Evidence map›Paper›PMID 27634756›Full record

ArticleCancer research2016

RK-33 Radiosensitizes Prostate Cancer Cells by Blocking the RNA Helicase DDX3.

Min Xie, Farhad Vesuna, Saritha Tantravedi, Guus M Bol, Marise R Heerma van Voss, Katriana Nugent, Reem Malek, Kathleen Gabrielson, Paul J van Diest, Phuoc T Tran and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

59 citing papers in PubMed, 82 citations in OpenAlex.

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  11. Role of DEAD/DEAH-box helicases in immunity, infection and cancers.Cell communication and signaling : CCS · 2025
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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

11 authors at 1 institution in 1 country.

Min XieDepartment of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Farhad VesunaDepartment of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Saritha TantravediDepartment of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Guus M BolDepartment of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Marise R Heerma van VossDepartment of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Katriana NugentDepartment of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Reem MalekDepartment of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Kathleen GabrielsonDepartment of Molecular and Comparative Pathobiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Paul J van DiestDepartment of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands.
Phuoc T TranDepartment of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Venu RamanDepartment of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland. vraman2@jhmi.edu.
Johns Hopkins Medicine · US

Funding

Structure-Functions Studies of Twist1-induced Radioresistance in Lung CancerR01CA166348 · NCI · JOHNS HOPKINS UNIVERSITY · PI TRAN, PHUOC T. · 2013 to 2017
$1.7M
Functional Imaging of Twist induced breast cancerR01CA140226 · NCI · JOHNS HOPKINS UNIVERSITY · PI RAMAN, VENU · 2010 to 2014
$1.6M
The role of Twist in inducing breast cancer initiating cells and metastasisR01CA131250 · NCI · JOHNS HOPKINS UNIVERSITY · PI RAMAN, VENU · 2011 to 2015
$1.2M
NCI NIH HHS R01 CA131250NCI NIH HHS R01 CA140226NCI NIH HHS R01 CA166348
6 · The paper itself

Abstract

Despite advances in diagnosis and treatment, prostate cancer is the most prevalent cancer in males and the second highest cause of cancer-related mortality. We identified an RNA helicase gene, DDX3 (DDX3X), which is overexpressed in prostate cancers, and whose expression is directly correlated with high Gleason scores. Knockdown of DDX3 in the aggressive prostate cancer cell lines DU145 and 22Rv1 resulted in significantly reduced clonogenicity. To target DDX3, we rationally designed a small molecule, RK-33, which docks into the ATP-binding domain of DDX3. Functional studies indicated that RK-33 preferentially bound to DDX3 and perturbed its activity. RK-33 treatment of prostate cancer cell lines DU145, 22Rv1, and LNCaP (which have high DDX3 levels) decreased proliferation and induced a G

Indexed as

AnimalsAzepinesCell Cycle CheckpointsCell Line, TumorCell MovementCell ProliferationDEAD-box RNA HelicasesDNA DamageHistonesHumansImidazolesMaleMiceProstatic NeoplasmsRadiation-Sensitizing Agents3,7-dihydro-3,7-bis((4-methoxyphenyl)methyl)-2H-diimidazo(4,5-d:4',5'-f)(1,3)diazepin-2-oneAzepinesDDX3X protein, humanDEAD-box RNA HelicasesH2AX protein, humanHistonesImidazolesRadiation-Sensitizing Agents

Identifiers

PMID27634756
PMCPMC5576499
OpenAlexW2520591314

What OpenQuestion holds

Textmetadata
LicenceTDM
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.