Evidence map›Paper›PMID 25015118›Full record

ArticleOncotarget2014

Sensitization of radio-resistant prostate cancer cells with a unique cytolethal distending toxin.

Chih-Ho Lai, Chia-Shuo Chang, Hsin-Ho Liu, Yuh-Shyan Tsai, Feng-Ming Hsu, Yung-Luen Yu, Cheng-Kuo Lai, Leah Gandee, Rey-Chen Pong, Heng-Wei Hsu and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.1field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  13. The Cytolethal Distending Toxin Subunit CdtB ofFrontiers in cellular and infection microbiology · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. DAB2IP in cancer.Oncotarget · 2016
    Review
  18. Review
  19. Article
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

13 authors at 3 institutions in 2 countries.

Chih-Ho LaiDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, Texas, USA. School of Medicine, China Medical University, Taichung, Taiwan.
Chia-Shuo ChangSchool of Medicine, China Medical University, Taichung, Taiwan.
Hsin-Ho LiuDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Yuh-Shyan TsaiDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, Texas, USA. Department of Urology, Medical College and Hospital, National Cheng Kung University, Tainan, Taiwan.
Feng-Ming HsuDepartment of Oncology, National Taiwan University Hospital, Taipei, Taiwan. Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Yung-Luen YuGraduate Institute of Cancer Biology, China Medical University, Taichung, Taiwan.
Cheng-Kuo LaiDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, Texas, USA. School of Medicine, China Medical University, Taichung, Taiwan.
Leah GandeeDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Rey-Chen PongDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Heng-Wei HsuDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Lan YuDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Debabrata SahaDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Jer-Tsong HsiehDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, Texas, USA. Graduate Institute of Cancer Biology, China Medical University, Taichung, Taiwan.
The University of Texas Southwestern Medical Center · USChina Medical University · TWNational Cheng Kung University · TW

Funding

Developing targeted therapy with prostate cancer specific nanomedicineR01CA182670 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HSIEH, JER-TSONG, YANG, JIAN · 2013 to 2017
$1.6M
NCI NIH HHS CA182670NCI NIH HHS R01 CA182670
6 · The paper itself

Abstract

Cytolethal distending toxin (CDT) produced by Campylobacter jejuni is a genotoxin that induces cell-cycle arrest and apoptosis in mammalian cells. Recent studies have demonstrated that prostate cancer (PCa) cells can acquire radio-resistance when DOC-2/DAB2 interactive protein (DAB2IP) is downregulated. In this study, we showed that CDT could induce cell death in DAB2IP-deficient PCa cells. A combination of CDT and radiotherapy significantly elicited cell death in DAB2IP-deficient PCa cells by inhibiting the repair of ionizing radiation (IR)-induced DNA double-strand break (DSB) during G2/M arrest, which is triggered by ataxia telangiectasia mutated (ATM)-dependent DNA damage checkpoint responses. We also found that CDT administration significantly increased the efficacy of radiotherapy in a xenograft mouse model. These results indicate that CDT can be a potent therapeutic agent for radio-resistant PCa.

Indexed as

AnimalsApoptosisBacterial ToxinsCell Cycle CheckpointsGene Knockdown TechniquesHumansMaleMiceMice, Inbred BALB CProstatic NeoplasmsRadiation, IonizingRadiation-Sensitizing Agentsras GTPase-Activating ProteinsXenograft Model Antitumor AssaysBacterial Toxinscytolethal distending toxinDAB2IP protein, humanRadiation-Sensitizing Agentsras GTPase-Activating Proteins

Identifiers

PMID25015118
PMCPMC4170639
OpenAlexW2106044868

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.