Evidence map›Paper›PMID 17263886›Full record

ArticleBMC cancer2007

E2F-1 induces melanoma cell apoptosis via PUMA up-regulation and Bax translocation.

Hongying Hao, Yanbin Dong, Maria T Bowling, Jorge G Gomez-Gutierrez, H Sam Zhou, Kelly M McMasters

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. A comprehensive review of the roles of E2F1 in colon cancer.American journal of cancer research · 2020
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
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  11. E2F-1- and E2Ftr-mediated apoptosis: the role of DREAM and HRK.Journal of cellular and molecular medicine · 2012
    Article
  12. Article
  13. Article
  14. BH3-based fusion artificial peptide induces apoptosis and targets human colon cancer.Molecular therapy : the journal of the American Society of Gene Therapy · 2009
    Article
  15. Article
  16. Melanoma biomarkers: current status and vision for the future.Nature clinical practice. Oncology · 2009
    Review
  17. Review
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 1 institution in 1 country.

Hongying HaoDepartment of Surgery, University of Louisville, Louisville, KY 40292, USA. h0hao001@louisville.edu <h0hao001@louisville.edu>
Yanbin Dong
Maria T Bowling
Jorge G Gomez-Gutierrez
H Sam Zhou
Kelly M McMasters
University of Louisville · US

Funding

E2F-1 Cancer Gene TherapyR01CA090784 · NCI · UNIVERSITY OF LOUISVILLE · PI MCMASTERS, KELLY M · 2002 to 2005
$970k
NCI NIH HHS R01 CA090784NCI NIH HHS R01 CA 90784-01A1
6 · The paper itself

Abstract

backgroundPUMA is a pro-apoptotic Bcl-2 family member that has been shown to be involved in apoptosis in many cell types. We sought to ascertain whether induction of PUMA plays a crucial role in E2F-1-induced apoptosis in melanoma cells.

methodsPUMA gene and protein expression levels were detected by real-time PCR and Western blot in SK-MEL-2 and HCT116 cell lines after Ad-E2F-1 infection. Activation of the PUMA promoter by E2F-1 overexpression was detected by dual luciferase reporter assay. E2F-1-induced Bax translocation was shown by immunocytochemistry. The induction of caspase-9 activity was measured by caspase-9 colorimetric assay kit.

resultsUp-regulation of the PUMA gene and protein by E2F-1 overexpression was detected by real-time PCR and Western blot analysis in the SK-MEL-2 melanoma cell line. In support of this finding, we found six putative E2F-1 binding sites within the PUMA promoter. Subsequent dual luciferase reporter assay showed that E2F-1 expression could increase the PUMA gene promoter activity 9.3 fold in SK-MEL-2 cells. The role of PUMA in E2F-1-induced apoptosis was further investigated in a PUMA knockout cell line. Cell viability assay showed that the HCT116 PUMA-/- cell line was more resistant to Ad-E2F-1-mediated cell death than the HCT116 PUMA+/+ cell line. Moreover, a 2.2-fold induction of the PUMA promoter was also noted in the HCT116 PUMA+/+ colon cancer cell line after Ad-E2F-1 infection. Overexpression of a truncated E2F-1 protein that lacks the transactivation domain failed to up-regulate PUMA promoter, suggesting that PUMA may be a transcriptional target of E2F-1. E2F-1-induced cancer cell apoptosis was accompanied by Bax translocation from the cytosol to mitochondria and the induction of caspase-9 activity, suggesting that E2F-1-induced apoptosis is mediated by PUMA through the cytochrome C/Apaf-1-dependent pathway.

conclusionOur studies strongly demonstrated that E2F-1 induces melanoma cell apoptosis via PUMA up-regulation and Bax translocation. The signaling pathways provided here will further enhance insights on the mechanisms of E2F-1-induced cancer cell apoptosis as a strategy for cancer therapy.

Indexed as

ApoptosisApoptosis Regulatory Proteinsbcl-2-Associated X ProteinBinding SitesCaspase 9Cell Line, TumorE2F1 Transcription FactorHumansMelanomaMitochondriaPromoter Regions, GeneticProtein TransportProto-Oncogene ProteinsTranscriptional ActivationUp-RegulationApoptosis Regulatory ProteinsBBC3 protein, humanbcl-2-Associated X ProteinCaspase 9E2F1 protein, humanE2F1 Transcription FactorProto-Oncogene Proteins

Identifiers

PMID17263886
PMCPMC1797184
OpenAlexW1951153742

What OpenQuestion holds

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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.