Evidence map›Paper›PMID 21429729›Full record

ArticleThe Journal of nutritional biochemistry2012

Gamma-tocotrienol induced apoptosis is associated with unfolded protein response in human breast cancer cells.

Dorrelyn Patacsil, Anh Thu Tran, Youn Sook Cho, Simeng Suy, Francisco Saenz, Irina Malyukova, Habtom Ressom, Sean P Collins, Robert Clarke, Deepak Kumar

Abstract read
In one paragraph

Article in The Journal of nutritional biochemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 18% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Revisiting the therapeutic potential of tocotrienol.BioFactors (Oxford, England) · 2022
    Review
  8. Article
  9. Vitamin E beyond Its Antioxidant Label.Antioxidants (Basel, Switzerland) · 2021
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Tocotrienols Modulate a Life or Death Decision in Cancers.International journal of molecular sciences · 2019
    Review
  19. Article
  20. Antioxidant Supplementation: A Linchpin in Radiation-Induced Enteritis.Technology in cancer research & treatment · 2017
    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

10 authors at 3 institutions in 1 country.

Dorrelyn PatacsilCancer Research Laboratory, Department of Biological and Environmental Sciences, University of the District of Columbia, Washington, DC 20008, USA.
Anh Thu Tran
Youn Sook Cho
Simeng Suy
Francisco Saenz
Irina Malyukova
Habtom Ressom
Sean P Collins
Robert Clarke
Deepak Kumar
Georgetown University Medical Center · USUniversity of the District of Columbia · USGeorgetown University · US

Funding

Functional Characterization of CCDC130 GeneSC1CA141935 · NCI · UNIVERSITY OF THE DISTRICT OF COLUMBIA · PI KUMAR, DEEPAK · 2009 to 2012
$1.4M
NCI NIH HHS SC1 CA141935
6 · The paper itself

Abstract

Gamma-tocotrienol (γ-T3) is a member of the vitamin E family. Tocotrienols (T3s) are powerful antioxidants and possess anticancer, neuroprotective and cholesterol-lowering properties. Tocotrienols inhibit the growth of various cancer cell lines without affecting normal cells. Less is known about the exact mechanisms of action of T3s on cell death and other growth inhibitory pathways. In the present study, we demonstrate that γ-T3 induces apoptosis in MDA-MB 231 and MCF-7 breast cancer cells as evident by PARP cleavage and caspase-7 activation. Gene expression analysis of MCF-7 cells treated with γ-T3 revealed alterations in the expression of multiple genes involved in cell growth and proliferation, cell death, cell cycle, cellular development, cellular movement and gene expression. Further analysis of differentially modulated genes using Ingenuity Pathway Analysis software suggested modulation of canonical signal transduction or metabolic pathways such as NRF-2-mediated oxidative stress response, TGF-β signaling and endoplasmic reticulum (ER) stress response. Analysis of ER-stress-related proteins in MCF-7 and MDA-MB 231 cells treated with γ-T3 demonstrated activation of PERK and pIRE1α pathway to induce ER stress. Activating transcription factor 3 (ATF3) was identified as the most up-regulated gene (16.8-fold) in response to γ-T3. Activating transcription factor 3 knockdown using siRNA suggested an essential role of ATF3 in γ-T3-induced apoptosis. In summary, we demonstrate that γ-T3 modulates ER stress signaling and have identified ATF3 as a molecular target for γ-T3 in breast cancer cells.

Indexed as

Activating Transcription Factor 3ApoptosisBreast NeoplasmsCaspase 7Cell CycleCell DeathCell Line, TumorCell ProliferationChromansEndoplasmic Reticulum StressFemaleGene Expression Regulation, NeoplasticHumansNF-E2-Related Factor 2Poly(ADP-ribose) PolymerasesSignal TransductionActivating Transcription Factor 3ATF3 protein, humanCaspase 7ChromansNFE2L2 protein, humanNF-E2-Related Factor 2plastochromanol 8Poly(ADP-ribose) PolymerasesVitamin E

Identifiers

PMID21429729
PMCPMC3123668
OpenAlexW2129352477

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.