Evidence map›Paper›PMID 17234809›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

An infectious retrovirus susceptible to an IFN antiviral pathway from human prostate tumors.

Beihua Dong, Sanggu Kim, Seunghee Hong, Jaydip Das Gupta, Krishnamurthy Malathi, Eric A Klein, Don Ganem, Joseph L Derisi, Samson A Chow, Robert H Silverman

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed
13.2field-weighted citation impact, top 1% 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

128 citing papers in PubMed, 217 citations in OpenAlex.

  1. Trial
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  8. Article
  9. Sites of retroviral DNA integration: From basic research to clinical applications.Critical reviews in biochemistry and molecular biology · 2016
    Review
  10. Article
  11. Review
  12. Could JC virus provoke metastasis in colon cancer?World journal of gastroenterology · 2014
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

68 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 3 countries.

Beihua DongDepartment of Cancer Biology, Lerner Research Institute, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
Sanggu Kim
Seunghee Hong
Jaydip Das Gupta
Krishnamurthy Malathi
Eric A Klein
Don Ganem
Joseph L Derisi
Samson A Chow
Robert H Silverman
Cleveland Clinic · USUniversity of California, Los Angeles · USCase Western Reserve University · USCzech Academy of Sciences, Institute of Microbiology · CZHoward Hughes Medical Institute · US

Funding

MOLECULAR MECHANISMS OF HIV1 DNA INTEGRATIONR01CA068859 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHOW, SAMSON A · 1995 to 2008
$2.5M
Role of RNase L in the Biology of Prostate CancerR01CA103943 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI SILVERMAN, ROBERT H. · 2004 to 2008
$1.5M
Role of small RNAs in innate immunity and inflammationR15AI089518 · NIAID · UNIVERSITY OF TOLEDO · PI KRISHNAMURTHY, MALATHI · 2010 to 2010
$430k
NCI NIH HHS CA103943NCI NIH HHS CA68859NCI NIH HHS R01 CA068859NCI NIH HHS R01 CA103943NIAID NIH HHS R15 AI089518
6 · The paper itself

Abstract

We recently reported identification of a previously undescribed gammaretrovirus genome, xenotropic murine leukemia virus-related virus (XMRV), in prostate cancer tissue from patients homozygous for a reduced activity variant of the antiviral enzyme RNase L. Here we constructed a full-length XMRV genome from prostate tissue RNA and showed that the molecular viral clone is replication-competent. XMRV replication in the prostate cancer cell line DU145 was sensitive to inhibition by IFN-beta. However, LNCaP prostate cancer cells, which are deficient in JAK1 and RNase L, were resistant to the effects of IFN-beta against XMRV. Furthermore, DU145 cells rendered deficient in RNase L with siRNA were partially resistant to IFN inhibition of XMRV. Expression in hamster cells of the xenotropic and polytropic retrovirus receptor 1 allowed these cells to be infected by XMRV. XMRV provirus integration sites were mapped in DNA isolated from human prostate tumor tissue to genes for two transcription factors (NFATc3 and CREB5) and to a gene encoding a suppressor of androgen receptor transactivation (APPBP2/PAT1/ARA67). Our studies demonstrate that XMRV is a virus that has infected humans and is susceptible to inhibition by IFN and its downstream effector, RNase L.

Indexed as

AnimalsCell Line, TumorCHO CellsCricetinaeCricetulusEndoribonucleasesHumansInterferonsJanus Kinase 1MaleMolecular Sequence DataOpen Reading FramesProstatic NeoplasmsRetroviridaeRNA, Small InterferingTranscriptional Activation2-5A-dependent ribonucleaseEndoribonucleasesInterferonsJanus Kinase 1RNA, Small Interfering

Identifiers

PMID17234809
PMCPMC1776164
OpenAlexW2037886449

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.