drug target in cancer types in which it contributes to tumor progression.

Indexed as

DNA MethylationGene Expression Regulation, NeoplasticTranscription, GeneticAzacitidineCells, CulturedCpG IslandsDecitabineHumansLeukemia, Erythroblastic, AcuteLung NeoplasmsPromoter Regions, GeneticReceptor Protein-Tyrosine KinasesTransgenesAzacitidineDecitabineReceptor Protein-Tyrosine KinasesRON protein

Identifiers

PMID17297469
OpenAlexW2137817937

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.