Evidence map›Paper›PMID 17876054›Full record

ArticleMolecular cancer therapeutics2007

Selenium inhibition of survivin expression by preventing Sp1 binding to its promoter.

Jae Yeon Chun, Yan Hu, Elaine Pinder, Jianguo Wu, Fengzhi Li, Allen C Gao

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Selenium Nanoparticles Synthesized UsingInternational journal of nanomedicine · 2020
    Article
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  10. Significant biological role of sp1 transactivation in multiple myeloma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2011
    Article
  11. Article
  12. Nutrigenetics, nutrigenomics, and selenium.Frontiers in genetics · 2011
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Induction of apoptosis of human colon cancer cells by siRNA recombinant expression vector targeting survivin gene.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2009
    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

6 authors at 2 institutions in 2 countries.

Jae Yeon ChunDepartment of Medicine, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USA.
Yan Hu
Elaine Pinder
Jianguo Wu
Fengzhi Li
Allen C Gao
Roswell Park Comprehensive Cancer Center · USImmunovaccine (Canada) · CA

Funding

Selenium regulates androgen receptor signaling in prostate cancerR01CA118887 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GAO, ALLEN C. · 2006 to 2010
$1.2M
Survivin expression and cancer cell drug resistanceR01CA109481 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI LI, FENGZHI · 2004 to 2008
$1.2M
IL-4 and androgen receptor signaling in prostate cancerR01CA109441 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GAO, ALLEN C. · 2005 to 2009
$1.1M
NCI NIH HHS CA 109441NCI NIH HHS CA109481NCI NIH HHS CA 118887NCI NIH HHS R01 CA109441NCI NIH HHS R01 CA109481NCI NIH HHS R01 CA118887
6 · The paper itself

Abstract

Survivin, an antiapoptotic protein highly expressed in cancer, regulates multiple cellular network associated with cancer cell viability and drug resistance. Inhibition of survivin expression has been pursued as a valid cancer therapeutic target. In this study, we showed that selenium, an effective chemopreventive agent for many types of cancers, down-regulated survivin expression. Selenium inhibited survivin expression in both mRNA and protein levels in a dose- and time-dependent manner. Using a series of survivin promoter-luciferase constructs, a 37-bp DNA element in the survivin core promoter region that mediates the ability of selenium to inhibit survivin transcription was identified. Gel mobility shift assays and chromatin immunoprecipitation analyses revealed that selenium prevents the binding of Sp1 or Sp1-like proteins to the 37-bp cis-acting DNA element in the survivin promoter. Furthermore, inhibition of survivin expression by small interfering RNA enhanced selenium's inhibitory effects on cell growth, whereas overexpression of survivin in LNCaP human prostate cancer cells desensitized cancer cells to selenium effect, suggesting that the expression of survivin plays an important role in determining the response of cancer cells to selenium. Taken together, these results suggest that selenium down-regulated survivin expression by preventing the binding of Sp1 or Sp1-like proteins to the promoter of survivin, which contributes at least in part to the inhibitory effect of selenium on survivin gene transcription. In addition, down-regulation of survivin expression may account for one of the molecular mechanisms of the anticancer effects of selenium.

Indexed as

AntioxidantsBlotting, NorthernBlotting, WesternCell Line, TumorChromatin ImmunoprecipitationDown-RegulationElectrophoretic Mobility Shift AssayGene Expression Regulation, NeoplasticHumansImmunoprecipitationInhibitor of Apoptosis ProteinsLuciferasesMaleMicrotubule-Associated ProteinsNeoplasm ProteinsPromoter Regions, GeneticAntioxidantsBIRC5 protein, humanInhibitor of Apoptosis ProteinsLuciferasesMicrotubule-Associated ProteinsNeoplasm ProteinsRNA, MessengerRNA, Small InterferingSeleniumSp1 Transcription FactorSurvivin

Identifiers

PMID17876054
PMCPMC2821810
OpenAlexW2112332697

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.