Evidence map›Paper›PMID 16909123›Full record

ArticleOncogene2007

Farnesyltransferase and geranylgeranyltransferase I inhibitors upregulate RhoB expression by HDAC1 dissociation, HAT association and histone acetylation of the RhoB promoter.

F L Delarue, J Adnane, B Joshi, M A Blaskovich, D-A Wang, J Hawker, F Bizouarn, J Ohkanda, K Zhu, A D Hamilton and 2 more

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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 60 citations in OpenAlex.

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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

12 authors at 4 institutions in 2 countries.

F L DelarueDrug Discovery Program at H Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.
J Adnane
B Joshi
M A Blaskovich
D-A Wang
J Hawker
F Bizouarn
J Ohkanda
K Zhu
A D Hamilton
S Chellappan
S M Sebti
University of South Florida · USMoffitt Cancer Center · USYale University · USUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, we have shown that RhoB suppresses EGFR-, ErbB2-, Ras- and Akt-mediated malignant transformation and metastasis. In this paper, we demonstrate that the novel antitumor agents farnesyltransferase inhibitors (FTIs) and geranylgeranyltransferase I inhibitors (GGTIs) upregulate RhoB expression in a wide spectrum of human cancer cells including those from pancreatic, breast, lung, colon, bladder and brain cancers. RhoB induction by FTI-277 and GGTI-298 occurs at the transcriptional level and is blocked by actinomycin D. Reverse transcription-PCR experiments documented that the increase in RhoB protein levels is due to an increase in RhoB transcription. Furthermore, treatment with FTIs and GGTIs of cancer cells results in HDAC1 dissociation, HAT association and histone acetylation of the RhoB promoter. Thus, promoter acetylation is a novel mechanism by which RhoB expression levels are regulated following treatment with the anticancer agents FTIs and GGTIs.

Indexed as

Promoter Regions, GeneticAcetylationAlkyl and Aryl TransferasesAntineoplastic AgentsBenzamidesEnzyme InhibitorsFarnesyltranstransferaseHistone AcetyltransferasesHistone Deacetylase 1Histone DeacetylasesHistonesHumansMethionineNeoplasmsProtein Processing, Post-TranslationalReverse Transcriptase Polymerase Chain ReactionAlkyl and Aryl TransferasesAntineoplastic AgentsBenzamidesEnzyme InhibitorsFarnesyltranstransferaseFTI 277geranylgeranyltransferase type-IGGTI 298HDAC1 protein, humanHistone AcetyltransferasesHistone Deacetylase 1Histone DeacetylasesHistonesMethioninerhoB GTP-Binding ProteinRNA, Neoplasm

Identifiers

PMID16909123
OpenAlexW2016806028

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.